摘要

Co-crystallization of p-N(CH3)(2)C6H4CHO and E-4-(4-dimethylaminostyryl)-1-methylpyridinium iodide ([DAMS]I) gives a new solid state form (A), characterized by high non-linear-optical (NLO) activity and quite different from the well known [DAMS]I salt (centrosymmetric and therefore inactive). The X-ray structural characterization, although affected by the extended disorder of p-N(CH3)(2)C6H4CHO, addresses a new kind of aggregation for the [DAMS(+)] chromophore molecules. In fact, together with the often encountered J-type aggregation, an unprecedented "fishbone'' coupling is observed. Calculations using time-dependent density functional theory (TDDFT) prove that the absence of a J-aggregation band in the electronic absorption spectrum is due to the additional intermolecular interaction that quenches the expected J-type signal. Correlation between supramolecular arrangements of the chromophores and NLO properties is also discussed.

  • 出版日期2010