Catalytic Properties of Zirconocene-Based Systems in 1-Hexene Oligomerization and Structure of Metal Hydride Reaction Centers

Despite large-scale investigations of homogeneous single-site metallocene catalysts and systems based on them, there are still unsolved problems related to the control of their activity and chemo- and stereoselectivity. A solution to these problems is required to develop efficient methods for the synthesis of practically useful products of alkene transformations, such as dimers, oligomers, and polymers. Here we studied the catalytic activity of structurally diverse zirconocenes (L2ZrCl2, L = Cp, C5Me5, Ind, L2 = Me2CCp2, Me2SiCp2, Me2C2Cp2, rac-Me2CInd2, rac-H4C2Ind2, BIPh(Ind)2, H4C2[THInd]2), and co-catalysts activating the system, namely HAlBui2, MMAO-12, and (Ph3C)[B(C6F5)4], at low activator/Zr ratios in a 1-hexene oligomerization reaction. The influence of catalyst structure and system composition on the alkene conversion, the type of products, and the reaction stereoselectivity were investigated. The composition of hydride intermediates formed in the L2ZrCl2–HAlBui2–activator system (L2 = ansa-Me2CCp2, Ind) was studied by NMR spectroscopy. Participation of the bis-zirconium hydride complex as the precursor of catalytically active sites of the alkene dimerization reaction was shown.


Introduction
Catalytic systems based on metallocenes, organoaluminum compounds (OACs), and activators are well known and have been studied for almost 70 years [1]. A large amount of research is related to the possibility of the efficient synthesis of practically important products: alkene dimers and oligomers, as well as polymers widely known as polyalphaolefins (PAO) [2][3][4][5][6][7]. The use of metallocene complexes in these reactions made it possible to transfer the classical Ziegler-Natta catalysis from a heterogeneous to a homogeneous medium. Hence, highly active and stereoselective single-site catalysts for the polymerization of unsaturated compounds became more controllable, and a detailed study of the reaction mechanism became possible. The high activity and chemo-and stereoselectivity of metallocene complexes are due to their structural features. They provide the most efficient stabilization of the electronic and steric environment of transition metal atoms owing to the high energy of metal-ligand bonds and allow variation of the electrophilicity and geometry of catalytically active sites due to broad possibilities of π-ligand modification. It has been shown that the electronic and steric features of the ligand, the nature of the activator, and the reaction conditions [8][9][10][11][12][13][14][15] determine the productivity and selectivity of catalytic systems.
Our interest in the structural features and reactivity of group 4B metal hydrides is due to the recent data on the alkene transformation reactions catalyzed by zirconocene dichloride Cp 2 ZrCl 2 or zirconocene dihydride [Cp 2 ZrH 2 ] 2 and OACs in the presence of aluminum-or boron-containing activators [32][33][34][35]. The formation of the bimetallic Zr,Zr-hydride intermediate in these systems was established, and its ability to serve as the precursor of the specific and selective catalytically active sites for alkene dimerization was demonstrated.
The present work is aimed at the study of the catalytic activity of structurally diverse zirconocenes (10 examples of cyclopentadienyl and indenyl complexes) in the presence of activators, namely HAlBu i 2 , MMAO-12, and (Ph 3 C)[B(C 6 F 5 ) 4 ], at low activator/Zr ratios in 1-hexene oligomerization. The influence of catalyst structure and system composition on the alkene conversion and reaction chemo-and stereoselectivity was investigated. The structure of hydride intermediates formed in the L 2 ZrCl 2 -HAlBu i 2 -activator system (L 2 = ansa-Me 2 CCp 2 , Ind) was studied by means of NMR spectroscopy.

