메뉴 건너뛰기




Volumn 105, Issue 37, 2001, Pages 8877-8884

Mechanism of the electrochemical reduction of 3,5-di-tert-butyl-1,2-benzoquinone. Evidence for a concerted electron and proton transfer reaction involving a hydrogen-bonded complex as reactant

Author keywords

[No Author keywords available]

Indexed keywords

PROTON TRANSFER;

EID: 0035922514     PISSN: 10895647     EISSN: None     Source Type: Journal    
DOI: 10.1021/jp0109269     Document Type: Article
Times cited : (73)

References (28)
  • 2
    • 84991970866 scopus 로고
    • Patai, S., Rappaport, Z., Eds.; Wiley: New York
    • For a review, see Chambers, J.Q. In The Chemistry of the Quininoid Compounds; Patai, S., Rappaport, Z., Eds.; Wiley: New York, 1988; Vol. 2, Part 1, pp 719-757.
    • (1988) The Chemistry of the Quininoid Compounds , vol.2 , Issue.PART 1 , pp. 719-757
    • Chambers, J.Q.1
  • 9
    • 0011339942 scopus 로고    scopus 로고
    • note
    • 7b,c.
  • 12
    • 0011332959 scopus 로고    scopus 로고
    • note
    • 8b.
  • 14
    • 0011300527 scopus 로고    scopus 로고
    • note
    • 6 described reactions 5 and 6 as a "water-catalyzed disproportionation" but "water-promoted disproportionation" might be better as the water molecule, unlike a true catalyst, is destroyed during the reaction.
  • 15
    • 0011374049 scopus 로고    scopus 로고
    • note
    • 2.
  • 26
    • 0011339944 scopus 로고    scopus 로고
    • note
    • -1.
  • 28
    • 0011374051 scopus 로고    scopus 로고
    • note
    • - that is formed is accompanied by one Q and one hydroxide (reaction 6). The reduction of Q would normally cause n to exceed one but the occurrence of reaction 22 would remove Q through its reaction with hydroxide.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.