Larger π-extended anti-/syn-aroylenediimidazole polyaromatic compounds: synthesis, physical properties, self-assembly, and quasi-linear conjugation effect-Reference-Cited by-同舟云学术

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Larger π-extended anti-/syn-aroylenediimidazole polyaromatic compounds: synthesis, physical properties, self-assembly, and quasi-linear conjugation effect

Published:2014 Issue:34 Volume:4 Page:17822-17831
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Zhao Jianfeng¹²³⁴⁵,Wong Jen It⁶⁷⁸,Gao Junkuo¹²³,Li Gang¹²³,Xing Guichuan⁹²¹⁰,Zhang Huacheng⁹²¹⁰,Sum Tze Chien⁹²¹⁰,Yang Hui Ying⁶⁷⁸,Zhao Yanli⁹²¹⁰,Ake Kjelleberg Staffan Lars¹¹²¹²,Huang Wei⁴⁵¹³,Joachim Loo Say Chye¹²³¹¹²,Zhang Qichun¹²³¹¹²

Affiliation:

1. School of Materials Science and Engineering

2. Nanyang Technological University

3. Singapore 639798, Singapore

4. Institute of Advanced Materials

5. Nanjing University of Technology

6. Pillar of Engineering Product Development

7. Singapore University of Technology and Design

8. Singapore 138682, Singapore

9. School of Physical and Mathematical Sciences

10. Singapore, Singapore

11. Singapore Centre on Environmental Life Sciences Engineering (SCELSE)

12. Singapore

13. Nanjing, China

Abstract

Four polyaromatic compounds with 11- or 13-fused rings have been synthesized and their physical properties have been studied.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA01049C

Reference136 articles.

1. Integrated Materials Design of Organic Semiconductors for Field-Effect Transistors

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

3. Macroscopic-Scale Assembled Nanowire Thin Films and Their Functionalities

4. Heptacene and Beyond: The Longest Characterized Acenes

5. Effects of electronegative substitution on the optical and electronic properties of acenes and diazaacenes

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