Why [6,6]- and 1,2-benzal-3-N-4-O-cyclic phenylimidate C60 undergo electrochemically induced retro-addition reactions while 1,4-dibenzyl-2,3-cyclic phenylimidate C60 does not? C-H⋯X (X = N, O) intramolecular interactions in organofullerenes

Journal of Organic Chemistry

Volumn 74, Issue 1, 2009, Pages 82-87

  Li, Fang Fang ^a   Gao, Xiang ^a   Zheng, Min ^a  

^a CHANGCHUN INSTITUTE OF APPLIED CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ANIONIC SPECIES; CHEMICAL EQUATIONS; CYCLOADDITION REACTIONS; DI ANIONS; ELECTROCHEMICAL STABILITIES; HETERO ATOMS; INTRAMOLECULAR HYDROGEN BONDINGS; INTRAMOLECULAR INTERACTIONS; NATURAL BOND ORBITALS; NBO ANALYSIS; SPECTROSCOPIC CHARACTERIZATIONS;

ADDITION REACTIONS; CHARGE DISTRIBUTION; CHARGED PARTICLES; CHEMICAL BONDS; CHEMICAL PROPERTIES; CHEMICAL REACTIONS; CRYSTAL STRUCTURE; CYCLOADDITION; ELECTROCHEMICAL PROPERTIES; HYDROGEN; LEAD COMPOUNDS;

HYDROGEN BONDS;

CRYSTALLOGRAPHY, X-RAY; CYCLIZATION; ELECTROCHEMISTRY; FULLERENES; HYDROGEN BONDING; MODELS, MOLECULAR; MOLECULAR STRUCTURE; OXAZOLES; STEREOISOMERISM;

EID: 58149308484     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo801769q     Document Type: Article

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