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作 者:杜福胜[1] 张昕[1] 陈广强[1] 李子臣[1] 李福绵[1] 潘卉[2] 高青雨[2]
机构地区:[1]北京大学化学与分子工程学院高分子科学与工程系,北京100871 [2]河南大学化学化工学院,开封475001
出 处:《高等学校化学学报》2003年第2期374-376,共3页Chemical Journal of Chinese Universities
基 金:国家自然科学基金 (批准号 :5 0 0 0 30 0 1);教育部博士学科点基金 (批准号 :990 0 0 131)资助
摘 要:A β-diketone-bridged chromophore-containing acrylic monomer, 1-(4-dimethylaminophenyl)-4-methyl-4-pentene-1,3-diketone(DMPDK) and its saturated model compound, 1-(4-dimethyl aminophenyl)-1,3-butanedione(DMBDK) were synthesized and investigated by spectroscopy. It was found that the fluorescence intensity of DMPDK was much lower than that of DMBDK at the same concentration, which indicates that DMPDK, a β-diketone-bridged acrylic monomer having chromophore moiety, also showed fluorescence structural self-quenching effect(SSQE). Photo-induced tautomerization of DMBDK in acetonitrile was studied by means of UV and fluorescence spectroscopy. The results imply that the fluorescence method is capable of monitoring tautomerization of some fluorescent β-diketones.A β-diketone-bridged chromophore-containing acrylic monomer, 1-(4-dimethylaminophenyl)-4-methyl-4-pentene-1,3-diketone(DMPDK) and its saturated model compound, 1-(4-dimethyl aminophenyl)-1,3-butanedione(DMBDK) were synthesized and investigated by spectroscopy. It was found that the fluorescence intensity of DMPDK was much lower than that of DMBDK at the same concentration, which indicates that DMPDK, a β-diketone-bridged acrylic monomer having chromophore moiety, also showed fluorescence structural self-quenching effect(SSQE). Photo-induced tautomerization of DMBDK in acetonitrile was studied by means of UV and fluorescence spectroscopy. The results imply that the fluorescence method is capable of monitoring tautomerization of some fluorescent β-diketones.
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