The subject of the invention are novel ruthenium complexes with CAAC type ligands (Cydic Alkyl Amino Carbene) which have found a widespread use as catalysts and/or (pre)catalysts of olefin metathesis reactions and their use in olefin metathesis reactions. The subject of the invention also includes intermediate compounds used to synthesize novel ruthenium complexes with CAAC ligands, as well as the method for synthesis of novel ruthenium complexes with CAAC ligands. This invention is used as desired tool in the widely understood organic synthesis, in the selective synthesis of olefins with a C=C bond, in particular in cross metathesis reaction with ethylene; ethenolysis.

Significant progress has been made in recent years in the use of olefin metathesis in organic synthesis [R. H. Grubbs (Editor), A G. Wenzel (Editor), D. J. O'Leary (Editor), E. Khosravi (Editor), Handbook of Olefin Metathesis, 2. Edition, 3 volumes, 2015, Wiley-VCH Verlag GmbH & Co. KGaA 1608 pages]. Many ruthenium-based homogeneous olefin metathesis catalysts are known in the state-of-the-art which show high activity in various types of metathesis reactions, as well as high tolerance to functional groups present in the substrate/product Due to the combination of these features, metathesis catalysts are of key importance in modem organic synthesis and in the industry. The most widely present ruthenium complexes in the literature and the ones finding the most widespread use in olefin metathesis reactions include Grubbs-type ruthenium complexes (Gru-I, Gru-Il and Gru-Ill), Hoveyda-Grubbs complexes (Hov-I and Hov-ll), as well as indenylidene complexes (lnd-1, Ind-Il and Ind-Ill), 1 ^st , 2 ^nd and 3 ^rd generation [Grubbs et al. Chem. Rev. 2010, 110, 1746-1787; Nolan et al. Chem. Commun. 2014, 50, 10355—10375]. In other cases, most structures of olefin metathesis catalysts are derived from the aforementioned ruthenium complexes.

Recently, the NHC ligand in the ruthenium catalyst structure has been replaced by a cyclic (alkyl) (amino) carbene ligand (CAAC), and resulted complexes occupy an important place in modem organic synthesis due to their use i.e. in cross metathesis reactions and in ring-closing metathesis [Grubbs et al. Chem. Rev, 2010, 110, 1746-1787; WO2017055945A1].

In modem organic synthesis, in an era of increasingly scarce resources, including fossil fuels, and the consequent risk of a shortage of raw materials for the synthesis for example, polymers based on products derived, for example, from crude oil, it is very important to develop new technologies and reactions that enable the synthesis of target compounds. Such processes include the ethenolysis reaction, particularly the ethenolysis of methyl/ethyl derivatives of long-chain fatty acids. In particular, ruthenium complexes with CAAC ligands in the ruthenium coordination sphere are used for this purpose. The first literature report on ruthenium catalysts for olefin metathesis with CAAC ligands dates back to 2005 [Bertrandt et al Angew. Chern. Int Ed., 2005, 44, 5705-5709]. In this scientific publication, Bertrandt described for the first time the CAAC ligands and their use in organic synthesis. In a subsequent publication from 2007 [Bertrandt et al. Angew. Chem. Int Ed., 2007, 46,7262-7265], Bertrandt described first method of the synthesis of ruthenium complexes with CAAC ligands. In both cases, the ligands contained 2,6- diisopropylbenzene at the nitrogen atom, and either two methyl (Ru5) or cyclohexyl substituent (Ru10) at the carbon atom C2. Next, the team of Prof. Bertrand, in cooperation with the team of Prof. Grubbs, synthesized and tested 17 catalysts in terms of their activity in the ethenolysis reaction of methyl oleate, in which the CAAC ligand contained symmetric substituents at the nitrogen atom: mesityl, 2,6-diisopropylbenzene, 2,6-diethylbenzene, as well as asymmetric ones 2- ethyl-6-methylbenzene, 2-isopropyl-6-methylbenzene, 2-methyl-6-tertbutylbenzene, while at the C2 carbon atom, two of the following substituents: methyl, ethyl, n-propyl, cyclohexyl, adamantyl or phenyl [Bertrandt et al. Angew. Chern. Int Ed., 2015, 54, 1919-1923]. These catalysts showed high activity towards the C-C double bond of methyl oleate in the presence of ethylene overpressure, leading to the formation of valuable industrial products in the olefin metathesis eaction: 1 -decene and 9-decenoic acid methyl ester. In 2017, Gawin et al. first published a method for a synthesis of indenylidene-type complexes with two CAAC ligands [Gawin et al., Angew. Chem. Int Ed. 2017, 56, 981-986; EP3356379B1]. The publication presents a method for the preparation of indenylidene complexes with two CAAC ligands, and tests the activity of the complexes in selected reactions including macrocyclisation, ethenolysis, and cross metathesis reaction of a-olefins. This document also discloses a novel approach to the synthesis of Hoveyda-Grubbs catalysts with CAAC ligands, involving thermal dissociation of one CAAC ligand in an indenylidene complex, followed by reaction of the intermediate with the relevant styrene.

Also in 2017, Gawin et al. published a method to synthesize Hoveyda-Grubbs analogues with a nitro group in the para position as substrates using bis-CAAC complexes [Gawin et al. ACS Catal. 2017, 7, 5443-5449]. The complexes proved to be effective in macrocyclization and cross-metathesis reactions with acrylonitrile. The European patent [EP3356379B1] discloses the structures Ru35-Ru37 with a modified benzylidene fragment

Subsequent modifications of ruthenium catalysts involved Hoveyda-Grubbs type complexes, wherein the hydrogen atom in the styrene part was replaced with an EWG or an EDG group. By modulating the nature of the styrenyl ether ligand, Mignagni et al. studied the reactivity of Ru38 and Ru39 catalysts [FR2947189A1; FR2934178A1]. It was shown that the presence of amino group donating electrons has a negative impact on the catalytic activity. On the other hand, the modification of Ru40 with an electron acceptor SO ₂ NMe ₂ group (Zhan type catalyst) enabled the synthesis of an extremely active catalyst in the ethenolysis reaction of fatty acids [EP1905777B1; US2011/0306815A1],

Verpoort et al. studied the impact of labile chelating groups: benzyl ether, benzyl thioether, and benzylamine [WO2017/185324A1]. All catalysis transformed methyl oleate with high selectivity and high TON values [Turnover number - the number of catalytic cycles, the number of moles of substrate undergoing reactions, calculated per one mole of the catalyst] (from 180,000 to 210,000). A reaction performed with ethylene (99.995%), in the presence of Ru43 chelated with benzylamine and an activator (HSiCb), yielded the highest recorded thus far TON value (390,000).

Lemcoff et al. showed that analogues of Hoveyda-Grubbs type catalysts chelated with sulfur in the benzylidene part are present in the cis/trans pairs Ru44-Ru47. The activity of complexes was studied i.e. in polymerization reactions of norbomene derivatives [Rozenberg, I. et al ACS CataL 2018, 8, 8182-8191].

The limited availability of a wide range of structurally various aldehydes used as substrates in the synthesis of CAAC ligands is a significant problem known in state-of-the-art Their use is mostly limited to simple aldehydes comprising isobutanal or 2-phenylpropanal. The high prices and low availability of other aldehyde derivatives, especially those with heterocyclic rings, as well as long and complicated synthesis pathways for these and other derivatives, in which the expected products are obtained with low yields, significantly limit the possibility of designing novel ruthenium catalysts containing modified CAAC ligands. These characteristics pose a significant limitation to the further development of organometallic catalysis based on ruthenium with novel CAAC ligands. Obtaining novel catalysts for olefin metathesis with ligands based, in particular, on various types of aldehydes with planned properties is becoming difficult to implement in chemical synthesis and economically unjustifiable in industrial scale-up.

In the search for novel ruthenium complexes with high catalytic activity and improved stability and selectivity enabling high TON values to be obtained, it is important that convenient synthetic paths based on easily available and inexpensive substrates lead to these compounds. From the point of view of industrial scaling, it is also important for the planned synthesis to be efficient at every stage and that the reaction products can be purified in a simple way, using techniques such as crystallization or distillation. It is also important to expand the library of ligands, the use of which will comprise an alternative and/or improved source of structures of ruthenium complexes used as catalysts in i.e. ethenolysis reactions of ester derivatives of fatty acids.

From an industrial point of view, it is extremely important that the activity of the new ruthenium complexes allows ethenolysis processes to be carried out with unpurified vegetable oils through a multi-step, laborious procedure of purifying raw materials from compounds that deactivate active catalyst molecules, such as oxygen, water, amines, sulfur compounds, halogenated compounds, peroxides, and others. It is equally important from an industrial point of view that the metathesis process can be carried out with ethylene available in an industrial installation, and not just commercially available high-purity ethylene (ethylene 3.0 = 99.9% purity or ethylene 43 = 99.995% purity). It is worth emphasizing that it is not possible to reproduce and apply under industrial conditions the procedures carried out in a glovebox under argon atmosphere, which are described in reputable journals by numerous respected scientists. Therefore, it is essential to search for novel ruthenium catalysts that, on the one hand, will be robust under reaction conditions, and at the same time active and efficient for performing the metathesis process.

Equally important is that transport and storage of catalysts should be easy and possible under normal atmospheric conditions, without the use of inert gases and low temperatures. Such properties of catalysts expected by the industry will enable their easy use on a large industrial scale, which will not require complex apparatus.

It was surprisingly discovered that complexes containing CAAC ligands with a heteroaromatic substituent were found to exhibit the properties desired and sought after by industry. Unexpectedly, it turned out that the ethenolysis processes catalyzed by the novel ruthenium complexes tolerate the presence of oxygen, so that the apparatus can be assembled in air, moreover, ethylene of lower purity than in the processes known in the literature can be used, as well as derivatives of fatty acids esters (oils of plant origin) without the need for a long purification process to high purity of raw materials.

