Abstract
A series of 10 (2−11) new chiral (salicylaldiminato)tin Schiff base complexes obtained from the Schiff base condensation of 4-(diethylamino)salicylaldehyde and various amino acids, in the presence of diphenyltin oxide, is reported together with the parent achiral (1) derivative. Compounds 2−7 crystallize in the P212121 orthorhombic space group, and their quadratic nonlinear optical properties are investigated. At the molecular level, the derivatives possess similar electronic spectra (λmax ≈ 395 nm), and hence molecular hyperpolarizabilities (β), in relation to the same π-conjugated “push−pull” electronic structure. In the solid state, they exhibit efficiencies in second-harmonic generation (SHG) up to 8 times that of urea. The SHG intensities of chromophores 2−6 appear largely correlated with a simple “degree of chirality” (dχ) parameter, defined from the molecular geometries. The intriguing issue of a possible quantification of chirality by means of SHG measurement is addressed.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.