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Alternated π‐conjugated polymers based on a 1,2‐diiminocyclohexane chiral unit for nitroaromatics sensing
Authors:Simon Clavaguera  Olivier J Dautel  Lionel Hairault  Christophe Méthivier  Pierre Montméat  Eric Pasquinet  Claire‐Marie Pradier  Françoise Serein‐Spirau  Salem Wakim  Florian Veignal  Joël J E Moreau  Jean‐Pierre Lère‐Porte
Institution:1. Institut Charles Gerhardt, UMR CNRS 5253, Equipe AM2N, Ecole Nationale Supérieure de Chimie de Montpellier, 8 Rue de l'Ecole Normale, 34296 Montpellier Cedex 05, France;2. CEA Le Ripault, BP 16, 37260 Monts, France;3. Laboratoire de Réactivité de Surface, UMR CNRS 7609, Université Pierre et Marie Curie, Case 178, 4 place Jussieu, 75252 Paris Cedex 05, France
Abstract:The detection of 2,4‐dinitrotoluene (DNT) by fluorescence quenching of a new class of polyimines consisting in π‐conjugated segments regularly alternated with chiral C2 symmetry units has been studied for solutions and thin films. Their photophysical properties and their sensitivity towards DNT detection has been compared to those of a small model molecule incorporating the same π‐conjugated segment. In solution, all the compounds exhibit the same photo‐physical properties and sensitivity towards DNT detection. In contrast, for thin films, better performances are observed in static conditions for this new class of polyimines compared to the small model molecule. It seems that C2 symmetry units prevent from the stacking of the π‐conjugated segments and provide in addition to high fluorescence signal an improved diffusion of the analyte inside the films. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 4141–4149, 2009
Keywords:chiral  chiral polymers  conjugated polymers  fluorescence  fluorescence nitroaromatics detection  infrared spectroscopy  polyimines  sensors
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