Twisted Thiophene-Based Chromophores with Enhanced Intramolecular Charge Transfer for Cooperative Amplification of Third-Order Optical Nonlinearity

Natasha B. Teran, Guang S. He, Alexander Baev, Yanrong Shi, Mark T. Swihart, Paras N. Prasad, Tobin J Marks, John R. Reynolds

Research output: Contribution to journalArticle

41 Citations (Scopus)

Abstract

Exploiting synergistic cooperation between multiple sources of optical nonlinearity, we report the design, synthesis, and nonlinear optical properties of a series of electron-rich thiophene-containing donor-acceptor chromophores with condensed π-systems and sterically regulated inter-aryl twist angles. These structures couple two key mechanisms underlying optical nonlinearity, namely, (i) intramolecular charge transfer, greatly enhanced by increased electron density and reduced aromaticity at chromophore thiophene rings and (ii) a twisted chromophore geometry, producing a manifold of close-lying excited states and dipole moment changes between ground and excited states that are nearly twice that of untwisted systems. Spectroscopic, electrochemical, and nonlinear Z-scan measurements, combined with quantum chemical calculations, illuminate relationships between molecular structure and mechanisms of enhancement of the nonlinear refractive index. Experiment and calculations together reveal ground-state structures that are strongly responsive to the solvent polarity, leading to substantial negative solvatochromism (- 102 nm) and prevailing zwitterionic/aromatic structures in the solid state and in polar solvents. Ground-to-excited-state energy gaps below 2.0 eV are obtained in condensed π-systems, with lower energy gaps for twisted versus untwisted systems. The real part of the second hyperpolarizability in the twisted structures is much greater than the imaginary part, with the highest twist angle chromophore giving |Re(γ)/Im(γ)| - 100, making such chromophores very promising for all-optical-switching applications.

Original languageEnglish
Pages (from-to)6975-6984
Number of pages10
JournalJournal of the American Chemical Society
Volume138
Issue number22
DOIs
Publication statusPublished - Jun 8 2016

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Thiophenes
Thiophene
Chromophores
Amplification
Charge transfer
Electrons
Refractometry
Excited states
Molecular Structure
Ground state
Energy gap
Dipole moment
Molecular structure
Carrier concentration
Refractive index
Optical properties
Geometry
Experiments

ASJC Scopus subject areas

  • Chemistry(all)
  • Catalysis
  • Biochemistry
  • Colloid and Surface Chemistry

Cite this

Twisted Thiophene-Based Chromophores with Enhanced Intramolecular Charge Transfer for Cooperative Amplification of Third-Order Optical Nonlinearity. / Teran, Natasha B.; He, Guang S.; Baev, Alexander; Shi, Yanrong; Swihart, Mark T.; Prasad, Paras N.; Marks, Tobin J; Reynolds, John R.

In: Journal of the American Chemical Society, Vol. 138, No. 22, 08.06.2016, p. 6975-6984.

Research output: Contribution to journalArticle

Teran, Natasha B. ; He, Guang S. ; Baev, Alexander ; Shi, Yanrong ; Swihart, Mark T. ; Prasad, Paras N. ; Marks, Tobin J ; Reynolds, John R. / Twisted Thiophene-Based Chromophores with Enhanced Intramolecular Charge Transfer for Cooperative Amplification of Third-Order Optical Nonlinearity. In: Journal of the American Chemical Society. 2016 ; Vol. 138, No. 22. pp. 6975-6984.
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