Enantioselective alternating copolymerization of carbon monoxide with ω undecylenic acid was carried out using cationic palladium catalyst modified by 1,4 3,6 dianhydro 2,5 dideoxy 2,5 bis(diphenylphosphino) L iditol...Enantioselective alternating copolymerization of carbon monoxide with ω undecylenic acid was carried out using cationic palladium catalyst modified by 1,4 3,6 dianhydro 2,5 dideoxy 2,5 bis(diphenylphosphino) L iditol (DDPPI). The chiral diphosphine was proved to be effective in the enantioselective copolymerization. The pure poly(1,4 ketone) was obtained by dissolving the copolymer containing spiroketal and 1,4 ketone units in 1,1,1,3,3,3 hexafluoro 2 propanol and reprecipitating with methanol. Optical rotation, elemental analysis, spectra of 1H, 13 C NMR and IR showed that our copolymer was an optically active, isotatic, alternating poly(1,4 ketone) structure. The copolymerization was carried out at 45 ℃ for 20 h. Molecular weight: n=1.1× 10 4 versus polystyrene, w/ n=1.84. Molar optical rotation: 20 589 =+43°(CH 3COOC 2H 5, 5.0 mg/mL). The productivity of the copolymer of ω undecylenic acid with carbon monoxide was 40.6 g copolymer/(g Pd·h).展开更多
Enantioselective alternating copolymerization of carbon monoxide with 1 heptene was carried out using palladium catalyst modified by 1,4 3,6 dianhydro 2,5 dideoxy 2,5 bis(diphenylphosphino) L iditol (DDPPI). The chira...Enantioselective alternating copolymerization of carbon monoxide with 1 heptene was carried out using palladium catalyst modified by 1,4 3,6 dianhydro 2,5 dideoxy 2,5 bis(diphenylphosphino) L iditol (DDPPI). The chiral diphosphine was proved to be effective at enantioselective copolymerization. The pure poly(1,4 ketone) was obtained by dissolving the copolymer containing spiroketal and 1,4 ketone units in 1,1,1,3,3,3 hexafluoro 2 propanol and reprecipitating with methanol. Optical rotation, elemental analysis, spectra of 1H\|NMR, 13 C NMR and IR showed that our copolymer was optically active, isotatic, alternating poly(1,4 ketone) structure. The copolymerization was carried out at 45℃ for 48?h. Molecular weight: M n=4 02×10 3, M w/ M n=1 55 (GPC measurements with polystyrene standards). Optical rotation:[ α ] 20 589 =+63° (CH 2Cl 2, 5 0?mg/mL). T m=194℃, T g=11℃.展开更多
文摘Enantioselective alternating copolymerization of carbon monoxide with ω undecylenic acid was carried out using cationic palladium catalyst modified by 1,4 3,6 dianhydro 2,5 dideoxy 2,5 bis(diphenylphosphino) L iditol (DDPPI). The chiral diphosphine was proved to be effective in the enantioselective copolymerization. The pure poly(1,4 ketone) was obtained by dissolving the copolymer containing spiroketal and 1,4 ketone units in 1,1,1,3,3,3 hexafluoro 2 propanol and reprecipitating with methanol. Optical rotation, elemental analysis, spectra of 1H, 13 C NMR and IR showed that our copolymer was an optically active, isotatic, alternating poly(1,4 ketone) structure. The copolymerization was carried out at 45 ℃ for 20 h. Molecular weight: n=1.1× 10 4 versus polystyrene, w/ n=1.84. Molar optical rotation: 20 589 =+43°(CH 3COOC 2H 5, 5.0 mg/mL). The productivity of the copolymer of ω undecylenic acid with carbon monoxide was 40.6 g copolymer/(g Pd·h).
文摘Enantioselective alternating copolymerization of carbon monoxide with 1 heptene was carried out using palladium catalyst modified by 1,4 3,6 dianhydro 2,5 dideoxy 2,5 bis(diphenylphosphino) L iditol (DDPPI). The chiral diphosphine was proved to be effective at enantioselective copolymerization. The pure poly(1,4 ketone) was obtained by dissolving the copolymer containing spiroketal and 1,4 ketone units in 1,1,1,3,3,3 hexafluoro 2 propanol and reprecipitating with methanol. Optical rotation, elemental analysis, spectra of 1H\|NMR, 13 C NMR and IR showed that our copolymer was optically active, isotatic, alternating poly(1,4 ketone) structure. The copolymerization was carried out at 45℃ for 48?h. Molecular weight: M n=4 02×10 3, M w/ M n=1 55 (GPC measurements with polystyrene standards). Optical rotation:[ α ] 20 589 =+63° (CH 2Cl 2, 5 0?mg/mL). T m=194℃, T g=11℃.
