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Electrophilic aromatic aroylation polycondensation synthesis of wholly aromatic polyketone composed of 2,2'-dimethoxy-1,1'-binaphthylylene moiety

机译:由2,2'-二甲氧基-1,1'-联萘撑部分组成的全芳族聚酮的亲电芳烃化缩聚反应

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摘要

A wholly aromatic polyketone containing 2,2'-dimethoxy-1,1 '-binaphthylylene moiety was successfully synthesized via electrophilic aromatic aroylation polycondensation with the aid of trifluoromethanesulfonic acid (TfOH) or phospho-rus(V) oxide-methanesulfonic acid mixture (P_2O_5-MsOH). The polycondensation reactions employing two sets of monomers of opposite combination that should afford the same structure of repeating unit showed distinct results. The polycondensation employing 2,2'-dimethoxy-1,1'-binaphthyl (4) as the acyl-acceptant monomer proceeded to give medium-molecular-weight polymer. The polymer synthesis via transformation of biaryl 4 into the corresponding acyl-donor monomer 12 followed by polycondensation with 2,2'-dimethoxybiphenyl (1) predominated the procedure of direct usage of biaryl 4 as the acyl-acceptant monomer. Acyl-acceptant monomer has been demonstrated to play a more crucial role in determination of polymerizability than acyl-donor one.
机译:借助三氟甲磺酸(TfOH)或磷-氧化(V)氧化物-甲磺酸混合物(P_2O_5),通过亲电芳族酰化缩聚反应成功合成了包含2,2'-二甲氧基-1,1'-联萘基部分的全芳族聚酮-MsOH)。使用应该提供相同结构重复单元的相反组合的两组单体的缩聚反应显示出不同的结果。使用2,2'-二甲氧基-1,1'-联萘基(4)作为酰基接受单体的缩聚反应进行,得到中等分子量的聚合物。通过将联芳基4转化成相应的酰基供体单体12,然后与2,2'-二甲氧基联苯(1)缩聚来进行的聚合物合成占主导地位,直接使用联芳基4作为酰基接受单体。事实证明,酰基接受单体在确定可聚合性方面比酰基供体更重要。

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