For Libraries For Publication Open Access Downloads About Us Contact Us
Paper Titles
Trifluoromethyl-Promoted Oxidation of Fischer N-Heterocyclic Carbene Complexes by DMSO
p.164
Study on Chemical Engineering with Evaluation of Efficiency of Safety Resources Invested in Chemical Enterprises Based on Accounting Information
p.168
Extraction and Characterization of Silk Fibroin from Waste Silk
p.174
A Novel Polymer Supported Catalyst for Preparation of Sydiopolystyrene
p.178
Synthesis, Photochromic Properties of an Unsymmetrical Diarylethene Bearing Fluorene Ring
p.182
Synthesis, Properties of a Photochromic Diarylethene Material Bearing Benzofuran and Thiazole Rings
p.186
Synthesis and Properties of a Novel Unsymmetrical Diarylethene with a Benzothiophene and a Thiazole Group
p.190
Synthesis and Properties of a New Unsymmetrical Diarylethene Bearing Benzothiophene and Thiophene Rings
p.194
Synthesis and Properties of a Novel Photochromic Diarylethene 1-(2,4-dimethyl-5-thiazolyl)-2-[2-methyl-5-(4-formylphenyl)-3-thienyl]perfluorocyclopentene
p.198

Synthesis, Photochromic Properties of an Unsymmetrical Diarylethene Bearing Fluorene Ring

Article Preview

Abstract:

A new unsymmetrical photochromic diarylethene compound was synthesized and its photochemical, fluorescence properties were investigated in detail in solution. The results showed that the compound exhibited remarkable photochromism and the emission intensity was quenched 87% at the photostationary state in solution. When the concentration arrived at 2 × 10-5 mol L-1, the fluorescence peak of the diarylethene had the maximum.

You might also be interested in these eBooks
Advanced Research on Material Engineering, Chemistry and Environment View Preview

Info:

Periodical:

Advanced Materials Research (Volume 788)

Pages:

182-185

DOI:

https://doi.org/10.4028/www.scientific.net/AMR.788.182

Citation:

Cite this paper

Online since:

September 2013

Authors:

Hai Chang Ding, Hong Yan Xu, Gang Liu

Keywords:

Diarylethene, Fluorene, Fluorescence, Photochromism

Export:

RIS, BibTeX

Price:

Permissions CCC:

Request Permissions

Permissions PLS:

Request Permissions

Сopyright:

© 2013 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

References

[1] R. Davis and N. Tamaoki: Chem. Eur. J. Vol. 13 (2007), p.626.

Google Scholar

[2] Y. Ishibashi, K. Tani, H. Miyasaka, S. Kobatake and M. Irie: Chemical Physics Letters. Vol. 437 (2007), p.243.

Google Scholar

[3] P. Sauer and R. E. Allen: Chemical Physics Letters Vol. 434 (2007), p.260.

Google Scholar

[4] S. Kobatake and I. Yamashita: Tetrahedron Vol. 64 (2008), p.7611.

Google Scholar

[5] S.Z. Pu, G. Liu, Q. Xiao, L. Shen and J.K. Xu: Org. Lett. Vol. 9 (2007), p.2139.

Google Scholar

[6] S.Z. Pu, C.H. Zheng, Z.G. Le, G. Liu and C.B. Fang: Tetrahedron Vol. 64 (2008), p.2576.

Google Scholar

[7] H. Tian and Y.L. Feng: J. Mater. Chem Vol. 18 (2008), p.1617.

Google Scholar

[8] S.Z. Pu, D.H. Jiang, W.J. Liu, G. Liu and S.Q. Cui. J. Mater. Chem. Vol. 22 (2012), p.3517.

Google Scholar

[9] Q.F. Luo, H. Cheng and H. Tian: Polym. Chem. Vol. 2 (2011), p.2435.

Google Scholar

[10] S.Z. Pu, H.H. Tang, B. Chen, J. K. Xu and W. H. Huang: Mater. Lett Vol. 60 (2006), p.3553.

Google Scholar

© 2025 Trans Tech Publications Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies. For open access content, terms of the Creative Commons licensing CC-BY are applied.
Scientific.Net is a registered trademark of Trans Tech Publications Ltd.