【摘要】 对反应性梯形聚氢基倍半硅氧烷 (H T)的合成方法进行了改进 .首先利用硅羟基与硅氯基之间的脱氯化氢缩聚来代替以前采用的硅羟基间脱水缩聚反应 ,进一步提高了作为梯撑的对苯二胺之间氢键在聚合反应中的模板作用 .另外利用三甲基氯硅烷与对苯二胺梯撑的聚硅氧烷中间体的末端硅羟基进行封端反应 ,从而保证在脱除对苯二胺梯撑模板分子过程中避免进一步的无规缩合导致支化或交联 ,得到的反应性梯形聚氢基倍半硅氧烷 (H T)的规整性有所改善 .热分析结果表明与单链聚二甲基硅氧烷的Tg(- 12 3℃ )相比 ,其Tg 高达 117 0℃ ,证明这种梯形高分子具有刚性链结构 .尤其是2 9Si NMR谱中代表梯形主链上硅原子 (SiO3 2 )峰的基线宽度Δ =5 ,而采用硅羟基间脱水缩合方法得到聚合物的Δ =8～ 10 .表明该反应性梯形聚氢基倍半硅氧烷H T的规整性得到了明显的提高 .而且 ,该聚合物又是第一个可溶性、反应性、纯梯形主链无机高分子 ,它可以进一步通过硅 氢侧基接枝反应制备不同类型的梯形无机主链功能高分子 .更多还原

【Abstract】 An ordered reactive ladderlike polyhydrosilsesquioxane （H-T） was successfully synthesized via a modified “stepwise coupling polymerization" process,which included two improvements in synthetic method.First,dehydrochlorination polycondensation between Si—OH and Si—Cl groups during polycondensation reaction is employed instead of the dehydration between Si\_OH groups used before,which improves the H-bonding template effect of the bridged-phenylene diamine.Meanwhile,trimethylchlorosilane is used to block the terminal silanol groups,avoiding the further intermolecular crosslinking of the phenylene diamine-bridged ladderlike macromolecular intermediates.Consequently,the regularity of H-T has been improved,and compared with a very low T_g （-123℃） of the single-chained polydimethylsiloxane,a significantly higher T_g （117.0℃） of H-T in DSC measurement confirms that the ordered reactive H-T macromolecule possesses comparatively stiff main chain.Above all,the peak of HSiO_3/2 （-84.8） with the baseline width （Δ） of about 5 in （）²⁹Si-NMR spectrum which is much narrower than that of the polysilsesquioxane （Δ=8～10） prepared by the usual dehydration condensation method shows that the regularity of H-T is obviously improved.Furthermore,H-T is the first soluble,reactive and purely inorganic ladderlike macromolecule,which can be grafted through hydrosilylation reaction and others to generate functional LPSs with different side groups.更多还原