Catalytic Effect of L 2 ZrCl 2 -HAlBu i 2 -Activator Systems in 1-Hexene Oligomerization
We studied the catalytic effect of complexes 1a-j in the oligomerization reaction in the presence of HAlBu i 2 and the activators MMAO-12 (modified methylaluminoxane) and [Ph 3 C][B(C 6 F 5 ) 4 ]. We used di(isobutyl)alane HAlBu i 2 as a co-catalyst similar to AlBu i 3 [6,7,[26][27][28]30] to initiate the formation of zirconocene hydrides, which act as catalytically active sites in these reactions [29,30,[33][34][35]. The reactant ratios were chosen on the basis of our earlier studies [33][34][35]. During the reaction under the selected conditions, the conversion of 1-hexene was approximately 99% in 1-3 h in most of the experiments. A decrease in the alkene conversion down to 85% was observed in the reaction catalyzed by complex 1e in the presence of MMAO-12. 1-Hexene dimer (5) and various oligomers (6) were formed as the major reaction products, which attests to predominant chain termination via β-H elimination mechanism [36] (Scheme 1, Figures S1 and S2). The presence of oligomers with various double bond positions may be due to the migration of zirconium cation upon the formation of allyl complexes [28,37]. Small amounts of M-C bonded oligomers 4 were generally observed in systems containing MMAO-12. In the same systems, oligomers with a methyl starting group were found. It should be noted that the application of other OACs (AlBu i 3 , AlEt 3 , or AlMe 3 ) in the reaction provided the identical nature of the dimerization and oligomerization products (see, for example, Refs. [26][27][28]31,33,34]). The origin of hydride intermediates in these systems is a result of the β-H elimination process in isobutyl and ethyl groups, as well as in branched alkyl chains bonded with Zr atoms [36].
It was shown that in the system based on zirconocene dichloride and [  4 ] concentration in the range of 0.3-1 equiv. resulted in a higher proportion of heavier oligomers with n = 1-5. Simultaneously, the selectivity of the reaction decreased, as follows from the GC-MS and NMR spectra of the products, representing a mixture of stereoisomers and isomers differing in the double bond position. The 13 C NMR spectra of the oligomers formed under these conditions exhibited signals for the internal double bond at δ C 124-131 ppm. When the reaction was carried out at the [Zr]:[B] ratio of 1:2, alkylation products, hexylsubstituted toluenes, were formed as the major products. An increase in the relative content of zirconocene and HAlBu i 2 provided the formation of heavier products with bimodal distribution (Mw 5571 and 1578 Da), along with dimers and light oligomers ( In the presence of MMAO-12, this system showed higher activity and selectivity to dimers (entry 5) [31]. decreased, as follows from the GC-MS and NMR spectra of the products, representing a mixture of stereoisomers and isomers differing in the double bond position. The 13 C NMR spectra of the oligomers formed under these conditions exhibited signals for the internal double bond at δC 124-131 ppm. When the reaction was carried out at the [Zr]:[B] ratio of 1:2, alkylation products, hexyl-substituted toluenes, were formed as the major products. An increase in the relative content of zirconocene and HAlBu i 2 provided the formation of heavier products with bimodal distribution (Mw 5571 and 1578 Da), along with dimers and light oligomers ( Table 1, entry 4). In the presence of MMAO-12, this system showed higher activity and selectivity to dimers (entry 5) [31]. In the presence of complexes 1c and 1e with hydrocarbon-bridged cyclopentadienyl ligands, dimer 5 was formed in >94% yield (entries 8, 10, and 14). The activity and chemoselectivity of complex 1e appeared to be higher with activator [Ph3C][B(C6F5)4] (98% dimer) compared to MMAO-12 (78% dimer) (entry 15).
Significant differences in the action of activators were also found when the reaction was carried out in the presence of Me2Si-bound complex 1d (entries 12,13). For example, the use of MMAO-12 promoted the formation of dimerization product 5 in up to 80% yield, whereas the application of [Ph3C][B(C6F5)4] resulted in the predominant formation of atactic oligomers 6, including heavy oligomers with Mw 6130.
Carrying out the reaction in the presence of bulky pentamethylcyclopentadienyl complex 1b gave mainly oligomer 6, whose mass distribution depended on the type of activator used (entries 6, 7). Under the action of [Ph3C][B(C6F5)4], short-chain oligomers with vinylidene end groups were formed predominantly ( 13 C NMR data). The heavy fraction obtained in the presence of MMAO-12 contained oligomers with a bimodal distribution (Mw 5605 and 861 Da). Moreover, the number of heavy oligomers was much higher in this case than in the experiment with sterically non-hindered Cp2ZrCl2. This indicates a significant predominance of the chain propagation rate over the chain termination rate under these conditions, which may be due to the steric hindrance of the catalytically active sites preventing β-H elimination or chain transfer to the monomer or OAC. Apparently, the steric hindrance is generated by not only the pentamethylsubstituted ligand on Zr but also the bulky methylaluminoxane counterion. In the presence of complexes 1c and 1e with hydrocarbon-bridged cyclopentadienyl ligands, dimer 5 was formed in >94% yield (entries 8, 10, and 14). The activity and chemoselectivity of complex 1e appeared to be higher with activator [Ph 3 C][B(C 6 F 5 ) 4 ] (98% dimer) compared to MMAO-12 (78% dimer) (entry 15).
