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10 G
₩236,698
About This Item
실험식(Hill 표기법):
C8H6S2
CAS Number:
Molecular Weight:
166.26
Beilstein:
3039
EC Number:
MDL number:
UNSPSC 코드:
12352103
PubChem Substance ID:
NACRES:
NA.23
추천 제품
![Thieno[3,2-b]thiophene 95%](/deepweb/assets/sigmaaldrich/product/structures/353/609/429fd4bf-e217-4371-80a3-9e5a4d88908b/640/429fd4bf-e217-4371-80a3-9e5a4d88908b.png)
![2,5-Bis(trimethylstannyl)-thieno[3,2-b]thiophene 97%](/deepweb/assets/sigmaaldrich/product/structures/126/532/26557e94-858e-4c96-90de-ca88d84a8727/640/26557e94-858e-4c96-90de-ca88d84a8727.png)
![Benzo[1,2-b:4,5-b′]dithiophene-4,8-dione 97%](/deepweb/assets/sigmaaldrich/product/structures/418/544/b7faac0b-ad09-4b42-a9fa-aeb38017a39e/640/b7faac0b-ad09-4b42-a9fa-aeb38017a39e.png)
분석
99%
bp
260 °C (lit.)
mp
32-33 °C (lit.)
SMILES string
c1csc(c1)-c2cccs2
InChI
1S/C8H6S2/c1-3-7(9-5-1)8-4-2-6-10-8/h1-6H
InChI key
OHZAHWOAMVVGEL-UHFFFAOYSA-N
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일반 설명
2,2′-Bithiophene is an electron transporting material with the π-electrons present in the system that facilitate charge mobility.[1]
애플리케이션
2,2′-Bithiophene can be polymerized to form poly(2,2′-Bithiophene) which can be electrodeposited on indium tin oxide (ITO) substrates for the fabrication of electrochromic devices.[2][3] It can also be used in the formation of electrode material for the development of supercapacitors.[4]
Substrate used in a rhodium-catalyzed C-H arylation of heteroarenes with aryl iodides.[5]
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
230.0 °F - closed cup
Flash Point (°C)
110 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
5, 5 `-Bis (dimesitylboryl)-2, 2 `-bithiophene and 5, 5 ``-bis (dimesitylboryl)-2, 2 `: 5 `, 2 ``-terthiophene as a novel family of electron-transporting amorphous molecular materials.
Noda T and Shirota Y
Journal of the American Chemical Society, 120(37), 9714-9715 (1998)
Weiying He et al.
Nature communications, 9(1), 3866-3866 (2018-09-27)
Nickel-catalyzed catalyst transfer polycondensation (CTP) of thiophenes is an efficient strategy for the controlled synthesis of polythiophenes. However, a detailed view of its reaction mechanism has remained elusive with unresolved questions regarding the geometry and bonding of critical Ni(0) thiophene intermediates.
Electrode material dependent p-or n-like thermoelectric behavior of single electrochemically synthesized poly (2, 2?-bithiophene) layer?application to thin film thermoelectric generator.
Kublitski J, et al.
Journal of Solid State Electrochemistry, 20(8), 2191-2196 (2016)
Ji He et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 16(7), 1049-1056 (2017-05-13)
Three D-D-π-A triphenylamine-coumarin sensitizers were designed and synthesized with a triphenylamine and coumarin double donor and a cyanoacrylic acid acceptor. Thiophene, bithiophene and phenylthiophene were used as π-bridges, respectively, and the effects of different π-bridges on the photophysical properties and
Applications of Poly (indole-6-carboxylic acid-co-2, 2?-bithiophene) Films in High-Contrast Electrochromic Devices.
Kuo C, et al.
Coatings, 8(3), 102-102 (2018)
문서
From Form to Function: Molding Porous Materials in Three Dimensions by Colloidal Crystal Templating
Professor Rivnay (Northwestern University, USA) discusses using organic mixed conductors as an alternative to efficiently bridge the ionic world of biology with contemporary microelectronics.
활성 필터
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.
