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Volumn 84, Issue 2, 2011, Pages 226-228

Heteroassociation of anions with acidic functionalities in acetonitrile

Author keywords

[No Author keywords available]

Indexed keywords

BORONIC ACID; SULFONAMIDE DERIVATIVES;

EID: 79951997652     PISSN: 00092673     EISSN: 13480634     Source Type: Journal    
DOI: 10.1246/bcsj.20100226     Document Type: Article
Times cited : (1)

References (24)
  • 16
    • 33745711873 scopus 로고    scopus 로고
    • - concentrations were sometimes observed: a) V. Amendola, D. Esteban-Gómez, L. Fabbrizzi, M. Licchelli, Acc. Chem. Res. 2006, 39, 343.
    • (2006) Acc. Chem. Res. , vol.39 , pp. 343
    • Amendola, V.1
  • 19
    • 79951988775 scopus 로고    scopus 로고
    • The values were cited from followings: a) For 1: CA database registry No. 19694-02-1
    • The values were cited from followings: a) For 1: CA database registry No. 19694-02-1.
  • 21
    • 79951983751 scopus 로고    scopus 로고
    • 3CN with an uncharged hydrogen donor, 3,5-dinitrophenol, was also reported, see Ref. 2c)
    • 3CN with an uncharged hydrogen donor, 3,5-dinitrophenol, was also reported, see Ref. 2c).
  • 22
    • 79951972327 scopus 로고    scopus 로고
    • note
    • 2-]) = ca. 0.4 and ca. 0.7 were barely recognized in the Job's plot. However, it is difficult to put a conclusive discussion for the complexation stoichiometry because of the uncertainty of the inflection points.
  • 23
    • 79951997875 scopus 로고    scopus 로고
    • See Supporting Information
    • See Supporting Information.
  • 24
    • 79951996441 scopus 로고    scopus 로고
    • note
    • 2. Thus, solvent effect is critical for the heteroassociation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.