Synthetic potential and limitations of o-quinones as acceptor groups in electron transfer compounds
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Model Reactions for Photosynthesis—Photoinduced Charge and Energy Transfer between Covalently Linked Porphyrin and Quinone Units
2. In photosynthetic reaction centers, the free energy difference for electron transfer between quinones bound at the primary and secondary quinone-binding sites governs the observed secondary site specificity.
3. Isomeric porphyrin phenanthrenequinones: synthesis, NMR spectroscopy, electrochemical properties, and in situ EPR/ENDOR studies of the o-semiquinone anion radicalsElectronic supplementary information (ESI) available: 1H and 13C NMR data for various phenanthrene derivatives. See http://www.rsc.org./suppdata/p2/b1/b110273g/
4. The chemistry of heterocyclic o-quinone cofactors
5. Oxidative reactions and schizophrenia: A review-discussion
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1. Highly electron deficient tetrabenzoquinone-appended Ni(ii) and Cu(ii) porphyrins: spectral, solvatochromatic, electrochemical redox and tuneable F−and CN−sensing properties;New Journal of Chemistry;2017
2. Synthetic methodologies leading to porphyrin-quinone conjugates;Journal of Porphyrins and Phthalocyanines;2016-01
3. Unexpected but convenient synthesis of soluble meso-tetrakis(3,4-benzoquinone)-substituted porphyrins;Journal of Porphyrins and Phthalocyanines;2014-03
4. Photochemical Transformations Involving Porphyrins and Phthalocyanines;CRC Handbook of Organic Photochemistry and Photobiology, Third Edition - Two Volume Set;2012-03-21
5. Photochemical Transformations Involving Zinc Porphyrins and Phthalocyanines;PATAI'S Chemistry of Functional Groups;2009-12-15
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