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Volumn 106, Issue 2, 2002, Pages 257-263

Spectral study and molecular modeling of the inclusion complexes of β-cyclodextrin with some phenoxathiin derivatives

Author keywords

[No Author keywords available]

Indexed keywords

ASSOCIATION REACTIONS; BINDING ENERGY; COMPLEXATION; DERIVATIVES; ELECTROSTATICS; FLUORESCENCE; HYDROGEN BONDS; QUANTUM THEORY; QUENCHING; RATE CONSTANTS; SOLUTIONS; SPECTROSCOPY; STOICHIOMETRY; SYNTHESIS (CHEMICAL); VAN DER WAALS FORCES;

EID: 0037123064     PISSN: 15206106     EISSN: None     Source Type: Journal    
DOI: 10.1021/jp012198v     Document Type: Article
Times cited : (52)

References (41)
  • 16
    • 84972996380 scopus 로고
    • Another phenomenological model based on the solvent effects on the complex stability was developed and applied for α-cyclodextrin. The authors inferred that the polarity of this host corresponds to a partition coefficient octanol/water, log P = -0.3. Mulski, M.J.; Connors K.A. Supramol. Chem. 1995, 4, 271.
    • (1995) Supramol. Chem. , vol.4 , pp. 271
    • Mulski, M.J.1    Connors, K.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.