Literature DB >> 15792481

An investigation on the role of the nature of sulfonate ancillary ligands on the strength and concentration dependence of the second-order NLO responses in CHCl3 of Zn(II) complexes with 4,4'-trans-NC5H4CH=CHC6H4NMe2 and 4,4'-trans,trans-NC5H4CH=CH)2C6H4NMe2.

Francesca Tessore1, Danika Locatelli, Stefania Righetto, Dominique Roberto, Renato Ugo, Patrizia Mussini.   

Abstract

To evidentiate the role of the nature of sulfonate ancillary ligands on the value of the quadratic hyperpolarizability of Zn(II) complexes with stilbazole-like ligands, the second-order nonlinear optical (NLO) properties of [ZnY(2)(4,4'-trans-NC5H4CH=CHC6H4NMe2)2] complexes (Y = CF3SO3, CH3SO3, or p-CH3C6H4SO3) are investigated. By working at relatively high concentrations (>3 x 10(-4) M), the positive effect of the triflate ligand remains unique while, with nonfluorinated sulfonate ligands, the second-order NLO response is comparable to that of the related complexes with acetate or trifluoroacetate as ancillary ligands. However, at dilutions higher than 10(-4) M, all of the sulfonate complexes reach huge quadratic hyperpolarizabilities because of solvolysis with the formation of cationic species such as [ZnY(4,4'-trans-NC5H4CH=CHC6H4NMe2)2]+, characterized by a large second-order NLO response. This view is supported by careful conductivity measurements. The same behavior occurs if 4,4'-trans-NC5H4CH=CHC6H4NMe2 is substituted by 4,4'-trans,trans-NC5H4(CH=CH)2C6H4NMe2.

Entities:  

Year:  2005        PMID: 15792481     DOI: 10.1021/ic0487124

Source DB:  PubMed          Journal:  Inorg Chem        ISSN: 0020-1669            Impact factor:   5.165


  1 in total

1.  Electric-Field-Induced Second Harmonic Generation Nonlinear Optic Response of A4 β-Pyrrolic-Substituted ZnII Porphyrins: When Cubic Contributions Cannot Be Neglected.

Authors:  Gabriele Di Carlo; Maddalena Pizzotti; Stefania Righetto; Alessandra Forni; Francesca Tessore
Journal:  Inorg Chem       Date:  2020-05-15       Impact factor: 5.165

  1 in total

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