作者: Lin-Lin Deng , Ling-Xiang Guo , Bao-Ping Lin , Xue-Qin Zhang , Ying Sun
DOI: 10.1039/C6PY01165A
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摘要: The known synthetic methods of preparing main-chain liquid crystalline polymers (MCLCPs) are rather limited to several polycondensation reactions. However, the nature step-growth endows corresponding MCLCPs with relatively low molecular weights and broad weight distributions. In this manuscript, an entropy-driven ring-opening metathesis polymerization (ED-ROMP) approach is for first time applied in producing a MCLCP by polymerizing macrocyclic olefin monomer containing one cyclohexanecarboxylic acid phenyl ester group as mesogenic core icos-10-enedicarbonyl flexible aliphatic chain. For comparison, Yamaguchi macrolactonization ring-closing (RCM) used synthesize monomer, it turns out that although method can prepare pure RCM strategy advantageous providing much higher overall reaction yield. Furthermore, compared traditional acyclic diene (ADMET) α,ω-diene, ED-ROMP starting same monomer-to-catalyst ratio, releases no heat or volatiles during reaction, efficiently provide over shorter time.