Zobrazeno 1 - 10
of 37
pro vyhledávání: '"R. Dubest"'
Autor:
Gaston Vermeersch, T. Couesnon, Jean Aubard, Stéphanie Delbaere, François Maurel, S. Lau Truong, R. Dubest
Publikováno v:
Journal of Physical Organic Chemistry. 20:944-952
Nuclear Magnetic Resonance (NMR), Surface-Enhanced Resonance Raman Scattering (SERRS), and Density Functional Theory (DFT) were used to study 8-substituted acetylene- and thienylacetylene-diphenylnaphthopyran photochromic compounds. The purpose of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e129e850de2702f6e0d59e2ff137ed26
https://doi.org/10.1002/poc.1212
https://doi.org/10.1002/poc.1212
Autor:
Abd Errahim Yassar, Corinne Moustrou, Robert Guglielmetti, Jean Aubard, N. Rebiere, André Samat, R. Dubest
Publikováno v:
Helvetica Chimica Acta. 81:1293-1302
The synthesis of 3H-naphtho[2,1-b]pyrans 9–21 linked to a thiophene moiety is described. Two different synthetic approaches were applied to prepare these novel functionalized compounds, and their spectrokinetic properties in solution are reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::822faf1d6fb54ad1d2eaaae62a425f4f
https://doi.org/10.1002/hlca.19980810540
https://doi.org/10.1002/hlca.19980810540
Publikováno v:
Helvetica Chimica Acta. 78:1887-1893
The synthesis of spiropyrans 11 and 12 and spirooxazines 13–17 containing a thiophene moiety is described. Two different synthetic approaches were used. The spectrokinetic properties of these new compounds are reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da9bb0a144969ff10b0239e2ab34bd41
https://doi.org/10.1002/hlca.19950780722
https://doi.org/10.1002/hlca.19950780722
Autor:
J. J. Meyer, Gilles Baillet, Robert Guglielmetti, P. Levoir, Jean Aubard, G. Giusti, R. Dubest
Publikováno v:
Review of Scientific Instruments. 64:1803-1808
In this paper, we describe a new, entirely computer‐controlled apparatus designed for degradation studies of photochromic compounds. Photodegradation can be performed in three different ways using, in addition to the usual flash mode, the cyclic an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c584bb887a17d09bb05cef77d28e154
https://doi.org/10.1063/1.1144014
https://doi.org/10.1063/1.1144014
Autor:
Pascale Tardieu, André Samat, A. Kellmann, F. Tfibel, J. Aubard, Robert Guglielmetti, R. Dubest
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c0d588b2b9b16c03646057bf529327c
https://doi.org/10.1002/chin.199241177
https://doi.org/10.1002/chin.199241177
Publikováno v:
ChemInform. 27
The synthesis of spiropyrans 11 and 12 and spirooxazines 13–17 containing a thiophene moiety is described. Two different synthetic approaches were used. The spectrokinetic properties of these new compounds are reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e5a0240ce47b06f7f6b6fe9a3b418b5
https://doi.org/10.1002/chin.199606175
https://doi.org/10.1002/chin.199606175
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a337351efdfb0770eb4ab2f65a2e88a
https://doi.org/10.1002/chin.199730133
https://doi.org/10.1002/chin.199730133
Autor:
R. Dubest, Robert Guglielmetti, N. Rebiere, André Samat, Abd Errahim Yassar, Corinne Moustrou, Jean Aubard
Publikováno v:
ChemInform. 29
The synthesis of 3H-naphtho[2,1-b]pyrans 9–21 linked to a thiophene moiety is described. Two different synthetic approaches were applied to prepare these novel functionalized compounds, and their spectrokinetic properties in solution are reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5d2dec3d994ba132a731b9ea5ef9cc6
https://doi.org/10.1002/chin.199840131
https://doi.org/10.1002/chin.199840131
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