Synthesis and properties of novel second-order NLO chromophores containing pyrrole as an auxiliary electron donor

2008 ◽  
Vol 18 (15) ◽  
pp. 1756 ◽  
Author(s):  
Xiaohua Ma ◽  
Ran Liang ◽  
Fan Yang ◽  
Zhenhua Zhao ◽  
Aixin Zhang ◽  
...  
RSC Advances ◽  
2014 ◽  
Vol 4 (63) ◽  
pp. 33312-33318 ◽  
Author(s):  
Maolin Zhang ◽  
Guowei Deng ◽  
Airui Zhang ◽  
Huajun Xu ◽  
Heyan Huang ◽  
...  

We have designed and synthesized a new chromophore having a 1,1,7,7-tetramethyljulolidine fused furan ring as the electron donor group to systematically investigate the role of the benzo[b]furan ring in NLO chromophores.


Tetrahedron ◽  
2012 ◽  
Vol 68 (39) ◽  
pp. 8147-8155 ◽  
Author(s):  
M. Cidália R. Castro ◽  
M. Belsley ◽  
A. Maurício C. Fonseca ◽  
M. Manuela M. Raposo

1995 ◽  
Vol 392 ◽  
Author(s):  
Xiaoguang Yang ◽  
Duncan McBranch ◽  
Basil Swanson ◽  
Dequan Li

AbstractThe design and synthesis of a family of calix[4]arene-based nonlinear optical (NLO) chromophores are discussed. The calixarene chromophores are macrocyclic compounds consisting of four simple D-π-A units bridged by methylene groups. These molecules were synthesized such that four D-π-A units of the calix[4]arene were aligned along the same direction with the calixarene in a cone conformation. These nonlinear optical super-chromophores were subsequently fabricated into covalently bound self-assembled monolayers on the surfaces of fused silica and silicon. Spectroscopic second harmonic generation (SHG) measurements were carried out to determine the absolute value of the dominant element of the second-order nonlinear susceptibility, d33, and the average molecular alignment, ψ. We find a value of d33 = 60 pm/V at a fundamental wavelength of 890 nm, and ψ˜ 36° with respect to the surface normal.


1995 ◽  
Vol 413 ◽  
Author(s):  
D. W. Cheong ◽  
J. -I Chen ◽  
J. Kumar ◽  
S. K. Tripathy

ABSTRACTNonlinear optical (NLO) LB films of polyamic acid containing a stable NLO dye were prepared and imidized either chemically or thermally. The optical properties and molecular orientation of these LB films were studied. From the absorption spectra, we infer that the derivative of the pnitroazobenzene chromophore covalently attatched to polyamic acid did not show significant aggregation. Quadratic dependence of SHG on the number of layers in polyamic acid films indicated the noncentrosymmetric organization of polar NLO chromophores. A second-order nonlinear coefficient (d33) of 23.4 pm/V was observed at 1064 nm after absorption correction. In polyimide films, SH intensity was dramatically reduced due to the collapse of the layered structure upon imidization process. In-plane isotropy of the LB films of polyamic acid and polyimide were lost upon irradiation of polarized light.


2018 ◽  
Vol 42 (18) ◽  
pp. 15052-15060 ◽  
Author(s):  
Emine Çatal ◽  
Ergin Keleş ◽  
Nurgül Seferoğlu ◽  
Sylvain Achelle ◽  
Alberto Barsella ◽  
...  

A series of NLO chromophores based on a mono-, di- or tri-substituted triphenylamine core and allylidenemalononitrile fragments has been designed.


2008 ◽  
Vol 587-588 ◽  
pp. 268-272 ◽  
Author(s):  
M. Manuela M. Raposo ◽  
Ana M. Ferreira ◽  
Michael Belsley ◽  
E. de Matos Gomes ◽  
J.C.V.P. Moura

The synthesis of 5-arylazo- substituted bithiophenes and their UV-visible, solvatochromic and nonlinear optical properties (NLO) are described. In agreement with the solvatochromic data and also with the second-order molecular NLO characterization, the new donor-acceptor systems could find application as suitable solvatochromic probes and also as new NLO materials.


2001 ◽  
Vol 13 (4) ◽  
pp. 1420-1427 ◽  
Author(s):  
Noëlla Lemaître ◽  
André-Jean Attias ◽  
Isabelle Ledoux ◽  
Joseph Zyss

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