4.7 Article

1, 3, 5-Triazine-cored derivatives dyes containing triphenylamine based two-photon absorption: Synthesis, optical characterization and bioimaging

Journal

DYES AND PIGMENTS
Volume 94, Issue 3, Pages 570-582

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.dyepig.2012.03.017

Keywords

Triazine dyes; Triphenylamine; sigma-Electron pair as a bridge; Photophysical properties; 2PA cross section; Two-photon fluorescence cell imaging

Funding

  1. Program for New Century Excellent Talents in University (China)
  2. Doctoral Program Foundation of Ministry of Education of China [20113401110004]
  3. Science and Technological Fund of Anhui Province for Outstanding Youth [10040606Y22]
  4. National Natural Science Foundation of China [21071001, 51142011, 21101001]
  5. Natural Science Foundation of Education Committee of Anhui Province [KJ2012A024, KJ2010A030]
  6. Anhui University [XJ103575023, KYXL201100337]
  7. Team for Scientific Innovation Foundation of Anhui Province [2006KJ007TD]
  8. Ministry of Education

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A series of new one, two and three-branched two-photon absorption triazine dyes containing triphenylamine with a pi-bond and a sigma-electron pair as a bridge, and different electron-donating groups, have been synthesized and their photophysical properties have been systematically investigated. These dyes showed obvious solvatochromic effects, i.e., significant bathochromic shifting of the emission spectra and larger Stokes shifts were observed in more polar solvents mainly due to intramolecular charge-transfer (ICT). The two-photon absorption (2PA) cross section values were determined by two-photon excited fluorescence (TPEF) measurements in DMF. This result further proved that a sigma-electron pair as a bridge is an efficient way to transfer charge as well as a pi bridge to provide a large 2PA cross section, and that their 2PA cross section values (delta) increase with increasing electron-donating strength of the end group and branch number. In addition, two-photon fluorescence cell imaging of dye 7a in HeLa and MCF-7 cancer cells was demonstrated. (C) 2012 Elsevier Ltd. All rights reserved.

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