N-Alkyl functionalized barbituric and thiobarbituric acid bithiophene derivatives for vacuum deposited n-channel OFETs-Reference-Cited by-同舟云学术

N-Alkyl functionalized barbituric and thiobarbituric acid bithiophene derivatives for vacuum deposited n-channel OFETs

Published:2014 Issue:20 Volume:2 Page:3895-3899
ISSN:2050-7526
Container-title:J. Mater. Chem. C
language:en
Short-container-title:J. Mater. Chem. C

Author:

Shu Ying¹²,Mikosch Annabel¹²,Winzenberg Kevin N.¹²,Kemppinen Peter¹²,Easton Christopher D.¹²,Bilic Ante³⁴,Forsyth Craig M.⁵⁶⁷,Dunn Christopher J.¹²,Singh Th. Birendra¹²,Collis Gavin E.¹²

Affiliation:

1. CSIRO Materials Science and Engineering

2. Clayton South MDC, Australia

3. CSIRO Computational Informatics

4. Clayton South, Australia

5. School of Chemistry

6. Monash University

7. Clayton, Australia

Abstract

Modification of the barbituric acid acceptor group results in structural and optoelectronic changes that provide electron mobilities nearing 0.3 cm² V⁻¹ s⁻¹.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/TC/C4TC00002A

Reference22 articles.

1. Semiconducting π-Conjugated Systems in Field-Effect Transistors: A Material Odyssey of Organic Electronics

2. n-Type Organic Semiconductors in Organic Electronics

3. Contents: (Adv. Mater. 8/2010)

4. Electron and Ambipolar Transport in Organic Field-Effect Transistors

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