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Volumn 47, Issue 24, 2008, Pages 4529-4532

Solvent effect on color, band shape, and charge-density distribution for merocyanine dyes close to the cyanine limit

Author keywords

Chromophores; Dyes pigments; Electrochromism; Nonlinear optics; Solvatochromism

Indexed keywords

ABSORPTION; OPTICAL PROPERTIES; SOLVENTS;

EID: 50149087702     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200800279     Document Type: Article
Times cited : (105)

References (42)
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    • For a comprehensive collection of solvatochromic probe molecules that have been introduced during more than half a century of research, see: a) C. Reichardt, Chem. Rev. 1994, 94, 2319-2358;
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    • Despite the fact that a change in the dipole moment of the dye by polarization was taken into account in determining the dipole moment of the dye by the Onsager theory, the solvent-dependent changes of these quantities have never been addressed in detail, and the studies were carried out almost exclusively in the weakly polar solvents cyclohexane, decalin, benzene, diisopropyl ether, and 1,4-dioxane: W. Baumann, Z. Naturforsch. A 1983, 38, 995-1002
    • Despite the fact that a change in the dipole moment of the dye by polarization was taken into account in determining the dipole moment of the dye by the Onsager theory, the solvent-dependent changes of these quantities have never been addressed in detail, and the studies were carried out almost exclusively in the weakly polar solvents cyclohexane, decalin, benzene, diisopropyl ether, and 1,4-dioxane: W. Baumann, Z. Naturforsch. A 1983, 38, 995-1002.
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    • For dyes with a similar behavior, see also reference [5] and G. Scheibe, E. Daltrozzo, O. Wörz, J. Heiss, Z. Phys. Chem. (Muenchen Ger.) Z. Phys. Chem. N. F. 1969, 64, 97-114.
    • For dyes with a similar behavior, see also reference [5] and G. Scheibe, E. Daltrozzo, O. Wörz, J. Heiss, Z. Phys. Chem. (Muenchen Ger.) Z. Phys. Chem. N. F. 1969, 64, 97-114.
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    • There is also a good linear correlation with the empirical π* solvent polarity scale (see reference [1]) for dye 1.
    • There is also a good linear correlation with the empirical π* solvent polarity scale (see reference [1]) for dye 1.
  • 41
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    • Based on a single-crystal X-ray analysis for dye 1 (to be published elsewhere) and NMR and molecular modeling studies for dyes 1-3, a planar X-S cis configuration is reasonable for these dyes.
    • Based on a single-crystal X-ray analysis for dye 1 (to be published elsewhere) and NMR and molecular modeling studies for dyes 1-3, a planar X-S cis configuration is reasonable for these dyes.
  • 42
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    • Owing to the very high field strength, such experiments must be carried out with caution and in carefully dried solvents, in particular for the more polar solvents
    • Owing to the very high field strength, such experiments must be carried out with caution and in carefully dried solvents, in particular for the more polar solvents.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.