The impact of vinylene bridges and side chain alkyl groups on the solid state structures of tricyanovinyl-substituted thiophenes
Author:
Affiliation:
1. Department of Chemistry
2. Penn State Worthington Scranton
3. USA
4. University of Minnesota
5. Minneapolis
6. Alfaisal University
7. Riyadh 11533
8. Saudi Arabia
Abstract
The goal of this work is to examine the solid state structures of compounds that have been designed for increased conjugation and solubility, as these factors are important if these compounds are to be used in the solid state.
Publisher
Royal Society of Chemistry (RSC)
Subject
Condensed Matter Physics,General Materials Science,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2018/CE/C7CE01574G
Reference50 articles.
1. Handbook of Thiophene-Based Materials: Applications in Organic Electronics and Photonics , ed. I. F. Perepichka and D. F. Perepichka , Wiley , Weinheim , 2009
2. Functional Oligothiophenes: Molecular Design for Multidimensional Nanoarchitectures and Their Applications
3. Synthesis, Electronic Structure, Molecular Packing/Morphology Evolution, and Carrier Mobilities of Pure Oligo-/Poly(alkylthiophenes)
4. Building Blocks for N-Type Molecular and Polymeric Electronics. Perfluoroalkyl- versus Alkyl-Functionalized Oligothiophenes (nTs; n = 2−6). Systematic Synthesis, Spectroscopy, Electrochemistry, and Solid-State Organization
5. Planar β-Linked Oligothiophenes Based on Thieno[3,2-b]thiophene and Dithieno[3,2-b:2‘,3‘-d]thiophene Fused Units
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1. Thiophenes Endowed with Electron-Accepting Groups: A Structural Study;Crystal Growth & Design;2024-01-18
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