4.6 Article

Second-Order Nonlinear Optical Properties of Multiaddressable Indolinooxazolidine Derivatives: Joint Computational and Hyper-Rayleigh Scattering Investigations

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 121, Issue 3, Pages 1851-1860

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.6b11082

Keywords

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Funding

  1. Region Aquitaine (INMERON Project) [2014-1R10102-00002867]
  2. University of Namur
  3. CNRS
  4. Region Aquitaine
  5. Belgian Government (IUAP) [P7/5]
  6. Francqui Foundation
  7. Programme IdEx Bordeaux LAPHIA [ANR-10-IDEX-03-02]
  8. FNRS-FRFC [2.4.617.07.F, 2.5020.11]
  9. Conseil Regional d'Aquitaine
  10. French Ministry of Research and Technology

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The linear and nonlinear optical (NLO) properties of two indolinooxazolidine derivatives acting as multiaddressable switches are reported. The second-order hyperpolarizability contrasts upon commutation between their closed and open forms are characterized using hyper-Rayleigh scattering (HRS) measurements, and rationalized by means of density functional theory and post Hartree-Fock ab initio calculations. It is evidenced that the addition of a withdrawing substituent on the indolinic subunit leads to a more effective photoinduced charge transfer while decreasing the transition energy of the S-0 -> S-1 transition, which induces a significant enhancement of the HRS response of the open form. This substitution is however detrimental to the NLO contrast, due to the concomitant increase of the HRS response of the closed form.

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