This paper is the first report on the atom transfer radical copolymerization of unsaturated cyclic acetal, 4,7 dimethyl 2 methylene 1,3 dioxepane(DMMDO) and styrene(St) in the presence of α bromobutyrate as the initi...This paper is the first report on the atom transfer radical copolymerization of unsaturated cyclic acetal, 4,7 dimethyl 2 methylene 1,3 dioxepane(DMMDO) and styrene(St) in the presence of α bromobutyrate as the initiator and CuBr/2,2 bipyridine as the catalyst/ligand at 110 ℃ was investigated. Both DMMDO and St components could be found in main chains of the obtained polymer, and the copolymer had a narrow molecular weight distribution. DMMDO component in the copolymer contained both addition and ring opening units, thus the ester bond was introduced into the main chain, and the copolymer could be chemically degradable and biologically degradable.展开更多
为了研究植物乳杆菌材料对黄曲霉毒素去除新方法,为黄曲霉毒素B_(1)的高效生物去除提供了新思路。本文采用基于聚多巴胺的原子转移自由基聚合方法(Polydopamine-based Atom Transfer Radical Polymerization,p-ATRP)和细胞自催化的无铜...为了研究植物乳杆菌材料对黄曲霉毒素去除新方法,为黄曲霉毒素B_(1)的高效生物去除提供了新思路。本文采用基于聚多巴胺的原子转移自由基聚合方法(Polydopamine-based Atom Transfer Radical Polymerization,p-ATRP)和细胞自催化的无铜添加原子转移自由基聚合方法(Cell-catalyzed Copper-free Atom Transfer Radical Polymerization,c-ATRP)对植物乳杆菌活细胞表面进行修饰,引导原子转移自由基聚合(Atom Transfer Radical Polymerization,ATRP)体系自组装聚合反应形成聚合物材料,对修饰后的植物乳杆菌进行表征,并比较修饰前后植物乳杆菌对黄曲霉毒素B_(1)吸附脱附能力。结果表明,未修饰的植物乳杆菌,细胞表面圆润光滑,经过p-ATRP修饰后的植物乳杆菌,细胞表面变得极为粗糙,经过c-ATRP修饰后的植物乳杆菌,细胞表面出现褶皱;未修饰的植物乳杆菌的Zeta点位为-8.43 mV,经过Dopamine和PNIPAAm修饰后的植物乳杆菌点位分别为1.791和13.767 mV;植物乳杆菌在0.1~100μg/mL黄曲霉毒素B_(1)吸附率为75.3%,p-ATRP和c-ATRP修饰的植物乳杆菌比未修饰的植物乳杆菌吸附能力分别提高了7.8%和6.4%。在相同黄曲霉毒素B_(1)浓度下,植物乳杆菌脱附率为6.1%,p-ATRP和c-ATRP修饰的植物乳杆菌脱附能力分别提高了14.4%和42%。经过修饰后的植物乳杆菌显著提升了植物乳杆菌对黄曲霉毒素的吸附和脱附能力。展开更多
In order to clarify whether Atom Transfer Radical Polymerization（ATRP） method could be extended to free radical ring-opening polymerization, the polymerization of a kind of unsaturated cyclic acetal: 5,6-benzo-2-met...In order to clarify whether Atom Transfer Radical Polymerization（ATRP） method could be extended to free radical ring-opening polymerization, the polymerization of a kind of unsaturated cyclic acetal: 5,6-benzo-2-methylene-1,3-dioxepane（BMDO） in the presence of α,α-dibromoxylene as the initiator and CuBr/2,2-bipyridine as the catalyst and ligand at 120 ℃ was investigated. IR, 1H NMR and 13C NMR spectra of the polymer obtained showed that BMDO underwent quantitatively ring-opening polymerization and linear polyesters were prepared. GPC curves indicated that the polyesters had a narrower molecular weight distribution. Molecular weight of the polyesters could be controlled by polymerization time and adjusting the molar ratio of monomer/intiator consumed. The polymers with narrower polydispersities were obtained, and first-order kinetics of polymerization was observed. These facts proved that BMDO underwent “living” free radical ring-opening polymerization. And this is the firsr report on the “living” free radical ring-opening polymerization of unsarurated cyclic acetal using atom transfer radical polymerization method. The results of ln（[M]0）/[M]) against polymerization time, Mn vs. conversion, and molecular weight distribution of the polymers are indicative of the “living” polymerization process.展开更多
Atom transfer radical polymerization (ATRP) of glycidyl methacrylate (GMA) at roomtemperature was carried out in a methylethyl ketone/1-propanol (in 7/3 volume ratio) solution,initiated and catalyzed by ethyl 2-bromop...Atom transfer radical polymerization (ATRP) of glycidyl methacrylate (GMA) at roomtemperature was carried out in a methylethyl ketone/1-propanol (in 7/3 volume ratio) solution,initiated and catalyzed by ethyl 2-bromopropionate (BRA)/CuC1/2,2＇ -bipyridine (BPY). Polymer ofGMA with planned molecular weight and narrow molecular weight distribution was obtained. In caseof bulk polymerization with the same initiator and catalyst the molecular weight of the polymerobtained was 1.5～2. 1 times greater than that of the above one. By using 1-phenylethyl chloride(PECl)/CuCl/BPY as catalyst controlled ATRP of GMA has failed whether it was in bulk or insolution.展开更多
文摘This paper is the first report on the atom transfer radical copolymerization of unsaturated cyclic acetal, 4,7 dimethyl 2 methylene 1,3 dioxepane(DMMDO) and styrene(St) in the presence of α bromobutyrate as the initiator and CuBr/2,2 bipyridine as the catalyst/ligand at 110 ℃ was investigated. Both DMMDO and St components could be found in main chains of the obtained polymer, and the copolymer had a narrow molecular weight distribution. DMMDO component in the copolymer contained both addition and ring opening units, thus the ester bond was introduced into the main chain, and the copolymer could be chemically degradable and biologically degradable.
