메뉴 건너뛰기




Volumn 107, Issue 21, 2003, Pages 4211-4216

Elimination of the hydrogen bonding effect on the solvatochromism of 3-hydroxyflavones

Author keywords

[No Author keywords available]

Indexed keywords

ABSORPTION SPECTROSCOPY; BENZENE; DERIVATIVES; ELECTRON ENERGY LEVELS; EMISSION SPECTROSCOPY; FLUORESCENCE; MOLECULAR DYNAMICS; MOLECULAR STRUCTURE; SYNTHESIS (CHEMICAL); THIN LAYER CHROMATOGRAPHY;

EID: 0037526227     PISSN: 10895639     EISSN: None     Source Type: Journal    
DOI: 10.1021/jp027315g     Document Type: Article
Times cited : (112)

References (34)
  • 26
    • 0038790248 scopus 로고
    • Lim, E. C., Ed.; Academic Press: New York; Chapter 1
    • Liptay, W. In Excited States; Lim, E. C., Ed.; Academic Press: New York, 1974; Chapter 1.
    • (1974) Excited States
    • Liptay, W.1
  • 29
    • 0038790249 scopus 로고    scopus 로고
    • note
    • 2 and DMSO possessing a high refractive index the absorption maxima are shifted to the red. The same is observed for BFE (Table 1).
  • 30
    • 0037775794 scopus 로고    scopus 로고
    • note
    • The position of the T* band of FE, especially for BFE in acetone, acetonitrile, DMF, and DMSO, is significantly shifted to the red. We expect that these solvents, because of their strong H-bond accepting ability and the steric availability of their oxygen or nitrogen atoms, may form H-bonds with the proton of the T* state, resulting in the spectral effects opposite to those of the protic solvents.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.