Homopolymerization of 4-vinyl pyridine（4-VP） and copolymerization of 4-VP with styrene（St） were performed by catalyst systems composed of calix[4]arene-neodymium complex 2,di-n-butylmagnesium and hexamethyl phosph...Homopolymerization of 4-vinyl pyridine（4-VP） and copolymerization of 4-VP with styrene（St） were performed by catalyst systems composed of calix[4]arene-neodymium complex 2,di-n-butylmagnesium and hexamethyl phosphoramide. The molecular weight of P（4-VP） was greatly affected by adding calix[4]arene-neodymium complex,and high molecular weight of P（4-VP） was got by using calix[4]arene-neodymium complex.The highest molecular weight of P（4-VP） was as high as 4.65×106 obtained by using a catalyst system with 2.0×10-4?mol/L of calix[4]arene-neodymium complex,while the molecular weight of P（4-VP） was only 5.62×105 without calix[4]arene-neodymium complex. In addition,4-VP-St copolymers with different 4-VP contents were obtained in good yield.When styrene was polymerized first for a time period,and then 4-VP was added,4-VP-St copolymers with 4.85?mol%～23.3?mol% of 4-VP units were obtained,but when 4-VP and styrene were added at the same time the resultant 4-VP-St copolymers had 44.0?mol%～66.3?mol% of 4-VP units.展开更多
Poly(4-diazosulfonate styrene-co-4-vinylpyridine) (P(DSS-co-VP)),containing both H-acceptor moieties of pyridine and photosensitive diazosulfonate groups,was synthesized and has been used for self-assembly as a new co...Poly(4-diazosulfonate styrene-co-4-vinylpyridine) (P(DSS-co-VP)),containing both H-acceptor moieties of pyridine and photosensitive diazosulfonate groups,was synthesized and has been used for self-assembly as a new component.The layer-by-layer deposition between P(DSS-co-VP)and m-methyl phenol formaldehyde resin (MPR) on a substrate via H-bonding interaction was investigated.After UV irradiation the stability of the multiplayer ultra thin film toward polar solvents is improved dramatically.The improvement of the solvent stability of the film should be attributed to the bond conversion between the layers of the film from H-bond to covalent bond under UV irradiation.展开更多
文摘Homopolymerization of 4-vinyl pyridine（4-VP） and copolymerization of 4-VP with styrene（St） were performed by catalyst systems composed of calix[4]arene-neodymium complex 2,di-n-butylmagnesium and hexamethyl phosphoramide. The molecular weight of P（4-VP） was greatly affected by adding calix[4]arene-neodymium complex,and high molecular weight of P（4-VP） was got by using calix[4]arene-neodymium complex.The highest molecular weight of P（4-VP） was as high as 4.65×106 obtained by using a catalyst system with 2.0×10-4?mol/L of calix[4]arene-neodymium complex,while the molecular weight of P（4-VP） was only 5.62×105 without calix[4]arene-neodymium complex. In addition,4-VP-St copolymers with different 4-VP contents were obtained in good yield.When styrene was polymerized first for a time period,and then 4-VP was added,4-VP-St copolymers with 4.85?mol%～23.3?mol% of 4-VP units were obtained,but when 4-VP and styrene were added at the same time the resultant 4-VP-St copolymers had 44.0?mol%～66.3?mol% of 4-VP units.
基金supported by the National Natural Science Foundation of China(21773215,J1210060)the Innovative Research Grant for Undergraduate Students of National/Zhengzhou University(201710459008)~~
文摘Poly(4-diazosulfonate styrene-co-4-vinylpyridine) (P(DSS-co-VP)),containing both H-acceptor moieties of pyridine and photosensitive diazosulfonate groups,was synthesized and has been used for self-assembly as a new component.The layer-by-layer deposition between P(DSS-co-VP)and m-methyl phenol formaldehyde resin (MPR) on a substrate via H-bonding interaction was investigated.After UV irradiation the stability of the multiplayer ultra thin film toward polar solvents is improved dramatically.The improvement of the solvent stability of the film should be attributed to the bond conversion between the layers of the film from H-bond to covalent bond under UV irradiation.
