Effect of alkylation of the pyrrole rings of the porphyrin molecule on the vibronic spectra
β Scribed by L. L. Gladkov; A. T. Gradyushko; K. N. Solov'ev; A. S. Starukhin; A. M. Shul'ga
- Publisher
- Springer US
- Year
- 1978
- Tongue
- English
- Weight
- 506 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0021-9037
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π SIMILAR VOLUMES
The connection is made between macrocycle deformations obtained from normal-coordinate structural decomposition (NSD) and the vibronic molecular states and spectra of porphyrins. NSD is a procedure that provides a description of the time-averaged distortion of a porphyrin in terms of normal-coordina
## Abstract The proton NMR spectra of tetraphenylporphyrin, octaethylporphyrin and the analogous chlorins (7,8βdihydroporphyrins) are presented, and the chemical shift changes on chlorin formation are interpreted using a ring current model. In these compounds a general 10% reduction in the ring cur