Quantum yields of photocoloration and molar absorption coefficients of ferrocenyl substituted benzo and dibenzochromenes. Comparison with their phenyl-homologues
The photochromic properties of three ferrocenyl-[2H]-benzopyrans were investigated under monochromatic irradiation and compared with those of their phenyl homologues. The UV/visible spectra of the closed and open forms are reported together with the quantum yields of photocoloration. It was shown th...
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| Format: | Article |
| Language: | English |
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Wiley
2003-01-01
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| Series: | International Journal of Photoenergy |
| Online Access: | http://dx.doi.org/10.1155/S1110662X03000394 |
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| author | Pierre Brun Robert Guglielmetti Jean Claude Micheau Véronique Pimienta Stéphane Anguille |
| author_facet | Pierre Brun Robert Guglielmetti Jean Claude Micheau Véronique Pimienta Stéphane Anguille |
| author_sort | Pierre Brun |
| collection | DOAJ |
| description | The photochromic properties of three ferrocenyl-[2H]-benzopyrans were investigated under
monochromatic irradiation and compared with those of their phenyl homologues. The UV/visible spectra of
the closed and open forms are reported together with the quantum yields of photocoloration. It was shown
that the ferrocenyl- substitution induces the formation of a new band in the 500–700 nm range in the open
forms, however, it does not affect significantly the UV spectra of the closed forms. Ferrocenyl- substitution
was also shown to increase the thermal bleaching rate constants and to decrease the photocoloration quantum
yields. For most compounds, photochromic behaviour was not sensitive to the irradiation wavelength.
However, for the methyl ferrocenyl chromene, the open form spectrum was slightly dependent of the irradiation
wavelength. The influence of the ferrocenyl group and other structural features on the photochromic
properties are discussed. |
| format | Article |
| id | doaj-art-8e2fb3f16f3d4cb7aab97f9f8ca25ed0 |
| institution | Kabale University |
| issn | 1110-662X |
| language | English |
| publishDate | 2003-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | International Journal of Photoenergy |
| spelling | doaj-art-8e2fb3f16f3d4cb7aab97f9f8ca25ed02025-02-03T05:45:42ZengWileyInternational Journal of Photoenergy1110-662X2003-01-015424324810.1155/S1110662X03000394Quantum yields of photocoloration and molar absorption coefficients of ferrocenyl substituted benzo and dibenzochromenes. Comparison with their phenyl-homologuesPierre Brun0Robert Guglielmetti1Jean Claude Micheau2Véronique Pimienta3Stéphane Anguille4UMR 6114, Université de la Méditerranée, 163 Avenue de Luminy, Marseille cedex 9 13288, FranceUMR 6114, Université de la Méditerranée, 163 Avenue de Luminy, Marseille cedex 9 13288, FranceUMR 5623, Université Paul Sabatier, 118 Route de Narbonne, Toulouse cedex 31062, FranceUMR 5623, Université Paul Sabatier, 118 Route de Narbonne, Toulouse cedex 31062, FranceUMR 6114, Université de la Méditerranée, 163 Avenue de Luminy, Marseille cedex 9 13288, FranceThe photochromic properties of three ferrocenyl-[2H]-benzopyrans were investigated under monochromatic irradiation and compared with those of their phenyl homologues. The UV/visible spectra of the closed and open forms are reported together with the quantum yields of photocoloration. It was shown that the ferrocenyl- substitution induces the formation of a new band in the 500–700 nm range in the open forms, however, it does not affect significantly the UV spectra of the closed forms. Ferrocenyl- substitution was also shown to increase the thermal bleaching rate constants and to decrease the photocoloration quantum yields. For most compounds, photochromic behaviour was not sensitive to the irradiation wavelength. However, for the methyl ferrocenyl chromene, the open form spectrum was slightly dependent of the irradiation wavelength. The influence of the ferrocenyl group and other structural features on the photochromic properties are discussed.http://dx.doi.org/10.1155/S1110662X03000394 |
| spellingShingle | Pierre Brun Robert Guglielmetti Jean Claude Micheau Véronique Pimienta Stéphane Anguille Quantum yields of photocoloration and molar absorption coefficients of ferrocenyl substituted benzo and dibenzochromenes. Comparison with their phenyl-homologues International Journal of Photoenergy |
| title | Quantum yields of photocoloration and molar absorption coefficients of ferrocenyl substituted benzo and dibenzochromenes. Comparison
with their phenyl-homologues |
| title_full | Quantum yields of photocoloration and molar absorption coefficients of ferrocenyl substituted benzo and dibenzochromenes. Comparison
with their phenyl-homologues |
| title_fullStr | Quantum yields of photocoloration and molar absorption coefficients of ferrocenyl substituted benzo and dibenzochromenes. Comparison
with their phenyl-homologues |
| title_full_unstemmed | Quantum yields of photocoloration and molar absorption coefficients of ferrocenyl substituted benzo and dibenzochromenes. Comparison
with their phenyl-homologues |
| title_short | Quantum yields of photocoloration and molar absorption coefficients of ferrocenyl substituted benzo and dibenzochromenes. Comparison
with their phenyl-homologues |
| title_sort | quantum yields of photocoloration and molar absorption coefficients of ferrocenyl substituted benzo and dibenzochromenes comparison with their phenyl homologues |
| url | http://dx.doi.org/10.1155/S1110662X03000394 |
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