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作 者:刘瑞源 Tong Zhang Xiao-dong Yang Yi-chen Yan 瞿金清
机构地区:[1]School of Pharmaceutical Sciences,Southern Medical University [2]School of Chemistry and Chemical Engineering,South China University of Technology
出 处:《Chinese Journal of Polymer Science》2014年第7期931-940,共10页高分子科学(英文版)
基 金:financially supported by the National Natural Science Foundation of China(Nos.21074073 and 51173050);The Guangdong Provincial Engineering Research Center of Green Fine Chemical Technology,China
摘 要:A novel phenylacetylene derivative containing urea groups was synthesized and polymerized with a Rh catalyst to give the corresponding polymer, poly(1) with moderate number-average molecular weights. The poly(1) was soluble in toluene, CHCI3, CH2C12, THF, DMF, and DMSO, but insoluble in hexane, diethyl ether and MeOH. The specific rotation and circular dichroism (CD) spectroscopic studies revealed that poly(1) took predominantly one-handed helical structures. The presence of intramolecular hydrogen bonding was confirmed by liquid-state IR spectroscopy. The helicity of poly(1) could be tuned by temperature and anion. The helical conformation of the polymer was stable against Br but susceptible to F.A novel phenylacetylene derivative containing urea groups was synthesized and polymerized with a Rh catalyst to give the corresponding polymer, poly(1) with moderate number-average molecular weights. The poly(1) was soluble in toluene, CHCI3, CH2C12, THF, DMF, and DMSO, but insoluble in hexane, diethyl ether and MeOH. The specific rotation and circular dichroism (CD) spectroscopic studies revealed that poly(1) took predominantly one-handed helical structures. The presence of intramolecular hydrogen bonding was confirmed by liquid-state IR spectroscopy. The helicity of poly(1) could be tuned by temperature and anion. The helical conformation of the polymer was stable against Br but susceptible to F.
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