Summary of the invention

The subject of this invention is a precursor of cyclic alkyl amine carbenes (CAAC) with the formula CAAC-1 in which X denotes an anion selected from a group comprising a halogen anion, BF ₄ -, PF ₆ -, CIO ₄ -, CF ₃ SO ₂ O-;

R ¹ , R ² , R ³ , R ⁴ and R ⁵ denote independently a hydrogen atom, a C ₁ -C ₁₂ alkyl group, a C ₃ -C ₁₂ cycloalkyl group, a C ₅ -C ₂₀ aryl group or a C ₅ -C ₂₀ heteroaryl group, a C ₅ -C ₂₅ aralkyl group, which may be independently substituted by one and/or more substituents selected from a group comprising a hydrogen atom, a halogen atom, a C ₁ -C ₁₂ alkyl group, a C ₁ -C ₁₂ perfluoroalkyl group, a C ₅ -C ₂₀ aryl group, a C ₅ -C ₂₀ perfluoroaryl group, a C ₅ -C ₂₀ heteroaryl group, a C ₁ -C ₁₂ alkoxy group, a C ₅ -C ₂₄ aryloxy group, a C ₅ -C ₂₀ heteroaryloxy group, a sulfide group (-SR''), an amino group (-NR'' ₂ ), in which the R'' group independently denotes a hydrogen atom, C ₁ -C ₅ alkyl, C ₆ -C ₂₄ aryl, C ₇ -C ₂₄ aralkyl, alternatively R ¹ , R ² , R ³ , R ⁴ and R ⁵ are connected and form a C ₅ -C ₂₅ ring wherein each substituent R ⁶ , R ⁷ , and R ⁸ denotes a hydrogen atom, a halogen atom, a C ₁ -C ₁₂ alkyl group or a C ₅ -C ₂₀ aryl group, which may be independently substituted by one and/or more substituents selected from a group comprising a hydrogen atom, a C ₁ -C ₁₂ alkyl group, a C ₁ -C ₁₂ perfluoroalkyl group, a C ₅ -C ₂₀ aryl group, a C ₅ -C ₂₀ perfluoroaryl group, a C ₅ -C ₂₀ heteroaryl group, a C ₁ -C ₁₂ alkoxy group, a C ₅ -C ₂₄ aryloxy group, a C ₅ -C ₂₀ heteroaryloxy group or a halogen atom, a sulfide group (-SR''), an amino group (-NR'' ₂ ), in which the R'' group independently denotes a hydrogen atom, C ₁ -C ₅ alkyl, C ₆ -C ₂₄ aryl, C ₇ -C ₂₄ aralkyl; substituent R ⁹ denotes a substituted or unsubstituted heterocyclic group or an organometallic complex group such as ferrocene, which may be independently substituted by one and/or more substituents selected from a group comprising a hydrogen atom, a hydrogen atom, a C ₁ -C ₁₂ alkyl group, a C ₁ -C ₁₂ perfluoroalkyl group, a C ₅ -C ₂₀ aryl group, a C ₅ -C ₂₀ perfluoroaryl group, a C ₅ -C ₂₀ heteroaryl group, a C ₁ -C ₁₂ alkoxy group, a C ₅ -C ₂₄ aryloxy group, a C ₅ -C ₂₀ heteroaryloxy group, a sulfide group (-SR''), an amino group (-NR'' ₂ ), in which the R'' group independently denotes a hydrogen atom, C ₁ -C ₅ alkyl, C ₆ -C ₂₄ aryl, C ₇ -C ₂₄ aralkyl, alternatively, R ⁶ and R ⁷ and/or R ⁸ and R ⁹ are connected and form a C ₅ -C ₂₅ ring

Preferably the substituent R ⁹ denotes a substituted or unsubstituted heterocyclic group selected from a heterocyclic group selected from thiophene, benzothiophene, furan, benzofuran, pyrrole, benzopyrrole, aziridine, oxirane, thiirane, azetidine, oxetane, thietane, pyrrolidine, tetrahydrofuran, tetrahydrothiophene, piperidine, tetrahydropyran, thiane, pyridine, azepane, oxepane, thiepane, azepine, oxepin, thiepine, oxazole, imidazole, thiazole, isoxazole, pyrazole, isothiazole, triazyne, pyrrolidine, pyridine, pyrimidine, hydantoin, quinoline, isoquinoline, chromonyl, coumarin, indole, indolysin, indazole, purine, quinolysine, isoquinol, quinol, phthalazine, naphthyridine, carbazole, β-carboline, or substitute R ⁹ denotes a substituted or unsubstituted organometallic complex group comprising cyclopentyl rings and metal atom selected from iron, cobalt, nickel, chromium, titanium, zirconium (metallocenes). Preferably the substituent R ⁹ denotes a substituted or unsubstituted heterocyclic group selected from thiophene, benzothiophene, furan, benzofuran or ferrocene.

Preferably, the precursor defined above has a structure represented by the formula L1, L2, L3, L4, L5, L6, L7, L8, L9, L10, L11, L12, L13, L14, L15, L16, L17, L18, L19, L20, L21 or L22:

The subject of the invention is also a ruthenium complex of formula 1-Ru

in which:

X ¹ and X ² independently from each other denote an anionic ligand selected from a group comprising a halogen anion, a group -CN, -SCN, -OR ^a , -SR ^a , -O(C=O)R ^a , -O(SO ₂ )R ^a and -OSi(R ^a ) ₃ , in which R ^a denotes C ₁ -C ₁₂ alkyl, C ₃ -C ₁₂ cycloalkyl, C ₂ -C ₁₂ alkenyl or C ₅ -C ₂₀ aryl, which is optionally substituted by at least one C ₁ -C ₁₂ alkyl, C ₁ -C ₁₂ perfluoroalkyl, C ₁ -C ₁₂ alkoxyl, C ₅ -C ₂₄ aryloxyl, C ₅ -C ₂₀ heteroaryloxyl or a halogen atom;

R ¹ , R ² , R ³ , R ⁴ and R ⁵ denote independently a hydrogen atom, a C ₁ -C ₁₂ alkyl group, a C ₃ -C ₁₂ cycloalkyl group, a C ₅ -C ₂₀ aryl group or a C ₅ -C ₂₀ heteroaryl group, a C ₅ -C ₂₅ aralkyl group, which may be independently substituted by one and/or more substituents selected from a group comprising a hydrogen atom, a halogen atom, a C ₁ -C ₁₂ alkyl group, a C ₁ -C ₁₂ perfluoroalkyl group, a C ₅ -C ₂₀ aryl group, a C ₅ -C ₂₀ perfluoroaryl group, a C ₅ -C ₂₀ heteroaryl group, a C ₁ -C ₁₂ alkoxy group, a C ₅ -C ₂₄ aryloxy group, a C ₅ -C ₂₀ heteroaryloxy group, a sulfide group (-SR''), an amino group (-NR'' ₂ ), in which the R'' group independently denotes a hydrogen atom, C ₁ -C ₅ alkyl, C ₆ - C ₂₄ aryl, C ₇ -C ₂₄ aralkyl, alternatively R ¹ , R ² , R ³ , R ⁴ and R ⁵ are connected and form a C ₅ -C ₂₅ ring each substituent R ⁶ , R ⁷ , and R ⁸ denotes a hydrogen atom, a halogen atom, an alkyl C ₁ -C ₁₂ group or a C ₅ -C ₂₀ aryl group, which may be substituted independently by one and/or more substituents selected from a group comprising a hydrogen atom, a C ₁ -C ₁₂ alkyl group, a C ₁ -C ₁₂ perfluoroalkyl group, a C ₅ -C ₂₀ aryl group, a C ₅ -C ₂₀ perfluoroaryl group, a C ₅ -C ₂₀ heteroaryl group, a C ₁ -C ₁₂ alkoxy group, a C ₅ -C ₂₄ aryloxy group, a C ₅ -C ₂₀ heteroaryloxy group or a halogen atom, a sulfide group (-SR''), an amino group (-NR'' ₂ ), in which the R'' group independently means a hydrogen atom, C ₁ -C ₅ alkyl, C ₆ -C ₂₄ aryl, C ₇ -C ₂₄ aralkyl; substituent R ⁹ denotes a substituted or unsubstituted heterocyclic group and/or organometallic complex group which may be independently substituted by one and/or more substituents selected from a group comprising a hydrogen atom, a halogen atom, a C ₁ - C ₁₂ alkyl group, a C ₁ - C ₁₂ perfluoroalkyl group, a C ₅ -C ₂₀ aryl group, a C ₅ -C ₂₀ perfluoroaryl group, a C ₅ -C ₂₀ heteroaryl group, a C ₁ -C ₁₂ alkoxy group, a C ₅ -C ₂₄ aryloxy group, a C ₅ -C ₂₀ heteroaryloxy group, a sulfide group (-SR''), an amino group (-NR'' ₂ ), in which the R'' group independently denotes a hydrogen atom, C ₁ -C ₅ alkyl, C ₆ -C ₂₄ aryl, C ₇ -C ₂₄ aralkyl, alternatively R ⁶ and R ⁷ and/or R ⁸ and R ⁹ are connected and form a C ₅ -C ₂₅ ring

R ¹⁶ and R ¹⁷ denote independently a hydrogen atom, a halogen atom, C ₁ -C ₂₅ alkyl, C ₃ -C ₁₂ cycloalkyl, C ₁ -C ₁₂ perfluoroalkyl, C ₂ -C ₂₅ alkene, C ₂ -C ₂₅ alkenyl, C ₃ -C ₂₅ cycloalkenyl, C ₂ -C ₂₅ alkynyl, C ₃ -C ₂₅ cycloallynyl, C ₁ -C ₂₅ alkoxyl, C ₅ -C ₂₅ aryl, C ₅ -C ₂₅ aryloxyl, C ₆ -C ₂₅ arylalkyl, C ₅ -C ₂₅ heteroaryl, C ₅ -C ₂₅ heteroaryloxyl, C ₅ -C ₂₅ perfluoroaryl, a 3-12-membered heterocycle comprising a sulfur, oxygen, nitrogen, selenium or a phosphorus atom; wherein the substituents R ¹⁶ and R ¹⁷ may be connected forming a ring selected from a group comprising C ₃ -C ₂₅ cycloalkyl, C ₃ -C ₂₅ cycloalkenyl, C ₃ -C ₂₅ cycloalkynyl, C ₅ -C ₂₅ aryl, C ₅ -C ₂₅ heteroaryl, C ₅ -C ₂₅ perfluoroaryl, a 3-12-membered heterocycle containing a sulfur, oxygen, nitrogen, selenium or phosphorus atom, which may be independently substituted by one or more substituents selected from a group comprising a hydrogen atom, a halogen atom, C ₁ -C ₂₅ alkyl, C ₃ -C ₂₅ cycloalkyl, C ₁ -C ₁₂ perfluoroalkyl, C ₂ -C ₂₅ alkene, C ₂ -C ₂₅ alkenyl, C ₃ -C ₂₅ cycloalkenyl, C ₂ -C ₂₅ alkynyl, C ₃ -C ₂₅ cycloallynyl, C ₁ -C ₂₅ alkoxyl, C ₅ -C ₂₅ aryl, C ₅ -C ₂₅ aryloxyl, C ₆ -C ₂₅ arylalkyl, C ₅ -C ₂₅ heteroaryl, C ₅ -C ₂₅ heteroaryloxyl, C ₅ -C ₂₅ perfluoroaryl, a 3-12-membered heterocycle;

G is selected from such as

- a ligand with the formula CAAC-1 in which X and the substituents R ¹ to R ⁹ have the meanings defined above or

