1160106-15-9

Basic information

• Product Name: 2,6-Di3MeTin-4,4-dioctyl-4H-silolo[3,2-b:4,5-b']dithiophene
• Synonyms: 2,6-Di3MeTin-4,4-dioctyl-4H-silolo[3,2-b:4,5-b']dithiophene;2,6-Di3MeTin-4,4-dioctyl-4H-silolo[3,2-b
• CAS NO: 1160106-15-9
• Molecular Formula: C30H54S2SiSn2
• Molecular Weight: 744.39
• EINECS: -0
• Mol File: 1160106-15-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 623.5±65.0 °C(Predicted)
• Appearance: /
• CAS DataBase Reference: 2,6-Di3MeTin-4,4-dioctyl-4H-silolo[3,2-b:4,5-b']dithiophene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Di3MeTin-4,4-dioctyl-4H-silolo[3,2-b:4,5-b']dithiophene(1160106-15-9)
• EPA Substance Registry System: 2,6-Di3MeTin-4,4-dioctyl-4H-silolo[3,2-b:4,5-b']dithiophene(1160106-15-9)

Safety Data

• Hazardous Substances Data: 1160106-15-9(Hazardous Substances Data)

Usage

Description

2,6-Di3MeTin-4,4-dioctyl-4H-silolo[3,2-b:4,5-b']dithiophene is a silole-based chemical compound with high electron mobility and excellent semiconductor properties, making it a valuable material for various electronic applications in the field of organic electronics.

Uses

Used in Organic Electronics Industry:
2,6-Di3MeTin-4,4-dioctyl-4H-silolo[3,2-b:4,5-b']dithiophene is used as a key component in the development of organic field-effect transistors, organic solar cells, and organic light-emitting diodes due to its favorable electronic and optical properties.
Used in Organic Field-Effect Transistors:
2,6-Di3MeTin-4,4-dioctyl-4H-silolo[3,2-b:4,5-b']dithiophene is used as a semiconductor material in organic field-effect transistors for its high electron mobility, which contributes to improved device performance and efficiency.
Used in Organic Solar Cells:
2,6-Di3MeTin-4,4-dioctyl-4H-silolo[3,2-b:4,5-b']dithiophene is used as an active layer material in organic solar cells, leveraging its semiconductor properties to enhance light absorption and charge transport, leading to increased power conversion efficiency.
Used in Organic Light-Emitting Diodes:
2,6-Di3MeTin-4,4-dioctyl-4H-silolo[3,2-b:4,5-b']dithiophene is used as an emissive layer material in organic light-emitting diodes, taking advantage of its electronic and optical properties to achieve high brightness and color purity.
Overall, 2,6-Di3MeTin-4,4-dioctyl-4H-silolo[3,2-b:4,5-b']dithiophene is a promising candidate for the development of efficient and cost-effective organic electronic devices, with potential applications in various industries such as consumer electronics, renewable energy, and display technology.

Upstream product

• 1160106-12-6 4,4′-bis-(n-octyl)-dithieno[3,2-b:2′,3′-d]silol 
• 1066-45-1 trimethyltin(IV)chloride 
• 1160106-14-8 4,4’-bis(octyl)-5,5’-dibromo-dithieno[3,2-b:2',3'-d]silole 
• 1203451-18-6 4,4-dioctyl-2,6-bis(trimethylsilyl)-4H-dithieno[3,2-b:2',3'-d]silole 
• 207742-50-5 3,3'-dibromo-5,5'-bis(trimethylsilyl)-2,2'-bithiophene 
• 125143-53-5 3,3',5,5'-tetrabromo-2,2'-bithiophene 
• 492-97-7 2,2'-Bithiophene 

Relevant articles and documents

Novel dithieno silicon heterocyclic pentadiene organic solar cell acceptor material, and preparation method, and applications thereof

The invention provides a novel dithieno silicon heterocyclic pentadiene organic solar cell acceptor material, and a preparation method and applications thereof. The novel dithieno silicon heterocyclicpentadiene organic solar cell acceptor material is a linear-type non-fullerene organic solar cell acceptor material with an A-D-A structure, and the structure general formula is disclosed in the invention, wherein m is used for representing a natural number selected from 2 or 3; R1 and R2 are used for representing alkyl straight chains or straight chains with a carbon atom number ranging from 1 to 20; and B1 and B2 are used for representing electron withdrawing terminals. The novel dithieno silicon heterocyclic pentadiene organic solar cell acceptor material is capable of solving problems inthe prior art that conventional non-fullerene small molecular acceptor material is simple in molecular structure, and low in molecular weight; the preparation method is simple; the synthesis raw materials are cheap and easily available; and it is beneficial for early commercialization applications of organic solar cells.

PROCESS FOR PRODUCING FUSED-RING AROMATIC COMPOUND, AND CONJUGATED POLYMER

The invention addresses a problem of purifying a monomer to be a precursor according to a simpler and milder method so as to obtain a polymer having a higher molecular weight. The invention relates to a method for producing a condensed polycyclic aromatic compound having n active groups (wherein n is an integer of 1 or more and 4 or less), which comprises bringing a composition containing the condensed polycyclic aromatic compound and a solvent into contact with zeolite.