Saltar al contenido
Merck

741027

Sigma-Aldrich

2,5-Bis(trimethylstannyl)-thieno[3,2-b]thiophene

97%

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización


About This Item

Fórmula empírica (notación de Hill):
C12H20S2Sn2
Peso molecular:
465.84
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

Quality Level

assay

97%

form

powder or crystals

mp

127-132 °C

SMILES string

C[Sn](C)(C)c1cc2sc(cc2s1)[Sn](C)(C)C

InChI

1S/C6H2S2.6CH3.2Sn/c1-3-7-6-2-4-8-5(1)6;;;;;;;;/h1-2H;6*1H3;;

InChI key

HDZULVYGCRXVNQ-UHFFFAOYSA-N

General description

2,5-Bis(trimethylstannyl)-thieno[3,2-b]thiophene is a conducting polymer that can be used in the formation of the hole transporting material (HTM) with improved charge mobility. It is a majorly utilized as a copolymer in the polymerization of new thieno(3,2-b)thiophene based polymers.

Application

2,5-Bis(trimethylstannyl)-thieno[3,2-b]thiophene can be used as a copolymer in the synthesis of thiophene based materials for the fabrication of organic electronic devices such as organic field effect transistors (OFETs), organic thin film transistors(OTFTs) and organic photovoltaic cells (OPVs).
2,5-Bis(trimethylstannyl)-thieno[3,2-b]thiophene is a synthetic intermediate, which can be used in the synthesis of polythiophenes based fluorinated polymers for the optoelectronic applications. It can also be used in the synthesis of PDBT-co-TT via Still coupling polymerization for the fabrication of organic thin film transistors (OTFTs)and photovoltaic devices.

pictograms

Skull and crossbonesEnvironment

signalword

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Thienoisoindigo-based copolymer with fused thieno (3, 2-b) thiophene as a donor in thin film transistor applications with high performance
Chen C, et al.
Journal of Material Chemistry C, 3(1), 33-36 (2015)
Dialkyl-Substituted Thieno [3, 2-b] thiophene-Based Polymers Containing 2, 2 `-Bithiophene, Thieno [3, 2-b] thiophene, and Ethynylene Spacers
San Miguel L and Matzger AJ
Macromolecules, 40(26), 9233-9237 (2007)
A High Mobility P-Type DPP-Thieno [3, 2-b] thiophene Copolymer for Organic Thin-Film Transistors
Li Y, et al.
Advanced Materials, 22(43), 4862-4866 (2010)
Using Molecular Design to Increase Hole Transport: Backbone Fluorination in the Benchmark Material Poly (2, 5-bis (3-alkylthiophen-2-yl) thieno [3, 2-b]-thiophene (pBTTT)
Boufflet P, et al.
Advances in Functional Materials, 25(45), 7038-7048 (2015)
Hugo Bronstein et al.
Journal of the American Chemical Society, 133(10), 3272-3275 (2011-02-22)
We report the synthesis and polymerization of a novel thieno[3,2-b]thiophene-diketopyrrolopyrrole-based monomer. Copolymerization with thiophene afforded a polymer with a maximum hole mobility of 1.95 cm(2) V(-1) s(-1), which is the highest mobility from a polymer-based OFET reported to date. Bulk-heterojunction

Artículos

Organic electronics promise renewable energy solutions surpassing silicon-based tech.

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico