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Aminas acíclicas como ligantes ancilares em catalisadores de rutênio para polimerização via metátese de olefinas cíclicas / Acyclic amines as ancillary ligands in ruthenium catalysts for ring opening metathesis polymerizationSilva, Tiago Breve da 17 February 2012 (has links)
As moléculas à base de nitrogênio, NH2Ph, NH2CH2Ph e NHnBuPh foram investigadas como ligantes ancilares nos novos complexos do tipo [RuCl2 (PPh3)2 (amina) x] para a polimerização via metátese por abertura de anel (ROMP) de norborneno (NBE), norbornadieno (NBD) e diciclopentadieno (DCPD). Os complexos foram obtidos da síntese com [RuCl2 (PPh3)3] com as respectivas moléculas. E eles foram caracterizados por análise elementar de CHN, FT-IR, RMN 31P{1H}, Espectroscopia eletrônica na região do uv-vis e voltametria cíclica. Os complexos isolados foram hexacoordenados (x = 2) com NH2Ph e NH2CH2Ph, e pentacoordenado com NHnBuPh (x = 1). Além disso, os resultados sugerem que todos os ligantes estão trans-posicionados no caso do complexo com NH2Ph (complex 1) e cis no caso do complexo com NH2CH2Ph (complex 2). O complexo com NHnBuPh ( complex 3) e sugerido estar na geometria pirâmide de base quadrada, com a amina no eixo axial. Quantitativos rendimentos foram obtidos na ROMP de NBE a 50°C com 1 por 30 min e com 2 por 5 minutos. Similar resultado foi obtido com 3 at 25°C por 5 min. O valor de Mw foram na faixa de 104 e 105 g/mol,com valores de IPD entre 1,6 e 3,5. Os valores de σc foram em torno de 0,40 a 0,52. ROMP de NBE e DCPD, bem como copolimerizações foram também realizadas com melhores resultados com 3. Os resultados são discutidos em termos de densidade eletrônica e impedimento estérico das aminas como ligantes ancilares nos complexos. As reações com o complexo 2 são favoráveis pelo caráter σ-doador, enquanto que o grande ângulo de cone da NHnBuPh prove a reatividade de 3. / The nitrogen-based molecules, NH2Ph, NH2CH2Ph and NHnBuPh were investigated as ancillary ligands in the new [RuCl2 (PPh3)2 (amine) x] complex types for Ring Opening Metathesis Polymerization (ROMP) of norbornene (NBE), norbornadiene (NBD) and dicyclopentadiene (DCPD). The complexes were obtained from syntheses with [RuCl2 (PPh3)3]of and the respectively molecules and they were characterized by elementar analysis of CHN, FT-IR, NMR 31P, uv-vis spectroscopy and cyclic voltammetry. The isolated complexes were sixcoordinated (x = 2) with NH2Ph and NH2CH2Ph and pentacoordinated with NHnBuPh (x = 1). Moreover, the data suggest that all the ligands are trans-positioned in the case of NH2Ph (complex 1) and cis-positioned in the case of NH2CH2Ph (complex 2). The complex with NHnBuPh (3) was suggested to present a square pyramidal geometry with the amine in the axial axis. Quantitative yields were obtained in the ROMP of NBE at 50 °C with 1 for 30 min and with 2 for 5 min. Similar result was obtained with 3 at 25 °C for 5 min. The Mw values were in the range of 104 to 105 g/mol with PDI values between 1.6 and 3.5. The σc values were 0.40 to 0.52. ROMP of NBD and DCPD, as well copolymerizations with NBE, NBD and DCPD, were also performed with better results with 3. The results are discussed in terms of the electronic density and steric hindrance from the amines as ancillary ligands in the complexes. The reactions with complex 2 are favored by the σ-donor character of NH2CH2Ph, whereas the large cone angle of NHnBuPh provided the reactivity with 3.
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Aminas acíclicas como ligantes ancilares em catalisadores de rutênio para polimerização via metátese de olefinas cíclicas / Acyclic amines as ancillary ligands in ruthenium catalysts for ring opening metathesis polymerizationTiago Breve da Silva 17 February 2012 (has links)
As moléculas à base de nitrogênio, NH2Ph, NH2CH2Ph e NHnBuPh foram investigadas como ligantes ancilares nos novos complexos do tipo [RuCl2 (PPh3)2 (amina) x] para a polimerização via metátese por abertura de anel (ROMP) de norborneno (NBE), norbornadieno (NBD) e diciclopentadieno (DCPD). Os complexos foram obtidos da síntese com [RuCl2 (PPh3)3] com as respectivas moléculas. E eles foram caracterizados por análise elementar de CHN, FT-IR, RMN 31P{1H}, Espectroscopia eletrônica na região do uv-vis e voltametria cíclica. Os complexos isolados foram hexacoordenados (x = 2) com NH2Ph e NH2CH2Ph, e pentacoordenado com NHnBuPh (x = 1). Além disso, os resultados sugerem que todos os ligantes estão trans-posicionados no caso do complexo com NH2Ph (complex 1) e cis no caso do complexo com NH2CH2Ph (complex 2). O complexo com NHnBuPh ( complex 3) e sugerido estar na geometria pirâmide de base quadrada, com a amina no eixo axial. Quantitativos rendimentos foram obtidos na ROMP de NBE a 50°C com 1 por 30 min e com 2 por 5 minutos. Similar resultado foi obtido com 3 at 25°C por 5 min. O valor de Mw foram na faixa de 104 e 105 g/mol,com valores de IPD entre 1,6 e 3,5. Os valores de σc foram em torno de 0,40 a 0,52. ROMP de NBE e DCPD, bem como copolimerizações foram também realizadas com melhores resultados com 3. Os resultados são discutidos em termos de densidade eletrônica e impedimento estérico das aminas como ligantes ancilares nos complexos. As reações com o complexo 2 são favoráveis pelo caráter σ-doador, enquanto que o grande ângulo de cone da NHnBuPh prove a reatividade de 3. / The nitrogen-based molecules, NH2Ph, NH2CH2Ph and NHnBuPh were investigated as ancillary ligands in the new [RuCl2 (PPh3)2 (amine) x] complex types for Ring Opening Metathesis Polymerization (ROMP) of norbornene (NBE), norbornadiene (NBD) and dicyclopentadiene (DCPD). The complexes were obtained from syntheses with [RuCl2 (PPh3)3]of and the respectively molecules and they were characterized by elementar analysis of CHN, FT-IR, NMR 31P, uv-vis spectroscopy and cyclic voltammetry. The isolated complexes were sixcoordinated (x = 2) with NH2Ph and NH2CH2Ph and pentacoordinated with NHnBuPh (x = 1). Moreover, the data suggest that all the ligands are trans-positioned in the case of NH2Ph (complex 1) and cis-positioned in the case of NH2CH2Ph (complex 2). The complex with NHnBuPh (3) was suggested to present a square pyramidal geometry with the amine in the axial axis. Quantitative yields were obtained in the ROMP of NBE at 50 °C with 1 for 30 min and with 2 for 5 min. Similar result was obtained with 3 at 25 °C for 5 min. The Mw values were in the range of 104 to 105 g/mol with PDI values between 1.6 and 3.5. The σc values were 0.40 to 0.52. ROMP of NBD and DCPD, as well copolymerizations with NBE, NBD and DCPD, were also performed with better results with 3. The results are discussed in terms of the electronic density and steric hindrance from the amines as ancillary ligands in the complexes. The reactions with complex 2 are favored by the σ-donor character of NH2CH2Ph, whereas the large cone angle of NHnBuPh provided the reactivity with 3.