- heteroatom 1 selected from a group comprising an oxygen, sulfur or selenium atom, substituted by a group selected from such as a hydrogen atom, a halogen atom, an oxygen atom, C ₁ -C ₂₅ alkyl, C ₁ -C ₂₅ perfluoroalkyl, C ₃ -C ₂₅ cycloalkyl, C ₅ -C ₂₀ alkoxyl, C ₅ -C ₂₀ aryl, C ₅ -C ₂₀ perfluoroaryl, C ₇ -C ₂₀ aralkyl, C ₅ -C ₂₄ aryloxyl, C ₂ -C ₁₂ alkenyl, C ₆ -C ₂₀ heteroaryl or heteroaryloxyl C ₅ -C ₂₄ a 3-12-membered heterocycle, optionally substituted by an acyl group (-COR'), a cyano group (-CN), a carboxyl group (-COOH), an ester group (-COOR'), an ester group (-CH ₂ COOR'), an ester group (-CHR'COOR'), an ester group (-C(R ^, ) ₂ COOR ^, ), an amide group (-CONR' ₂ ), a Weinreb-type amide (-CON(R')(OR')), a sulfone group (-SO ₂ R'), a formyl group (-CHO), a sulfonamide group (-SOiNR' ₂ ), a ketone group (-COR'), a thioamide group (-CSNR' ₂ ), a thioketone (-CSR'), a thionoester group (-CSOR'), a thioester group (-COSR'), a dithioester group (-CS2R'), in which the group R' denotes independently C ₁ -C ₂₅ alkyl, C ₁ -C ₂₅ perfluoroalkyl, C ₃ -C ₂₅ cycloalkyl, C ₅ -C ₂₀ alkoxyl, C ₅ -C ₂₀ aryl, C ₅ -C ₂₀ perfluoroaryl, C ₇ -C ₂₀ aralkyl, C ₅ -C ₂₄ aryloxyi, C ₂ -C ₁₂ alkenyl, C ₆ -C ₂₀ heteroaryl, C ₅ -C ₂₄ heteroaryloxyl and then the dashed line denotes a direct bond between a heteroatom and the substituent R ¹⁷ or it denotes a bond between the substituent R ¹⁷ and a heteroatom via a methylene bridge -CH ₂ -, -CHR’-, or -CR'2- wherein the substituent R ¹⁴ is C ₅ -C ₁₅ aryl, optionally substituted by 1-4 substituents independently selected from a group comprising a hydrogen atom, a halogen atom, C ₁ -C ₂₅ alkyl, C ₃ -C ₂₅ cycloalkyl, C ₂ -C ₂₅ alkenyl, C ₃ -C ₂₅ cycloalkenyl, C ₂ -C ₂₅ alkynyl, C ₃ -C ₂₅ cycloalkynyl, C ₁ -C ₂₅ perfluoroalkyl, C ₅ -C ₂₀ alkoxyl, C ₅ -C ₂₀ aryl, C ₅ -C ₂₀ perfluoroaryl, C ₇ -C ₂₀ aralkyl, C ₅ -C ₂₄ aryloxyi, C ₆ -C ₂₀ heteroaryl or C ₅ -C ₂₄ heteroaryloxyl, a 3-12-membered heterocycle, an alkoxyl group (-OR"), a sulfide group (-SR**), a sulfoxide group (-S(O)R"), a sulfonium group (-S ⁺ R'' ₂ ), a sulfone group (-SO ₂ R**), a sulfonamide group (-SO ₂ NR'' ₂ ), an amino group (-NR'' ₂ ), an ammonium group (-N ⁺ R'' ₃ ), a nitro group (-NO ₂ ), a cyano group (-CN), a phosphinous group (-P(O)(OR**) ₂ ), a phosphinic group (-P(O)R**(OR**)), a phosphonine group (-P(OR**) ₂ ), a phosphine group (-PR'' ₂ ), a phosphine oxide group (-P(O)R'' ₂ ), a phosphonium group (-P ⁺ R'' ₃ ), a carboxyl group (-COOH), an ester group (-COOR**), an amide group (-CONR'' ₂ ), an amide group (-NR**C(O)R**), a formyl group (-CHO), a ketone group (-COR**), a thioamide group (-CSNR'' ₂ ), a thioketone group (-CSR**), a thionoester group (-CSOR**), a thioester group (-COSR**), a dithioester group (-CS2R**), in which the R'' group denotes C ₁ -C ₅ alkyl, C ₁ -C ₅ perfluoroalkyl, C ₆ -C ₂₄ aryl, C ₇ -C ₂₄ aralkyl, C ₅ -C ₂₄ perfluoroaryl, or

— heteroatom 2 selected from a group comprising a nitrogen or a phosphorus atom, substituted by the group selected from such as a hydrogen atom, methylidene, optionally substituted by the substitute R’, C ₁ -C ₂₅ alkyl, C ₁ -C ₂₅ perfluoroalkyl, C ₃ -C ₂₅ cycloalkyl, C ₅ -C ₂₀ alkoxyl, C ₅ -C ₂₀ aryl, C ₅ -C ₂₀ perfluoroaryl, C ₇ -C ₂₀ aralkyl, C ₅ -C ₂₄ aryloxyi, C ₂ -C ₁₂ alkenyl, C ₆ -C ₂₀ heteroaryl or C ₅ -C ₂₄ heteroaryloxyl, a 3-12-membered heterocycle, an acyl group (-COR'), an ester group (-COOR'), a tert-butyloxycarbonyl group (t-Boc) or a 9-fluorenylmethoxycarbonyla group (Fmoc), a carbamine group (-CONR'2), a sulfone group (-SO ₂ R'), a formyl group (-CHO), in which the R' group denotes C ₁ -C ₂₅ alkyl, C ₁ -C ₂₅ perfluoroalkyl, C ₃ -C ₂₅ cycloalkyl, C ₅ -C ₂₀ alkoxyl, C ₅ -C ₂₀ aryl, C ₅ -C ₂₀ perfluoroaryl, C ₇ -C ₂₀ aralkyl, C ₅ -C ₂₄ aryloxyi, C ₂ -C ₁₂ alkenyl, C ₆ -C ₂₀ heteroaryl or C ₅ -C ₂₄ heteroaryloxyl, optionally substituted with an acyl group (-COR'), a cyano group (-CN), a carboxyl group (-COOH), an ester group (-COOR'), an ester group (-CH ₂ COOR'), an ester group (-CHR'COOR'), an ester group (-C(R') ₂ COOR'), an amide group (-CONR' ₂ ), a sulfone group

(-SOiR'), a formyl group (-CHO), a sulfonamide group (-SO ₂ NR' ₂ ), a ketone group (-COR'), a thioamide group (-CSNR' ₂ ), a thioketone group (-CSR'), a thionoester group (-CSOR'), a thioester group (-COSR') or a dithioester group (-CS ₂ R'), in which the R' group denotes C ₁ -C ₂₅ alkyl, C ₁ -C ₂₅ perfluoroalkyl, C ₃ -C ₂₅ cycloalkyl, C ₅ -C ₂₀ alkoxyl, C ₅ -C ₂₀ aryl, C ₅ -C ₂₀ perfluoroaryl, C ₇ - C ₂₀ aralkyl, C ₅ -C ₂₄ aryloxyl, C ₂ -C ₁₂ alkenyl, C ₆ -C ₁₀ heteroaryl or C ₅ -C ₂₄ heteroaryloxyl, and then the dashed line denotes a direct bond between the heteroatom and the substituent R ¹⁴ or it denotes a bond between the substituent R ¹⁷ with a heteroatom via methylene bridge (CH ₂ )- , -(CHR')-, or -(CR' ₂ )-; wherein the substituent R ¹⁷ is C ₅ -C ₁₅ aryl, optionally substituted with 1-4 substituents independently selected from the group comprising a hydrogen atom, a halogen atom, C ₁ -C ₂₅ alkyl, C ₃ -C ₂₅ cycloalkyl, C ₂ -C ₂₅ alkenyl, C ₃ -C ₂₅ cycloalkenyl, C ₂ -C ₂₅ alkynyl, C ₃ -C ₂₅ cycloalkynyl, C ₁ -C ₂₅ perfluoroalkyl, C ₅ -C ₂₀ alkoxyl, C ₅ -C ₂₀ aryl, C ₅ -C ₂₀ perfluoroaryl, C ₇ -C ₂₀ aralkyl, C ₅ -C ₂₄ aryloxyl, C ₆ -C ₂₀ heteroaryl or C ₅ -C ₂₄ heteroaryloxyl, a 3-12-membered heterocycle, an alkoxyl group (-OR''), a sulfide group (-SR"), a sulfoxide group (-S(O)R''), a sulfonium group (-S ⁺ R'' ₂ ), a sulfone group (-SO ₂ R''), a sulfonamide group (-SO ₂ NR'' ₂ ), an amino group (-NR'' ₂ ), an ammonium group (-N ⁺ R'' ₃ ), a nitro group (-NO ₂ ), a cyano group (-CN), a phosphinous group (-P(O)(OR'') ₂ ), a phosphinic group (-P(O)R''(OR'')), a phosphonine group (-P(OR'') ₂ ), a phosphine group (-PR'' ₂ ), a phosphine oxide group (-P(O)R'' ₂ ), a phosphonium group (-P ⁺ R'' ₃ ), a carboxyl group (-COOH), an ester group (-COOR''), an amide group (-CONR'' ₂ ), an amide group (-NR''C(O)R''), a formyl group (-CHO), a ketone group (-COR''), a thioamide group (-CSNR'' ₂ ), a thioketone group (-CSR''), a thionoester group (-CSOR''), a thioester group (-COSR'') or a dithioester group (-CS2R''), in which the group R'' denotes C ₁ -C ₅ alkyl, C ₁ -C ₅ perfluoroalkyl, C ₆ - C ₂₄ aryl, C ₇ -C ₂₄ aralkyl, C ₅ -C ₂₄ perfluoroaryl, or

- heteroatom 3 selected from a group comprising a halogen atom and then the dashed line denotes a direct bond between the heteroatom and the R ¹⁷ substituent, wherein the R ¹⁷ substituent is C ₅ -C ₁₅ aryl, or C ₅ -C ₂₅ polyaryl, optionally substituted with 1-4 substituents selected independently from a group comprising a hydrogen atom, a halogen atom, C ₁ -C ₂₅ alkyl, C ₃ -C ₂₅ cycloalkyl, C ₂ -C ₂₅ alkenyl, C ₃ -C ₂₅ cycloalkenyl, C ₂ -C ₂₅ alkynyl, C ₃ -C ₂₅ cycloalkynyl, C ₁ -C ₂₅ perfluoroalkyl, C ₅ -C ₂₀ alkoxyl, C ₅ -C ₂₀ aryl, C ₅ -C ₂₀ perfluoroaryl, C ₇ -C ₂₀ aralkyl, C ₅ -C ₂₄ aryloxyl, C ₆ -C ₂₀ heteroaryl or C ₅ -C ₂₄ heteroaryloxyl, a 3-12-membered heterocycle, an alkoxy group (-OR''), a sulfide group (-SR'), a sulfoxide group (-S(O)R''), a sulfonium group (-S ⁺ R'' ₂ ), a sulfone group (-SO ₂ R''), a sulfonamide group (-SO ₂ NR'' ₂ ), an amino group (-NR'' ₂ ), an ammonium group (-N ⁺ R'' ₃ ), a nitro group (-NO ₂ ), a cyano group (-CN), a phosphonous group (-P(O)(OR'') ₂ ), a phosphinous group (-P(O)R''(OR'')), a phosphonine group (-P(OR'') ₂ ), a phosphine group (-PR'' ₂ ), a phosphine oxide group (-P(O)R'' ₂ ), a phosphonium group (-P ⁺ R'' ₃ ), a carboxyl group (-COOH), an ester group (-COOR''), an amide group (-CONR'' ₂ ) , an amide group (-NR''C(O)R''), a formyl group (-CHO), a ketone group (-COR''), a thioamide group (-CSNR'' ₂ ), a thioketone group (-CSR''), a thionoester group (-CSOR''), a thioester group (-COSR''), a dithioester group (-CS2R''), in which the R'' group denotes C ₁ -C ₅ alkyl, C ₁ -C ₅ perfluoroalkyl, C ₆ -C ₂₄ aryl, C ₇ -C ₂₄ aralkyl, C ₅ -C ₂₄ perfluoroaryl.