Significant differences in the action of activators were also found when the reaction was carried out in the presence of Me 2 Si-bound complex 1d (entries 12,13). For example, the use of MMAO-12 promoted the formation of dimerization product 5 in up to 80% yield, whereas the application of [Ph 3 C][B(C 6 F 5 ) 4 ] resulted in the predominant formation of atactic oligomers 6, including heavy oligomers with Mw 6130.
Carrying out the reaction in the presence of bulky pentamethylcyclopentadienyl complex 1b gave mainly oligomer 6, whose mass distribution depended on the type of activator used (entries 6, 7). Under the action of [Ph 3 C][B(C 6 F 5 ) 4 ], short-chain oligomers with vinylidene end groups were formed predominantly ( 13 C NMR data). The heavy fraction obtained in the presence of MMAO-12 contained oligomers with a bimodal distribution (M w 5605 and 861 Da). Moreover, the number of heavy oligomers was much higher in this case than in the experiment with sterically non-hindered Cp 2 ZrCl 2 . This indicates a significant predominance of the chain propagation rate over the chain termination rate under these conditions, which may be due to the steric hindrance of the catalytically active sites preventing β-H elimination or chain transfer to the monomer or OAC. Apparently, the steric hindrance is generated by not only the pentamethyl-substituted ligand on Zr but also the bulky methylaluminoxane counterion.
The appearance of indeneyl ligands (1f), in particular bridged ligands (1g-j), in the complexes also led to an increased yield of oligomeric products, both for MMAO-12 and for [Ph 3 C][B(C 6 F 5 ) 4 ] (entries [16][17][18][19][20][21][22][23][24][25][26][27][28][29][30][31][32][33]. The reaction catalyzed by Me 2 CInd 2 ZrCl 2 (1g) mainly afforded dimers and light oligomers with n = 1-4 (entries [23][24][25]. Heavy oligomers were formed in the system based on rac-H 4 C 2 Ind 2 ZrCl 2 (1h) and [Ph 3 C][B(C 6 F 5 ) 4 ] or MMAO-12 activator (entries 26,27). Hydrogenation of the ligand benzene rings in complex 1h and the transition to 1j resulted in a considerable decrease in the catalytic system activity: an alkene conversion at the 90-99% level was achieved in 3 h (entries [31][32][33]. Moreover, the oligomeric products obtained in these experiments had, as a rule, a multimodal distribution. a Monoalkyl-substituted toluene (77%), dialkyl-substituted toluene (19%), and trialkyl-substituted toluene (4%) were detected; b tetramers, that is, "dimer of dimers" (15%), were formed in the presence of both activators; c the yield of oligomers with n = 6 were up to 7%; d Me starting group; e reaction was carried out in an NMR tube at 20 For the isolated higher hexene oligomers, the isotacticity in mmmm% was determined using 13 C NMR spectroscopy [37][38][39][40]. The highest stereoselectivity was found for zirconocenes with indenyl ligands. For example, complexes 1f, 1g, and 1h showed isotacticities of 67, 93, and 71% mmmm, respectively (Table 1, entries 20, 23, and 26) ( Figures S3 and S4). The stereoselectivity of the catalytic systems based on zirconocenes 1i and 1j was below 58% mmmm. It is noteworthy that the stereoselectivity of this reaction depended on the nature of the activator used. Under the action of complex 1f, an oligomer with isotacticity of 67% was obtained in the presence of MMAO-12, while [Ph 3 C][B(C 6 F 5 ) 4 ] furnished an atactic product. The opposite trend was observed for complex 1g with bound ligands: the highest stereoselectivity was attained in the presence of [Ph 3 C][B(C 6 F 5 ) 4 ]. The complex H 4 C 2 Ind 2 ZrCl 2 (1h) provides the formation of isotactic oligohexenes (61-71% mmmm) regardless of the activator type. For complexes 1i and 1j, some increase in the stereoselectivity was found in the presence of MMAO-12. The observed dependence indicates a fine-tuning of the catalytically active sites in the homogeneous Ziegler-Natta type systems. Probably, the stereocontrol may be provided by not only the ligand on the transition metal atom (site control) or the growing chain (chain control) but also the activator occurring as a part of the active site and determining its structure and dynamics on an equal basis with other factors. As stated earlier [12], the complete separation of the cation-anion pair may increase the activity of the system but may lead to the loss of stereoselectivity. Strong cation-anion interactions could minimize the epimerization of the last inserted unit and thus increase the stereoselectivity, but at the same time, they cause a decrease in the activity by hampering the monomer insertion.