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Desenvolvimento de sulfóxido complexos de Ru(II) para aplicação em polimerização via metátese de olefinas cíclicas por abertura do anel / Development of Ru(II) complex sulphoxide for polymerization application via ring-opening cyclic olefin metathesisMartins, Daniele Maria 22 February 2018 (has links)
Este trabalho apresenta as sínteses do complexo fac-[RuCl2(Sdmso3(O-dmso)] (1) e de dois novos complexos, trans,cis,cis- [RuCl2(S-dmso)2(NH2Ph)2] (2) e fac-[RuCl2(Sdmso)3(NH2Ph)] (3). Estes compostos foram caracterizados por espectroscopia de absorção na região do infravermelho, espectroscopia de absorção na região do ultravioleta e visível, análise elementar (CHN), RMN (1H e 13C{1H}) e por difração de raios X em monocristal, confirmando a formação de complexos hexacoordenados. As atividades catalíticas destes complexos como pré-catalisadores nas reações de polimerização via metátese por abertura de anel (ROMP) de norborneno (NBE), norbornadieno (NBD), diciclopentadieno (DCPD) e seus copolímeros foram investigadas. As polimerizações foram realizadas na presença de etil diazoacetato (EDA) em diferentes razões molares de [monômero]/[Ru], tempos e temperaturas de reação. Estudos em função da variação da razão molar [monômero]/[Ru] mostraram que, em geral, a melhor condição para reação via ROMP é a de 5000 equivalentes na presença de [EDA]/[Ru] = 28. Valores de massas moleculares com ordem de magnitude de 105 g.mol-1 para todos os poliNBE e poli(NBE-co-DCPD) foram medidos por cromatografia por permeação em gel (GPC). Os demais polímeros foram insolúveis em CHCl3. Em polimerizações com NBE a 25 °C por 50 min, obtiveram-se rendimentos de 91, 83 e 99 % usando os complexos 1, 2 e 3, respectivamente. Nas polimerizações de NBD, o complexo 1 rendeu 8 % de poliNBD a 50 °C em 30 min. Nestas mesmas condições, os complexos 2 e 3 renderam 42 e 34 % de poliNBD, respectivamente. Na ROMP de DCPD a 50 °C em 30 min, os três complexos sintetizaram poliDCPD com rendimentos em torno de 16 %. A 50 °C por 30 min, poli(NBE-co-NBD) com maior concentração de NBD (80NBD: 20NBE) usando os complexos 2 ou 3 foram obtidos com 35 % de rendimento, enquanto com o complexo 1 os rendimentos são de 15 %. Copolímeros do tipo poli(NBE-co-DCPD) foram obtidos com maiores rendimentos com o complexo 3 e com maiores valores de Mw usando o complexo 2. A influência do tipo de complexo e dos efeitos cooperativos dos ligantes foi avaliada neste tipo de reação com implicações nas características dos polímeros. / This work presents the syntheses of the complex fac-[RuCl2(Sdmso)3(O-dmso)] (1) and of the two new complexes trans,cis,cis- [RuCl2(S-dmso)2(NH2Ph)2] (2) and fac-[RuCl2(Sdmso)3(NH2Ph)] (3). These compounds were characterized by infrared absorption spectroscopy, ultraviolet-visible absorption spectroscopy, elemental analysis (CHN), NMR (1H and 13C{1H}) and by X-ray diffraction in single crystals, confirming the formation of hexacoordinate complexes. The catalytic activities of these complexes as pre-catalysts in ring-opening metathesis polymerization (ROMP) reactions of norbornene (NBE), norbornadiene (NBD), dicyclopentadiene (DCPD) and its copolymers were investigated. The polymerizations were carried out in presence of ethyl diazoacetate (EDA), in different molar ratios of [monomer]/[Ru], as a function of reaction time and temperature. Studies on the variation of the [monomer]/[Ru] molar ratio have shown that, in general, the best condition for the ROMP reaction is 5000 equivalents, in the presence of [EDA]/[Ru] = 28.Values of molecular weights with order of magnitude of 105 g.mol-1 for all polyNBE and poly(NBE-co-DCPD) were measured by gel permeation chromatography (GPC). The other polymers were insoluble in CHCl3. In polymerizations with NBE at 25 °C for 50 min, yields of 91, 83 and 99 % were obtained using complexes 1, 2 and 3, respectively. In the NBD polymerizations, complex 1 yielded 8 % of polyNBD at 50 °C for 30 min. Under these same conditions, complexes 2 and 3 yielded 42 and 34 % of polyNBD, respectively. In the ROMP of DCPD at 50 °C for 30 min, the three complexes synthesized polyDCPD in yields of about 16 %. At 50 °C for 30 min, poly(NBE-co-NBD) with higher concentration of NBD (80NBD : 20NBE) using complexes 2 or 3 were obtained in 35% yield, while with complex 1 the yields were 15 %. Poly(NBE-co-DCPD) copolymers were obtained in higher yields with complex 3 and higher Mw values using complex 2. The influence of the type of complex and the cooperative effects of the ligands were evaluated in this type of reaction with implications in the characteristics of the polymers.