The ruthenium complex is preferably represented by the formula1a-Ru in which X ¹ and X ² and the R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ substituents have the meanings defined above

'n' means 1 or 0

Z is selected from a group comprising halogen atoms, O atom, S atom, Se atom, or a NR''' group, in which R''' denotes methylidene, C ₁ -C ₂₅ alkyl, C ₁ -C ₂₅ perfluoroalkyl, C ₃ -C ₂₅ cycloalkyl, C ₅ -C ₂₀ alkoxyl, C ₅ -C ₂₀ aryl, C ₅ -C ₂₀ perfluoroaryl, C ₇ -C ₂₀ aralkyl, C ₅ -C ₂₄ aryloxyl, C ₂ -C ₁₂ alkenyl, C ₆ -C ₂₀ heteroaryl or C ₅ -C ₂₄ heteroaryloxyl, a 3-12-membered heterocycle, an acyl group (-COR'), an ester group (-COOR'), a tert-butylcarboxycarbon group (t-Boc) or a 9-fluorenylmethoxycarbonyl group (Fmoc), a carbamine group (-CONR' ₂ ), a sulfone group (-SO ₂ R'), a formyl group (-CHO), in which the R' group denotes C ₁ -C ₂₅ alkyl, C ₁ -C ₂₅ perfluoroalkyl, C ₃ -C ₂₅ cycloalkyl, C ₅ -C ₂₀ alkoxyl, C ₅ -C ₂₀ aryl, C ₅ -C ₂₀ perfluoroaryl, C ₇ -C ₂₀ aralkyl, C ₅ -C ₂₄ aryloxyi, C ₂ -C ₁₂ alkenyl, C ₄ -C ₂₀ heteroaryl or C ₅ -C ₂₄ heteroaryloxyl, or a halogen atom, wherein if Z denotes a halogen atom, R ¹⁸ is absent;

R ¹⁸ means independently a hydrogen atom, C ₁ -C ₂₅ alkyl, C ₁ -C ₂₅ cycloalkyl, C ₅ -C ₂₀ alkoxyl, C ₅ -C ₂₀ aryl, C ₅ -C ₂₄ aryloxyi, a -COOR''' group, a -CH ₂ COOR''' group, a -CONR''' ₂ group, a -CH ₂ CONR''' ₂ group, a -COR''' group, a -CH ₂ COR''' group, a -CON(OR''’)(R''’) group, a -CH ₂ CON(OR''’)(R''’) group or a halogen atom, wherein R''' denotes C ₁ -C ₁₂ alkyl, C ₃ -C ₁₂ cycloalkyl, C ₂ -C ₁₂ alkenyl, C ₄ -C ₂₀ aryl, which are optionally substituted with at least one C ₁ -C ₁₂ alkyl, C ₁ -C ₁₂ perfluoroalkyl, C ₁ -C ₁₂ alkoxyl, C ₆ -C ₂₄ aryloxyi, or a halogen atom;

R ¹ ’, R ²⁰ , R ²¹ , and R ²² denote independently a hydrogen atom, a halogen atom, a C ₁ -C ₂₅ alkyl group, a C ₂ -C ₂₅ alkenyl group, a C ₅ -C ₂₅ aryl group, an alkoxy group (-OR''), a sulfide group (-SR"), a sulfoxide (-S(O)R''), a sulfonium group (-S ⁺ R'' ₂ ), a sulfone group (-SO ₂ R''), a sulfonamide group (-SO ₂ NR'' ₂ ), an amino group (-NR'' ₂ ), an ammonium group (-N ⁺ R'' ₃ ), a nitro group (-NO ₂ ), a cyano group (-CN), a phosphonous group (-P(O)(OR'') ₂ ), a phosphinous group (-P(O)R''(OR'')), a phosphonine group (-P(OR'') ₂ ), a phosphine group (-PR'' ₂ ), a phosphine oxide group (-P(O)R'' ₂ ), a phosphonium group (-P ⁺ R'' ₃ ), a carboxyl group (-COOH), an ester group (-COOR''), an amide group (-CONR'' ₂ ), an amide group (-NR''C(O)R'), a formyl group (-CHO), a ketone group (-COR''), a thioamide group (-CSNR'' ₂ ), a thioketone group (-CSR''), a thionoester group (-CSOR''), a thioester group (-COSR''), a dithioester group (-CS ₂ R''), in which the R'' group denotes C ₁ -C ₅ alkyl, C ₁ -C ₅ perfluoroalkyl, C ₆ -C ₂₄ aryl, C ₇ -C ₂₄ aralkyl, C ₅ -C ₂₄ perfluoroaryl, wherein the R ¹⁶ , R ¹⁷ , R ¹⁸ and R ¹⁹ substituents may be connected, thus forming a substituted or unsubstituted C ₄ -C10 cyclic or C ₄ -C ₁₂ polycyclic system.

The ruthenium complex is preferably represented by the formula1b-Ru in which X ¹ and X ² and the R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ substituents have the meanings defined above

R ¹⁶ and R ¹⁷ independently denote a hydrogen atom, a halogen atom, C ₁ -C ₂₅ alkyl, optionally substituted; C ₃ -C ₂₅ cycloalkyl, optionally substituted; C ₁ -C ₁₂ perfluoroalkyl, optionally substituted; C ₂ -C ₂₅ alkene, optionally substituted; C ₂ -C ₂₅ alkenyl, optionally substituted; C ₃ -C ₂₅ cycloalkenyl, optionally substituted; C ₂ -C ₂₅ alkynyl, optionally substituted; C ₃ -C ₂₅ cycloalkynyl, optionally substituted; C ₁ -C ₂₅ alkoxyl, optionally substituted; C ₅ -C ₂₅ aryl, optionally substituted; C ₅ -C ₂₅ aryloxyl, optionally substituted; C ₆ -C ₂₅ arylalkyl, optionally substituted; C ₅ -C ₂₅ heteroaryl, optionally substituted; C ₅ -C ₂₅ heteroaryloxyl, optionally substituted; C ₅ -C ₂₅ perfluoroaryl, optionally substituted; a 3-12-membered heterocycle containing a sulfur, oxygen, nitrogen, selenium or a phosphorus atom, optionally substituted; wherein the R ¹⁶ and R ¹⁷ substituents may be connected, forming a ring selected from a group comprising C ₃ -C ₂₅ cycloalkyl, cycloalkenyl C ₃ -C ₂₅ , C ₃ -C ₂₅ cycloalkynyi, C ₅ -C ₂₅ aryl, C ₅ -C ₂₅ heteroaryl, C ₅ -C ₂₅ perfluoroaryl, a 3-12-membered heterocycle comprising a sulfur, oxygen, nitrogen, selenium or a phosphorus atom, which may be independently substituted with one or more substituents selected from a group comprising a hydrogen atom, a halogen atom, C ₁ -C ₂₅ alkyl, C ₃ -C ₂₅ cycloalkyl, C ₁ -C ₁₂ perfluoroalkyl, C ₂ -C ₂₅ alkene, C ₂ -C ₂₅ alkenyl, C ₃ -C ₂₅ cycloalkenyl, C ₂ -C ₂₅ alkynyl, C ₃ -C ₂₅ cycloalkynyi, C ₁ -C ₂₅ alkoxyl, C ₅ -C ₂₅ aryl, C ₅ -C ₂₅ aryloxyl, C ₆ -C ₂₅ arylalkyl, C ₅ -C ₂₅ heteroaryl, C ₅ -C ₂₅ heteroaryloxyl, C ₅ -C ₂₅ perfluoroaryl, a 3-12-membered heterocycle.

The ruthenium complex is preferably represented with the formulas Ru1a, Ru2a, Ru3a, Ru4a, Ru5a, Ru6a, Ru7a, Ru8a, Ru9a, Ru10a, Ru11a, Ru11a, Ru12a, Ru13a, Ru14a, Ru15a, Ru16a, Ru17a, Ru18a, Ru19a, Ru20a, Ru21aa Ru22a:

The subject of the invention is also a method of obtaining a ruthenium complex of formula

1a-Ru defined above, in which the alkylidene ruthenium complex with the formula 10 in which:

L ¹ denotes a neutral ligand selected from a group comprising pyridine or substituted pyridine, P(R') ₃ , P(OR') ₃ , O(R') ₂ , N(R') ₃ , wherein each R' independently denotes C ₁ -C ₁₂ alkyl, C ₃ -C ₁₂ cycloalkyl, C ₅ -C ₂₀ aryl, C ₇ -C ₂₄ aralkyl, C ₅ -C ₂₄ perfluoroaryl, a 5-12-membered heteroaryl;

N, Z, X ¹ , X ² and the substituents R ¹⁸ , R ¹ ’, R ²⁰ , R ²¹ and R ²² have the meanings defined above undergoes reaction with carbene of formula 8 in which the substituents R ¹ to R ⁹ have the meanings defined above.

The subject of the invention also relates to the use of the compound of formula 1-Ru, defined above, as a precatalyst and/or a catalyst in olefin metathesis reactions, in particular in ring-closing metathesis (RCM), cross-metathesis (CM), homometathesis (cross-metathesis between two molecules of the same olefin), ethenolysis, isomerization, in the reaction of diastereoselective ring-rearrangement metathesis (DRRM) reactions, 'alkene-aHyne' (en-yn) metathesis or ROMP or ADMET polymerization reactions.

The reaction is preferably carried out in an organic solvent, such as toluene, mesitylene, hexane, cyclohexane, ethyl acetate, methyl acetate, methyl carbonate, ethyl carbonate, tert-butyl-methyl ether, cyclopentyl-methyl ether, diethyl ether, THF, 2-Me-THF, 4-Me-THP, dioxane, DME, PAO. PEG, paraffin, esters of saturated fatty acids.

The reaction is preferably carried out in a solvent-free system.

The reaction is preferably carried out at a temperature between 20 °C and 200 °C.

The reaction is preferably carried out over a period between 5 minutes and 48 hours.

The 1-Ru compound is preferably used in a quantity not greater than 10 mol%. The 1-Ru compound is preferably used in a quantity not greater than 0.1 mol%.

The 1-Ru compound is preferably added to the reaction mixture in aliquots, as a solid and/or continuously, using a pump, as a solution in an organic solvent

The gaseous by-product of the reaction, selected from ethylene, propylene, butylene, is preferably actively removed from the reaction mixture using inert gas barbotage or under reduced pressure.

