• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于空气稳定杂芳烃的薄膜有机晶体管:蒽[1,2-b:4,3-b':5,6-b'':8,7-b''']四噻吩衍生物

Thin film organic transistors from air-stable heteroarenes: anthra[1,2-b:4,3-b':5,6-b'':8,7-b''']tetrathiophene derivatives.

作者信息

Liu Wen-Jun, Zhou Yan, Ma Yuguo, Cao Yong, Wang Jian, Pei Jian

机构信息

The Key Laboratory of Bioorganic Chemistry and Molecular Engineering and Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.

出版信息

Org Lett. 2007 Oct 11;9(21):4187-90. doi: 10.1021/ol701690y. Epub 2007 Sep 13.

DOI:10.1021/ol701690y
PMID:17850155
Abstract

A facile synthesis of air-stable anthra[1,2-b:4,3-b':5,6-b'':8,7-b''']tetrathiophene derivatives 1a and 1b has been developed for applications in organic thin film transistors. Both molecules tend to self-associate through pi-pi stacking in solution and in different films. The hole mobility of 0.012 cm2 V(-1) s(-1) is obtained from 1a due to morphology changes in films from less ordered to highly ordered structures after thermal annealing. Good performance remained persistent over a period of 14 days, indicating the high stability of such transistors.

摘要

已开发出一种简便的方法来合成空气稳定的蒽[1,2-b:4,3-b':5,6-b'':8,7-b''']四噻吩衍生物1a和1b,用于有机薄膜晶体管。这两种分子在溶液和不同薄膜中都倾向于通过π-π堆积进行自缔合。由于热退火后薄膜形态从无序结构变为高度有序结构,1a的空穴迁移率为0.012 cm2 V(-1) s(-1)。在14天的时间里,器件性能一直保持良好,表明此类晶体管具有很高的稳定性。

相似文献

1
Thin film organic transistors from air-stable heteroarenes: anthra[1,2-b:4,3-b':5,6-b'':8,7-b''']tetrathiophene derivatives.基于空气稳定杂芳烃的薄膜有机晶体管:蒽[1,2-b:4,3-b':5,6-b'':8,7-b''']四噻吩衍生物
Org Lett. 2007 Oct 11;9(21):4187-90. doi: 10.1021/ol701690y. Epub 2007 Sep 13.
2
A highly pi-stacked organic semiconductor for field-effect transistors based on linearly condensed pentathienoacene.一种基于线性稠合五噻吩并苯的用于场效应晶体管的高度π堆积有机半导体。
J Am Chem Soc. 2005 Sep 28;127(38):13281-6. doi: 10.1021/ja052816b.
3
Benzo[1,2-b:4,5-b']bis[b]benzothiophene as solution processible organic semiconductor for field-effect transistors.用于场效应晶体管的溶液可加工有机半导体苯并[1,2 - b:4,5 - b']双[b]苯并噻吩
Chem Commun (Camb). 2008 Apr 7(13):1548-50. doi: 10.1039/b717608b. Epub 2008 Jan 25.
4
High-performance air-stable n-channel organic thin film transistors based on halogenated perylene bisimide semiconductors.基于卤化苝二酰亚胺半导体的高性能空气稳定型n沟道有机薄膜晶体管。
J Am Chem Soc. 2009 May 6;131(17):6215-28. doi: 10.1021/ja901077a.
5
High-mobility semiconducting naphthodithiophene copolymers.高分子迁移率半导体萘并二噻吩共聚物。
J Am Chem Soc. 2010 Apr 14;132(14):5000-1. doi: 10.1021/ja101125p.
6
Linear- and angular-shaped naphthodithiophenes: selective synthesis, properties, and application to organic field-effect transistors.线性和角型萘并二噻吩:选择性合成、性质及其在有机场效应晶体管中的应用。
J Am Chem Soc. 2011 Apr 6;133(13):5024-35. doi: 10.1021/ja110973m. Epub 2011 Mar 9.
7
n-Channel semiconductor materials design for organic complementary circuits.用于有机互补电路的 n 通道半导体材料设计。
Acc Chem Res. 2011 Jul 19;44(7):501-10. doi: 10.1021/ar200006r. Epub 2011 May 26.
8
Indacenodithiophene semiconducting polymers for high-performance, air-stable transistors.用于高性能、空气稳定晶体管的茚并二噻吩半导体聚合物。
J Am Chem Soc. 2010 Aug 25;132(33):11437-9. doi: 10.1021/ja1049324.
9
Sigma-pi molecular dielectric multilayers for low-voltage organic thin-film transistors.用于低压有机薄膜晶体管的西格玛-派分子介电多层膜
Proc Natl Acad Sci U S A. 2005 Mar 29;102(13):4678-82. doi: 10.1073/pnas.0501027102. Epub 2005 Mar 21.
10
Design, synthesis, and characterization of ladder-type molecules and polymers. Air-stable, solution-processable n-channel and ambipolar semiconductors for thin-film transistors via experiment and theory.梯形分子和聚合物的设计、合成与表征。通过实验和理论研究,开发出空气稳定、溶液可加工的 n 型和双极性半导体薄膜晶体管。
J Am Chem Soc. 2009 Apr 22;131(15):5586-608. doi: 10.1021/ja809555c.