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Alternating Ring-Opening Metathesis Copolymerization by Grubbs-Type Initiators with Unsymmetrical N-Heterocyclic Carbenes

A series of RuIV–alkylidenes based on unsymmetrical imidazolin‐2‐ylidenes, that is, [RuCl2{1‐(2,4,6‐trimethylphenyl)‐3‐R‐4,5‐dihydro‐(3H)‐imidazol‐1‐ylidene}(CHPh)(pyridin)] (R=CH2Ph (5), Ph (6), ethyl (7), methyl (8)), have been synthesized. These and the parent initiators [RuCl2(PCy3){1‐(2,4,6‐tri...

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Published in:Chemistry : a European journal 2009-09, Vol.15 (37), p.9451-9457
Main Authors: Lichtenheldt, Martin, Wang, Dongren, Vehlow, Kati, Reinhardt, Ingrid, Kühnel, Christa, Decker, Ulrich, Blechert, Siegfried, Buchmeiser, Michael R.
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cited_by cdi_FETCH-LOGICAL-c3824-9345963ec08d5361567437f795ab940bd2e191ea4e3be114caf7ea802550c3043
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container_issue 37
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creator Lichtenheldt, Martin
Wang, Dongren
Vehlow, Kati
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Blechert, Siegfried
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description A series of RuIV–alkylidenes based on unsymmetrical imidazolin‐2‐ylidenes, that is, [RuCl2{1‐(2,4,6‐trimethylphenyl)‐3‐R‐4,5‐dihydro‐(3H)‐imidazol‐1‐ylidene}(CHPh)(pyridin)] (R=CH2Ph (5), Ph (6), ethyl (7), methyl (8)), have been synthesized. These and the parent initiators [RuCl2(PCy3){1‐(2,4,6‐trimethylphenyl)‐3‐R‐4,5‐dihydro‐(3H)‐imidazol‐1‐ylidene}(CHC6H5)] (R=CH2C6H5 (1), C6H5 (2), ethyl (3)) were used for the alternating copolymerization of norborn‐2‐ene (NBE) with cis‐cyclooctene (COE) and cyclopentene (CPE), respectively. Alternating copolymers, that is, poly(NBE‐alt‐COE)n and poly(NBE‐alt‐CPE)n containing up to 97 and 91 % alternating diads, respectively, were obtained. The copolymerization parameters of the alternating copolymerization of NBE with CPE under the action of initiators 1–3 and 5–8 were determined by using both a zero‐ and first‐order Markov model. Finally, kinetic investigations using initiators 1–3, 6, and 7 were carried out. These revealed that in contrast to the 2nd‐generation Grubbs‐type initiators 1–3 the corresponding pyridine derivatives 6 and 7 represent fast and quantitative initiating systems. Hydrogenation of poly(NBE‐alt‐COE)n yielded a fully saturated, hydrocarbon‐based polymer. Its backbone can formally be derived by 1‐olefin polymerization of CPE (1,3‐insertion) followed by five ethylene units and thus serves as an excellent model compound for 1‐olefin polymerization‐derived copolymers. Alternate your chemistry! RuIV–alkylidenes based on unsymmetrical imidazolin‐2‐ylidenes (see figure) were used for the alternating copolymerization of norborn‐2‐ene with cis‐cyclooctene and cyclopentene. Alternating copolymers, that is, poly(norborn‐2‐ene‐alt‐cyclooctene)n and poly(norborn‐2‐ene‐alt‐cyclopentene)n containing up to 97 and 91 % alternating diads, were obtained.