The subject of the invention is explained in embodiments in the Figures, in which:

Fig. 1 presents the structure of the Ru17a compound obtained on the basis of X-ray structural analysis;

Fig. 2 presents a summary of precatalysts and catalysts of olefin metathesis available on the market and of novel precatalysts and catalysts according to the invention;

Fig. 3 presents a photography showing: (A) the set up and closed reaction system - autoclave, and (B) the reaction system (autoclave), which is open prior to the ethenolysis reaction and does not require a glovebox at any stage of the reaction process.

In this description, terms used have the following meanings.

Terms undefined in this document have meanings which are provided and understood by the specialist in the field in light of the best knowledge available, this disclosure and the context of the patent application description.

Unless otherwise stated, the following conventions of chemical terms are used in this description and have the meanings indicated as in the definitions below:

As used in this description, the term "halogen atom" means an element selected from F, Cl, Br, I.

The term "carbene" means an electrically inert molecule in which the carbon atom has two nonbonding electrons occurring in the singlet or triplet state and is linked by a single covalent bond to two groups or linked by a double covalent bond to one group. The term 'carbene' also includes carbene analogues in which the carbene carbon atom is replaced by another chemical element such as boron, silicon, germanium, tin, lead, nitrogen, phosphorus, sulfur, selenium or tellurium.

The term “alkyl” refers to a saturated, linear or branched hydrocarbon substituent with the indicated number of carbon atoms. Examples of alkyl substituents include -methyl, -ethyl, -n-propyl, -n-butyl, -n-pentyl, -n-hexyl, -n-heptyl, -n-octyl, -n-nonyl and -n-decyl. Representative branched -(C ₁ -C ₁₀ ) alkyls include -isopropyl, -sec-butyl, -isobutyl, -tertbutyl, -isopentyl, -neopentyl, -1 -methylbutyl, -2-methylbutyl, -3-methylbutyl, -1,1 -dimethylpropyl, -1,2-dimethylpropyl, -1 -methylpentyl, -2-methylpentyl, -3-methylpentyl, -4-methylpentyl, -1 -ethylbutyl, -2-ethylbutyl, -1,1 -dimethylbutyl, -1,2-dimethylbutyl, -1,3 -di methyl butyl, -2,2-dimethylbutyl, -2,3-dimethylbutyl, -3,3-dimethylbutyl, -1 -methylhexyl, -2-methylhexyl, -3-methylhexyl, -4-methylhexyl, -1,2-di methyl pentyl, -1,3-dimethyipentyl, -5-methylhexyl, -1,2-di methyl hexyl, -1,3-dimethylhexyl, -3,3-dimethyihexyl, -1,2-di methyl heptyl, -1,3-dimethylheptyl, -3,3-dimethylheptyl and the like.

The term “alkox/T refers to an alkyl substituent as defined above, connected via an oxygen atom.

The term “perfluoroalkyF denotes an alkyl group as defined above, in which all the hydrogen atoms have been replaced with the same or different halogen atoms.

The term “cydoalk/T refers to a saturated, mono- or polycyclic hydrocarbon substituent with the indicated number of carbon atoms. Examples of cycloalkyl substituent include -cyclopropyl, -cyclobutyl, -cyclopentyl, -cyclohexyl, -cycloheptyl, -cyclooctyl, -cyclononyl, -cyclodecyl and the like.

The term “alkenyl” refers to an unsaturated, linear or branched, acyclic hydrocarbon substituent with the indicated number of hydrogen atoms and containing at least one double carbon-carbon bond. Examples of alkenyl substituents include -vinyl, -allyl, -1-butenyl, -2-butenyl, -isobutenyl, -1 -pentenyl, -2-pentenyl, -3-methyl-1-butenyl, -2-methyl-2-butenyl, -2,3-dimethyl-2-butenyl, -1 -hexenyl, -2-hexenyl, -3-hexenyl, -1 -heptenyl, -2-heptenyl, -3-heptenyl, -1 -octenyl, -2-octenyl, -3-octenyl, -1-nonenyl, -2-nonenyl, -3-nonenyl, -1 -decenyl, -2-decenyl, -3-decenyl and the like.

The term “cycloalkenyl” refers to an unsaturated, cyclic or branched, cyclic hydrocarbon substituent with the indicated number of hydrogen atoms and containing at least one double carbon-carbon bond. Examples of cycloalkenyl substituents include -cyclopropene, -cyclobutene, -cyclopentene, -cyclohexene, -cycloheptene, -cyclooctene, -cyclononene, -cyclodecene, -metylcyclopropene, -ethylcyclobutene, -isopropylcyclo pentene, -methylcyclohexene and the like.

The term “aryl" refers to an aromatic, mono- or polycyclic hydrocarbon substituent with the indicated number of carbon atoms. Examples of aryl substituents include -phenyl, -tolyl, -xylyl, -naphthtyl, -2,4,6-trimethylphenyl, -2-fluorophenyl, -4-fluorophenyl, -2,4,6-trifluorophenyl, -2,6-difluorophenyl, -4-nitrophenyl and the like.

The term “aralkyl" refers to an alkyl substituent as defined above, substituted with at least one aryl as defined above. Examples of aralkyl substituents include -benzyl, -diphenylmethyl, -triphenylmethyl and the like.

The term “heteroaryl” refers to an aromatic mono- or polycyclic hydrocarbon substituent with the indicated number of carbon atoms, in which at least one carbon atom has been replaced with a heteroatom selected from O, N and S atoms. Examples of heteroaryl substituents include -furyl, -thienyl, -imidazolyl, -oxazolyi, -thiazolyl, -isoxazolyl, -triazolyl, -oxadiazolyl, -thiadiazolyl, - tetrazolyl, -pyridyl, -pyrimidyl, -triazinyl, -indolyl, -benzo[b]furyl, -benzo[b]thienyl, -indazolyl, - benzoimidazolyl, -azaindolyl, -quinolyl, -isoquinolyl, -carbazolyl and the like.

The term ..heterocycle" refers to a saturated, unsaturated or partially unsaturated hydrocarbon substituent, with the indicated number of carbon atoms, in which at least one carbon atom has been replaced with a heteroatom selected from O, N and S atoms. Example heterocycle substituents include -furyl, -thiophenyl, -pyrrolyl, -oxazolyl, -imidazolyl, -thiazolyl, -isoxazolyl, -pyrazolyl, -isothiazolyl, -triazinyl, -pyrrolidinonyl, -pyrrolidinyl, -hydantoinyl, -oxiranyl, -oxetanyl, -tetrahydrofuranyl, -tetrahydrothiophenyl, -quinolinyl, -isoquinolinyl, -chromonyl, -coumarinyl, -indolyl, -indolysinyl, -benzo[b]furanyl, -benzo[b]thiophenyl, -indazolyl, -purinyl, -4H-quinolysinyl, - isoquinolyl, -quinolyl, -phtalazinyl, -naphtyridinyl, -carbazolyl, -β-carbolinyl and the like.

The term “neutral ligand” refers to an non-charged substituent capable of coordinating with a metallic center (transition metal atom). Examples of such ligands may include: N-heterocydic carbenes (NHC), cyclic (alkyl) (amino) carbenes (CAAC), amines, phosphines and their oxides, alkyl and aryl phosphites and phosphates, arsines and their oxides, ethers, alkyl and aryl sulfides, coordinated unsaturated or aromatic hydrocarbons, alkyl and aryl halides, nitriles, isonitriles, sulfides, sulfoxides, sulfones, thioketones, thioamides, thioester, thionoesters and dithioesters.

The term “anionic ligand” refers to a substituent capable of coordinating with a charged metallic center (transition metal atom), which can partially or fully compensate the charge of the metallic center. Examples of such ligands may include fluoride, chloride, bromide, iodide, cyanide, cyanate and thiocyanate anions, carboxylic acid anions, alcohol anions, phenol anions, thiol and thiophenol anions, anions of hydrocarbons with delocalized charge (e.g. cyclopentadiene anion), anions of (organo)sulfuric acids and (organo)phosphoric acids and their esters (such as e.g. anions of alkylsulfonic and arylsulfonic acids, anions of alkylphosphoric and arylphosphoric acids, anions of alkyl and aryl esters of sulfuric acid, anions of alkyl and aryl esters of phosphoric acids, anions of alkyl and aryl esters of alkylphosphoric and arylphosphoric acids).

The term “heteroatom” means an atom selected from the group comprising oxygen sulfur, nitrogen, phosphorous, boron, silicon, arsenic, selenium, tellurium.

The term "PAO" stands for polyolefins, an abbreviation for Poly-Alpha-Olefins, in the case of the present invention, an abbreviation used for low molecular weight polyolefins used as high boiling point solvents. It also denotes a class of solvents and/or lubricants that are the product of the polymerization of ethylene derivatives, leading to the formation of branched, saturated hydrocarbons, used here as heat-resistant, non-polar, high boiling point solvents.

Embodiments of the invention

The following examples are included only to illustrate the invention and to clarify particular aspects of the invention, not to limit it, and should not be equated with the entire scope of the invention as defined in the appended claims. In the following examples, unless otherwise indicated, standard materials and methods used in the field were used or followed manufacturers' recommendations for specific reactants and methods.

When necessary, model compounds for the metathesis reaction were purified by fractional distillation and then stored under inert gas atmosphere over activated neutral aluminum oxide. Tetrahydrofuran was purified by sodium-potassium alloy distillation in the presence of benzophenone, and then stored over 4Å molecular sieves. When expedient, selected reactions were carried out under an argon atmosphere using reaction vessels heated at 130 °C. Aluminum oxide (AI ₂ O ₃ , neutral, Brockman Grade I) was activated by heating at 150 °C under reduced pressure for 16 hours.

Starting compounds for the synthesis of aldehyde derivatives were commercially available.

Example I

Synthesis of new aldehydes, precursors of CAAC ligands

The following Scheme 9 illustrates the first three steps in the synthesis of CAAC ligand precursors to synthesize ruthenium catalysts for olefin metathesis (with the general formulae Ru1a to Ru21a, Scheme 9), which are the subject of the present invention.

Scheme 9. Synthesis of the aldehydes A6 - A10

Reactions R1 through R5, shown in Scheme 9, were carried out using commercially available substrates based on procedures described in the literature with modifications developed by the authors of the invention. Unless otherwise written, the reactions described used commercially available solvents and paid no attention to the presence of oxygen and/or moisture. Reaction R1

In the R1 step (Scheme 9), the synthesis of an epoxide with the general formula BX is carried out. For this purpose, a ketone of the general formula AX and a trimethyl sulfonyl salt, preferably either trimethyl sulfonyl bromide (Me ₃ SBr) or iodide (Me ₃ SI), are used. The transformation is carried out in an organic solvent, preferably acetonitrile (MeCN) or another organic solvent, using a stoichiometric amount of the sulfonium salt and using a metal hydroxide, preferably potassium hydroxide (KOH). The reaction mixture is carried out at an elevated temperature, preferably 60 °C for 2 to 16 hours. The product is separated by filtration from the reaction mixture and distillation of the solvent

Embodiment of R1

Scheme 10. Synthesis of the epoxide

Into a reaction vessel equipped with a stirring element, 2-acetylthiophene (7.01 g, 6.00 mL, 55.0 mmol, 1.0 equiv.), MeiSI (14.9 g, 71.5 mmol, 1.3 equiv.), KOH (9.44 g, 0.14 mmol, 2.6 equiv.), distilled water (0.25 mL) and MeCN (55 mL) were placed under an argon atmosphere. The contents of the vessel were stirred for 16 hours at 60 °C. After the reaction was completed, 15 mL of diethyl ether (Et ₂ O) was added, the precipitate was filtered off and washed again with diethyl ether (40 mL), the solvent was evaporated under reduced pressure. The remaining dark pink oil was washed with diethyl ether (40 mL), the solvent was evaporated and washed with n-hexane (40 mL), the solvent was evaporated under reduced pressure to give the expected product as a yellow oil in 91% yield (6.98 g, 49.8 mmol).

