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Photoisomerization of the azobenzenes included in Langmuir-Blodgett films of cyclodextrins
Authors:Akira Yabe  Yasujiro Kawabata  Hiroyuki Niino  Mutsuyoshi Matsumoto  Akihiko Ouchi  Hisao Takahashi  Shoji Tamura  Waichiro Tagaki  Hiroo Nakahara  Kiyoshige Fukuda
Affiliation:

National Chemical Laboratory for Industry, Yatabe, Tsukuba, Ibaraki 305, Japan

Department of Applied Chemistry, Faculty of Engineering, Osaka City University, Sumiyoshiku, Osaka 558, Japan

Department of Chemistry, Faculty of Science, Saitama University, Urawa, Saitama 338, Japan

Abstract:A new type of photochemical Langmuir-Blodgett (LB) film containing azobenzenes (p-phenylazobenzoic acid (PAB), methyl red (MR) and methyl orange (MO)) without long alkyl chains was prepared by the host-guest interaction with an amphiphilic cyclodextrin derivative. The azobenzenes in the LB film of the host- guest complex exhibited an excellent cis-trans photoisomerization, while trans-to- cis photoisomerization was restricted for LB films of long chain azobenzene derivatives alone. The cavity of cyclodextrin provides a favourable environment for the photochemical reaction leading to an increase in the molecular area in the rigid LB film. The half-life times of cis isomers of PAB, MR and MO in the host-guest complex LB films were 35 h, 55 s and 13 min respectively at 20°C.
Keywords:
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