Literature DB >> 17658741

Two-photon transitions in quadrupolar and branched chromophores: experiment and theory.

Claudine Katan1, Sergei Tretiak, Martinus H V Werts, Angus J Bain, Richard J Marsh, Nicholas Leonczek, Nicholas Nicolaou, Ekaterina Badaeva, Olivier Mongin, Mireille Blanchard-Desce.   

Abstract

A combined experimental and theoretical study is conducted on a series of model compounds in order to assess the combined role of branching and charge symmetry on absorption, photoluminescence, and two-photon absorption (TPA) properties. The main issue of this study is to examine how branching of quadrupolar chomophores can lead to different consequences as compared to branching of dipolar chromophores. Hence, three structurally related pi-conjugated quadrupolar chromophores symmetrically substituted with donor end groups and one branched structure built from the assembly of three quadrupolar branches via a common donor moiety are used as model compounds. Their photophysical properties are studied using UV-vis spectroscopy, and the TPA spectra are determined through two-photon excited fluorescence experiments using femtosecond pulses in the 500-1000 nm range. Experimental studies are complemented by theoretical calculations. The applied theoretical methodology is based on time-dependent density functional theory, the Frenkel exciton model, and analysis in terms of the natural transition orbitals of relevant electronic states. Theory reveals that a symmetrical intramolecular charge transfer from the terminal donating groups to the middle of the molecule takes place in all quadrupolar chromophores upon photoexcitation. In contrast, branching via a central electron-donating triphenylamine moiety breaks the quadrupolar symmetry of the branches. Consequently, all Frank-Condon excited states have significant asymmetric multidimensional charge-transfer character upon excitation. Subsequent vibrational relaxation of the branched chromophore in the excited state leads to a localization of the excitation and fluorescence stemming from a single branch. As opposed to what was earlier observed when dipolar chromophores are branched via the same common electron-donating moiety, we find only a slight enhancement of the maximum TPA response of the branched compound with respect to an additive contribution of its quadrupolar branches. In contrast, substantial modifications of the spectral shape are observed. This is attributed to the subtle interplay of interbranch electronic coupling and asymmetry caused by branching.

Entities:  

Year:  2007        PMID: 17658741     DOI: 10.1021/jp071069x

Source DB:  PubMed          Journal:  J Phys Chem B        ISSN: 1520-5207            Impact factor:   2.991


  6 in total

1.  Fluorescence anisotropy of branched molecules containing 1-aminopyrene chromophores.

Authors:  Miroslav Dvořák; Martin Michl; Numan Almonasy; Miloš Nepraš; Nemiah Ladd; Vlastimil Fidler
Journal:  J Fluoresc       Date:  2010-05-04       Impact factor: 2.217

2.  Synthesis, structural, thermal and photo-physical properties of triazine based NLO material.

Authors:  M Shyamala Devi; P Tharmaraj; C D Sheela; R Ebenezer
Journal:  J Fluoresc       Date:  2012-12-22       Impact factor: 2.217

3.  Rational design of small indolic squaraine dyes with large two-photon absorption cross section.

Authors:  Chun-Lin Sun; Qing Liao; Ting Li; Jun Li; Jian-Qiao Jiang; Zhen-Zhen Xu; Xue-Dong Wang; Rong Shen; De-Cheng Bai; Qiang Wang; Sheng-Xiang Zhang; Hong-Bing Fu; Hao-Li Zhang
Journal:  Chem Sci       Date:  2014-10-07       Impact factor: 9.825

4.  A biocompatible macromolecular two-photon initiator based on hyaluronan.

Authors:  Maximilian Tromayer; Peter Gruber; Marica Markovic; Arnulf Rosspeintner; Eric Vauthey; Heinz Redl; Aleksandr Ovsianikov; Robert Liska
Journal:  Polym Chem       Date:  2016-11-29       Impact factor: 5.582

5.  Two-Photon Absorption Cooperative Effects within Multi-Dipolar Ruthenium Complexes: The Decisive Influence of Charge Transfers.

Authors:  Nicolas Durand; Anissa Amar; Rana Mhanna; Huriye Akdas-Kiliç; Olivier Soppera; Jean-Pierre Malval; Abdou Boucekkine; Jean-Luc Fillaut
Journal:  Molecules       Date:  2022-02-23       Impact factor: 4.411

6.  Effects of Hydroxyl Group on the Interaction of Carboxylated Flavonoid Derivatives with S. Cerevisiae α-Glucosidase.

Authors:  Huining Lu; Yanjiao Qi; Yaming Zhao; Nengzhi Jin
Journal:  Curr Comput Aided Drug Des       Date:  2020       Impact factor: 1.606

  6 in total

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