4.7 Article

Synthesis, crystal structures and two-photon absorption properties of a series of terpyridine-based chromophores

Journal

DYES AND PIGMENTS
Volume 95, Issue 1, Pages 149-160

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.dyepig.2012.03.020

Keywords

Terpyridine derivatives; Synthesis; Single-photon-excited fluorescence; Two-photon-excited fluorescence; Photophysical properties; Density functional theory

Funding

  1. National Natural Science Foundation of China [21071001, 51142011, 21101001]
  2. Department of Education of Anhui Province [KJ2010A030]
  3. Foundation for the Scientific Innovation Team of Anhui Province [2006KJ007TD]
  4. Anhui University
  5. Ministry of Education
  6. Fundation for Outstanding Youth of the Department of Science and Technology of Anhui Province [10040606Y22]

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A series of 2, 2': 6', 2 ''-terpyridine-based chromophores (L1, L2, L3 and L4) with intramolecular 'push-pull' structure have been designed and synthesized. The single crystals of L1, L2 and L4 were obtained and solved by X-ray diffraction analysis. The photophysical behavior and the connections between structure and properties of the chromophores were investigated both experimentally and theoretically. It is revealed that the chromophores exhibit sensitive single-photon-excited fluorescence emission with high quantum yields, strong two-photon-excited fluorescence and large two-photon absorption cross sections, especially in DMF solution. It was also found that methylformate units as a peripheral groups attached to the triphenylamine moiety influence the structures, photophysical properties of the chromophores obviously. (C) 2012 Elsevier Ltd. All rights reserved.

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