所有图片(2)
About This Item
经验公式（希尔记法）:
C18H12S3
CAS号:
分子量:
324.48
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.23
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方案
97%
表单
solid
mp
154-160 °C
SMILES字符串
c1csc(c1)-c2cc(cc(c2)-c3cccs3)-c4cccs4
InChI
1S/C18H12S3/c1-4-16(19-7-1)13-10-14(17-5-2-8-20-17)12-15(11-13)18-6-3-9-21-18/h1-12H
InChI key
UBHPRZXDFVCNHZ-UHFFFAOYSA-N
一般描述
1,3,5-Tris(2-thienyl)benzene is a 1,3,5 tris substituted benzene that has a three dimensional structure which facilitates the preparation of conjugating polymers. It is a branched conductive monomer with electronically attached nodes that provide a suitable support to increase the conductivity of the synthesized polymers.
应用
1,3,5-Tris(2-thienyl)benzene is a trifunctionalized monomer that can be used in the synthesis of conjugated C3-symmetric poly(arylbenzene) polymers. These polymeric materials can further be used in organic photovoltaic devices as well as organic field effect transistors (OFETs) and organic light emitting diodes (OLED) systems.
警示用语：
Danger
危险声明
预防措施声明
危险分类
Acute Tox. 3 Oral
储存分类代码
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Idzik, K. R.; Beckert, R.; Golba, S.; Ledwon, P.; Lapkowski, M.
Tetrahedron Letters, 51, 2396-2396 (2010)
Synthesis and Electrochemical Properties of Novel 1, 3, 5-Tris (oligothienyl) benzenes: A New Generation of 3D Reticulating Agents
Cherioux F and Guyard L
Advances in Functional Materials, 11(4), 305-309 (2001)
Electrochemical and spectral properties of meta-linked 1, 3, 5-tris (aryl) benzenes and 2, 4, 6-tris (aryl)-1-phenoles, and their polymers
Idzik KR, et al.
Electrochimica Acta, 55(24), 7419-7426 (2010)
Shape and size effects in the crystal structures of complexes of 1, 3, 5-trinitrobenzene with some trigonal donors: the benzene-thiophene exchange rule
Thallapally PK, et al.
Tetrahedron, 56(36), 6721-6728 (2000)
Synthesis of C3-Symmetric Nano-Sized Polyaromatic Compounds by Trimerization and Suzuki- Miyaura Cross-Coupling Reactions
Kotha S, et al.
European Journal of Organic Chemistry, 2004(19), 4003-4013 (2004)
商品
Organic materials in optoelectronic devices like LEDs and solar cells are of significant academic and commercial interest.
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