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I CRYSTAL GROWTH AND CHARACTERIZATION OF NLO ACTIVE ORGANIC INCLUSION COMPOUNDS. Jürg Hulliger, Olaf König, Vera Kramer-Hoss, Institute of Inorg., Analyt. and Physical Chemistry, University of Berne, Switzerland.

Design of efficient organic nonlinear optical (NLO) materials attempts a molecular hyperpolarizability ßzzz up to a value close to 10'000 10-40m4/V and seeks for an orientation of ßzzz- axes that optimizes either frequency doubling (SHG) or the electro-optic (EO) effect of macroscopic I crystals [1-3].

On account of a low yield [1-3] of crystal structures providing a parallel alignment of dipoles (max. EO effect), recent interest focused on the packing of NLO molecules along parallel channels of inclusion type lattices [4]. When compared to other host materials [5], perhydrotriphenylene (PHTP) worked out to be ideally suited [6,7] to include a variety of linearly shaped NLO entities of the A-[[pi]]-D type (A, D: acceptor, donor group, respectively; [[pi]]: thiophene, stilbene, polyphenyl, polyacetylene). SHG powder tests revealed that PHTP-(A-[[pi]]-D) inclusion formation produces polar materials at a yield of around 75% that is 3 times higher than found for corresponding single component systems. Crystals of PHTP-(A-[[pi]]-D) were grown by (i) controlled isothermal evaporation of 2-butanone or paraldehyde, (ii) the temperature difference technique, and (iii) by sublimation [8].

[1] D S. Chemla, J. Zyss (Eds.), Nonlinear Optical Properties of Organic Molecules

and Crystals, Vol. 1,2, Academic Press (1987).

[2] J. Zyss (Ed.), Molecular Nonlinear Optics, Academic Press (1994).

[3] Ch. Bosshard, K. Sutter, Ph. Pretre, J. Hulliger, M. Florsheimer, P. Kaatz, P.

Gunter, Organic Nonlinear Optical Materials, Gordon and Breach (1995).

[4] V. Ramamurthy, D.F. Eaton, Chem. Mater., 6, 1128 (1994).

[5] E. Weber, Topics in Current Chemistry, Vol. 140, Springer (1987).

[6] J. Hulliger, O. Konig, R. Hoss, Adv. Mater., 7, 719-721 (1995).

[7] R. Hoss, O. Konig, V. Kramer-Hoss, U. Berger, P. Rogin, J. Hulliger, Angew.

Chem., submitted.

[8] J. Hulliger, Angew. Chem. Int. Ed. Engl. 33, 143-163 (1994).