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Desenvolvimento de catalisadores de rutênio coordenados a toluilfosfinas para polimerização via metátese / Development of ruthenium catalysts coordinated with tolylphosphines for metathesis polymerizationFerreira, Marcella de Sousa 20 February 2014 (has links)
Este trabalho investigou a influência das propriedades estéricas e eletrônicas de ligantes ancilares em complexos do tipo [RuCl2(PR3)3] e [RuCl2(PR3)xLy], onde R = p-toluil e L = piperidina, N-butilamina e isonicotinamida, em reações de polimerização via metátese por abertura de anel (ROMP) e de copolimerização via metátese por abertura de anel (ROMCP) de norborneno (NBE) e norbornadieno (NBD). O objetivo foi observar como o efeito estéreo (dado em função do ângulo de cone, θ) e eletrônico (dado em função de pKa) da PpTol3 pode influenciar a reatividade em ROMP e ROMCP quando está sozinha ou combinada com amina. <br /> O complexo [RuCl2(PpTol3)3] (1) produziu rendimentos melhores que 70% por 10 min a 23 °C, com Mw na ordem de 104 g.mol-1 e IPD de 2,2. O melhor rendimento obtido quando o complexo [RuCl2(PpTol3)2(pip)] (2) é utilizado foi observado nas reações por 30 min a 50 °C (80,2%) com Mw de 1,5 x 105 g.mol-1. IPD de 2,0 foi obtido com 2 por 60 min a 23 °C. O complexo 2 demonstrou ser mais reativo que o complexo 1 nas reações de ROMP de NBD, com rendimento de 60,1% por 60 min a 50 °C. O impedimento estéreo de PpTol3 em 1, provavelmente é o responsável pelo melhor desempenho com NBE, com um período de indução mais curto para iniciar a ROMP. Por outro lado, o sinergismo amina→Ru→olefina deve contribuir para a ativação de NBD com 2. <br /> Os rendimentos para poliNBE com os complexos contendo N-butilamina e isonicotinamida foram de 68 e 35%, respectivamente, por 60 min a 50 °C, isso mostra que a atividade catalítica para estes complexos sobrepõe o baixo ângulo de cone da Nbutilamina e a capacidade de retrodoação da isonicotinamida. Os rendimentos para o poliNBD foram de 30,9 e 9,1, respectivamente. <br /> As reações de copolimerizações com NBE e NBD (ROMCP) foram realizadas com uma quantidade fixa de NBE ([NBE]/[Ru] = 5000) e diferentes concentrações de NBD ([NBD]/[Ru] = 1000, 2000 ou 3000), por 60 min a 50°C. Para ambos os complexos 1 e 2, os rendimentos foram acima de 80% quando aumentou-se a [NBD] e os materiais poliméricos apresentaram microestruturas lisas. Os valores de Tg (acima de 60 °C) obtidos quando o complexo 1 foi utilizado, sugerem a presença de NBD nas cadeias poliméricas. Com o complexo 2, os valores de Tg foram entre 33 e 37 °C, indicando a possibilidade de polimerização apenas do NBE. / This study investigated the influence of steric and electronic properties of ancillary ligands in complexes of the type [RuCl2(PR3)3] and [RuCl2(PR3)xLy], with R = p-tolyl and L = piperidine, N-butylamine and isonicotinamide, for ring-opening metathesis polymerization (ROMP) and ring-opening metathesis copolymerization of norbornene (NBE) and norbornadiene (NBD). The aim was to observe how the steric (in terms of the cone angle, θ) and electronic (in terms of pKa) effects of PpTol3 can tune the reactivity in ROMP and ROMCP when alone or combining with an amine. <br /> The [RuCl2(PpTol3)3] complex (1) produced yields better than 70% for 10 min at 23 °C, with Mw in the order of 104 g.mol-1 and PDI of 2,2. The best yields obtained when the complex [RuCl2(PpTol3)2(pip)] (2) was used was observed in the reactions 30 min at 50 °C (80%), with Mw of 1.5 x 105 g.mol-1. PDI of 2.0 was obtained with 2 for 60 min at 23 °C. The complex 2 proved to be more reactive than complex 1 for ROMP of NBD, with yield of 60.1% for 60 min at 50 °C. The steric hindrance of PpTol3 in 1 probable provided the difference in the reactive for NBE, with a short