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Synthesis and second-order optical nonlinearity of carbazolyl-substituted furan chromophores with high thermal stability and good transparency
A series of new chromophores, in which N-hexylcarbazole acts as an electron donor and a furan ring is part of a conjugation bridge, are synthesised, and exhibit similar values of the first molecular hyperpolarisability, but better transparency compared with their analogues which contain diethylamino...
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Published in: | Journal of chemical research 2001-10, Vol.2001 (10), p.418-420 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A series of new chromophores, in which N-hexylcarbazole acts as an electron donor and a furan ring is part of a conjugation bridge, are synthesised, and exhibit similar values of the first molecular hyperpolarisability, but better transparency compared with their analogues which contain diethylaminophenyl instead of N-hexylcarbazole as the donor, in addition to high thermal stability. |
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ISSN: | 1747-5198 2047-6507 |
DOI: | 10.3184/030823401103168514 |