Abstract
Here we report on the synthesis and photochromism of a group of newly designed phenanthrene-bridged diarylethenes. The structure of one diarylethene derivative was determined by single crystal X-ray diffraction analysis. The photochromic dyes cyclize smoothly in polar organic solvents and water upon UV light irradiation while undergo fading under visible light. These photochromic materials have non-destructive readout capability through fluorescent modulation. Fluorescent read-out lights of them are 390 and 385 nm respectively. The non-destructive read out capability of them was studied with density functional theory and the results indicated that the cyclization probably took place at the second rather than the first excited states.
| Original language | English |
|---|---|
| Pages (from-to) | 45-52 |
| Number of pages | 8 |
| Journal | Journal of Photochemistry and Photobiology A: Chemistry |
| Volume | 277 |
| DOIs | |
| Publication status | Published - Mar 1 2014 |
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Keywords
- Diarylethene
- Non-destructive readout
- Phenanthrene
- Photochromism
- Solvent effect
ASJC Scopus subject areas
- Chemistry(all)
- Chemical Engineering(all)
- Physics and Astronomy(all)
Cite this
Phenanthrene-bridged diarylethenes : Synthesis, photochromism and non-destructive readout. / He, Junjie; Wang, Tingting; Chen, Shuxin; Zheng, Ruiping; Chen, Huiyuan; Li, Jing; Zeng, Heping.
In: Journal of Photochemistry and Photobiology A: Chemistry, Vol. 277, 01.03.2014, p. 45-52.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Phenanthrene-bridged diarylethenes
T2 - Synthesis, photochromism and non-destructive readout
AU - He, Junjie
AU - Wang, Tingting
AU - Chen, Shuxin
AU - Zheng, Ruiping
AU - Chen, Huiyuan
AU - Li, Jing
AU - Zeng, Heping
PY - 2014/3/1
Y1 - 2014/3/1
N2 - Here we report on the synthesis and photochromism of a group of newly designed phenanthrene-bridged diarylethenes. The structure of one diarylethene derivative was determined by single crystal X-ray diffraction analysis. The photochromic dyes cyclize smoothly in polar organic solvents and water upon UV light irradiation while undergo fading under visible light. These photochromic materials have non-destructive readout capability through fluorescent modulation. Fluorescent read-out lights of them are 390 and 385 nm respectively. The non-destructive read out capability of them was studied with density functional theory and the results indicated that the cyclization probably took place at the second rather than the first excited states.
AB - Here we report on the synthesis and photochromism of a group of newly designed phenanthrene-bridged diarylethenes. The structure of one diarylethene derivative was determined by single crystal X-ray diffraction analysis. The photochromic dyes cyclize smoothly in polar organic solvents and water upon UV light irradiation while undergo fading under visible light. These photochromic materials have non-destructive readout capability through fluorescent modulation. Fluorescent read-out lights of them are 390 and 385 nm respectively. The non-destructive read out capability of them was studied with density functional theory and the results indicated that the cyclization probably took place at the second rather than the first excited states.
KW - Diarylethene
KW - Non-destructive readout
KW - Phenanthrene
KW - Photochromism
KW - Solvent effect
UR - http://www.scopus.com/inward/record.url?scp=84891853728&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84891853728&partnerID=8YFLogxK
U2 - 10.1016/j.jphotochem.2013.11.016
DO - 10.1016/j.jphotochem.2013.11.016
M3 - Article
AN - SCOPUS:84891853728
VL - 277
SP - 45
EP - 52
JO - Journal of Photochemistry and Photobiology A: Chemistry
JF - Journal of Photochemistry and Photobiology A: Chemistry
SN - 1010-6030
ER -