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Updated: May 7, 2026

Effect of Bending on the Electrical Characteristics of Flexible Organic Single Crystal-based Field-effect Transistors
08:43

Effect of Bending on the Electrical Characteristics of Flexible Organic Single Crystal-based Field-effect Transistors

Published on: November 7, 2016

オーガニック・エレクトロニクス用,電子欠乏のテトラアザベンゾジジフローランテネ二ミドを基にした高流動性n型結合ポリマー

Haiyan Li1, Felix Sunjoo Kim, Guoqiang Ren

  • 1Department of Chemical Engineering and Department of Chemistry, University of Washington , Seattle, Washington 98195-1750, United States.

Journal of the American Chemical Society
|September 27, 2013
PubMed
まとめ

研究者らは,2D π 結合による新しい結合ポリマーである,ポリ・テトラアザベンゾジフッ素アンテナ二酸化物 (PBFI-T と PBFI-BT) を開発した. これらのポリマーは,高流動性のnチャネル輸送を実現し,有機電子工学を進歩させています.

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関連する概念動画

Stability of Conjugated Dienes01:28

Stability of Conjugated Dienes

Introduction
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
Structure of Conjugated Dienes01:16

Structure of Conjugated Dienes

Introduction
Conjugated dienes are compounds characterized by the presence of alternating double and single bonds. In a conjugated system like 1,3-butadiene, the unhybridized 2p orbital on each carbon overlaps continuously, allowing the π electrons to be delocalized across the entire molecule. In contrast, this type of overlap does not occur in cumulated and isolated dienes, such as 2,3-pentadiene and 1,4-pentadiene, respectively. Instead, the π electrons remain localized between the double...
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction01:16

[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction

The Diels–Alder reaction is an example of a thermal pericyclic reaction between a conjugated diene and an alkene or alkyne, commonly referred to as a dienophile. The reaction involves a concerted movement of six π electrons, four from the diene and two from the dienophile, forming an unsaturated six-membered ring. As a result, these reactions are classified as [4+2] cycloadditions.