Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Quentin Verolet"'
Publikováno v:
CHEMISTRY-A EUROPEAN JOURNAL
Chemistry-A European Journal, Vol. 21, No 16 (2015) pp. 6012-6021
Chemistry-A European Journal, Vol. 21, No 16 (2015) pp. 6012-6021
This article assembles pertinent insights behind the concept of planarizable push-pull probes. As a response to the planarization of their polarized ground state, a red shift of their excitation maximum is expected to report on either the disorder, t
Autor:
Alessio Carmine, Cristina Stefaniu, Pierre-Léonard Zaffalon, Samuel Fernandez, Andreas Zumbuehl, Quentin Verolet, Gerald Brezesinski, Tomasz Adam Wesolowski
Publikováno v:
Langmuir : the ACS journal of surfaces and colloids
Langmuir, Vol. 31, No 4 (2015) pp. 1296-1302
Langmuir, Vol. 31, No 4 (2015) pp. 1296-1302
A series of long-tail alkyl ethanolamine analogs containing amide-, urea-, and thiourea moieties was synthesized and the behavior of the corresponding monolayers was assessed on the Langmuir-Pockels trough combined with grazing incidence X-ray diffra
Autor:
Adai Colom, Laure Guénée, Naomi Sakai, Marta Dal Molin, Quentin Verolet, Aurélien Roux, Stefan Matile
Publikováno v:
Helvetica Chimica Acta, Vol. 100, No 2 (2017) P. e1600328
Planarizable and polarizable dithieno[3,2-b;2′,3′-d]thiophene (DTT) dimers have been introduced recently as fluorescent probes that report on membrane fluidity with red shifts in excitation, i.e. planarization in the ground state. In this study,
Publikováno v:
Angewandte Chemie. 125:9117-9120
Publikováno v:
Journal of the American Chemical Society, Vol. 138, No 29 (2016) pp. 9093-9096
In this report, we introduce synthetic anion transporters that operate with chalcogen bonds. Electron-deficient dithieno[3,2-b;2',3'-d]thiophenes (DTTs) are identified as ideal to bind anions in the focal point of the σ holes on the cofacial endocyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ad2f755065a98c90e956857850606a8
https://archive-ouverte.unige.ch/unige:85614
https://archive-ouverte.unige.ch/unige:85614
Publikováno v:
Chemistry - A European Journal. 19:372-381
New p-type, n-type, and ambipolar molecules were synthesized from commercially available 4,10-dibromoanthanthrone dye. Substitution at the 4,10- and 6,12-positions with different electron-rich and electron-poor units allowed the modulation of the opt
Autor:
Romain Letrun, Naomi Sakai, Quentin Verolet, Aurélien Roux, Adai Colom, Emmanuel Derivery, Marta Dal Molin, Stefan Matile, Eric Vauthey, Marcos González-Gaitán
Publikováno v:
Journal of the American Chemical Society, Vol. 137, No 2 (2015) pp. 568-571
Journal of the American Chemical Society
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Journal of the American Chemical Society
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
In this report, “fluorescent flippers” are introduced to create planarizable push–pull probes with the mechanosensitivity and fluorescence lifetime needed for practical use in biology. Twisted push–pull scaffolds with large and bright dithien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29214fc4200f7b9082441bd82e766fe3
https://archive-ouverte.unige.ch/unige:55060
https://archive-ouverte.unige.ch/unige:55060
Autor:
Stefan Matile, Eric Vauthey, Arnulf Rosspeintner, Naomi Sakai, Quentin Verolet, Saeideh Soleimanpour
Publikováno v:
Journal of the American Chemical Society, Vol. 137, No 50 (2015) pp. 15644-15647
Attached to electron-rich aromatic systems, sulfides are very weak acceptors; however, attached to electron-poor aromatics, they turn into quite strong donors. Here, we show that this underappreciated dual nature of sulfides deserves full considerati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8a324c6ef229c467f8bf65f2f1d819a
https://archive-ouverte.unige.ch/unige:79049
https://archive-ouverte.unige.ch/unige:79049
Autor:
Quentin Verolet, Marta Dal Molin, Stefan Matile, Naomi Sakai, Saeideh Soleimanpour, Kaori Fujisawa
Publikováno v:
ChemistryOpen, Vol. 4, No 3 (2015) pp. 264-267
CHEMISTRYOPEN
ChemistryOpen
CHEMISTRYOPEN
ChemistryOpen
Monomers with large surface area and high quantum yield, that is fluorescent flippers, have been engineered into twisted push–pull oligomers to create membrane probes with high mechanosensitivity and long fluorescence lifetime. Here, the synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5650fccdab960f67f7cc054e09167b6
https://archive-ouverte.unige.ch/unige:73189
https://archive-ouverte.unige.ch/unige:73189
Autor:
Sebastian Malkusch, Steven F. Lee, Mike Heilemann, Alexandre Fuerstenberg, Ulrike Endesfelder, Christoph Spahn, Kathrin Klehs, Quentin Verolet
Publikováno v:
Biophysical Journal. 106(2)
Advanced fluorescence microscopy techniques including single-molecule and super-resolution imaging require bright and photostable dyes that can be selectively targeted to biomolecules. There is therefore an ongoing interest in the development of impr