induction period to initiate the ROMP. However, the amine→Ru→olefin synergism in 2 probable contributed to the better activation of NBD. <br /> The yields for polyNBE with the N-butylamine and isonicotinamide derivative complexes were 68 and 35%, respectively, for 60 min at 50 °C., it shows that the catalytic activity of these complexes to overlap the low cone angle of the N-butylamine and the ability of the backdonation of the isonicotinamide. Proceeds to poliNBD were 30.9 and 9.1, respectively. <br /> Copolymerizations with NBE and NBD (ROMCP) were performed with a fixed quantity of NBE ([NBE]/[Ru] = 5000) and different concentrations of NBD ([NBD]/[Ru] = 1000, 2000 or 3000), for 60 min at 50 ° C. The yields were better than 80% when increasing the [NBD] and the polymeric materials showed smooth microstructures. The obtained Tg values (60 °C) obtained when the complex 1 was used, indicated the presence of NBD in the polymer chains. With the complex 2, the Tg values were in the range of 33 - 37 °C, indicating the possibility of polymerization of only NBE.
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Desenvolvimento de sulfóxido complexos de Ru(II) para aplicação em polimerização via metátese de olefinas cíclicas por abertura do anel / Development of Ru(II) complex sulphoxide for polymerization application via ring-opening cyclic olefin metathesisDaniele Maria Martins 22 February 2018 (has links)
Este trabalho apresenta as sínteses do complexo fac-[RuCl2(Sdmso3(O-dmso)] (1) e de dois novos complexos, trans,cis,cis- [RuCl2(S-dmso)2(NH2Ph)2] (2) e fac-[RuCl2(Sdmso)3(NH2Ph)] (3). Estes compostos foram caracterizados por espectroscopia de absorção na região do infravermelho, espectroscopia de absorção na região do ultravioleta e visível, análise elementar (CHN), RMN (1H e 13C{1H}) e por difração de raios X em monocristal, confirmando a formação de complexos hexacoordenados. As atividades catalíticas destes complexos como pré-catalisadores nas reações de polimerização via metátese por abertura de anel (ROMP) de norborneno (NBE), norbornadieno (NBD), diciclopentadieno (DCPD) e seus copolímeros foram investigadas. As polimerizações foram realizadas na presença de etil diazoacetato (EDA) em diferentes razões molares de [monômero]/[Ru], tempos e temperaturas de reação. Estudos em função da variação da razão molar [monômero]/[Ru] mostraram que, em geral, a melhor condição para reação via ROMP é a de 5000 equivalentes na presença de [EDA]/[Ru] = 28. Valores de massas moleculares com ordem de magnitude de 105 g.mol-1 para todos os poliNBE e poli(NBE-co-DCPD) foram medidos por cromatografia por permeação em gel (GPC). Os demais polímeros foram insolúveis em CHCl3. Em polimerizações com NBE a 25 °C por 50 min, obtiveram-se rendimentos de 91, 83 e 99 % usando os complexos 1, 2 e 3, respectivamente. Nas polimerizações de NBD, o complexo 1 rendeu 8 % de poliNBD a 50 °C em 30 min. Nestas mesmas condições, os complexos 2 e 3 renderam 42 e 34 % de poliNBD, respectivamente. Na ROMP de DCPD a 50 °C em 30 min, os três complexos sintetizaram poliDCPD com rendimentos em torno de 16 %. A 50 °C por 30 min, poli(NBE-co-NBD) com maior concentração de NBD (80NBD: 20NBE) usando os complexos 2 ou 3 foram obtidos com 35 % de rendimento, enquanto com o complexo 1 os rendimentos são de 15 %. Copolímeros do tipo poli(NBE-co-DCPD) foram obtidos com maiores rendimentos com o complexo 3 e com maiores valores de Mw usando o complexo 2. A influência do tipo de complexo e dos efeitos cooperativos dos ligantes foi avaliada neste tipo de reação com implicações nas características dos polímeros. / This work presents the syntheses of the complex fac-[RuCl2(Sdmso)3(O-dmso)] (1) and of the two new complexes trans,cis,cis- [RuCl2(S-dmso)2(NH2Ph)2] (2) and fac-[RuCl2(Sdmso)3(NH2Ph)] (3). These