A new environmental friendly catalyst, HaSiWrMo6O40/PAn was prepared and identified by means of FT-IR, XRD and TG/DTA. The optimum conditions have been found, that was, mass ratio of m（PAn）： m（HaSiW6Mo6On.） was 1...A new environmental friendly catalyst, HaSiWrMo6O40/PAn was prepared and identified by means of FT-IR, XRD and TG/DTA. The optimum conditions have been found, that was, mass ratio of m（PAn）： m（HaSiW6Mo6On.） was 1：1.25, volume of methanol was 20 mL, and the reflux reaction time was 2h. The structural identity of Keggin units was preserved after the incorporation into polyaniline matrix. H4SiW6Mo6040/PAn was used as catalyst in catalytic synthesis of acetals and ketals. Effects of n（aldehyde（ketone ））： n（glycol）, catalyst dosage and reaction time on yield were investingated. Optimal conditions were： n（aldehyde（ketone））： n（glycol）=1.0： 1.5; mass fraction of catalyst to reactants, 0.5%; reaction time, 1.0 h and cyclohexane as water-stripped reagent, 15 mL. Under these conditions, yields of actels and ketals were 31.9%-91.6%.展开更多
A novel copolymer network with acetal structure was prepared using bis[4-(vinyloxy)butyl](4-methyl-1,3-phenylene)biscarbamate(BECT)as the crosslinking agent.Firstly,a tri-copolymer of maleic anhydride(MAn),n-butyl vin...A novel copolymer network with acetal structure was prepared using bis[4-(vinyloxy)butyl](4-methyl-1,3-phenylene)biscarbamate(BECT)as the crosslinking agent.Firstly,a tri-copolymer of maleic anhydride(MAn),n-butyl vinyl ether(BVE)and 4-hydroxybutyl vinyl ether(HBVE)was synthesized via free-radical polymerization with 2,2′-azobisisobutyronitrile as the initiator.The tri-copolymer consisted of two sorts of alternating units,MAn-alt-BVE and MAn-alt-HBVE.The linear copolymer Poly((MAn-alt-BVE)-co-(MAn-alt-HBVE))with pending hydroxyl groups was then combined with BECT in the presence of pyridinium p-toluenesulfonate,generating a copolymer network comprising acetal components in the crosslinking segment. This polymer network exhibited degradation in acid conditions.展开更多
文摘A new environmental friendly catalyst, HaSiWrMo6O40/PAn was prepared and identified by means of FT-IR, XRD and TG/DTA. The optimum conditions have been found, that was, mass ratio of m（PAn）： m（HaSiW6Mo6On.） was 1：1.25, volume of methanol was 20 mL, and the reflux reaction time was 2h. The structural identity of Keggin units was preserved after the incorporation into polyaniline matrix. H4SiW6Mo6040/PAn was used as catalyst in catalytic synthesis of acetals and ketals. Effects of n（aldehyde（ketone ））： n（glycol）, catalyst dosage and reaction time on yield were investingated. Optimal conditions were： n（aldehyde（ketone））： n（glycol）=1.0： 1.5; mass fraction of catalyst to reactants, 0.5%; reaction time, 1.0 h and cyclohexane as water-stripped reagent, 15 mL. Under these conditions, yields of actels and ketals were 31.9%-91.6%.
基金the support from Innovative Research Team in Universities (IRT0706)the Polymer Chemistry and Physics, Beijing Municipal Education Commission (XK100100640)
文摘A novel copolymer network with acetal structure was prepared using bis[4-(vinyloxy)butyl](4-methyl-1,3-phenylene)biscarbamate(BECT)as the crosslinking agent.Firstly,a tri-copolymer of maleic anhydride(MAn),n-butyl vinyl ether(BVE)and 4-hydroxybutyl vinyl ether(HBVE)was synthesized via free-radical polymerization with 2,2′-azobisisobutyronitrile as the initiator.The tri-copolymer consisted of two sorts of alternating units,MAn-alt-BVE and MAn-alt-HBVE.The linear copolymer Poly((MAn-alt-BVE)-co-(MAn-alt-HBVE))with pending hydroxyl groups was then combined with BECT in the presence of pyridinium p-toluenesulfonate,generating a copolymer network comprising acetal components in the crosslinking segment. This polymer network exhibited degradation in acid conditions.
