The photophysics and two-photon absorption of a series of quadrupolar and tribranched molecules: The role of the edge substituent

Fakis, M; Fitilis, I; Stefanatos, S; Vellis, P; Mikroyannidis, J; Giannetas, V; Persephonis, P

HERO ID

3575456

Reference Type

Journal Article

Year

2009

HERO ID 3575456
In Press No
Year 2009
Title The photophysics and two-photon absorption of a series of quadrupolar and tribranched molecules: The role of the edge substituent
Authors Fakis, M; Fitilis, I; Stefanatos, S; Vellis, P; Mikroyannidis, J; Giannetas, V; Persephonis, P
Journal Dyes and Pigments
Volume 81
Issue 1
Page Numbers 63-68
Abstract A series of quadrupolar and tribranched molecules were synthesized in order to examine the role of the edge substituents on their photophysical and two-photon absorption properties. Two-photon absorption cross sections, delta, of the molecules were determined in THF solution using a two-photon excited fluorescence technique with femtosecond pulsed excitation. The quadrupolar molecules contained a fluorene or alcoxy-substituted phenylene central core together with various electron accepting edge substituents such as pyridine, terpyridine, phthalimide and naphthalimide. The tribranched molecules contained triphenylamine at the center and terpyridine or phthalimide substituents at the periphery. It was found that edge phthalimide substituent favour high h values. 6 Values as high as 1660 GM and 1500 GM were obtained from the phthalimide-fluorene-phthalimide and phthalimide-phenylene-phthalimide molecules. respectively; in the case of the tribranched molecule with a phthalimide substituent, a delta-value of 1200 GM was found. (C) 2008 Elsevier Ltd. All rights reserved.
Doi 10.1016/j.dyepig.2008.08.014
Wosid WOS:000261911600010
Is Certified Translation No
Dupe Override No
Is Public Yes
Keyword Two-photon absorption; Two-photon excited fluorescence; Fluorene molecules; Tribranched molecules