compounds were characterized by infrared absorption spectroscopy, ultraviolet-visible absorption spectroscopy, elemental analysis (CHN), NMR (1H and 13C{1H}) and by X-ray diffraction in single crystals, confirming the formation of hexacoordinate complexes. The catalytic activities of these complexes as pre-catalysts in ring-opening metathesis polymerization (ROMP) reactions of norbornene (NBE), norbornadiene (NBD), dicyclopentadiene (DCPD) and its copolymers were investigated. The polymerizations were carried out in presence of ethyl diazoacetate (EDA), in different molar ratios of [monomer]/[Ru], as a function of reaction time and temperature. Studies on the variation of the [monomer]/[Ru] molar ratio have shown that, in general, the best condition for the ROMP reaction is 5000 equivalents, in the presence of [EDA]/[Ru] = 28.Values of molecular weights with order of magnitude of 105 g.mol-1 for all polyNBE and poly(NBE-co-DCPD) were measured by gel permeation chromatography (GPC). The other polymers were insoluble in CHCl3. In polymerizations with NBE at 25 °C for 50 min, yields of 91, 83 and 99 % were obtained using complexes 1, 2 and 3, respectively. In the NBD polymerizations, complex 1 yielded 8 % of polyNBD at 50 °C for 30 min. Under these same conditions, complexes 2 and 3 yielded 42 and 34 % of polyNBD, respectively. In the ROMP of DCPD at 50 °C for 30 min, the three complexes synthesized polyDCPD in yields of about 16 %. At 50 °C for 30 min, poly(NBE-co-NBD) with higher concentration of NBD (80NBD : 20NBE) using complexes 2 or 3 were obtained in 35% yield, while with complex 1 the yields were 15 %. Poly(NBE-co-DCPD) copolymers were obtained in higher yields with complex 3 and higher Mw values using complex 2. The influence of the type of complex and the cooperative effects of the ligands were evaluated in this type of reaction with implications in the characteristics of the polymers.
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Desenvolvimento de catalisadores de rutênio coordenados a toluilfosfinas para polimerização via metátese / Development of ruthenium catalysts coordinated with tolylphosphines for metathesis polymerizationMarcella de Sousa Ferreira 20 February 2014 (has links)
Este trabalho investigou a influência das propriedades estéricas e eletrônicas de ligantes ancilares em complexos do tipo [RuCl2(PR3)3] e [RuCl2(PR3)xLy], onde R = p-toluil e L = piperidina, N-butilamina e isonicotinamida, em reações de polimerização via metátese por abertura de anel (ROMP) e de copolimerização via metátese por abertura de anel (ROMCP) de norborneno (NBE) e norbornadieno (NBD). O objetivo foi observar como o efeito estéreo (dado em função do ângulo de cone, θ) e eletrônico (dado em função de pKa) da PpTol3 pode influenciar a reatividade em ROMP e ROMCP quando está sozinha ou combinada com amina. <br /> O complexo [RuCl2(PpTol3)3] (1) produziu rendimentos melhores que 70% por 10 min a 23 °C, com Mw na ordem de 104 g.mol-1 e IPD de 2,2. O melhor rendimento obtido quando o complexo [RuCl2(PpTol3)2(pip)] (2) é utilizado foi observado nas reações por 30 min a 50 °C (80,2%) com Mw de 1,5 x 105 g.mol-1. IPD de 2,0 foi obtido com 2 por 60 min a 23 °C. O complexo 2 demonstrou ser mais reativo que o complexo 1 nas reações de ROMP de NBD, com rendimento de 60,1% por 60 min a 50 °C. O impedimento estéreo de PpTol3 em 1, provavelmente é o responsável pelo melhor desempenho com NBE, com um período de indução mais curto para iniciar a ROMP. Por outro lado, o sinergismo amina→Ru→olefina deve contribuir para a ativação de NBD com 2. <br /> Os rendimentos para poliNBE com os complexos contendo N-butilamina e isonicotinamida foram de 68 e 35%, respectivamente, por 60 min a 50 °C, isso mostra que a atividade catalítica para estes