Structural features of 11 synthetic bacteriochlorins — comparisons with chlorins and porphyrins

As part of a program to develop the fundamental science of synthetic bacteriochlorins — analogues of Nature’s light-harvesting pigments in anoxygenic photosynthesis — 11 synthetic free base bacteriochlorins have been examined by single-crystal X-ray diffraction analysis. In each bacteriochlorin, each pyrroline ring contains a gem-dimethyl group to block adventitious (aerobic) dehydrogenation. The structural features of the bacteriochlorins (tetrahydroporphyrins) are compared with the less saturated counterparts, chlorins (dihydroporphyrins) and porphyrins. Only slight structural perturbation accrues due to the presence of the gem-dimethyl groups. The results presented herein may aid in understanding metal chelation processes and underpin the development of functional solid-state molecular assemblies.

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Publication Details

Journal
Journal of Porphyrins and Phthalocyanines
Published
2025-09-01
DOI
https://doi.org/10.1142/s1088424625500786
Primary Topic
Porphyrin and Phthalocyanine Chemistry
Type
article
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article

Structural features of 11 synthetic bacteriochlorins — comparisons with chlorins and porphyrins

Roger D. Sommer, Phattananawee Nalaoh, Paul D. Boyle, Masahiko Taniguchi et al.
Journal of Porphyrins and Phthalocyanines
Porphyrin and Phthalocyanine Chemistry
article

Structural features of 11 synthetic bacteriochlorins — comparisons with chlorins and porphyrins

Roger D. Sommer, Phattananawee Nalaoh, Paul D. Boyle, Masahiko Taniguchi, Jonathan S. Lindsey, Vy-Phuong Tran
article en

Abstract

As part of a program to develop the fundamental science of synthetic bacteriochlorins — analogues of Nature’s light-harvesting pigments in anoxygenic photosynthesis — 11 synthetic free base bacteriochlorins have been examined by single-crystal X-ray diffraction analysis. In each bacteriochlorin, each pyrroline ring contains a gem-dimethyl group to block adventitious (aerobic) dehydrogenation. The structural features of the bacteriochlorins (tetrahydroporphyrins) are compared with the less saturated counterparts, chlorins (dihydroporphyrins) and porphyrins. Only slight structural perturbation accrues due to the presence of the gem-dimethyl groups. The results presented herein may aid in understanding metal chelation processes and underpin the development of functional solid-state molecular assemblies.

Journal of Porphyrins and PhthalocyaninesVol. 29(09)
North Carolina State University (US), University of Tennessee at Knoxville (US)
Openalex Percentile: Top 82%
Porphyrin and Phthalocyanine Chemistry
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