Relative stability and diatropic character of carbaporphyrin, dicarbaporphyrin, tricarbaporphyrin, and quatyrin tautomers

Journal of Organic Chemistry

Volumn 78, Issue 22, 2013, Pages 11535-11548

  Abusalim, Deyaa I ^a   Lash, Timothy D ^a  

^a ILLINOIS STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC STRUCTURES; CARBAPORPHYRINOID; ELECTRON DELOCALIZATION; METHYLENE GROUPS; NUCLEUS-INDEPENDENT CHEMICAL SHIFTS; RELATIVE STABILITIES; SYNTHETIC ROUTES; TAUTOMERIC FORMS;

AROMATIZATION; COMPLEXATION;

AROMATIC COMPOUNDS;

DICARBAPORPHYRIN; MACROCYCLIC COMPOUND; MONOCARBAPORPHYRIN; PORPHYRIN DERIVATIVE; PYRROLE DERIVATIVE; QUATYRIN; TRICARBAPORPHYRIN; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CONFORMATION; CONJUGATION; CONTROLLED STUDY; CRYSTAL STRUCTURE; DENSITY FUNCTIONAL THEORY; ENERGY; HYDROGEN BOND; MOLECULAR STABILITY; PROTON NUCLEAR MAGNETIC RESONANCE; TAUTOMER; ULTRAVIOLET RADIATION;

MODELS, MOLECULAR; MOLECULAR STRUCTURE; PORPHYRINS; QUANTUM THEORY;

EID: 84887935594     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo4021198     Document Type: Article

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