doi_str_mv 10.1002/chem.200900384
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These and the parent initiators [RuCl2(PCy3){1‐(2,4,6‐trimethylphenyl)‐3‐R‐4,5‐dihydro‐(3H)‐imidazol‐1‐ylidene}(CHC6H5)] (R=CH2C6H5 (1), C6H5 (2), ethyl (3)) were used for the alternating copolymerization of norborn‐2‐ene (NBE) with cis‐cyclooctene (COE) and cyclopentene (CPE), respectively. Alternating copolymers, that is, poly(NBE‐alt‐COE)n and poly(NBE‐alt‐CPE)n containing up to 97 and 91 % alternating diads, respectively, were obtained. The copolymerization parameters of the alternating copolymerization of NBE with CPE under the action of initiators 1–3 and 5–8 were determined by using both a zero‐ and first‐order Markov model. Finally, kinetic investigations using initiators 1–3, 6, and 7 were carried out. These revealed that in contrast to the 2nd‐generation Grubbs‐type initiators 1–3 the corresponding pyridine derivatives 6 and 7 represent fast and quantitative initiating systems. Hydrogenation of poly(NBE‐alt‐COE)n yielded a fully saturated, hydrocarbon‐based polymer. Its backbone can formally be derived by 1‐olefin polymerization of CPE (1,3‐insertion) followed by five ethylene units and thus serves as an excellent model compound for 1‐olefin polymerization‐derived copolymers. Alternate your chemistry! RuIV–alkylidenes based on unsymmetrical imidazolin‐2‐ylidenes (see figure) were used for the alternating copolymerization of norborn‐2‐ene with cis‐cyclooctene and cyclopentene. 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These and the parent initiators [RuCl2(PCy3){1‐(2,4,6‐trimethylphenyl)‐3‐R‐4,5‐dihydro‐(3H)‐imidazol‐1‐ylidene}(CHC6H5)] (R=CH2C6H5 (1), C6H5 (2), ethyl (3)) were used for the alternating copolymerization of norborn‐2‐ene (NBE) with cis‐cyclooctene (COE) and cyclopentene (CPE), respectively. Alternating copolymers, that is, poly(NBE‐alt‐COE)n and poly(NBE‐alt‐CPE)n containing up to 97 and 91 % alternating diads, respectively, were obtained. The copolymerization parameters of the alternating copolymerization of NBE with CPE under the action of initiators 1–3 and 5–8 were determined by using both a zero‐ and first‐order Markov model. Finally, kinetic investigations using initiators 1–3, 6, and 7 were carried out. These revealed that in contrast to the 2nd‐generation Grubbs‐type initiators 1–3 the corresponding pyridine derivatives 6 and 7 represent fast and quantitative initiating systems. Hydrogenation of poly(NBE‐alt‐COE)n yielded a fully saturated, hydrocarbon‐based polymer. Its backbone can formally be derived by 1‐olefin polymerization of CPE (1,3‐insertion) followed by five ethylene units and thus serves as an excellent model compound for 1‐olefin polymerization‐derived copolymers. Alternate your chemistry! RuIV–alkylidenes based on unsymmetrical imidazolin‐2‐ylidenes (see figure) were used for the alternating copolymerization of norborn‐2‐ene with cis‐cyclooctene and cyclopentene. 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These and the parent initiators [RuCl2(PCy3){1‐(2,4,6‐trimethylphenyl)‐3‐R‐4,5‐dihydro‐(3H)‐imidazol‐1‐ylidene}(CHC6H5)] (R=CH2C6H5 (1), C6H5 (2), ethyl (3)) were used for the alternating copolymerization of norborn‐2‐ene (NBE) with cis‐cyclooctene (COE) and cyclopentene (CPE), respectively. Alternating copolymers, that is, poly(NBE‐alt‐COE)n and poly(NBE‐alt‐CPE)n containing up to 97 and 91 % alternating diads, respectively, were obtained. The copolymerization parameters of the alternating copolymerization of NBE with CPE under the action of initiators 1–3 and 5–8 were determined by using both a zero‐ and first‐order Markov model. Finally, kinetic investigations using initiators 1–3, 6, and 7 were carried out. These revealed that in contrast to the 2nd‐generation Grubbs‐type initiators 1–3 the corresponding pyridine derivatives 6 and 7 represent fast and quantitative initiating systems. Hydrogenation of poly(NBE‐alt‐COE)n yielded a fully saturated, hydrocarbon‐based polymer. Its backbone can formally be derived by 1‐olefin polymerization of CPE (1,3‐insertion) followed by five ethylene units and thus serves as an excellent model compound for 1‐olefin polymerization‐derived copolymers. Alternate your chemistry! RuIV–alkylidenes based on unsymmetrical imidazolin‐2‐ylidenes (see figure) were used for the alternating copolymerization of norborn‐2‐ene with cis‐cyclooctene and cyclopentene. Alternating copolymers, that is, poly(norborn‐2‐ene‐alt‐cyclooctene)n and poly(norborn‐2‐ene‐alt‐cyclopentene)n containing up to 97 and 91 % alternating diads, were obtained.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>19670196</pmid><doi>10.1002/chem.200900384</doi><tpages>7</tpages></addata></record>
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subjects metathesis
polymerization
ring-opening polymerization
ruthenium
synthesis design
title Alternating Ring-Opening Metathesis Copolymerization by Grubbs-Type Initiators with Unsymmetrical N-Heterocyclic Carbenes
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