Correlation between the molecular structure and transcis isomerization characteristics of azobenzenes  

Correlation between the molecular structure and transcis isomerization characteristics of azobenzenes

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作  者:HAN Mina HONDA Takumu 

机构地区:[1]Department of Chemistry and Department of Electronic Chemistry,Tokyo Institute of Technology

出  处:《Science China Chemistry》2011年第12期1955-1961,共7页中国科学(化学英文版)

基  金:supported by the Global COE Program from the Ministry of Education,Culture,Sports,Science,and Technology of Japanese Government

摘  要:Photochemical and thermal isomerization of various azobenzenes was systematically investigated to understand the correlation between the molecular structure and trans → cis isomerization characteristics of azobenzenes. A blue shift in π-π absorption band of ortho-alkylated azobenzenes (1o and 2o) was observed together with a reduction in molar extinction coefficient (e) in comparison with both meta-alkylated azobenzenes (4m and 5m) and 7p lacking the meta and ortho substituents. For orthoalkylated azobenzene, photochemical trans-to-cis isomerization and thermal back cis-to-trans isomerization in solution oc- curred slowly when compared with 4m, 5m and 7p. The half-life time of the cis form of 20 was found to be 380 h, which is about 8-50 times longer than those of comparable 4m, 5m (43-13 h) and 7p (7 h). Furthermore, comparison of the molecular structure and isomerization characteristics of azobenzene thiol (20 and 5m) self-assembled monolayers on flat gold surfaces indicates that the trans-to-cis photoconversion in monolayer systems is influenced by steric hindrance and strong intermoleculax interaction between azobenzene units.Photochemical and thermal isomerization of various azobenzenes was systematically investigated to understand the correlation between the molecular structure and trans ? cis isomerization characteristics of azobenzenes.A blue shift in πDπ* absorption band of ortho-alkylated azobenzenes(1o and 2o) was observed together with a reduction in molar extinction coefficient in comparison with both meta-alkylated azobenzenes(4m and 5m) and 7p lacking the meta and ortho substituents.For ortho-alkylated azobenzene,photochemical trans-to-cis isomerization and thermal back cis-to-trans isomerization in solution occurred slowly when compared with 4m,5m and 7p.The half-life time of the cis form of 2o was found to be 380 h,which is about 8-50 times longer than those of comparable 4m,5m(43-13 h) and 7p(7 h).Furthermore,comparison of the molecular structure and isomerization characteristics of azobenzene thiol(2o and 5m) self-assembled monolayers on flat gold surfaces indicates that the trans-to-cis photoconversion in monolayer systems is influenced by steric hindrance and strong intermolecular interaction between azobenzene units.

关 键 词:AZOBENZENE ISOMERIZATION lifetime of cis form molecular structure 

分 类 号:O621.13[理学—有机化学]

 

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