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Photoswitchable molecular wires

Authors :
Ben L. Feringa
Maaike T.W. Milder
Jennifer Lynn Herek
Jetsuda Areephong
Wesley R. Browne
Stratingh Institute of Chemistry
Zernike Institute for Advanced Materials
Synthetic Organic Chemistry
Chemistry of (Bio)organic Materials and Devices
Faculty of Science and Engineering
Faculty of Science and Technology
Optical Sciences
Source :
Chemical Physics Letters, 479(1-3), 137-139. ELSEVIER SCIENCE BV, Chemical physics letters, 479(1-3), 137-139. Elsevier
Publication Year :
2009

Abstract

Photoswitchable dithienylethene groups, added to both alpha-ends of a sexithiophene molecular wire, switch reversibly between their open and closed forms upon irradiation. The open form has an excited state lifetime of 500 ps and is highly fluorescent, as is typical for oligothiophenes. In contrast the closed form is non-fluorescent and the excited state lifetime is a shorter by a factor of 100, reminiscent of a dithienylethene. In this system, we control the fundamental character of a molecular system through optical switching; toggling between a sexithiophene molecular wire and a dithienylethene reversibly. (C) 2009 Published by Elsevier B.V.

Details

Language :
English
ISSN :
18734448 and 00092614
Volume :
479
Issue :
1-3
Database :
OpenAIRE
Journal :
Chemical Physics Letters
Accession number :
edsair.doi.dedup.....5f37d5547fe4b93a8904088df3addcc2
Full Text :
https://doi.org/10.1016/j.cplett.2009.08.013