This submission belongs to the session c. Bioorganic Chemistry and Natural Products of the event The 4th International Electronic Conference on Synthetic Organic Chemistry
Published date
11 Sep, 2000
Citation
H. Kurreck, M. O. Senge, M. Speck, Synthesis and Characterization of Porphyrin-o-Quinones - A New Group of Model Compounds for Photosynthesis, in Proceedings of The 4th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2000, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-4-01923
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Synthesis and Characterization of Porphyrin-o-Quinones - A New Group of Model Compounds for Photosynthesis
M. Speck 1
M. O. Senge 1
H. Kurreck 1
1. Institut für Chemie, Organische Chemie, Freie Universität Berlin, Takustrasse 3,D-14195 Berlin, Germany
Abstract
Photosynthesis is the most important energy conversion process for life on earth. Thus, many research groups attempt the synthesis of covalently linked porphyrin quinones to mimic the underlying electron transfer processes occurring in the primary step of photosynthesis. In order to study the influence of different acceptor strengths and geometrical parameters on the electron transfer properties a few hundred porphyrin-p-quinones with different bridging and acceptor units were synthesized.[1] In this context we became interested in the synthesis of stabilized porphyrin-o-quinones, which have not been described by other groups.
Keywords
n/a
Conformationally Designed Biomimetic Macrocycles - Synthesis of Porphyrins and Porphodimethenes with Mixed Substitution Pattern and Distortion Modes
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