文摘为了研究植物乳杆菌材料对黄曲霉毒素去除新方法,为黄曲霉毒素B_(1)的高效生物去除提供了新思路。本文采用基于聚多巴胺的原子转移自由基聚合方法(Polydopamine-based Atom Transfer Radical Polymerization,p-ATRP)和细胞自催化的无铜添加原子转移自由基聚合方法(Cell-catalyzed Copper-free Atom Transfer Radical Polymerization,c-ATRP)对植物乳杆菌活细胞表面进行修饰,引导原子转移自由基聚合(Atom Transfer Radical Polymerization,ATRP)体系自组装聚合反应形成聚合物材料,对修饰后的植物乳杆菌进行表征,并比较修饰前后植物乳杆菌对黄曲霉毒素B_(1)吸附脱附能力。结果表明,未修饰的植物乳杆菌,细胞表面圆润光滑,经过p-ATRP修饰后的植物乳杆菌,细胞表面变得极为粗糙,经过c-ATRP修饰后的植物乳杆菌,细胞表面出现褶皱;未修饰的植物乳杆菌的Zeta点位为-8.43 mV,经过Dopamine和PNIPAAm修饰后的植物乳杆菌点位分别为1.791和13.767 mV;植物乳杆菌在0.1~100μg/mL黄曲霉毒素B_(1)吸附率为75.3%,p-ATRP和c-ATRP修饰的植物乳杆菌比未修饰的植物乳杆菌吸附能力分别提高了7.8%和6.4%。在相同黄曲霉毒素B_(1)浓度下,植物乳杆菌脱附率为6.1%,p-ATRP和c-ATRP修饰的植物乳杆菌脱附能力分别提高了14.4%和42%。经过修饰后的植物乳杆菌显著提升了植物乳杆菌对黄曲霉毒素的吸附和脱附能力。
文摘In order to clarify whether Atom Transfer Radical Polymerization（ATRP） method could be extended to free radical ring-opening polymerization, the polymerization of a kind of unsaturated cyclic acetal: 5,6-benzo-2-methylene-1,3-dioxepane（BMDO） in the presence of α,α-dibromoxylene as the initiator and CuBr/2,2-bipyridine as the catalyst and ligand at 120 ℃ was investigated. IR, 1H NMR and 13C NMR spectra of the polymer obtained showed that BMDO underwent quantitatively ring-opening polymerization and linear polyesters were prepared. GPC curves indicated that the polyesters had a narrower molecular weight distribution. Molecular weight of the polyesters could be controlled by polymerization time and adjusting the molar ratio of monomer/intiator consumed. The polymers with narrower polydispersities were obtained, and first-order kinetics of polymerization was observed. These facts proved that BMDO underwent “living” free radical ring-opening polymerization. And this is the firsr report on the “living” free radical ring-opening polymerization of unsarurated cyclic acetal using atom transfer radical polymerization method. The results of ln（[M]0）/[M]) against polymerization time, Mn vs. conversion, and molecular weight distribution of the polymers are indicative of the “living” polymerization process.
文摘Atom transfer radical polymerization (ATRP) of glycidyl methacrylate (GMA) at roomtemperature was carried out in a methylethyl ketone/1-propanol (in 7/3 volume ratio) solution,initiated and catalyzed by ethyl 2-bromopropionate (BRA)/CuC1/2,2＇ -bipyridine (BPY). Polymer ofGMA with planned molecular weight and narrow molecular weight distribution was obtained. In caseof bulk polymerization with the same initiator and catalyst the molecular weight of the polymerobtained was 1.5～2. 1 times greater than that of the above one. By using 1-phenylethyl chloride(PECl)/CuCl/BPY as catalyst controlled ATRP of GMA has failed whether it was in bulk or insolution.
