Electrochemical switch based on the photoisomerization of a diarylethene derivative

Nan Xie; De X. Zeng; Yi Chen

doi:10.1016/j.jelechem.2007.06.009

Electrochemical switch based on the photoisomerization of a diarylethene derivative

Nan Xie, De X. Zeng, Yi Chen

Research output: Contribution to journal › Article › peer-review

11 Scopus citations

Abstract

3,4-Bis[5-(2′-thiophene)-2-methylthien-3-yl]-2,5-dihydrothiophene 1a was synthesized and underwent excellent ring-opening and ring-closing photoisomerization in solution with UV/Vis light irradiation. Both ring-open isomer and ring-closed isomer of diarylethene showed electrochemical behavior, and the oxidation/reduction potential was reversible based on the ring-opening and ring-closing photoisomerization of diarylethene with UV/Vis light irradiation. Besides, a combination of photochromism and electrochromism of 1a was also observed.

Original language	English (US)
Pages (from-to)	27-30
Number of pages	4
Journal	Journal of Electroanalytical Chemistry
Volume	609
Issue number	1
DOIs	https://doi.org/10.1016/j.jelechem.2007.06.009
State	Published - Oct 15 2007
Externally published	Yes

Keywords

Diarylethene
Electrochemical switch
Electrochromism
Photochromism
Photoisomerization

ASJC Scopus subject areas

Analytical Chemistry
Chemical Engineering(all)
Electrochemistry

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10.1016/j.jelechem.2007.06.009

Cite this

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title = "Electrochemical switch based on the photoisomerization of a diarylethene derivative",

abstract = "3,4-Bis[5-(2′-thiophene)-2-methylthien-3-yl]-2,5-dihydrothiophene 1a was synthesized and underwent excellent ring-opening and ring-closing photoisomerization in solution with UV/Vis light irradiation. Both ring-open isomer and ring-closed isomer of diarylethene showed electrochemical behavior, and the oxidation/reduction potential was reversible based on the ring-opening and ring-closing photoisomerization of diarylethene with UV/Vis light irradiation. Besides, a combination of photochromism and electrochromism of 1a was also observed.",

keywords = "Diarylethene, Electrochemical switch, Electrochromism, Photochromism, Photoisomerization",

author = "Nan Xie and Zeng, {De X.} and Yi Chen",

note = "Funding Information: This work was supported by the National Science Foundation of China (No. 60337020).",

year = "2007",

month = oct,

day = "15",

doi = "10.1016/j.jelechem.2007.06.009",

language = "English (US)",

volume = "609",

pages = "27--30",

journal = "Journal of Electroanalytical Chemistry",

issn = "1572-6657",

publisher = "Elsevier Sequoia",

number = "1",

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TY - JOUR

T1 - Electrochemical switch based on the photoisomerization of a diarylethene derivative

AU - Xie, Nan

AU - Zeng, De X.

AU - Chen, Yi

N1 - Funding Information: This work was supported by the National Science Foundation of China (No. 60337020).

PY - 2007/10/15

Y1 - 2007/10/15

N2 - 3,4-Bis[5-(2′-thiophene)-2-methylthien-3-yl]-2,5-dihydrothiophene 1a was synthesized and underwent excellent ring-opening and ring-closing photoisomerization in solution with UV/Vis light irradiation. Both ring-open isomer and ring-closed isomer of diarylethene showed electrochemical behavior, and the oxidation/reduction potential was reversible based on the ring-opening and ring-closing photoisomerization of diarylethene with UV/Vis light irradiation. Besides, a combination of photochromism and electrochromism of 1a was also observed.

AB - 3,4-Bis[5-(2′-thiophene)-2-methylthien-3-yl]-2,5-dihydrothiophene 1a was synthesized and underwent excellent ring-opening and ring-closing photoisomerization in solution with UV/Vis light irradiation. Both ring-open isomer and ring-closed isomer of diarylethene showed electrochemical behavior, and the oxidation/reduction potential was reversible based on the ring-opening and ring-closing photoisomerization of diarylethene with UV/Vis light irradiation. Besides, a combination of photochromism and electrochromism of 1a was also observed.

KW - Diarylethene

KW - Electrochemical switch

KW - Electrochromism

KW - Photochromism

KW - Photoisomerization

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U2 - 10.1016/j.jelechem.2007.06.009

DO - 10.1016/j.jelechem.2007.06.009

M3 - Article

AN - SCOPUS:34948903844

SN - 1572-6657

VL - 609

SP - 27

EP - 30

JO - Journal of Electroanalytical Chemistry

JF - Journal of Electroanalytical Chemistry

IS - 1

ER -

Electrochemical switch based on the photoisomerization of a diarylethene derivative

Abstract

Keywords

ASJC Scopus subject areas

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