Zobrazeno 1 - 10
of 22
pro vyhledávání: '"T. Nozdryn"'
Publikováno v:
Synthetic Metals. 115:261-264
From DFWM efficiency measurements, we deduce third-order susceptibility of polyfluroalkylsulfanyl-substituted TTF derivatives. To know the physical nature of the optical non-linearities, we separate the electronic and nuclear contributions in w h3i .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6367b279a645daf9567fd4a08a342f5
https://doi.org/10.1016/s0379-6779(00)00323-4
https://doi.org/10.1016/s0379-6779(00)00323-4
Publikováno v:
Thin Solid Films. 300:228-233
New semifluorinated tetrathiafulvalene (TTF) derivatives were prepared and used in Langmuir and Langmuir-Blodgett (LB) films. Transfer onto a solid substrate of such pure monolayers can be easily achieved leading to organized LB films in which the fl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cde7dcad04f773bb71b11c2b4155652d
https://doi.org/10.1016/s0040-6090(96)09521-1
https://doi.org/10.1016/s0040-6090(96)09521-1
Autor:
Javier Garín, Marc Sallé, T. Nozdryn, Michel Jubault, Alain Gorgues, Yann Siqot, Pierre Frère, Jack Cousseau, Jesús Orduna
Publikováno v:
Tetrahedron Letters. 38:1919-1922
The synthesis of the first fused [3,4]furano-TTFs has been accomplished starting from the 4-formyl-5-diethoxymethyl-2-thioxo-1,3-dithiole. Two routes have been explored involving either the furan ring or the TTF core. In particular, the first proceed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09b55fc21c897cb4f0e42b4412867d38
https://doi.org/10.1016/s0040-4039(97)00244-x
https://doi.org/10.1016/s0040-4039(97)00244-x
Autor:
T. Nozdryn, Peter J. Skabara, Jan Becher, Rasmus P. Clausen, Alain Gorgues, Wim Dehaen, V. Morisson, Martin R. Bryce, Javier Garín, Jack Cousseau, Jesús Orduna, María Savirón, Raquel Andreu
Publikováno v:
Scopus-Elsevier
The synthesis of the title compound 9, by three different routes, is described for the first time.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12e27e90786e3f3f32972ce58deb94cb
https://doi.org/10.1016/0040-4039(94)88478-1
https://doi.org/10.1016/0040-4039(94)88478-1
Autor:
Jesús Orduna, T. Nozdryn, Alain Gorgues, Javier Garín, Santiago Uriel, Michel Jubault, Jack Cousseau
Publikováno v:
ChemInform. 24
DIBALH reduction of the methyl ester group of 2-(thi)oxo-1.3-dithioles 1a and 1b selectively affords the corresponding alcohols 3a and 3b which are readily converted into the title compounds 6a and 6b under standard conditions; the latter behave as u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff3e78f1fa03020d29f2c8f0e9005353
https://doi.org/10.1002/chin.199350196
https://doi.org/10.1002/chin.199350196
Autor:
Michel Jubault, T. Nozdryn, Y. Siquot, Javier Garín, Jack Cousseau, Jesús Orduna, Marc Sallé, Pierre Frère, Alain Gorgues
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29d41478a3a67c5827efb62d564710c6
https://doi.org/10.1002/chin.199727134
https://doi.org/10.1002/chin.199727134
Autor:
Alain Gorgues, T. Nozdryn, Jesús Orduna, Michel Jubault, Javier Garín, Jack Cousseau, Jean-François Favard
Publikováno v:
ChemInform. 29
Polyfluoroalkylsulfanyl-substituted tetrathiafulvalene derivatives have been synthesised via self- or cross-coupling of suitable 2-(thi)oxo-1, 3-dithioles. Key intermediates are 4,5-bis(polyfluoroalkyl-sulfanyl)-2-thioxo-1,3-dithioles, formed from re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7d7850f19e8d050b41065e75d5ddd02
https://doi.org/10.1002/chin.199819126
https://doi.org/10.1002/chin.199819126
Publikováno v:
Synthetic Metals. 102:1637
The synthesis, electrochemical and mesomorphic properties of 4,5-ethylenedithio-4′-[2-(perfluorohexyl)ethoxycarbonyl] tetrathiafulvalene are reported. This compound is the first semifluorinated mesogenic tetrathiafulvalene derivative.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8f077bcab6250afb0140b8e56953f9f
https://doi.org/10.1016/s0379-6779(98)00519-0
https://doi.org/10.1016/s0379-6779(98)00519-0
Autor:
Michel Jubault, Jack Cousseau, Jesús Orduna, Javier Garín, T. Nozdryn, Santiago Uriel, Alain Gorgues
Publikováno v:
Scopus-Elsevier
DIBALH reduction of the methyl ester group of 2-(thi)oxo-1.3-dithioles 1a and 1b selectively affords the corresponding alcohols 3a and 3b which are readily converted into the title compounds 6a and 6b under standard conditions; the latter behave as u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c411eef5277a0305efb67403e5a660a
http://www.scopus.com/inward/record.url?eid=2-s2.0-37049069395&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-37049069395&partnerID=MN8TOARS
Autor:
Jesús Orduna, Alain Gorgues, Javier Garín, Jack Cousseau, Jean-François Favard, Michel Jubault, T. Nozdryn
Publikováno v:
Scopus-Elsevier
Polyfluoroalkylsulfanyl-substituted tetrathiafulvalene derivatives have been synthesised via self- or cross-coupling of suitable 2-(thi)oxo-1, 3-dithioles. Key intermediates are 4,5-bis(polyfluoroalkyl-sulfanyl)-2-thioxo-1,3-dithioles, formed from re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a018ef63787ce77eb96ff720368ed39b
http://www.scopus.com/inward/record.url?eid=2-s2.0-0031555426&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0031555426&partnerID=MN8TOARS