Triisopropylsilylethynyl-substituted indenofluorenes: carbonyl versus dicyanovinylene functionalization in one-dimensional molecular crystals and solution-processed n-channel OFETs-Reference-Cited by-同舟云学术

Triisopropylsilylethynyl-substituted indenofluorenes: carbonyl versus dicyanovinylene functionalization in one-dimensional molecular crystals and solution-processed n-channel OFETs

Published:2018 Issue:20 Volume:5 Page:2912-2924
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Ozdemir Resul¹²³⁴^ORCID,Park Sangyun⁵⁶⁷⁸,Deneme İbrahim¹²³⁴,Park Yonghan⁵⁶⁷⁸,Zorlu Yunus⁹¹⁰¹¹⁴,Alidagi Husniye Ardic¹²³⁴⁹,Harmandar Kevser⁹¹⁰¹¹⁴,Kim Choongik⁵⁶⁷⁸,Usta Hakan¹²³⁴^ORCID

Affiliation:

1. Department of Materials Science and Nanotechnology Engineering

2. Abdullah Gül University

3. Kayseri

4. Turkey

5. Department of Chemical and Biomolecular Engineering

6. Sogang University

7. Mapo-gu

8. Republic of Korea

9. Department of Chemistry

10. Gebze Technical University

11. Gebze

Abstract

Carbonyl vs. dicyanovinylene functionalization in indenofluorenes leads to substantial differences in solid-state packings and results in significant variations (×1000) in electron mobilities.

Funder

Türkiye Bilimler Akademisi

Ministry of Science, ICT and Future Planning

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/QO/C8QO00856F

Reference66 articles.

1. Slip-Stacked Perylenediimides as an Alternative Strategy for High Efficiency Nonfullerene Acceptors in Organic Photovoltaics

2. Solution-Processed High-Performance Tetrathienothiophene-Based Small Molecular Blends for Ambipolar Charge Transport

3. Ring-Fusion of Perylene Diimide Acceptor Enabling Efficient Nonfullerene Organic Solar Cells with a Small Voltage Loss

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