2003
DOI: 10.1021/ol027343h
|View full text |Cite
|
Sign up to set email alerts
|

Bis-1,4-(p-diarylaminostryl)-2,5-dicyanobenzene Derivatives with Large Two-Photon Absorption Cross-Sections

Abstract: Synthesis and physical properties of novel multibranched two-photon materials are reported. The compound with three units of 4-(p-diphenylaminostyryl)-2,5-dicyanostyryl moieties attached to the central triphenylamine core exhibits a very large two-photon absorption cross-section.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

3
84
0

Year Published

2005
2005
2009
2009

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 156 publications
(87 citation statements)
references
References 35 publications
3
84
0
Order By: Relevance
“…[33,36,57] In turn, exploitation of intermolecular interactions through branching strategies and the supramolecular approaches offers even more possibilities to tune or enhance TPA properties. This has already been demonstrated for branched chromophores built from the gathering of either dipolar [108][109][110][111][112][113][114][115][116][117][118][119][120][121][122][123] or quadrupolar [97,102,[124][125][126] sub-chromophores via common conjugated core moieties and multichromophore structures in which subchromophores interact only via electrostatic interactions. [127] Alternative routes such as those based on porphyrins, [128][129][130][131][132][133][134][135][136] oligomers and polymers [103,[137][138][139] have been explored as well.…”
Section: Introductionmentioning
confidence: 86%
See 2 more Smart Citations
“…[33,36,57] In turn, exploitation of intermolecular interactions through branching strategies and the supramolecular approaches offers even more possibilities to tune or enhance TPA properties. This has already been demonstrated for branched chromophores built from the gathering of either dipolar [108][109][110][111][112][113][114][115][116][117][118][119][120][121][122][123] or quadrupolar [97,102,[124][125][126] sub-chromophores via common conjugated core moieties and multichromophore structures in which subchromophores interact only via electrostatic interactions. [127] Alternative routes such as those based on porphyrins, [128][129][130][131][132][133][134][135][136] oligomers and polymers [103,[137][138][139] have been explored as well.…”
Section: Introductionmentioning
confidence: 86%
“…A large body of experimental data is available for many families of quadrupolar systems. [3,33,36,57,58,63,76,78,81,85,86,[89][90][91][92][93][94][95][96][97][98][99][100][101][102][103][104][105][106][107] Their nonlinear response is a non-trivial function of terminal donor and acceptor strength, π-conjugated bridge length and type, nature of the conjugated core, torsional disorder, symmetry and topology. [58] In this subsection we exemplify some of these relationships using two different families of quadrupoles to derive general trends in terms of TPA cross sections and peak positions.…”
Section: Quadrupolar Chromophoresmentioning
confidence: 99%
See 1 more Smart Citation
“…Lately, attention has turned toward multipolar [22][23][24][25][26][27][28][29][30][31][32][33] and branched structures including dendrimers. 23,24,28,[33][34][35][36][37][38][39][40][41][42][43] Given the huge synthetic effort needed to build such supramolecular structures, a detailed understanding of the effect of branching of molecular entities on the linear and nonlinear optical properties is of major interest. Thus, further development of approaches for rational design of NLO assemblies is needed in order to focus the synthesis on knowledgebased materials.…”
Section: Introductionmentioning
confidence: 99%
“…Triphenylamine is a well-known electrondonating moiety, which has been used both in the design of octupoles for second-order NLO effects [58][59][60][61] and in branched and dendritic structures for molecular TPA. [23][24][25][29][30][31][32][36][37][38]41,42 In this paper, we first briefly describe the synthesis of the studied chromophores, as well as experimental and computational details (section 2). Linear absorption and fluorescence properties of the compounds are then thoroughly explored through a combined analysis of both experimental and theoretical results (section 3).…”
Section: Introductionmentioning
confidence: 99%