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Fluorinated β-Diketonate Diglyme Lanthanide Complexes as New Second-Order Nonlinear Optical Chromophores: The Role of f Electrons in the Dipolar and Octupolar Contribution to Quadratic Hyperpolarizability.

Authors :
Valore, Adriana
Cariati, Elena
Righetto, Stefania
Roberto, Dominique
Tessore, Francesca
Ugo, Renato
Fragalà, lgnazio L.
Fragalà, Maria Elena
Malandrino, Graziella
De Angelis, Filippo
Belpassi, Leonardo
Ledoux-Rak, Isabelle
Khuyen Hoang Thi
Zyss, Joseph
Source :
Journal of the American Chemical Society. 4/7/2010, Vol. 132 Issue 13, p4966-4970. 5p.
Publication Year :
2010

Abstract

The second-order nonlinear optical (NLO) properties of [Ln(hfac)3(diglyme)] (hfac = hexafluo- roacetylacetonate; diglyme = bis(2-methoxyethyl)ether; Ln = La, Ce, Pr, Sm, Eu, Gd, Er, Lu) complexes have been investigated by a combination of electric-field second harmonic generation (EFISH) and harmonic light scattering (HLS) techniques, providing evidence for the relevant role of I electrons in tuning the second- order NLO response dominated by the octupolar contribution. These lanthanide NLO chromophores allow a clean valuation of the influence of f electrons on the quadratic hyperpolarizability and on its dipolar and octupolar contributions. Molecular quadratic hyperpolarizability values measured by the EFISH method, βEFISH, initially increase rapidly with the number of f electrons, the value for the Gd complex being 11 times that of the La complex, whereas this increase is much lower for the last seven f electrons, the βEFISH value of the Lu complex being only 1.2 times that of the Gd complex. The increase of (βHLS), which is dominated by an octupolar contribution, is much lower along the Ln series. Remarkably, the good (βHLS) values of these simple systems, well known for their luminescence properties, are reached at no cost of transparency. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00027863
Volume :
132
Issue :
13
Database :
Academic Search Index
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
49755427
Full Text :
https://doi.org/10.1021/ja101081q