Thus, it was shown that the dimerization pathway is implemented with the participation of Zr complexes with sterically non-hindered cyclopentadienyl ligands (L = Cp, ansa-Me 2 CCp 2 , ansa-(Me 2 C) 2 Cp 2 , and ansa-Me 2 SiCp 2 ), whereas the oligomerization is determined by the action of complexes with bulky cyclopentadienyl (L = C 5 Me 5 , rac-H 4 C 2 [THInd] 2 ) or electron-withdrawing indenyl (L = Ind, Me 2 CInd 2 , H 4 C 2 Ind 2 , BIPh(Ind) 2 ) ligands. The difference between the behaviors of the complexes is primarily determined by the composition and reactivity of the intermediates. It was assumed that hydride bimetallic intermediates may act as the active sites of dimerization and oligomerization reactions [29,30,[33][34][35]. Our previous NMR study of the reaction of Cp 2 ZrCl 2 or [Cp 2 ZrH 2 ] 2 with OACs showed the existence of Zr,Zr-hydride complexes, which are activated by MMAO-12 or organoboron compound ([Ph 3 C][B(C 6 F 5 ) 4 ] or B(C 6 F 5 ) 3 ), being thus converted to active species responsible for dimer formation [32][33][34][35].  (Figures S5 and S6, Table 2). The H 1 :H Cp :H Cp ratio of signal intensities was 1:2:2. The NOESY spectrum exhibited opposite phase cross-peaks of these protons with Cp ring signals at δ H 6.11 and 5.19 ppm, and a signal for the methyl group of the isopropylidene bridge at δ H 1.03 ppm ( Figure S7). At 298 K, the hydride signals were significantly broadened, and peaks corresponding to the chemical exchange between H 1 , H 2 , and HAlBu i 2 monomers and oligomers appeared in the NOESY spectra ( Figure S8). Considering these results and literature data for similar molecules with other π-ligands [41][42][43][44], we assigned the observed signals to the trihydride complex 8c as the most probable structure (Scheme 2, Table 2). Moreover, the C 2v symmetry of the complex was also in line with the observed NMR pattern. , the spectrum exhibited highfield signals at δ H −1.10 (H 1 ) and −0.81 (H 2 ) ppm, correlated with each other in the COSY HH spectrum, in addition to the signals of unreacted complex 1c (Figures S9 and S10). The low-field region of the spectrum contained signals of four non-equivalent protons of the cyclopentadienyl ligand at δ H 6.28, 6.23, 5.66, and 5.37 ppm. The observed decrease in the symmetry of the structure, the H 1 :H 2 :H Cp :H Cp :H Cp :H Cp intensity ratio of 1:1:2:2:2, and literature data [42,44] make it possible to identify the structure as 9c. Additionally, the 1 H NMR spectrum showed a low-intensity triplet at δ H −3.58 ppm, which was correlated with a doublet at δ H −1.34 ppm in the COSY HH spectra ( Figure S10). The spin-spin coupling constants 2 J = 17.9 Hz for these signals are typical of the bis-zirconium structures [Cp 2 ZrH 2 ·Cp 2 ZrHCl·ClAlR 2 ], which we detected earlier [32][33][34][35]. Therefore, these resonance lines were attributed to complex 10c.
