Highly stable C60/poly(vinylpyrrolidone) charge-transfer complexes afford new predictions for biological applications of underivatized fullerenes

Journal of Medicinal Chemistry

Volumn 43, Issue 16, 2000, Pages 3186-3188

  Ungurenasu, C ^a   Airinei, A ^a  

^a PETRU PONI INSTITUTE OF MACROMOLECULAR CHEMISTRY   (Romania)

Author keywords

[No Author keywords available]

Indexed keywords

FULLERENE DERIVATIVE; POVIDONE;

ARTICLE; BASE PAIRING; COMPLEX FORMATION; EQUILIBRIUM CONSTANT; LIGAND BINDING; ROMANIA; SYNTHESIS;

CARBON; FULLERENES; POVIDONE; PYRROLIDINONES; SPECTROPHOTOMETRY, ULTRAVIOLET; WATER;

EID: 0034632767     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm991175q     Document Type: Article

References (10)

1. Enthalpically driven cyclophan-arene inclusion complexation: Solvent-dependent calorimetric studies
2. Intramolecular charge-transfer interaction in 1,3-diphenyl-2-pyrazoline ring-fused C60
3. 60 with aromatic hydrocarbons
4. Photophysical properties of fullerenes and fullerene/ N,N-diethylaniline charge-transfer complexes
5. 60 with substituted anilines
6. 60
7. 60 on agonist-induced responses in various tissues of K guinea pig and rat
8. 2 adduct in a reversibly formed and structurally characterized peroxo-dicopper complex
9. Molecular complexes and their spectra. Contact charge-transfer spectra