期刊
CHEMISTRY-A EUROPEAN JOURNAL
卷 21, 期 5, 页码 2182-2192出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201404784
关键词
boron; density functional calculations; dithienylethene; multi-addressable functions; photochromic systems
资金
- University of Hong Kong
- URC Strategic Research Theme on New Materials
- University Grants Committee Areas of Excellence Scheme [AoE/P-03/08]
- General Research Fund (GRF) Grant from the Research Grants Council of Hong Kong Special Administrative Region, China [HKU 7060/12P]
A series of dithienylethene-containing triarylboranes has been designed, synthesized, and characterized. The electrochemistry, photophysics, and photochromic behavior have also been studied. The photophysical and photochromic properties could be facilely tuned in this system by varying the thiophene spacers (thiophene, thienothiophene, and bithiophene) between the dithienylethene and the dimesitylboron (BMes(2)) or the position of the BMes(2) substitution in the thiophene spacers. The absorption of closed form has been found to be more sensitive towards the structural modification upon incorporation of the BMes(2) unit. Moreover, multi-addressable photochromic reactivity is obtained upon addition of Lewis base (F-), which is due to the formation of boron-Lewis base adduct. The dependence of the photophysical and photochromic properties on the thiophene spacers and the position of the BMes(2) substitution has been further supported by computational studies.
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