Syntheses and 1H NMR Spectroscopy of Rigid, Cofacially Aligned, Porphyrin−Bridge−Quinone Systems in Which the Interplanar Separations between the Porphyrin, Aromatic Bridge, and Quinone Are Less than the Sum of Their Respective van der Waals Radii
- 26 August 2000
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 122 (36) , 8717-8727
- https://doi.org/10.1021/ja000759a
Abstract
No abstract availableThis publication has 57 references indexed in Scilit:
- Evidence for Interacting Gas Flows and an Extended Volatile Source Distribution in the Coma of Comet C/1996 B2 (Hyakutake)Science, 1997
- Intramolecular “Through-Bond” and “Through-Space” Electron Transfer Pathways in Covalently Linked Porphyrin-Quinone MoleculesBulletin of the Chemical Society of Japan, 1996
- Long-Range Photoinduced Electron Transfer Through a DNA HelixScience, 1993
- Catalytic conversion of simple haloporphyrins into alkyl-, aryl-, pyridyl-, and vinyl-substituted porphyrinsJournal of the American Chemical Society, 1993
- Accelerated Electron Transfer Between Metal Complexes Mediated by DNAScience, 1988
- Synthesis of a Porphyrin Sandwiched between Two Parallel p‐Benzoquinone UnitsAngewandte Chemie International Edition in English, 1984
- Synthesis of a cofacial porphyrin-quinone via entropically favored macropolycyclizationJournal of the American Chemical Society, 1982
- Nickel and palladium complex catalyzed cross-coupling reactions of organometallic reagents with organic halidesPure and Applied Chemistry, 1980
- The Mechanism of Fluorination. III.1 Fluorine Atom Reactions. The Olefin Dimerization Reaction2,3Journal of the American Chemical Society, 1957
- Brassicasterol. I. Empirical Formula and HydrogenationJournal of the American Chemical Society, 1939