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Volumn 10, Issue 4, 2004, Pages 933-939

A Critical Evaluation of the Factors Determining the Effect of Intramolecular Hydrogen Bonding on the O-H Bond Dissociation Enthalpy of Catechol and of Flavonoid Antioxidants

Author keywords

Ab initio calculations; Antioxidants; EPR spectroscopy; Flavonoids; Radicals

Indexed keywords

ANTIOXIDANTS; DISSOCIATION; ENTHALPY; HYDROGEN BONDS; IRRADIATION; PARAMAGNETIC RESONANCE;

EID: 1542378822     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200305311     Document Type: Article
Times cited : (92)

References (39)
  • 20
    • 85039565700 scopus 로고    scopus 로고
    • note
    • It should be emphasised that the solvated hydroxyl group of catechol is not that one involved in the intramolecular hydrogen bonding, which is characterised by a lower BDE value, but the free hydroxyl substituent in position 1.
  • 27
    • 85039565001 scopus 로고    scopus 로고
    • note
    • 1.
  • 30
    • 0037350212 scopus 로고    scopus 로고
    • -1) of the relative bond dissociation enthalpy of catechol based on kinetic data appeared in the literature (H. Y. Zhang, New J. Chem. 2003, 27, 453-454).
    • (2003) New J. Chem. , vol.27 , pp. 453-454
    • Zhang, H.Y.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.