710172
Dithieno[3,2-b:2′,3′-d]thiophene
97% (HPLC)
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About This Item
Formula empirica (notazione di Hill):
C8H4S3
Numero CAS:
Peso molecolare:
196.31
Numero MDL:
Codice UNSPSC:
12352103
ID PubChem:
NACRES:
NA.23
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Saggio
97% (HPLC)
Stato
powder
Punto di fusione
65-70 °C
Stringa SMILE
c1cc2sc3ccsc3c2s1
InChI
1S/C8H4S3/c1-3-9-7-5(1)11-6-2-4-10-8(6)7/h1-4H
VGWBXRXNERKBSJ-UHFFFAOYSA-N
Descrizione generale
Dithieno[3,2-b:2′,3′-d]thiophene (DTT) is a conductive material that acts as a donor building block for synthesizing a variety of optoelectronic materials. It can be used as an active layer with high charge mobility and environmental stability for development of organic electronic devices.
Applicazioni
DTT can be used for a wide range of applications which include electro-luminescence, organic thin film transistors, photochromism, and organic photovoltaic (OPV) solar cells.
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Acute Tox. 4 Oral - Eye Irrit. 2
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 2
Punto d’infiammabilità (°F)
247.1 °F - closed cup
Punto d’infiammabilità (°C)
119.5 °C - closed cup
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Improved synthesis of dithieno [3, 2-b: 2?, 3?-d] thiophene (DTT) and derivatives for cross coupling.
Frey J, et al.
Chemical Communications (Cambridge, England), 10(20), 2424-2425 (2002)
A facile synthesis of low-band-gap donor-acceptor copolymers based on dithieno [3, 2-b: 2?, 3?-d] thiophene.
Ku S, et al.
Macromolecules, 44(24), 9533-9538 (2011)
A new reaction of P4S10 and Lawesson's reagent; a new method for the synthesis of dithieno [3, 2-b; 2?, 3?-d] thiophenes.
Ertas E and Ozturk T
Tetrahedron Letters, 45(17), 3405-3407 (2004)
Novel copolymers incorporating dithieno [3, 2-b: 2?, 3?-d] thiophene moieties for air-stable and high performance organic field-effect transistors.
Lu K, et al.
Journal of Materials Chemistry, 18(29), 3426-3432 (2008)
Highly luminescent p-conjugated dithienometalloles: photophysical properties and their application in organic light-emitting diodes
Kondo, R.;Yasuda, T.; Adachi, C.; et al.
Journal of Materials Chemistry, 22, 16810-16816 (2012)
Articoli
Optoelectronic Devices Based on Diketopyrrolopyrrole (DPP)-containing Conjugated Small Molecules
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