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CONCERTED H-BONDING TEMPLATE SYNTHESIS OF AN ORDERED LADDER POLYSILSESQUIOXANE

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【作者】 张榕本

【Author】 Kui-lin Deng, Tao-yi Zhang, Xiao-jing Zhang, Ai-qin Zhang, Ping Xie and Rong-ben Zhang PCLCC (Polym. Chem. Lab. Chinese Academy of Sciences & China Petro-Chemical Corp.), State Key Laboratory on Polymer Physics & Chemistry, Joint Laboratory of Polymer Science & Materials Institute of Chemistry, Chinese Academy of Sciences, Beijing 100080, China Graduate School of the Chinese Academy of Sciences, Beijing 100039, China College of Chemistry & Environmental Science, Hebei University, Baoding 071002, China

【机构】 PCLCC (Polym. Chem. Lab. Chinese Academy of Sciences & China Petro-Chemical Corp.) State Key Laboratory on Polymer Physics & Chemistry Joint Laboratory of Polymer Science & Materials Institute of Chemistry Chinese Academy of Sciences Beijing 100080 China

【摘要】 <正>A novel soluble regular ladder poly(benzoyl-3-aminopropyl) silsesquioxane (LPBAS) was facilely prepared under effective assistance of concerted H-bonding self-assembly of amido groups of side chains and silanol groups, respectively, of a new template monomer [1,3-bis(benzoyl-3-aminopropyl)-1,1,3,3-tetraethoxydisiloxane] (M). The ordered ladder structure of LPBAS is manifested in: (1) the presence of two Bragg peaks representing the ladder width (d) and ladder thickness (t) in X-ray diffraction (XRD) pattern; (2) narrow base-line width (w = 6) of resonance absorption for -CH2SiO3/2 moiety in 29Si-NMR and (3) high glass transition temperature Tg = 112℃in differential scanning calorimetry (DSC) analysis.

【Abstract】 A novel soluble regular ladder poly(benzoyl-3-aminopropyl) silsesquioxane (LPBAS) was facilely prepared under effective assistance of concerted H-bonding self-assembly of amido groups of side chains and silanol groups, respectively, of a new template monomer [1,3-bis(benzoyl-3-aminopropyl)-1,1,3,3-tetraethoxydisiloxane] (M). The ordered ladder structure of LPBAS is manifested in: (1) the presence of two Bragg peaks representing the ladder width (d) and ladder thickness (t) in X-ray diffraction (XRD) pattern; (2) narrow base-line width (w = 6) of resonance absorption for -CH2SiO3/2 moiety in 29Si-NMR and (3) high glass transition temperature Tg = 112℃in differential scanning calorimetry (DSC) analysis.

【基金】 This work was financially supported by NSFC (Nos. 50073028, 29974036 and 20174047).
  • 【文献出处】 Chinese Journal of Polymer Science ,高分子科学(英文版) , 编辑部邮箱 ,2006年05期
  • 【分类号】O631.3
  • 【被引频次】1
  • 【下载频次】73
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