The addition of MMAO-12 to the mixture obtained in the reaction of Me 2 CCp 2 ZrCl 2 and HAlBu i 2 in a ratio of 1:(3-8) and containing the trihydride intermediate 8c induced broadening of both hydride signals and cyclopentadienyl ring signals of complex 8c (Figures 1 and S13), which may indicate its association with methylaluminoxane. According to theoretical data, zirconium hydride complexes have a high affinity for this activator and are able to produce stable adducts [45]. In addition, it is known that methy-laluminoxane tends to absorb hydrides, which exchange with methyl groups to provide H-substituted MAO (methylaluminoxane) [46]. This was also confirmed in our study. The NOESY spectra of a mixture of MMAO-12 and HAlBu i 2 showed a negative effect for methyl groups (−0.14 ppm), isobutyl groups (0.56 and 1.29 ppm), and H-Al(MAO) (3.26-4.11 ppm) ( Figures S11 and S12), indicating that these groups belong to the macromolecule. It also follows from the NOESY spectra that the association of 8c with MAO preserves the possibility of hydride exchange with H-Al(MAO) ( Figure S14). zirconocenes with HAlBu i 2 largely depends on the starting reactant ratio. For example, the 1 H NMR spectrum of the mixture of 1c and HAlBu i 2 taken in the molar ratio [Zr]:[Al] = 1:3 showed hydride signals at δH −1.44 (H 1 ) and 1.29-1.43 ppm (H 2 ). These signals were correlated with each other in the COSY HH experiment (at 250 K) ( Figure S5 and Figure  S6, Table 2). The H 1 :H Cp :H Cp ratio of signal intensities was 1:2:2. The NOESY spectrum exhibited opposite phase cross-peaks of these protons with Cp ring signals at δH 6.11 and 5.19 ppm, and a signal for the methyl group of the isopropylidene bridge at δH 1.03 ppm ( Figure S7). At 298 K, the hydride signals were significantly broadened, and peaks corresponding to the chemical exchange between H 1 , H 2 , and HAlBu i 2 monomers and oligomers appeared in the NOESY spectra ( Figure S8). Considering these results and literature data for similar molecules with other π-ligands [41,42,43,44], we assigned the observed signals to the trihydride complex 8c as the most probable structure (Scheme 2, Table 2). Moreover, the C2v symmetry of the complex was also in line with the observed NMR pattern.  Figure S9 and Figure S10). The low-field region of the spectrum contained signals of four non-equivalent protons of the cyclopentadienyl ligand at δH 6.28, 6.23, 5.66, and 5.37 ppm. The observed decrease in the symmetry of the structure, the H 1 :H 2 :H Cp :H Cp :H Cp :H Cp intensity ratio of 1:1:2:2:2, and literature data [42,44] make it possible to identify the structure as 9c. Additionally, the 1 H NMR spectrum showed a low-intensity triplet at δH −3.58 ppm, which was correlated with a doublet at δH −1.34 ppm in the COSY HH spectra ( Figure S10). The spin-spin coupling constants 2 J = 17.9 Hz for these signals are typical of the bis-zirconium  (Figure 1 and Figure S13), which may indicate its association with methylaluminoxane. According to theoretical data, zirconium hydride complexes have a high affinity for this activator and are able to produce stable adducts [45]. In addition, it is known that methylaluminoxane tends to absorb hydrides, which exchange with methyl groups to provide H-substituted MAO (methylaluminoxane) [46]. This was also confirmed in our study. The NOESY spectra of a mixture of MMAO-12 and HAlBu i 2 showed a negative effect for methyl groups (−0.14 ppm), isobutyl groups (0.56 and 1.29 ppm), and H-Al(MAO) (3.26-4.11 ppm) ( Figure S11 and Figure S12), indicating that these groups belong to the macromolecule. It also follows from the NOESY spectra that the association of 8c with MAO preserves the possibility of hydride exchange with H-Al(MAO) ( Figure  S14). Under conditions of HAlBu i 2 deficiency, when complexes 9c and 10c existed in the catalytic system, the addition of MMAO-12 was accompanied by the appearance of a heavy fraction and by doubling of the triplet at δH −3.58 ppm belonging to 10c, whereas the signals of complex 9c remained virtually unchanged ( Figure S15 and Figure S16). The  Under conditions of HAlBu i 2 deficiency, when complexes 9c and 10c existed in the catalytic system, the addition of MMAO-12 was accompanied by the appearance of a heavy fraction and by doubling of the triplet at δ H −3.58 ppm belonging to 10c, whereas the signals of complex 9c remained virtually unchanged (Figures S15 and S16). The negative NOE indicated an increase in the molecular weight of the complex, which may be due to the formation of a stable 10c·MAO conjugate similar to the bis-cyclopentadienyl complex [33,35] (Figure S17).
