Second-order nonlinear optical activity of dipolar chromophores based on pyrrole-hydrazono donor moieties.

A series of highly efficient and thermally stable second-order nonlinear optical (NLO) dipolar donor-auxiliary donor-acceptor chromophores have been synthesised in which a hydrazono group and a pyrrole ring act as donor and auxiliary donor components, respectively, in combination with different aromatic and heteroaromatic acceptors. The new dyes have been systematically investigated by NMR spectroscopy, absorption spectroscopy, NLO measurements and thermal stability studies. NLO properties have been studied in detail by electro-optical absorption (EOA) and hyper-Rayleigh scattering (HRS) measurements in 1,4-dioxane and DMSO, respectively. The results originating from the two different methods have been compared and analysed in detail. We found that the NLO properties measured by the EOA and HRS methods correlate with each other and converge to reveal the dye with the acceptor 2-dicyanomethylene-3-cyano-4,5,5-trimethyl-2,5-dihydrofuran as the most efficient system. The unprecedented combination of a strong donor hydrazono group and the auxiliary donor effects of pi-excessive heteroaromatic rings afforded NLO chromophores with very high values (mu(g)beta0(EOA) up to 2038 x 10(-48) esu and beta(HRS) up to 3980 x 10(-30) esu at 1.5 microm).

Three-branched dendritic dipolar nonlinear optical chromophores, more than three times a single-strand chromophore?

To elucidate the dependence of the nonlinear optical (NLO) response on the conformation of triply branched derivatives, a new series of D-pi-A dendrimers has been synthesized. A combined approach of experiments (UV-vis and EOA measurements) and computational predictions (semiempirical and ab initio) was applied both on the dendrimers and on the corresponding single-strand chromophores. It has been shown that depending on the surrounding media the NLO activity of a flexible dendrimer can be very different. Two limiting cases are proposed: (i) the dendrimer resembles a solution of the corresponding single-strand chromophores with about 3-fold concentration, where the hyperpolarizability is the sum of the effect of three noninteracting single-strand subunits ("independent chromophores" limit); (ii) the dendrimers show nearly parallel or helical alignments of the single-strand subunits. Because of this change of conformation the NLO activity can be enhanced up to nine times the value of the "independent chromophores" limit and, thus, are more than a single strand chromophore. Conformers of dendrimers with interacting single-strand chromophores have been identified experimentally in nonpolar solutions by the EOA spectroscopy and possible structures have been revealed by numerical calculations, which could moreover show the tendency of the effects on the hyperpolarizability due to structural changes of the flexible dendritic architecture. Implications for future research developments are given to implement the "more than three times" concept.