¹ H NMR (400 MHz, CDCl ₃ ) 6 ppm: 7.21 (dd, j = 5.1, 1.2 Hz, 1H), 7.04 (dd, J = 3.7, 1.3 Hz, 1H), 6.96 (dd, J = 5.1, 3.6 Hz, 1H), 3.07 - 3.03 (m, 2H), 1.78 - 1.78 (m, 3H);

¹³ C NMR (101 MHz, CDCl ₃ ) 5 ppm: 145.9, 127.2, 125.0, 124.8, 58.7, 55.2, 22.2;

Reaction R2

In step R2 (Scheme 9), the synthesis of an aldehyde of the general formula CX is carried out For this purpose, an epoxide of the general formula BX and Lewis acid, preferably SiO ₂ , chloroform, ZnC ₂ or ZnBr ₂ are used. The transformation is carried out in an organic solvent preferably ethyl acetate (EtOAc), chloroform or toluene (PhMe). The reaction mixture is carried out at room temperature until full conversion of the substrate (2.5 - 48 hours). The product is purified by distillation of the solvent and then used in the next step without further purification. Embodiment of performing reaction R2

2-Methyl-2-(thiophen-2-yl)epoxide (6.6 g, 47.0 mmol, 1.0 equiv.), silicon oxide (3.76 g) and EtOAc (90 mb) were placed in a reaction vessel equipped with a stirring element The reaction was carried out for 2.5 hours at room temperature. Silicon oxide was filtered off and solvent was distilled off under reduced pressure, to give the expected product as a yellow oil in 69% yield (2.60 g, 18.5 mmol).

Alternative embodiment of performing reaction R2

2-Methyl-2-(thiophen-2-yl)epoxide (6.6 g, 47.0 mmol, 1.0 equiv.) and chloroform (60 mL) were placed in a reaction vessel equipped with a stirring element The reaction was carried out for 2 hours at room temperature. The solvent was distilled off under reduced pressure to give the expected product as a yellow oil in >99% yield (6.59 g, 47.0 mmol).

Alternative embodiment of performing reaction R2

2-Methyl-2-(benzothiophen-2-yl)epoxide (5.32 g, 28.0 mmol, 1 equiv.), zinc chloride (3.81 g, 28.0 mmol, 1 equiv.) and toluene (119 mL) were placed in a reaction vessel equipped with a stirring element The reaction was carried out for 2 hours at room temperature. The reaction mixture was filtered off on a Schott funnel, the solvent was distilled off under reduced pressure, and the crude product was sublimed under reduced pressure using a Kugelrohr glass oven, to give the expected product as a colorless solid in 97% yield (5.17 g, 27.2 mmol). Reaction R3

In step R3 (Scheme 9), the synthesis of an aldehyde with the general formula FX is carried out. For this purpose, an aldehyde of the general formula CX and an alkenyl halide, preferably chloride, a metal hydroxide, preferably NaOH, a quaternary ammonium salt, preferably tetra-N- butylammonium bromide, are used. The transformation is carried out in an organic solvent, preferably toluene. The reaction mixture is carried out at an elevated temperature, preferably 40 - 60 °C for 30 minutes to 5 hours. The product is separated by extraction from the reaction mixture. It is then dried over a drying agent, preferably sodium sulfate or magnesium sulfate, solid is filtered off, and the solvent is distilled off under reduced pressure. The product is used in the next step without additional purification.

Embodiment of performing reaction R3

Into a reaction vessel equipped with a stirring element were placed thiophene-2-ylpropanal (6.4 g, 46.0 mmol, 1.00 equiv.), 3-chloro-2-methylpropene (5.1 g, 55.0 mmol, 1.20 equiv.), potassium hydroxide (2.7 g, 69.0 mmol, 1.50 equiv.), tetrabutylammonium bromide (0.6 g, 1.8 mmol, 0.04 equiv.), toluene (60 mL) and water (3 mL). The reaction was carried out for 3 hours at 60 °C. The mixture was cooled to room temperature, 15 mL of water was added and extracted with toluene (4 x 25 mL), dried over sodium sulfate. The drying agent was filtered off and the solvent was distilled off under reduced pressure, to give the expected product as a yellow oil in 68% yield (7.3 g, 31.0 mmol,).

Table 1. The obtained aldehydes

Reaction R4

In step R4 (Scheme 9), the synthesis of an enol ether of the general formula EX is carried out. For this purpose, DX ketone and a suitable Wittig reagent, preferably chloride, a strong base, preferably potassium tert-butoxide, are used. The transformation is carried out in an anhydrous organic solvent, preferably tetrahydrofuran. The reaction mixture is carried out in the temperature range -78 °C - RT for 16 hours. Then n-heptane is added to precipitate phosphine oxide. After filtering off solids and distilling off the solvent, the product is separated by column chromatography.

Alternative embodiment of performing reaction R4

Wittig's reagent (13.2 g, 385 mmol, 1.35 equiv.), potassium tert-butoxide (20.4 g, 38.5 mmol, 1.35 equiv.) and anhydrous tetrahydrofuran (57 mL) were placed in a reaction vessel equipped with a stirring element under an argon atmosphere. The reaction was carried out for one hour at -78 °C. The mixture was then warmed to room temperature and allowed to stir vigorously for 30 minutes. The mixture was cooled again to -78 °C, after which a solution of acetylferrocene (6.50 g, 285 mmol, 1 equiv.) in anhydrous tetrahydrofuran (10 mL) was added dropwise. After 30 minutes, the mixture was warmed to room temperature and the reaction was carried out for 16 hours at this temperature. The solvent was then evaporated under reduced pressure, to the residue n-heptane (250 mL) was added, the phosphine oxide was precipitated and filtered off. The solvent was distilled off under reduced pressure, the crude product was purified by column chromatography (Al ₂ O ₃ ×5%H ₂ O) collecting fractions using eluent from 0 to 20% ethyl acetate in n-hexane. The expected product was obtained as a red-orange oil with a yield of 96% (6.98 g, 27.2 mmol). ¹ H NMR (400 MHz, CDCl ₃ ) 6 ppm: 6.22 - 6.20 (m, 0.53x1 H), 5.96 - 5.94 (m, 0.47x1 H), 4.60 - 4.56 (m, 0.47×2H), 4.25 - 4.22 (m, 0.53×2H), 4.19 - 4.16 (m, 0.47x2H), 4.16 - 4.14 (m, 0.53×2H), 4.12 (s, 0.53x5H), 4.08 (s, 0.47x5H), 3.65 (s, 0.47x3H), 3.64 (s, O.53x3H), 1.93 (d, j = 1.4 Hz, O.53×3H), 1.84 (d, j = 1.4 Hz, 0.47x3H).

¹³ C NMR (101 MHz, CDCl ₃ ) 5 ppm: 142.8, 141.5, 11.0, 109.3, 87.8, 83.6, 69.1, 68.9, 67.9, 67.7, 67.6, 64.2, 59.9, 59.8, 17.5, 12.8.

Reaction R5

In step R5 (Scheme 9), the synthesis of an aldehyde of the general formula CX is carried out For this purpose, an enol ether EX and a suitable inorganic acid, preferably hydrobromic acid, are used. The transformation is carried out in a mixture of organic solvent - water, preferably acetone - water (4 - 1 v/v). The acid is added dropwise at a temperature below -50 °C, using a dry ice-acetone cooling bath, and then the mixture is heated to 45 °C and stirred vigorously for another 2 hours until full conversion of the substrate is achieved. Next, a weak base, preferably sodium bicarbonate, is added until a pH of 8 is obtained, the product is extracted with an organic solvent, preferably methylene chloride, then dried over a drying agent, preferably sodium or magnesium sulfate. After filtering off solids and evaporating the solvent under reduced pressure, the product is obtained.

Embodiment of performing reaction R5

Into a reaction vessel equipped with a stirring element, ether (2.60 g, 10.2 mmol, 1 equiv.), acetone (12 mL) and water (3 mL) were placed. The mixture was cooled below -50 °C and HBr (48% aqueous solution, 2.30 mL, 2 equiv.) was added dropwise under an argon atmosphere. The reaction was then carried out for 2 hours at 45 °C. An aqueous solution of NaHCOi was added to the reaction mixture until a pH of 8. The product was extracted with methylene chloride, dried over magnesium sulfate, which was then filtered off. The solvent was distilled off under reduced pressure to give the expected product as a maroon oil in 93% yield (2.30 g, 9.50 mmol).

¹ H NMR (400 MHz, CDCl ₃ ) 6 ppm: 9.72 (d, j = 2.2 Hz, 1H), 4.21 - 4.19 (m, 2H), 4.16 (s, 4H), 4.12 - 4.09 (m, 2H), 3.26 (qd, J = 7.0, 2.3 Hz, 1H), 1.36 (d, J = 7.0 Hz, 3H).

¹³ C NMR (101 MHz, CDCl ₃ ) 6 ppm: 201.0, 85.0, 68.8, 68.3, 68.3, 67.1, 67.0, 45.7, 14.7. Example II

Synthesis of CAAC ligands

The following Scheme 15 illustrates the synthesis of CAAC ligands allowing the preparation of ruthenium catalysts for olefin metathesis (general formula Ru1a to Ru21a, Scheme 18), which are the subject of the present invention.

The R6 and R8 reactions shown in Scheme 15 were carried out using commercially available compounds based on procedures described in the literature with modifications developed by the authors. Unless otherwise written, the reactions described used commercially available solvents and paid no attention to the presence of oxygen and/or moisture.

In step R6 (Scheme 15), the synthesis of imine HX is carried out, for this purpose a suitable aniline and an aldehyde of the general formula FX are used, in the presence of an acid, preferably p-toluenesulfonic acid (PTSA). The reaction is carried out preferably in toluene or other organic solvent The reaction mixture is carried out at the boiling point of the solvent The product is separated by filtration through neutral AI ₂ O ₃ and distillation of the solvent The product is used in the next step without additional purification.

In step R7 (Scheme 15), the synthesis of a CAAC ligand of the general formula LX is carried out, for this purpose imine of the general formula HX from step R6 or R9 is used in the presence of an acid, preferably 4 normal hydrochloric acid in dioxane. The reactions are carried out under an argon atmosphere in anhydrous toluene at 85 °C. Chloride ions are then exchanged, preferably to tetrafluoroborate ions, and the crude product is precipitated from a mixture of organic solvents, preferably methanolidiethyl ether.

