메뉴 건너뛰기




Volumn , Issue 9, 2006, Pages 2201-2209

Dediazoniation of 4-nitrobenzenediazonium ions in acidic MeOH/H 2O mixtures: Role of acidity and MeOH concentration on the formation of transient diazo ethers that initiate homolytic dediazoniation

Author keywords

Alcohols; Arenediazonium ions; Dediazoniation; Kinetics; Solvolysis

Indexed keywords


EID: 33646436181     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200500946     Document Type: Article
Times cited : (38)

References (50)
  • 1
    • 0001540489 scopus 로고
    • Synthetic Applications of Diazonium Ions
    • (Eds.: S. Patai), John Wiley & Sons
    • D. S. Wulfman, Synthetic Applications of Diazonium Ions, in The Chemistry of Diazonium and Diazo Compounds (Eds.: S. Patai), John Wiley & Sons, 1978.
    • (1978) The Chemistry of Diazonium and Diazo Compounds
    • Wulfman, D.S.1
  • 5
    • 0003197230 scopus 로고
    • Kinetics and Mechanisms of Reactions Involving Diazonium and Diazo Groups
    • (Ed.: S. Patai), John Wiley & Sons, NY
    • A. F. Hegarty, Kinetics and Mechanisms of Reactions Involving Diazonium and Diazo Groups, in The Chemistry of Diazonium and Diazo Compounds (Ed.: S. Patai), John Wiley & Sons, NY, 1978.
    • (1978) The Chemistry of Diazonium and Diazo Compounds
    • Hegarty, A.F.1
  • 12
    • 0002040709 scopus 로고    scopus 로고
    • Interfacial Compositions of Surfactant Assemblies by Chemical Trapping with Arenediazonium Ions: Method and Applications
    • (Ed.: J. Texter), Marcel Dekker, New York
    • L. S. Romsted, Interfacial Compositions of Surfactant Assemblies by Chemical Trapping with Arenediazonium Ions: Method and Applications, in Reactions and Synthethis in Surfactant Systems (Ed.: J. Texter), Marcel Dekker, New York, 2001.
    • (2001) Reactions and Synthethis in Surfactant Systems
    • Romsted, L.S.1
  • 40
    • 0004041546 scopus 로고
    • Mc-Graw-Hill, NY
    • HOM = (yields of heterolytic products)/(yields of homolytic products), see for example: J. H. Espenson, Chemical kinetics and reaction mechanisms, 2nd ed., Mc-Graw-Hill, NY, 1995; however, our data clearly show that the product yields depends on both the acidity and MeOH concentration, i.e., Scheme 2, and hence the above relationships are no longer valid.
    • (1995) Chemical Kinetics and Reaction Mechanisms, 2nd Ed.
    • Espenson, J.H.1
  • 41
    • 0037518642 scopus 로고    scopus 로고
    • Reactivity of Arenediazonium Ions in Micellar and Macromolecular Systems
    • Trivandum, India, ISSN 0972-4494.
    • C. Bravo-Díaz, E. González-Romero, "Reactivity of Arenediazonium Ions in Micellar and Macromolecular Systems", in: Current Topics in Colloid and Interface Science, Trivandum, India, 2001, ISSN 0972-4494.
    • (2001) Current Topics in Colloid and Interface Science
    • Bravo-Díaz, C.1    González-Romero, E.2
  • 50
    • 0001540489 scopus 로고
    • Synthetic Applications of Diazonium Ions
    • (Ed.: S. Patai), John Wiley & Sons
    • D. S. Wulfman, Synthetic Applications of Diazonium Ions, in: The Chemistry of Diazonium and Diazo Compounds (Ed.: S. Patai), John Wiley & Sons, 1978.
    • (1978) The Chemistry of Diazonium and Diazo Compounds
    • Wulfman, D.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.