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Volumn 19, Issue 16-17, 2000, Pages 1961-1966
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Electronic and NMR properties of meso-monosubstituted ferrocenylporphyrin: Evidence of π-conjugation between porphyrin and ferrocene
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Author keywords
Electrochemical communication; Ferrocenylporphyrin; Intramolecular hydrogen bonding; NH tautomerism; Conjugation
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Indexed keywords
HYDROGEN;
HYDROGEN BONDS;
IRON COMPOUNDS;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
ORGANOMETALLICS;
TRICHLOROACETIC ACID;
ELECTROCHEMICAL COMMUNICATION;
ELECTROCHEMICALS;
EQUIMOLAR MIXTURES;
FERROCENECARBOXALDEHYDE;
FERROCENES;
FERROCENYLPORPHYRIN;
INTRAMOLECULAR HYDROGEN BONDING;
NH TAUTOMERISM;
PROPERTY;
Π-CONJUGATION;
MANGANESE COMPOUNDS;
5 FERROCENYL 15 PHENYL 2,8,12,18 TETRAETHYL 3,7,13,17 TETRAMETHYLPORPHYRIN;
ACETONITRILE;
ALDEHYDE;
AMINE;
BENZALDEHYDE;
FERROCENE DERIVATIVE;
MANGANESE CHLORIDE;
METHANE;
PORPHYRIN DERIVATIVE;
TOLUENE;
TRICHLOROACETIC ACID;
UNCLASSIFIED DRUG;
ZINC ACETATE;
ARTICLE;
CATALYSIS;
CHEMICAL REACTION;
CONJUGATION;
CYCLIC POTENTIOMETRY;
ELECTROCHEMISTRY;
HYDROGEN BOND;
ISOMERISM;
NUCLEAR MAGNETIC RESONANCE;
OXIDATION;
PROTON NUCLEAR MAGNETIC RESONANCE;
STOICHIOMETRY;
TEMPERATURE;
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EID: 0034664968
PISSN: 02775387
EISSN: None
Source Type: Journal
DOI: 10.1016/S0277-5387(00)00481-2 Document Type: Article |
Times cited : (26)
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References (33)
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