Title
Models for the Photosynthetic Reaction Center—Synthesis and Structure of Porphyrin Dimers with cis‐ and trans‐Ethene and Skewed Hydroxymethylene Bridges
Document Type
Article
Publication Date
1-1-1993
Abstract
TiCl3‐induced coupling of meso‐forrnylporphyrins provides cofacial porphyrin dimers such as 1 (M Cu, Ni) with bridging cis‐CHCH units. These compounds show strong interactions between the porphyrin rings; in the case of M Ni, the dimer can be easily transformed into the corresponding trans isomer. Similar reactions with β‐formyl‐porphyrins lead to a third type of dimer, a skewed hydroxymethylene‐bridged bisporphyrin. These dimeric compounds are models for the photosynthetic reaction center and should facilitate studies on the influence of the dimer geometry on the photophysical properties. (Figure Presented.) Copyright © 1993 by VCH Verlagsgesellschaft mbH, Germany
Publication Source (Journal or Book title)
Angewandte Chemie International Edition in English
First Page
750
Last Page
753
Recommended Citation
Senge, M., Gerzevske, K., Vicente, M., Forsyth, T., & Smith, K. (1993). Models for the Photosynthetic Reaction Center—Synthesis and Structure of Porphyrin Dimers with cis‐ and trans‐Ethene and Skewed Hydroxymethylene Bridges. Angewandte Chemie International Edition in English, 32 (5), 750-753. https://doi.org/10.1002/anie.199307501