Affiliation:
1. Departamento de Química Orgánica, Universidad Autãnoma de Madrid, Cantoblanco, 28049-Madrid, Spain
2. Laboratoire de Photonique Quantique et Moléculaire, Ecole Normale Supérieure de Cachan, 94235 Cachan, France
Abstract
The EFISH and HRS responses of a push-pull bisphthalocyanine-[2,2]paracyclophane compound have been measured at 1.9 and 1.06 μm, respectively, obtaining a remarkably high hyperpolarizability β HRS value. Since the two electronically different phthalocyanine chromophores are connected through a non π-conjugated and rigid [2,2]paracyclophane spacer, this result implies an efficient through-space intramolecular charge transfer between them. The results have been compared to that of structurally related, unsymmetrically substituted phthalocyanines 2-5, bearing either [2,2]paracyclophane or phenyl substituents. In these cases, the [2,2]paracycloplane does not play a significant role in the NLO response, being that the nature of the peripheral sustituents on the phthalocyanine is the most influent structural feature.
Publisher
World Scientific Pub Co Pte Lt
Cited by
11 articles.
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