The addition of [Ph 3 C][B(C 6 F 5 ) 4 ] to complex 8c formed in the Me 2 CCp 2 ZrCl 2 -HAlBu i 2 system (1:1) led to an equilibrium shift due to the reaction of HAlBu i 2 with the organoboron reagent, resulting in the recovery of the original zirconocene dichloride and the appearance of complexes 9c and 10c (Figures S18 and S19). The NMR signals of complex 9c disappeared over time.
In the reaction of Ind 2 ZrCl 2 (1f) with HAlBu i 2 , taken in a ratio of [Zr]:[Al] = 1:(3-8), complex 8f was formed [43]. The complex was characterized by the presence of broadened high-field signals of hydride atoms in the 1 H NMR spectra at room temperature, which indicated the participation of the molecule in exchange processes ( Figures S21 and S22). The addition of the ionic activator [Ph 3 C][B(C 6 F 5 ) 4 ] to 8f, obtained in the 1f-HAlBu i 2 system (1:3), provided complex 10f and initial 1f by analogy with the ansa-bis-cyclopentadienyl complex (Figures 2, S23 and S24, Table 2). Moreover, the spectra exhibited a set of indenyl proton signals at δ H 4.2-7.8 ppm and hydride atom signals at δ H −3-0 ppm, which can be tentatively assigned to the cationic hydride species. Their content increased as the concentration of HAlBu i 2 increased in the system (Figures 2 and S25).
Molecules 2023, 28, x FOR PEER REVIEW 10 of 15 the appearance of complexes 9c and 10c ( Figure S18 and Figure S19). The NMR signals of complex 9c disappeared over time.
In the reaction of Ind2ZrCl2 (1f) with HAlBu i 2, taken in a ratio of [Zr]:[Al] = 1:(3-8), complex 8f was formed [43]. The complex was characterized by the presence of broadened high-field signals of hydride atoms in the 1 H NMR spectra at room temperature, which indicated the participation of the molecule in exchange processes ( Figure S21 and Figure  S22). The addition of the ionic activator [Ph3C][B(C6F5)4] to 8f, obtained in the 1f-HAlBu i 2 system (1:3), provided complex 10f and initial 1f by analogy with the ansa-biscyclopentadienyl complex (Figure 2, Figure S23 and Figure S24, Table 2). Moreover, the spectra exhibited a set of indenyl proton signals at δH 4.2-7.8 ppm and hydride atom signals at δH −3-0 ppm, which can be tentatively assigned to the cationic hydride species. Their content increased as the concentration of HAlBu i 2 increased in the system ( Figure 2 and Figure S25). As in the case of the cyclopentadienyl complex 8c, the addition of MMAO-12 to 8f, obtained in the reaction of 1f with an excess of HAlBu i 2 (1:3), gave the associate 10f•MAO, which was characterized by hydride signals at -6.11 and 0.05 ppm in the 1 H NMR spectra ( Figure S26 and Figure S27)  Figure S25 and Figure S28). It should be noted that under conditions of a large excess of HAlBu i 2 (1:8), the complex 8f did not provide associates with methylalumoxane similar to 8c, which followed from the permanence of the shape and width of NMR spectral lines with the appearance of the activator.
To clarify the reactivity of the complexes towards the alkene, 1-hexene was added to As in the case of the cyclopentadienyl complex 8c, the addition of MMAO-12 to 8f, obtained in the reaction of 1f with an excess of HAlBu i 2 (1:3), gave the associate 10f·MAO, which was characterized by hydride signals at -6.11 and 0.05 ppm in the 1 H NMR spectra ( Figures S26 and S27).  (Figures 2b, S25 and S28). It should be noted that under conditions of a large excess of HAlBu i 2 (1:8), the complex 8f did not provide associates with methylalumoxane similar to 8c, which followed from the permanence of the shape and width of NMR spectral lines with the appearance of the activator.