complexos sobrepõe o baixo ângulo de cone da Nbutilamina e a capacidade de retrodoação da isonicotinamida. Os rendimentos para o poliNBD foram de 30,9 e 9,1, respectivamente. <br /> As reações de copolimerizações com NBE e NBD (ROMCP) foram realizadas com uma quantidade fixa de NBE ([NBE]/[Ru] = 5000) e diferentes concentrações de NBD ([NBD]/[Ru] = 1000, 2000 ou 3000), por 60 min a 50°C. Para ambos os complexos 1 e 2, os rendimentos foram acima de 80% quando aumentou-se a [NBD] e os materiais poliméricos apresentaram microestruturas lisas. Os valores de Tg (acima de 60 °C) obtidos quando o complexo 1 foi utilizado, sugerem a presença de NBD nas cadeias poliméricas. Com o complexo 2, os valores de Tg foram entre 33 e 37 °C, indicando a possibilidade de polimerização apenas do NBE. / This study investigated the influence of steric and electronic properties of ancillary ligands in complexes of the type [RuCl2(PR3)3] and [RuCl2(PR3)xLy], with R = p-tolyl and L = piperidine, N-butylamine and isonicotinamide, for ring-opening metathesis polymerization (ROMP) and ring-opening metathesis copolymerization of norbornene (NBE) and norbornadiene (NBD). The aim was to observe how the steric (in terms of the cone angle, θ) and electronic (in terms of pKa) effects of PpTol3 can tune the reactivity in ROMP and ROMCP when alone or combining with an amine. <br /> The [RuCl2(PpTol3)3] complex (1) produced yields better than 70% for 10 min at 23 °C, with Mw in the order of 104 g.mol-1 and PDI of 2,2. The best yields obtained when the complex [RuCl2(PpTol3)2(pip)] (2) was used was observed in the reactions 30 min at 50 °C (80%), with Mw of 1.5 x 105 g.mol-1. PDI of 2.0 was obtained with 2 for 60 min at 23 °C. The complex 2 proved to be more reactive than complex 1 for ROMP of NBD, with yield of 60.1% for 60 min at 50 °C. The steric hindrance of PpTol3 in 1 probable provided the difference in the reactive for NBE, with a short induction period to initiate the ROMP. However, the amine→Ru→olefin synergism in 2 probable contributed to the better activation of NBD. <br /> The yields for polyNBE with the N-butylamine and isonicotinamide derivative complexes were 68 and 35%, respectively, for 60 min at 50 °C., it shows that the catalytic activity of these complexes to overlap the low cone angle of the N-butylamine and the ability of the backdonation of the isonicotinamide. Proceeds to poliNBD were 30.9 and 9.1, respectively. <br /> Copolymerizations with NBE and NBD (ROMCP) were performed with a fixed quantity of NBE ([NBE]/[Ru] = 5000) and different concentrations of NBD ([NBD]/[Ru] = 1000, 2000 or 3000), for 60 min at 50 ° C. The yields were better than 80% when increasing the [NBD] and the polymeric materials showed smooth microstructures. The obtained Tg values (60 °C) obtained when the complex 1 was used, indicated the presence of NBD in the polymer chains. With the complex 2, the Tg values were in the range of 33 - 37 °C, indicating the possibility of polymerization of only NBE.
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Influence of Ancillary Ligands in the Chemistry of Transition Metal σ-ComplexesBera, Barun January 2014 (has links) (PDF)
This thesis work is based on an investigation of intermediates involved in various metal mediated catalytic reactions such as hydrogenation, hydroboration, functionalization of methane etc. An intermediate dictates the energetics of the catalytic cycle of these reactions. Therefore, it is important to study such types of intermediates in order to design a better catalyst. These intermediates are called σ-complexes in which a σ-bond is coordinated to the metal center at some stage of the reaction coordinate. These species are rarely stable at ambient conditions which create difficulties in exploring their chemistry.
