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品質水準
アッセイ
98%
形状
solid
bp
139-140 °C (lit.)
mp
37-41 °C (lit.)
官能基
iodo
保管温度
2-8°C
SMILES記法
Ic1ccc(I)s1
InChI
1S/C4H2I2S/c5-3-1-2-4(6)7-3/h1-2H
InChI Key
PNYWRAHWEIOAGK-UHFFFAOYSA-N
関連するカテゴリー
詳細
The multilayer desorption behavior of 2,5-diidothiophene was studied.
アプリケーション
2,5-Diiodothiophene was used in the preparation of oligothiophene films. It was used in maskless fabrication of periodic patterns of a conjugated polymer. It was also used in fabrication of oligothiophene and polythiophene micropatterns.
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
204.8 °F - closed cup
引火点(℃)
96.00 °C - closed cup
個人用保護具 (PPE)
Eyeshields, Gloves, type N95 (US)
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
労働安全衛生法名称等を表示すべき危険物及び有害物
名称等を表示すべき危険物及び有害物
労働安全衛生法名称等を通知すべき危険物及び有害物
名称等を通知すべき危険物及び有害物
Jan Code
331570-BULK:
331570-5G:4548173988016
331570-VAR:
331570-1G:4548173988023
Photochemical production of oligothiophene and polythiophene micropatterns from 2, 5-diiodothiophene on Au in UHV.
Surface Science, 592(1), L305-L309 (2005)
The journal of physical chemistry. B, 110(41), 20197-20201 (2006-10-13)
The multilayer desorption behavior of 2,5-diidothiophene and the dendritic aggregation of photochemical reaction products during the desorption of 2,5-diiodothiophene multilayers have been studied. Like many other aromatic compounds, 2,5-diiodothiophene shows a multilayer desorption behavior different from the typical zeroth-order kinetics
The journal of physical chemistry. B, 110(15), 8047-8051 (2006-04-14)
This paper describes the details of surface reactions producing >100-nm-thick conjugated polymer films. When 2,5-diiodothiophene films deposited on copper are irradiated with UV at room temperature in Ar environments, oligothiophene films are synthesized. The average conjugation length of the produced
Langmuir : the ACS journal of surfaces and colloids, 21(15), 7052-7056 (2005-07-13)
Maskless fabrication of periodic patterns of a conjugated polymer is achieved by regioselective condensation of 2,5-diiodothiophene on chemically patterned substrate surfaces followed by in situ photochemical conversion of the condensed molecules into oligothiophenes and polythiophenes. This approach utilizes preferential aggregation
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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