2,2':5',2''-TERTHIOPHENE

Catalog Number

ACM1081341-3

CAS

1081-34-1

Structure

Synonyms

2,5-Di(thien-2-yl)thiophene

IUPAC Name

2,5-Dithiophen-2-ylthiophene

Molecular Weight

248.4

Molecular Formula

C12H8S3

Description

2,2':5',2''-Terthiophene (TTh) may be prepared by nickel catalysed coupling reaction of grignard's reagent derived from 2-bromothiophene and magnesium. It generates singlet oxygen. In nature, it is found in the floral extract of Tagetes minuta and Echinops grijisii. It is known to be toxic to mosquitoes. It also exihibits antifungal activity.; 2,2':5',2''-Terthiophene (3T) is a tri-thiophene based low band conductive polymer that is prepared by reacting 2,5-dibromothiophene and thienylmagnesium bromide in the presence of nickel catalyst.

Canonical SMILES

C1=CSC(=C1)C2=CC=C(S2)C3=CC=CS3

InChI

InChI=1S/C12H8S3/c1-3-9(13-7-1)11-5-6-12(15-11)10-4-2-8-14-10/h1-8H

InChI Key

KXSFECAJUBPPFE-UHFFFAOYSA-N

Boiling Point

361.3±32.0 °C/760mmHg (lit.)

Melting Point

93-95 °C

Flash Point

128.4±11.3 °C

Purity

95%+

Density

1.3±0.1 g/cm³

Solubility

Insoluble in water

Appearance

Light yellow solid

Application

3T can be combined with 3,4-ethylenedioxythiophene (EDOT) in a tetrabutylammonium perchlorate solution for use as an electrochromic copolymer for a wide range of s like photovoltaics and polymer light emitting diodes (LEDs). It can also be used to form metal-organic based thin films with metals like aluminum, silver, and calcium which can potentially be used for optoelectronics based s.; Electrochemical copolymerization of carbazole and TTh in sodium perchlorate/acetonitrile was reported. Electrochromic copolymer based on TTh and 3, 4-ethylenedioxythiophene has been reported. TTh acts as a monomer precursor for polythiophene and as a dopant for polycarbonate. It may function as a photosensitizer.

Storage

Keep in dark place,sealed in dry,Room Temperature

Packaging

Packaging; 1 g in glass bottle

• Catalog Number: ACM1081341-3
• CAS: 1081-34-1
• Synonyms: 2,5-Di(thien-2-yl)thiophene
• IUPAC Name: 2,5-Dithiophen-2-ylthiophene
• Molecular Weight: 248.4
• Molecular Formula: C12H8S3
• Description: 2,2':5',2''-Terthiophene (TTh) may be prepared by nickel catalysed coupling reaction of grignard's reagent derived from 2-bromothiophene and magnesium. It generates singlet oxygen. In nature, it is found in the floral extract of Tagetes minuta and Echinops grijisii. It is known to be toxic to mosquitoes. It also exihibits antifungal activity.; 2,2':5',2''-Terthiophene (3T) is a tri-thiophene based low band conductive polymer that is prepared by reacting 2,5-dibromothiophene and thienylmagnesium bromide in the presence of nickel catalyst.
• Canonical SMILES: C1=CSC(=C1)C2=CC=C(S2)C3=CC=CS3
• InChI: InChI=1S/C12H8S3/c1-3-9(13-7-1)11-5-6-12(15-11)10-4-2-8-14-10/h1-8H
• InChI Key: KXSFECAJUBPPFE-UHFFFAOYSA-N
• Boiling Point: 361.3±32.0 °C/760mmHg (lit.)
• Melting Point: 93-95 °C
• Flash Point: 128.4±11.3 °C
• Purity: 95%+
• Density: 1.3±0.1 g/cm³
• Solubility: Insoluble in water
• Appearance: Light yellow solid
• Application: 3T can be combined with 3,4-ethylenedioxythiophene (EDOT) in a tetrabutylammonium perchlorate solution for use as an electrochromic copolymer for a wide range of s like photovoltaics and polymer light emitting diodes (LEDs). It can also be used to form metal-organic based thin films with metals like aluminum, silver, and calcium which can potentially be used for optoelectronics based s.; Electrochemical copolymerization of carbazole and TTh in sodium perchlorate/acetonitrile was reported. Electrochromic copolymer based on TTh and 3, 4-ethylenedioxythiophene has been reported. TTh acts as a monomer precursor for polythiophene and as a dopant for polycarbonate. It may function as a photosensitizer.
• Storage: Keep in dark place,sealed in dry,Room Temperature
• Packaging: Packaging; 1 g in glass bottle