Structure engineering: extending the length of azaacene derivatives through quinone bridges-Reference-Cited by-同舟云学术

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Structure engineering: extending the length of azaacene derivatives through quinone bridges

Published:2018 Issue:14 Volume:6 Page:3628-3633
ISSN:2050-7526
Container-title:Journal of Materials Chemistry C
language:en
Short-container-title:J. Mater. Chem. C

Author:

Wang Zilong¹²³⁴,Wang Zongrui¹²³⁴,Zhou Yecheng⁵⁶⁷⁸,Gu Peiyang¹²³⁴,Liu Guangfeng¹²³⁴,Zhao Kexiang¹²³⁴,Nie Lina¹²³⁴,Zeng Qingsheng¹²³⁴,Zhang Jing¹²³⁴,Li Yongxin⁹¹⁰¹¹³⁴,Ganguly Rakesh⁹¹⁰¹¹³⁴^ORCID,Aratani Naoki¹²¹³¹⁴¹⁵^ORCID,Huang Li⁵⁶⁷⁸,Liu Zheng¹²³⁴^ORCID,Yamada Hiroko¹²¹³¹⁴¹⁵^ORCID,Hu Wenping¹⁶¹⁷¹⁸¹⁹²⁰,Zhang Qichun¹²³⁴⁹^ORCID

Affiliation:

1. School of Materials Science and Engineering

2. Nanyang Technological University Singapore

3. Singapore 639798

4. Singapore

5. Department of Physics

6. South University of Science and Technology of China

7. Shenzhen 518055

8. China

9. Division of Chemistry and Biological Chemistry

10. School of Physical and Mathematical Sciences

11. Nanyang Technological University

12. Graduate School of Materials Science

13. Nara Institute of Science and Technology

14. Ikoma 630-0192

15. Japan

16. Tianjin Key Laboratory of Molecular Optoelectronic Sciences

17. Department of Chemistry

18. School of Science & Collaborative Innovation Center of Chemical Science and Engineering (Tianjin)

19. Tianjin University

20. Tianjin 300072

Abstract

A novel quinone bridged large azaacene exhibits an electron mobility of 0.22 cm² V⁻¹ s⁻¹ through molecular stacking structure engineering.

Funder

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/TC/C8TC00628H

Reference46 articles.

1. Dibenzobarrelene-Based Azaacenes: Emitters in Organic Light-Emitting Diodes

2. The Radical Anion and Dianion of Tetraazapentacene

3. Synthesis, Physical Properties, and Light-Emitting Diode Performance of Phenazine-Based Derivatives with Three, Five, and Nine Fused Six-Membered Rings

4. Linearly Fused Azaacenes: Novel Approaches and New Applications Beyond Field-Effect Transistors (FETs)

5. Synthesis, Characterization, and Nonvolatile Ternary Memory Behavior of a Larger Heteroacene with Nine Linearly Fused Rings and Two Different Heteroatoms

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1. Using azaacene as an acceptor unit to construct an ultraefficient red fluorophore with an EQE over 40%;Materials Horizons;2023

2. Boron-based non-fullerene small molecule acceptors via nitrogen substitution: a theoretical study;Materials Advances;2022

3. Tuning the π–π overlap and charge transport in single crystals of an organic semiconductor via solvation and polymorphism;Physical Chemistry Chemical Physics;2020

4. 5,7,12,14‐Tetrafunctionalized 6,13‐Diazapentacenes;Chemistry – A European Journal;2019-12-16

5. Mono‐ and Dianion of a Bis(benzobuta)tetraazapentacene Derivative;Chemistry – A European Journal;2019-07-03

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