Symmetry Breaking in Pyrrolo[3,2‐b]pyrroles: Synthesis, Solvatofluorochromism and Two‐photon Absorption

Abstract

Five centrosymmetric and one dipolar pyrrolo[3,2‐b]pyrroles, possessing either two or one strongly electron‐withdrawing nitro group have been synthesized in a straightforward manner from simple building blocks. For the symmetric compounds, the nitroaryl groups induced spontaneous breaking of inversion symmetry in the excited state, thereby leading to large solvatofluorochromism. To study the origin of this effect, the series employed peripheral structural motifs that control the degree of conjugation via altering of dihedral angle between the 4‐nitrophenyl moiety and the electron‐rich core. We observed that for compounds with a larger dihedral angle, the fluorescence quantum yield decreased quickly when exposed to even moderately polar solvents. Reducing the dihedral angle (i.e., placing the nitrobenzene moiety in the same plane as the rest of the molecule) moderated the dependence on solvent polarity so that the dye exhibited significant emission, even in THF. To investigate at what stage the symmetry breaking occurs, we measured two‐photon absorption (2PA) spectra and 2PA cross‐sections (σ2PA) for all six compounds. The 2PA transition profile of the dipolar pyrrolo[3,2‐b]pyrrole, followed the corresponding one‐photon absorption (1PA) spectrum, which provided an estimate of the change of the permanent electric dipole upon transition, ≈18 D. The nominally symmetric compounds displayed an allowed 2PA transition in the wavelength range of 700–900 nm. The expansion via a triple bond resulted in the largest peak value, σ2PA=770 GM, whereas altering the dihedral angle had no effect other than reducing the peak value two‐ or even three‐fold. In the S0→S1 transition region, the symmetric structures also showed a partial overlap between 2PA and 1PA transitions in the long‐wavelength wing of the band, from which a tentative, relatively small dipole moment change, 2–7 D, was deduced, thus suggesting that some small symmetry breaking may be possible in the ground state, even before major symmetry breaking occurs in the excited state.

Document Details

Document Type
Pub Defense Publication
Publication Date
Jun 08, 2017
Source ID
10.1002/asia.201700159

Entities

People

  • Aleksander Rebane
  • Alexander Mikhaylov
  • Bolesław Kozankiewicz
  • Cloé Azarias
  • Daniel Gryko
  • Denis Jacquemin
  • Hye Gun Ryu
  • Kyo Han Ahn
  • Marzena Banasiewicz
  • Łukasz G. Łukasiewicz

Organizations

  • Agence Nationale de la Recherche
  • Air Force Office of Scientific Research
  • European Regional Development Fund
  • Institut Universitaire de France
  • Institute of Physics
  • Montana State University
  • Nantes University
  • National Institute of Chemical Physics and Biophysics
  • National Research Foundation of Korea
  • National Science Centre Poland
  • Pohang University of Science and Technology
  • Polish Academy of Sciences

Tags

Fields of Study

  • Physics

Readers

  • Molecular Photonics/Laser Physics
  • Organic Chemistry
  • Quantum spin resonance or Electron Paramagnetic Resonance spectroscopy.

Technology Areas

  • Microelectronics
  • Microelectronics - Graphene
  • Quantum Computing