In step R8 (Scheme 15), the synthesis of imine GX is carried out, For this purpose, a suitable aniline and an aldehyde of the general formula CX are used, in the presence of Lewis acid, preferably titanium(IV) isopropanolate. The reaction is carried out in an anhydrous organic solvent, preferably in methanol or another organic solvent at a temperature in the range of 25 - 45 °C. The product is separated by precipitation and filtration through neutral Celite and distillation of the solvent The product is used in the next step without additional purification.

In step R9 (Scheme 15), the synthesis of imine HX is carried out, and for this purpose imine GX, an alkyl halide, preferably a chloride, a base, preferably n-BuLi, and an organic solvent, preferably tetrahydrofuran (THF) or another organic solvent are used. The reaction is carried out at -78 °C - RT for 10 minutes, cooled to -20 °C, the alkyl halide is added, then warmed to room temperature and the reaction is carried out for 16 hours. The product is separated by filtration through neutral Celite and distillation of the solvent The product is used in the next step without additional purification.

In a round-bottom flask equipped with a stirring element 2,4-dimethyl-2-thiophenylpent-4-enal (2.11 g, 9.00 mmol, 1.00 equiv.), aniline (1.87 g, 9.00 mmol, 1.00 equiv.) and PTSA (17 mg, 0.09 mmol, 1 mol%) dissolved in PhMe (C=0.30 M) were placed. The reaction was carried out at boiling temperature of toluene until the full conversion of the substrates (collecting water in a Dean-Stark apparatus). The solvent was evaporated under reduced pressure, the crude reaction mixture was dissolved in n-hexane, filtered through neutral alumina ( AI ₂ O ₃ , neutral, Brockman Grade I), washed with a mixture of n-hexane:ethyl acetate (98:2, v/v), and dried under reduced pressure to give imine in 44% yield (1.50 g, 3.94 mmol), which was used in the next step without further purification.

The imine from the previous step, 4 M HCI (solution in dioxane, 2.53 g, 2.46 mL, 9.83 mmol, 2.5 equiv.) and anhydrous PhMe (C=0.50 M) were placed in a round-bottom flask under an argon atmosphere. The reaction was carried out for 16 hours at 85 °C. The solvent was evaporated under reduced pressure. The crude product was dissolved in a methylene chloride water mixture, NaBF ₄ (0.86 g, 7.86 mmol, 2.0 equiv.) was added and ion exchange was carried out for 2 h. The organic fraction was collected, washed with water and dried over sodium sulfate. The product was precipitated from the MeOH: Et ₂ O mixture, to give final product as a colorless crystals in 39% yield (0.72 g, 133 mmol).

¹ H NMR (400 MHz, CDCl ₃ ): 9.62 - 9.55 (m, 1H), 8.94 (s, 1H), 7.68 - 7.62 (m, 1H), 7.56 - 7.47 (m, 3H), 7.39 - 7.31 (m, 5H), 7.29 - 7.27 (m, 1H), 7.16 - 7.07 (m, 2H), 6.71 - 6.61 (m, 1H), 3.08 = 23.3, 13.9 Hz, 2H), 2.72 = 54.9, 14.0 Hz, 2H), 2.16 (s, 3H), 1.95 (s, 3H), 1.85 (s, 3H), 1.57 - 132 (m, 5H), 1.45 (s, 4H), 1.34 (s, 5H), 1.27 (s, 4H), 1.17 (s, 5H).

¹³ C NMR (101 MHz, CDCl ₃ ): δ 184.9, 184.5, 151.0, 150.5, 142.2, 142.0, 142.0, 141.2, 132.1, 131.0, 130.7, 130.6, 129.2, 128.9, 128.6, 127.0, 126.6, 126.3, 125.5, 125.5, 123.1, 82.5, 823, 81.9,

81.9, 52.6, 52.4, 503, 49.2, 37.7, 37.1, 34.7, 34.5, 33.8, 33.7, 31.0, 30.9, 30.7, 29.4, 29.0, 28.9, 27.2,

26.6.

Embodiment of carrying out reactions R8 - R9 - R7

In a round-bottomed flask under an argon atmosphere, 2-ferrocenylpropanal (5.45 g, 22.5 mmol, 1.00 equiv.) and anhydrous methanol (150 mL) were placed, followed by the addition of titanium(IV) isopropanolate (13.3 mL, 45 mmol, 2.00 equiv.). To the reaction mixture thus prepared, 2,6-diethylaniline (4.27 mL, 25.8 mmol, 1.15 equiv.) was added dropwise. The reaction was carried out for 16 h at 45 °C. The solvent was evaporated under reduced pressure. The crude product was dissolved in n-pentane and then filtered through neutral Celite. The solvent was evaporated to give the crude product as a maroon oily liquid in 73% yield (6.15 g, 16.5 mmol).

Imine (6.36 g, 17.1 mmol, 1.00 equiv.) and anhydrous tetrahydrofuran (835 mL) were placed in a round-bottom flask — previously heated under reduced pressure — under an argon atmosphere. The mixture was then cooled to -78 °C in a dry ice - acetone cooling bath. A solution of n-BuLi (2.35 M solution in n-hexane, 8.72 mL, 20.5 mmol, 1.20 equiv.) was then added dropwise with intense stirring, followed by warming to room temperature. After one hour, the reaction mixture was cooled again to -78 °C in a dry ice-acetone cooling bath and 3-chloro-2-methylpropene (2.50 mL, 25.6 mmol, 1.50 eqn.) was added dropwise. The reaction was carried out for 16 h at room temperature. The solvent was evaporated under reduced pressure. The crude product was purified by distillation to give a maroon oily liquid in 100% yield (7.30 g, 17.1 mmol).

The imine from the previous step (7.30 g, 17.1 mmol, 1 equiv.) dissolved in anhydrous PhMe (C=500 mM) was placed in a round-bottom flask under an argon atmosphere. The mixture was cooled to -78 °C in a dry ice-acetone cooling bath. HCI solution (4 M solution in dioxane, 12.8 mL, 51.2 mmol, 3 equiv.) was then added dropwise and the reaction was carried out for 16 h at 85 °C with vigorous stirring. The solvent was evaporated under reduced pressure. The crude product was dissolved in methylene chloride (about 10 mL), a saturated aqueous solution of NaBF ₄ (3.75 g, 34.1 mmol, 2 equiv.) was added and the ion exchange was carried out for 2 h with vigorous stirring. The mixture was extracted three times with methylene chloride, dried with anhydrous magnesium sulfate and filtered through neutral Celite, after which the solvent was evaporated under reduced pressure. The product was precipitated from the DCM:Et ₂ O mixture to give red crystals in 47% yield (4.14 g, 8.05 mmol).

Table 2. Summary of CAAC ligands obtained according to the general procedure from Example III.

Scheme 18. Synthesis of the complexes Ru1a- Ru21a

Example III

Synthesis of the complexes Ru1a - Ru20a by using CAAC ligands

Embodiment of the invention

Under an argon atmosphere, the CAACxBFt ligand (430 mg, 916 pmol, 2.20 equiv.), first- generation Hoveyda-Grubbs complex (250 mg, 416 pmol, 1.00 equiv.), and anhydrous THF (C _CAAC =0.1 M) were placed in a heated Schlenk vessel and stirred for 1 min. UHMDS (153 mg, 916 pmol, 2.20 equiv.) was then added and stirred until full conversion was achieved (20 min). The crude mixture was filtered through neutral alumina (AI ₂ O ₃ , neutral, Brockman Grade I) with methylene chloride as eluent The green fraction was collected and evaporated under reduced pressure. A small amount of n-pentane was then added and the mixture was placed in an ultrasonic bath. The product was filtered off and washed with cold n-pentane. The process was repeated twice and then three times using diethyl ether. After drying under vacuum, a green crystalline solid was obtained in 91% yield (267 mg, 380 pmol).

Using the method presented in Example III, a series of complexes from Ru1a to Ru21a were obtained, the structures of which are shown below.

All complexes in the table below were characterized by nuclear magnetic resonance spectroscopy. Table 3 summarizes the benzylidene proton shifts of each complex in the ¹ H NMR spectrum in a given solvent

Table 3. Summary of the obtained structures of the ruthenium complexes according to Example IV general procedure and the shifts of their benzylidene proton in the ¹ H NMR spectrum.

Example V

Study of the activity of complexes in the ethenolysis reaction of methyl oleate

Methyl oleate was degassed by stirring for a minimum of 30 minutes under reduced pressure (oil pump). During this time, a closed Schlenk vessel was prepared and weighed to obtain tare. The oil was then filtered through a syringe filter into the Schlenk vessel and the vessel was weighed together with the oil, thus obtaining the weight of the oil. The vessel with the substrate was subjected to reduced pressure. In a separate vessel, a catalyst solution (~3 mg in 2 mL of degassed toluene) was prepared. A preheated glass insert for the Amar reactor equipped with a stirring element was placed in the Amar reactor immersed in a preheated oil bath. The reactor was closed and the gas inside was evacuated using an oil pump. A portion of the catalyst (10 ppm or 3 ppm or 500 ppb) was added to the Schlenk vessel containing the oil and the mixture was immediately transferred into the reactor using a Teflon tube. The reactor was filled with ethylene to a dynamic pressure of 10 bar, then stirring was started and the reaction was run for 3 hours or 6 hours. The glovebox and inert gas atmosphere (argon) were not used during the reaction.

After that time, pressure was normalized and the autoclave was disassembled. SnatchCat metal scavenger (scavenger) solution was immediately added and the contents of the vessel were stirred for several minutes. A sample was then taken and, after dilution with toluene, subjected to GC analysis.

The results of the model reaction are shown in Table 2.

Table 4. Comparison of the selectivity of the new ruthenium complexes and ruthenium complexes known from the literature in the process of ethenolysis

Example 1: ethylene 99.9%, <30 min, 40 °C, pressure of 10 bar

Example 2: 4 hours, 40 °C, pressure of 10 bar

Examples 3 and 4: ethylene 99.95%, 3 hours, 40 °C, pressure of 10 bar

Examples 5 and 6: ethylene , 99.99%, 4 hours, 40 °C, pressure of 10 bar

Examples 7 - 17: reactions for 10 ppm: ethylene 99.95%, 3 hours, 40 °C; reactions for 3 ppm: ethylene 99.95%, 3 - 6 hours, 40 °C; reactions for 0.5 ppm: ethylene 99.995%, 6 hours, 40 °C (ethylene pressure of 10 bar) ¹ Grubbs et al. Organometallic 2008, 27, 563-566.

¹ Zhang et al. Chem. Commun., 2013, 49, 9491-9493.

³ Bertrandt et al. Angew. Chem. Int Ed., 2015, 54, 1919-1923.

⁴ Gawin et al. Angew. Chem. Int Ed. 2017, 56, 981-986.

Example VI

Testing the activity of the ruthenium complex in the ethenolysis reaction of methyl oleate outside the glovebox under conditions that do not require an inert gas protective atmosphere (Fig. 3). Fig. 3 shows A) the autoclave assembled in air, B) the open autoclave before the ethenolysis reaction.

