Afficher la notice abrégée

dc.rights.licenseopen
dc.contributor.authorPIELAK, Kornelia
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorTONNELÉ, Claire
hal.structure.identifierMOLTECH-Anjou
dc.contributor.authorSANGUINET, Lionel
dc.contributor.authorCARIATI, Elena
hal.structure.identifierDipartimento di Chimica
dc.contributor.authorRIGHETTO, Stefania
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
dc.contributor.authorMUCCIOLI, Luca
hal.structure.identifierInstitut des Sciences Moléculaires [ISM]
dc.contributor.authorCASTET, Frédéric
hal.structure.identifierLaboratoire de Chimie Théorique appliquée
dc.contributor.authorCHAMPAGNE, Benoît
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2018
dc.identifier.issn1932-7447
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/19689
dc.description.abstractEnSecond-order nonlinear optical molecular switches are systems displaying marked variations of their second harmonic generation (SHG) responses upon external stimulation. In this article, we combine a multiscale computational method and experimental characterizations to provide a full description of the SHG responses of molecular switches built from the association of the indolino-oxazolidine unit to a bithiophene donor. In chloroform solutions, the addition of trifluoroacetic acid triggers the switching from a neutral closed form to a protonated open form, making an ion pair with the trifluoroacetate counterion and induces a strong enhancement of the SHG responses. The numerical simulations (i) evidence how the large and rapid thermally induced geometrical fluctuations lead to broadening the SHG responses distributions, making even difficult the determination of their sign, (ii) rationalize the variations of these responses as a function of the closure/opening of the oxazolidine ring and of the nature of its chemical substitution, and (iii) call into question common assumptions employed when analyzing the experimental SHG responses.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.title.enDynamical Behavior and Second Harmonic Generation Responses in Acido-Triggered Molecular Switches
dc.typeArticle de revue
dc.identifier.doi10.1021/acs.jpcc.8b08697
dc.subject.halChimie
bordeaux.journalJournal of Physical Chemistry C
bordeaux.page26160-26168
bordeaux.volume122
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue45
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-02564573
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-02564573v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal%20of%20Physical%20Chemistry%20C&rft.date=2018&rft.volume=122&rft.issue=45&rft.spage=26160-26168&rft.epage=26160-26168&rft.eissn=1932-7447&rft.issn=1932-7447&rft.au=PIELAK,%20Kornelia&TONNEL%C3%89,%20Claire&SANGUINET,%20Lionel&CARIATI,%20Elena&RIGHETTO,%20Stefania&rft.genre=article


Fichier(s) constituant ce document

FichiersTailleFormatVue

Il n'y a pas de fichiers associés à ce document.

Ce document figure dans la(les) collection(s) suivante(s)

Afficher la notice abrégée