To clarify the reactivity of the complexes towards the alkene, 1-hexene was added to the systems containing various intermediates in different ratios. After the addition of alkene to the reaction media containing an associate of 8c with MAO, hydrometalation products were formed ( Figure S20). The formation of dimers was detected only in systems containing intermediate 10c when the reaction mixture was heated to 60 • C for several minutes (Figure 3). It is noteworthy that the reaction catalyzed by the cyclopentadienyl complex 1c at the ratio of reagents [Zr]:[HAlBu i 2 ]:[(Ph 3 C)(B(C 6 F 5 ) 4 )] (MMAO-12) = 1:1:0.1 (11), when complexes 9c and 10c are present in the catalytic system, was accompanied by a lower conversion of the alkene and the yield of the reaction product 5 (Table 1, entries 9, 10). Apparently, an additional amount of HAlBu i 2 is required both for the preparation of active forms of co-catalysts [34] and for their subsequent reaction with 10c to give reactive species.  (11), when complexes 9c and 10c are present in the catalytic system, was accompanied by a lower conversion of the alkene and the yield of the reaction product 5 (Table 1, entries 9,10). Apparently, an additional amount of HAlBu i 2 is required both for the preparation of active forms of co-catalysts [34] and for their subsequent reaction with 10c to give reactive species. A more pronounced dependency of the reactivity and chemoselectivity of the catalytic system on the composition of the intermediates was observed in the case of the indenyl complex. At a lower content of HAlBu i 2, when both 10f and cationic species were present in the systems, both dimers and oligomers were found (Table 1, entries 18,21; Figure S29 and Figure S30). With an increase HAlBu i 2 concentration and, consequently, cationic intermediates, the proportion of oligomers in the reaction products increased (

General Procedures
All operations for organometallic compounds were performed under argon according to the Schlenk technique. The complexes Cp2ZrCl2 (1a) [47], Me2CCpZrCl2 (1c) [48], Me2SiCp2ZrCl2 (1d) [49], (Me2C)2CpZrCl2 (1e) [50], Ind2ZrCl2 (1f) [51], rac- A more pronounced dependency of the reactivity and chemoselectivity of the catalytic system on the composition of the intermediates was observed in the case of the indenyl complex. At a lower content of HAlBu i 2 , when both 10f and cationic species were present in the systems, both dimers and oligomers were found (Table 1, entries 18, 21; Figures S29 and S30). With an increase HAlBu i 2 concentration and, consequently, cationic intermediates, the proportion of oligomers in the reaction products increased (Table 1,  entries 19, 22).
Thus, the NMR study of L 2 ZrCl 2 -HAlBu i 2 -activator systems demonstrated the formation of various hydride clusters, among which the bis-zirconium hydride intermediate [L 2 ZrH 2 ·L 2 ZrHCl·ClAlR 2 ] may be the precursor of the active sites responsible for dimerization.
ing on the composition of the catalytic system, the formation of 1-hexene vinylidene dimer and oligomers, 1,2-insertion products with different double bond positions, were observed.
Indenyl complexes (L = Ind, Me 2 CInd 2 , H 4 C 2 [Ind] 2 ) showed the highest values of isotacticity at 67, 93, 71% mmmm, respectively. Moreover, stereoselectivity was notably dependent on the type of activator, suggesting a significant influence of the co-catalyst on the stereoregulation process in the course of alkene coordination by the catalytically active species.
Considerable differences in catalyst action are indicative of the realization of dimerization and oligomerization processes through different active centers, including hydride intermediates. In the example of the reaction of ansa-Me 2 CCp 2 ZrCl 2 and Ind 2 ZrCl 2 with HAlBu i 2 and activators, the composition of hydride intermediates was studied by NMR spectroscopy. As a result, the bis-zirconium complex of type [L 2 ZrH 2 ·L 2 ZrHCl·ClAlR 2 ], which is the precursor of catalytically active centers of the alkene dimerization, was found.