Synthetic, Optical and Theoretical Study of Alternating Ethylenedioxythiophene-Pyridine Oligomers: Evolution from Planar Conjugated to Helicoidal Structure towards a Chiral Configuration-Reference-Cited by-同舟云学术

Synthetic, Optical and Theoretical Study of Alternating Ethylenedioxythiophene-Pyridine Oligomers: Evolution from Planar Conjugated to Helicoidal Structure towards a Chiral Configuration

Published:2016-11-15 Issue:24 Volume:17 Page:4090-4101
ISSN:1439-4235
Container-title:ChemPhysChem
language:en
Short-container-title:ChemPhysChem

Author:

Chevallier Floris¹²,Charlot Marina¹,Mongin Florence¹²,Champagne Benoît³,Franz Edith⁴,Clays Koen⁴,Blanchard-Desce Mireille¹⁵

Affiliation:

1. Chimie et Photonique Moléculaires; UMR 6510 CNRS; Université de Rennes 1; 35042 Rennes France

2. Institut des Sciences Chimiques de Rennes; UMR 6226 CNRS; Université de Rennes 1; 35042 Rennes France

3. Laboratoire de Chimie Théorique; Université de Namur; 5000 Namur Belgium

4. Department of Chemistry; University of Leuven; 3001 Leuven Belgium

5. Université de Bordeaux; Institut des Sciences Moléculaires; UMR 5255 CNRS; 33405 Talence France

Publisher

Wiley

Subject

Physical and Theoretical Chemistry,Atomic and Molecular Physics, and Optics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/cphc.201601057/fullpdf

Reference90 articles.

1. Design, Synthesis, Linear, and Nonlinear Optical Properties of Conjugated (Porphinato)zinc(II)-Based Donor−Acceptor Chromophores Featuring Nitrothiophenyl and Nitrooligothiophenyl Electron-Accepting Moieties

2. Theoretical Investigations on the Electronic and Optical Properties of Bridged Oligothiophenes

3. 3,4-Ethylenedioxythiophene (EDOT) as a versatile building block for advanced functional π-conjugated systems

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