[60]Fullerene-motivated organogel formation in a porphyrin derivative bearing programmed hydrogen-bonding sites

Journal of the American Chemical Society

Volumn 125, Issue 33, 2003, Pages 9902-9903

  Shirakawa, Michihiro ^a   Fujita, Norifumi ^a   Shinkai, Seiji ^a  

^a KYUSHU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

FULLERENE; ORGANIC COMPOUND; PORPHYRIN DERIVATIVE;

ARTICLE; BINDING SITE; CHEMICAL STRUCTURE; GEL; HYDROGEN BOND; MOLECULAR INTERACTION; SCANNING ELECTRON MICROSCOPY; STOICHIOMETRY; SYNTHESIS; TRANSMISSION ELECTRON MICROSCOPY;

EID: 0043023446     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja035933k     Document Type: Article

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13. In the computational processes, the nitrogen-oxygen distance in the amide-amide hydrogen bonds was restrained to 0.28 nm which is generally obtained from crystal data of amide-containing compounds.
14. 60 complexes as determined by X-ray crystallographic analysis and computational energy-minimization: see refs 6 and 7.
15. See Supporting Information.