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Volumn 136, Issue 47, 2014, Pages 16643-16650

The catalytic mechanism of diarylamine radical-trapping antioxidants

Author keywords

[No Author keywords available]

Indexed keywords

ANILINE; ANTIOXIDANTS; CARBONYL COMPOUNDS; CATALYST ACTIVITY; PETROLEUM ADDITIVES; REACTION INTERMEDIATES;

EID: 84913553462     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja509391u     Document Type: Article
Times cited : (49)

References (34)
  • 9
    • 84864704522 scopus 로고    scopus 로고
    • In contrast, the reaction of N, N -dialkylalkoxyamines with peroxyl radicals is believed to be the reaction responsible for the catalytic activities of the significantly less reactive hindered amine light stabilizers; see
    • In contrast, the reaction of N, N -dialkylalkoxyamines with peroxyl radicals is believed to be the reaction responsible for the catalytic activities of the significantly less reactive hindered amine light stabilizers; see: Grynova, G.; Ingold, K. U.; Coote, M. L. J. Am. Chem. Soc. 2012, 134, 12979
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 12979
    • Grynova, G.1    Ingold, K.U.2    Coote, M.L.3
  • 33
    • 0001794160 scopus 로고
    • Kochi, J. K. Wiley: New Work, Vol
    • Howard, J. A. In Free Radicals; Kochi, J. K., Ed.; Wiley: New Work, 1973; Vol. 2, pp 3-62.
    • (1973) Free Radicals , vol.2 , pp. 3-62
    • Howard, J.A.1
  • 34
    • 34547691131 scopus 로고    scopus 로고
    • N -Phenyl-β-naphthylamine was, at one time, among the most widely used diarylamine RTAs, but is now used sparingly owing to its carcinogenic potential. See
    • N -Phenyl-β-naphthylamine was, at one time, among the most widely used diarylamine RTAs, but is now used sparingly owing to its carcinogenic potential. See: Weiss, T.; Brüning, T.; Bolt, H. M. Crit. Rev. Toxicol. 2007, 37, 553
    • (2007) Crit. Rev. Toxicol. , vol.37 , pp. 553
    • Weiss, T.1    Brüning, T.2    Bolt, H.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.