Our aim is to study the effect of ancillary ligands on the coordination properties of a σ-bond ligand. We chose two different classes of σ-complexes – one contains a B–H σ-bond as a ligand, i.e., σ-borane complex and another contains a H–H σ-bond as a ligand, i.e., σ-dihydrogen complex. Both M–H–B and M–H2 interactions are 3-center-2-electron coordination bonds comprised of two bonding components. One is σ-donation, which is present in both and another is π-back donation from the metal center, which is negligible in the σ-borane complexes contrary to the σ-dihydrogen complexes. The bonding characteristics of M–H–B and M–H2 interactions suggest that an electron deficient metal center is necessary to study the σ-borane complexes with reasonable stability. Thus, we selected an early transition metal, i.e., Cr(0) bearing arene and CO ancillary ligands, for studying the σ-borane complexes. On the other hand, the cis-dihydrogen/hydride and cis-dihydrogen chloride complexes were studied on a late transition metal center, i.e., Ru(II) bearing phosphine and N–N bidentate ligands.
Ammonia-borane is known to be a potential hydrogen storage material. Therefore, we picked up the catalytic dehydrogenation reaction of this compound and intended to investigate the interaction between a metal center and the BH σ-bonds of amine-boranes. We characterized the σ-borane complexes [(η6-arene)Cr(CO)2(η1-H–BH2•NMe3)] (arene = fluorobenzene, benzene, and mesitylene), and observed an interesting correlation between the electronics and stability of these species. This was the first report of σ-borane systems possessing an η6-arene ligand. A prototype homobimetallic σ-borane complex, [(η6-C6H5CH2NMe2•BH2–HCr(CO)5)Cr(CO)3] was characterized using single crystal X-ray crystallography. An intramolecular σ-borane complex, (η1-(η6-C6H5CH2NMe2•BH2–H))Cr(CO)2 was found to possess an interesting chelation of the η6-arene, and BH coordination sites of its amine-borane moiety with the Cr(0) center. These σ-borane complexes showed an interesting dynamics in the binding interface between the metal center and the borane ligand. Free energy of activation (ΔG#) for this process was estimated to be 30-40 kJ/mol.
To explore certain σ-dihydrogen complexes we investigated the chemistry of cis-dihydrogen/hydride complexes of Ru(II) bearing phosphine and N-N bidentate ligands cis,trans-[RuH(η2-H2)(PPh3)2(N-N)][OTf] (N-N = 2, 2′-bipyridyl, 2, 2′-bipyrimidine) in detail. In those cases, we established that the adjacent hydride ligand has large influence on the dihydrogen coordination. The η2-H2 and hydride ligands showed a single 1H NMR spectral signal due to fast site exchange among each other. We established the mechanism and calculated the free energy of activation (ΔG# = 8-13 kJ/mol) of this dynamics. These complexes were found to be stable at ambient conditions although, a labile dihydrogen ligand is present in the coordination sphere of the metal center. In fact, we could obtain the single crystals of cis,trans-[RuH(η2-H2)(PPh3)2(bpy)][OTf]. The molecular structure of a σ-complex in which a σ-bond (before it gets completely formed or broken) acts as a ligand is what fascinates this area in chemistry. A cis-dihydrogen chloride complex, cis,trans-[RuCl(η2-H2)(PPh3)2(bpm)][OTf] was characterized unambiguously using NMR spectroscopy. The H-H distance (dHH) for the η2-H2 ligand of these complexes were estimated to be 0.9-1.0 Å.
We attempted to observe some σ-methane species spectroscopically at low temperatures. Unfortunately, these species were quite unstable for exhibiting the NMR spectral signals even at low temperatures. Nevertheless, we investigated the reactivity of cis,trans-[RuHX(PPh3)2(N-N)] (X = H, Cl; N-N = 2, 2′-bipyridyl, 2, 2′-bipyrimidine) towards a methylating agent, CH3OTf. This reaction resulted in methane evolution by the combination of the hydride ligand of a Ru(II) complex and the CH3+ moiety of CH3OTf. This reaction was carried out in a sealed tube inside a NMR probe at ~183 K and monitored for a long period of time; however, the methane bound metal species was not observed. Perhaps, the longevity of this class of σ-methane complex falls below the NMR time scale.
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