Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Teresa M. Figueira Duarte"'
Autor:
Teresa M. Figueira-Duarte, Martin Baumgarten, Manfred Wagner, Ashok Keerthi, Dominik Lorbach, Klaus Müllen
Publikováno v:
Angewandte Chemie International Edition. 55:418-421
First synthesis of the macrocycle cyclohexa(1,3-pyrenylene) is achieved in six steps starting with pyrene, leading to a non-aggregating highly twisted blue-light-emitting material. The cyclodehydrogenation of the macrocycle offers a promising synthes
Autor:
Martin Baumgarten, Manfred Wagner, Teresa M. Figueira-Duarte, Ashok Keerthi, Klaus Müllen, Dominik Lorbach
Publikováno v:
Angewandte Chemie. 128:427-431
Die Synthese des Makrocyclus Cyclohexa-1,3-pyrenylen uber sechs Schritte ausgehend von Pyren wird beschrieben. Der nicht aggregierende und stark verdrillte Makrocyclus ist ein blau emittierendes Material. Die Cyclodehydrierung bietet einen vielverspr
Autor:
Stefan Sax, Teresa M. Figueira-Duarte, Pablo G. Del Rosso, Emil J. W. List, Roman Trattnig, Klaus Müllen
Publikováno v:
Advanced Materials. 22:990-993
Autor:
Teresa M. Figueira-Duarte, José Vidal-Gancedo, Concepció Rovira, Béatrice Delavaux-Nicot, Vega Lloveras, Jaume Veciana, Jean-François Nierengarten, Carine Duhayon
Publikováno v:
European Journal of Organic Chemistry. 2009:5779-5787
Macrocyclic C60-(π-conjugated oligomer) dyads have been prepared from the corresponding bis-malonates by a macrocyclization reaction on the C60 sphere. In both multicomponent systems, the fullerene moiety and the π-conjugated oligomer subunit are a
Autor:
François Cardinali, Jean Olivier, Jean-François Nierengarten, Aline Gégout, Teresa M. Figueira-Duarte
Publikováno v:
European Journal of Organic Chemistry. 2009:3879-3884
Hexaphenylbenzene derivatives bearing two aldehyde groups were prepared by reaction of 4,4′-(ethyne-1,2-diyl)dibenzaldehyde with bisarylalkynes in the presence of a catalytic amount of Co2(CO)8. These synthetic intermediates were used to produce th
Autor:
Teresa M, Figueira-Duarte, Sascha C, Simon, Manfred, Wagner, Sergey I, Druzhinin, Klaas A, Zachariasse, Klaus, Müllen
Publikováno v:
Angewandte Chemie. 120:10329-10332
Publikováno v:
European Journal of Organic Chemistry. 2008:3627-3634
Oligophenylenevinylene (OPV) derivatives substituted with one or two fullerene subunits have been prepared starting from a fullerene carboxylic acid derivative and OPV heptamers bearing one or two alcohol functions. The electrochemical properties of
Autor:
Ali Trabolsi, Nathalie Solladié, Haiko Herschbach, Uwe Hahn, Mathieu E. Walther, Anne Marie Albrecht-Gary, Mourad Elhabiri, Jean-François Nierengarten, Emmanuelle Leize, Teresa M. Figueira Duarte, Alain Van Dorsselaer, François Cardinali
Publikováno v:
Comptes Rendus Chimie. 9:1022-1030
Here, we report our recent progresses in the synthesis and the study of fullerene-containing supramolecular photoactive devices. Our approach is based on the self-assembly of C 60 derivatives bearing an ammonium unit with functionalized crown ethers.
Autor:
Alain Van Dorsselaer, Jean-François Nierengarten, Nathalie Solladié, Emmanuelle Leize, Haiko Herschbach, Mathieu E. Walther, Teresa M. Figueira Duarte
Publikováno v:
Tetrahedron. 62:1979-1987
A methanofullerene derivative with an ammonium subunit ( 1 ) has been prepared and its ability to form a supramolecular complex with a porphyrin–crown ether conjugate evidenced by NMR, UV–vis, electrospray mass spectrometry (ES-MS) and luminescen
Autor:
Fettah Ajamaa, Michel Holler, Teresa M. Figueira Duarte, Patrick W. Fowler, Cyril Bourgogne, Jean-François Nierengarten
Publikováno v:
European Journal of Organic Chemistry. 2005:3766-3774
A complete series of (phenylpyrrolidino)fullerene derivatives has been prepared. A detailed conformational analysis of these compounds has been carried out by variable-temperature 1H NMR experiments and computational studies. In the case of (phenylpy