18042-57-4

Basic information

• Product Name: Silane, triethenylphenyl-
• CAS NO: 18042-57-4
• Molecular Formula: C12H14Si
• Molecular Weight: 186.329
• Mol File: 18042-57-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Silane, triethenylphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, triethenylphenyl-(18042-57-4)
• EPA Substance Registry System: Silane, triethenylphenyl-(18042-57-4)

Safety Data

• Hazardous Substances Data: 18042-57-4(Hazardous Substances Data)

Usage

General Description

Silane, triethenylphenyl- is a chemical compound with the molecular formula C14H18Si. It is a silane derivative with three ethenyl groups and a phenyl group bonded to a silicon atom. Silane, triethenylphenyl- is commonly used as a coupling agent in the production of polymers and composite materials. It promotes adhesion between organic and inorganic materials and enhances the physical and mechanical properties of the resulting products. Silane, triethenylphenyl- is also used as a crosslinking agent in the formulation of adhesives, coatings, and sealants, where it helps improve the durability and performance of these materials. Additionally, it is utilized in the manufacturing of electronic components, plastics, and rubber products. Despite its beneficial applications, it is important to handle silane, triethenylphenyl- with caution due to its flammability and potential health hazards.

Upstream product

• 1826-67-1 vinyl magnesium bromide 
• 98-13-5 Phenyltrichlorosilane 
• 3536-96-7 vinylmagnesium chloride 

Downstream Products

• 1445998-17-3 C₆₆H₅₃N₃Si 
• 578740-38-2 1-trihydridoborato-4-(2-iodoethyl)-1,4-diphenyl-1-phosphonia-4-silacyclohexane 
• 578740-40-6 tris(2-iodoethyl)(phenyl)silane 
• 578740-42-8 4-phenyl-1-thioxo-1-phospha-4-silabicyclo[2.2.2]octane 
• 578740-37-1 4-phenyl-1-phospha-4-silabicyclo[2.2.2]octane 
• 578740-39-3 tris(2-hydroxyethyl)(phenyl)silane 

Relevant articles and documents

Bi- and tridentate silicon-based acceptor molecules

Triethynylphenylsilane (1), trivinylphenylsilane (2), diethynyldiphenylsilane (3) and diphenyldivinylsilane (4) were reacted with chlorodimethylsilane yielding the corresponding hydrosilylation products. To increase their Lewis acidity, the Si-Cl functions were directly transferred into Si-C6F5 units by salt elimination reactions leading to the (semi-) flexible molecules 5-8 bearing two or three Lewis-acidic sidearms. With the aim of providing host-guest complexes, the air-stable and readily soluble compounds 5-8 were converted with N- and O-Lewis bases of different size and geometry. In all cases, NMR spectroscopic investigations reveal no formation of Lewis acid-base complexes. X-ray diffraction experiments of host compounds 5-7 show intermolecular aryl perfluoroaryl interactions of dispersion nature in the solid state. By hydrosilylation of 1 with trichlorosilane the more Lewisacidic all-trans-tris[(trichlorosilyl)vinyl]phenylsilane (9) was obtained. Its Lewis acidity was further increased by fluorination to yield all-trans-tris[(trifluorosilyl)vinyl] phenylsilane (10); the conversion with nitrogen containing Lewis bases ends up in the formation of insoluble precipitates.

NOVEL COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

Compounds represented by Formula 1 and organic light-emitting devices including an organic layer including the compounds are disclosed.