Panda, Pradeepta K and Krishnan, V (2005) Meso-functionalized octamethoxyporphyrins: A new class of nonasubstituted porphyrins. In: Journal of Chemical Sciences, 117 (2). pp. 73-84.
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Abstract
Octamethoxyporphyrin containing multiple-donor substituents has been functionalized for the first time. A large number of its mono- meso-substituted derivatives with substituents such as nitro, amino,N-methylamino, formyl, hydroxymethyl, oxime, cyano and carboxy functional groups have been synthesized and characterized. They form anew class of nonasubstituted porphyrins. Crystallographic studies on the cyano derivative show that the -C=N group is in conjugation with the prophyrin pi-system The calculated optical transition energies and the electron densities on the imino nitrogens of the synthesised porphyrins using AMI calculations correlate well with the experimentally observed data. Meso-substituted porphyrins are found tobe essentially planar.
Item Type: | Journal Article |
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Publication: | Journal of Chemical Sciences |
Publisher: | Indian Academy of Sciences |
Additional Information: | Copyright for this article belongs to Indian Academy of Sciences. |
Keywords: | Octamethoxyporphyrin;meso-functionalization;nonasubstituted porphyrins;basicity;AM1 semi-empirical correlation |
Department/Centre: | Division of Chemical Sciences > Inorganic & Physical Chemistry |
Date Deposited: | 05 May 2005 |
Last Modified: | 19 Sep 2010 04:18 |
URI: | http://eprints.iisc.ac.in/id/eprint/3157 |
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