The corresponding ethenolysis reactions described in Example V were performed outside the glovebox in an autoclave apparatus placed under the fume hood and located in the air - the reaction system shown in Fig. 3. Subsequent reaction steps were performed in the air without an inert gas protective atmosphere. Ethylene of different purities was used during the reaction, with the purity of ethylene being lower than that described in previous literature reports. Using the new ruthenium complexes Ru1a - Ru22a was observed to be resistant to the use of lower quality ethylene, which did not impair the reaction results as determined by TON and selectivity.

Example VII

Synthesis of a CAAC ligand and a spiro carbon catalyst

Scheme 20. Synthesis of ligand and catalyst with spiro carbon. Synthesis of compound I

Aluminium(lll) chloride (14.3 g, 105 mmol, 1.00 equiv.) and anhydrous DCM (100 mL) were placed under an argon atmosphere in a three-neck flask equipped with a stirring element and the suspension was cooled to -40 °C. In a two-neck flask under an argon atmosphere equipped with a stirring element ferrocene (20.0 g, 105 mmol, 1.00 equiv.) was dissolved in anhydrous DCM (155 mL) and added dropwise into the aluminum(lll) chloride suspension in DCM at -40 °C with stirring. The mixture was then cooled to -78 °C and acryloyl chloride (9.81 mL, 116 mmol,

1.10 equiv.) was added dropwise for 30 min at -78 °C. The reaction was carried out for 18 hours at -78 °C, then the contents of the flask were poured into water at 0 °C. The organic layer was separated, washed with brine, dried over MgSO* the drying agent was filtered through neutral Celite and the solvent was evaporated. The crude product was purified by column chromatography (AI ₂ O ₃ × 5% H ₂ O) to give the product as an orange solid (7.99 g, 33.3 mmol, 31%).

¹ H NMR (400 MHz, CDCl ₃ ): δ 4.87 - 4.79 (m, 2H), 4.66 - 4.56 (m, 2H), 4.43 - 4.30 (m, 2H),

4.10 - 3.94 (m, 2H), 3.06 - 2.86 (m, 4H).

¹³ C NMR (101 MHz, CDCl ₃ ): δ 212.0, 88.2, 74.1, 72.8, 71.2, 70.4, 69.4, 44.3, 31.9.

Synthesis of compound II

Ketone I (1.16 g, 4.83 mmol, 1.0 equiv.), MeiSBr (0.98 g, 6.28 mmol, 1.3 equiv.), KOH (0.70 g, 12.6 mmol, 2.6 equiv.), distilled water (0.25 mL), and MeCN (10 mL) were placed in a reaction vessel equipped with a stirring element under an argon atmosphere. The contents of the vessel were stirred for 16 h at 60 °C. After completion of the reaction, 5 mL of diethyl ether (Et ₂ O) was added, the precipitate was filtered off ,and the precipitate was washed again with diethyl ether (10 mL), the solvent was evaporated under reduced pressure. The residue was washed with diethyl ether (10 mL), the solvent evaporated and washed with n-hexane (10 mL), the solvent evaporated under reduced pressure to give the product as an orange solid (1.02 g, 4.01 mmol, 83%).

¹ H NMR (400 MHz, CDCl ₃ ): δ 4.44 - 4.35 (m, 1H), 4.25 - 4.22 (m, 1H), 4.19 - 4.16 (m, 2H),

4.10 - 4.04 (m, 4H), 2.95 (d, J = 5.5 Hz, 1H), 2.90 (dd, J = 0.6, 5.4 Hz, 1H), 2.33 - 2.16 (m, 3H), 2.09 - 1.99 (m, 1H).

¹³ C NMR (101 MHz, CDCl ₃ ): δ 86.6, 81.8, 70.9, 69.1, 68.9, 68.8, 68.7, 68.5, 68.4, 67.7, 56.4, 55.0, 42.5, 22.9.

Synthesis of compound III

Epoxide II (0.94 g, 3.68 mmol, 1 equiv.), zinc(ll) chloride (0.50 g, 3.68 mmol, 1 equiv.) and toluene (16 mL) were placed in a reaction vessel equipped with a stirring element The reaction was carried out for 2 hours at room temperature. The reaction mixture was filtered off on a Schott funnel, the solvent was distilled off under reduced pressure to give the product as a bright orange solid (0.77 g, 3.04 mmol, 82%).

¹ H NMR (400 MHz, CDCl ₃ ): δ 9.82 (d, j = 1.5 Hz, 1H), 4.22 - 4.19 (m, 1H), 4.18 - 4.15 (m, 1H), 4.14 - 4.11 (m, 3H), 4.10 - 4.07 (m, 1H), 4.06 - 4.01 (m, 2H), 2.82 - 2.74 (m, 1H), 2.54 - 2.39 (m, 2H), 2.05 - 1.93 (m, 1H), 1.86 - 1.72 (m, 1H).

¹³ C NMR (101 MHz, CDCl ₃ ): δ 201.4, 86.4, 81.4, 71.5, 71.4, 70.0, 69.8, 68.9, 68.1, 68.0, 67.3, 50.4, 35.8, 23.9.

Synthesis of compound IV

In a round-bottom flask — previously heated under reduced pressure — under an argon atmosphere, aldehyde III (0.7 g, 2.76 mmol, 1.0 equiv.), 2-ethyl-6-methylaniline (0.38 g, 2.76 mmol, 1.0 equiv.), 4A molecular sieves (0.7 g), and methylene chloride (5.5 mL) were placed. The reaction was carried out for 16 h at room temperature. The molecular sieves were filtered off, the solvent was evaporated under reduced pressure to give the product as an orange solid. (0.56 g, 1.49 mmol, 54%).

¹ H NMR (400 MHz, CD ₂ Ch): δ 7.75 (d, j = 4.7 Hz, 1H), 7.05 - 6.96 (m, 2H), 6.91 (t, J = 7.5 Hz, 1H), 4.22 - 4.18 (m, 1H), 4.16 - 4.12 (m, 2H), 4.13 - 4.05 (m, 4H), 4.06 - 4.00 (m, 1H), 3.08 - 2.94 (m, 1H), 2.57 - 2.47 (m, 2H), 2.43 (q, J = 7.5 Hz, 2H), 2.30 - 2.16 (m, 1H), 2.04 (s, 3H), 2.01 - 1.90 (m, 1H), 1.08 (t, j = 7.5 Hz, 3H).

¹³ C NMR (101 MHz, CD ₂ Ch): δ 169.2, 151.0, 133.5, 128.2, 127.0, 126.6, 123.7, 86.9, 85.2, 71.6, 71.0, 69.6, 68.5, 68.2, 68.1, 67.2, 43.9, 39.2, 24.9, 24.4, 18.5, 14.9.

Synthesis of compound V

Imine IV (0.55 g, 1.47 mmol, 1.00 equiv.) and anhydrous tetrahydrofuran (3.0 mL) were placed in a round-bottom flask — previously heated under reduced pressure — under an argon atmosphere. The mixture was then cooled to -78 °C in a dry ice - acetone cooling bath. A solution of n-BuLi (2.30 M solution in n-hexane, 0.77 mL, 1.76 mmol, 1.20 equiv.) was then added dropwise with intense stirring, followed by heating to room temperature. After one hour, the reaction mixture was cooled again to -78 °C in a dry ice - acetone cooling bath and 3-chloro-2-methylpropene (0.22 mL, 2.2 mmol, 1.50 equiv.) was added dropwise. The reaction was carried out for 16 h at room temperature. The solvent was evaporated under reduced pressure. The crude product was filtered through a syringe filter to give the product as a red oil.(0.51 g, 1.19 mmol, 80%).

¹ H NMR (400 MHz, CDCl ₃ ): δ 7.84 (s, 1H), 7.10 - 7.03 (m, 1H), 7.06 - 6.99 (m, 1H), 7.00 - 6.92 (m, 1H), 4.85 - 4.80 (m, 1H), 4.80 - 4.75 (m, 1H), 4.25 - 4.18 (m, 2H), 4.16 - 4.11 (m, 3H), 4.11 - 4.05 (m, 1H), 4.08 - 4.03 (m, 2H), 2.76 (d, J = 14.5 Hz, 1H), 2.70 - 2.64 (m, 1H), 2.58 (d, J = 14.5 Hz, 1H), 2.5 1 (qd, J = 1.6, 7.5 Hz, 2H), 2.43 - 2.32 (m, 2H), 2.24 - 2.19 (m, 1H), 2.15 (s, 3H), 1.69 (s, 3H), 1.16 (t J = 7.5 Hz, 3H).

¹³ C NMR (101 MHz, CDCl ₃ ): δ 171.3, 150.4, 142.0, 133.3, 128.2, 127.0, 126.3, 123.7, 115.3, 89.6, 87.4, 68.8, 68.8, 683, 68.5, 68.4, 68.4, 67.7, 67.7, 46.2, 42.9, 29.8, 25.1, 24.6, 20.6, 19.1, 14.9.

Synthesis of compound L22

The imine from the previous step (0.49 g, 1.15 mmol, 1 equiv.) dissolved in anhydrous PhMe (C=500 mH) was placed in a round-bottom flask under an argon atmosphere. The mixture was cooled to -78 °C in a dry ice - acetone cooling bath. HCI solution (0.7 mL, 4 M solution in dioxane, 2.88 mmol, 2.5 equiv.) was then added dropwise and the reaction was carried out for 16 h at 85 °C with vigorous stirring. The solvent was evaporated under reduced pressure. The crude product was dissolved in methylene chloride (about 5 mL), a saturated aqueous solution of NaBF« (0.25 g, 2.30 mmol, 2 equiv.) was added and the ion exchange was carried out for 2 h with vigorous stirring. The mixture was extracted three times with methylene chloride, dried with anhydrous magnesium sulfate and filtered through neutral Celite, after which the solvent was evaporated under reduced pressure. The product was precipitated from the DCM:Et ₂ O mixture to give the product as a light brown solid (0.27 g, 0.53 mmol, 45%).

Synthesis of compound Ru22a

Under an argon atmosphere, the CAAC×BF ₄ ligand L22 (174 mg, 340 pmol, 1.20 equiv.), the first-generation Hoveyda-Grubbs complex (170 mg, 283 pmol, 1.00 equiv.) and anhydrous THF (C _CAAC =0.1 M) were placed in a preheated Schlenk flask and stirred for 1 min. LiHMDS (56 mg, 340 pmol, 1.20 equiv.) was then added and stirred until full conversion was achieved (5 min). After this time, copper(l) chloride (56 mg, 566 pmol, 2.00 equiv.) was added. The crude mixture was filtered through neutral alumina (AI ₂ O ₃ , neutral, Brockman Grade I) with methylene chloride as eluent The green fraction was collected and the solvent was evaporated under reduced pressure. A small amount of n-pentane was then added and the mixture was placed in an ultrasonic bath. The product was drained and washed with cold n-pentane. The process was repeated twice and then using diethyl ether. After drying under vacuum, a green crystalline solid was obtained (164 mg, 220 pmol, 77%).