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氮杂对环吩CP44与萘衍生物超分子体系研究

Study on Supramolecular Systems of Naphthalene Derivative with the Host CP44
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摘要 用紫外吸收光谱法、荧光光谱法和同步扫描荧光光谱法对主体分子CP44与α-萘酚、β-萘酚、2, 6-二羟基茶和6,7-二羟基-2-萘磺酸客体分子形成超分子体系进行了研究.化学计量法表明:主体分子 CP44与萘衍生物客体分子形成1:1的超分子体系;CP44与α-萘酚的包结配位反应是热焓驱动的包结配位反 应,CP44与β-萘酚,2,6-二羟基萘或6,7-二羟基-2-萘磺酸是熵驱动包结配位反应.荧光探针表明:主体 CP44能对α-萘酚、β-萘酚同分异构体进行分子识别. Supramolecular systems of the host CP44 with α-naphthol, β-naphtho1, 2, 6-dihydroxyl naphthalene and 2,3 -dihydroxyl naphthalen-6-sulfonic acid were studied by UV spectroscopy, fluorescence spectroscopy and syn-chronous fluorimetry. The supramolecular system stoichiometry is 1: 1 for all naphthalene derivative complex guests with host CP44. The complex formation reaction of CP44 with β-naphthol was promoted by heat content, where as the complex formation reactions of CP44 with β- naphthol, 2, 6-dihydroxyl naphthalene and 2, 3-dihydroxyl naph-thalen-6-sulfonic acid were promoted by entropy increase. It was proved that host CP44 can recognize the isomers, α-naphthol and β-naphthol by fluorescence probe.
出处 《中山大学学报(自然科学版)》 CAS CSCD 北大核心 2001年第1期118-120,共3页 Acta Scientiarum Naturalium Universitatis Sunyatseni
基金 中山大学科研基金资助项目(3200901)
关键词 氮杂对环吩 超分子体系 分子识别 包结配位反应 CP44 萘衍生物 1 6 20 25-四氮杂[6.1.6.1]对环吩 焓驱动 熵驱动 azaparacyclophane supramolecular systems molecular recognition △H0 △S0
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