TY - JOUR
T1 - Dynamical Behavior and Second Harmonic Generation Responses in Acido-Triggered Molecular Switches
AU - Pielak, Kornelia
AU - Tonnelé, Claire
AU - Sanguinet, Lionel
AU - Cariati, Elena
AU - Righetto, Stefania
AU - Muccioli, Luca
AU - Castet, Frédéric
AU - Champagne, Benoît
N1 - Funding Information:
K.P. acknowledges the Reǵ ion Aquitaine (INMERON Project, Convention 2014-1R10102-00002867) and the University of Namur for her Ph.D. grant. This work was supported by funds from the Francqui Foundation. It was also carried out in the frame of the Centre of Excellence LAPHIA (Investments for the future: Programme IdEx BordeauxLAPHIA (ANR-10-IDEX-03-02)). The calculations were performed on the computing facilities of the Consortium des Équipements de Calcul Intensif (CÉCI, http://www.ceci-hpc.be), and particularly those of the Technological Platform on High-Performance Computing, for which the authors gratefully acknowledge the financial support of the FNRS-FRFC (Conventions No. 2.4.617.07.F and 2.5020.11) and of the University of Namur, on zenobe, the Tier-1 facility of the Walloon Region (Convention 1117545), as well as by the Pôle Modeĺ isation HPC facilities of the Institut des Sciences Molećulaires UMR 5255 CNRSUniversité de Bordeaux, co-funded by the Nouvelle Aquitaine region as well as the MCIA (Meś ocentre de Calcul Intensif Aquitain) ressources of the Université de Bordeaux and of the Université de Pau et des Pays de l’Adour.
Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/11/15
Y1 - 2018/11/15
N2 - Second-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.
AB - Second-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.
UR - http://www.scopus.com/inward/record.url?scp=85056374349&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.8b08697
DO - 10.1021/acs.jpcc.8b08697
M3 - Article
AN - SCOPUS:85056374349
SN - 1932-7447
VL - 122
SP - 26160
EP - 26168
JO - Journal of Physical Chemistry C: Nanomaterials and interfaces
JF - Journal of Physical Chemistry C: Nanomaterials and interfaces
IS - 45
ER -