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Merck
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Principaux documents

754080

Sigma-Aldrich

ADT

sublimed, 97%

Synonyme(s) :

Anthra[2,3-b:6,7-b′]dithiophene

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About This Item

Formule empirique (notation de Hill):
C18H10S2
Numéro CAS:
Poids moléculaire :
290.40
Numéro MDL:
Code UNSPSC :
12352103
ID de substance PubChem :

Essai

97%

Forme

sublimed

Perte

0.5 wt. %, 280 °C

Propriétés du semi-conducteur

P-type (mobility=0.3 cm2/V·s)

Chaîne SMILES 

c1cc2cc3cc4cc5sccc5cc4cc3cc2s1

InChI

1S/C18H10S2/c1-3-19-17-9-15-8-14-6-12-2-4-20-18(12)10-16(14)7-13(15)5-11(1)17/h1-10H

Clé InChI

DAMUWSYTQPWFIY-UHFFFAOYSA-N

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Description générale

ADT is an anthradithiophene based small molecule semiconductor that contributes to a new class of heteroacenes, which has a 22-electron π-conjugated system. It can be majorly used in a variety of organic electronic applications.

Application

ADT can be used as a conducting polymer in the fabrication of organic field effect transistors (OFETs) and organic photovoltaics (OPVs).

Pictogrammes

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Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Acute Tox. 4 Oral

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Consulter la Bibliothèque de documents

Physical Properties of Anthra [2, 3-b; 6, 7-b'] Dithiophene Organic Material
Hamad H
Journal of Physical Chemistry and Functional Materials, 2(1), 37-39 (2019)
Non-classical heteroacenes: synthesis and properties of anthra [2, 3-c: 6, 7-c?] dithiophene derivatives
Djukic B and Perepichka DF
Chemical Communications (Cambridge, England), 47(47), 12619-12621 (2011)
Synthesis of 2, 2?-[2, 2?-(arenediyl) bis (anthra [2, 3-b] thiophene-5, 10-diylidene)] tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
Baranov DS, et al.
Synthetic Metals, 255(18), 116097-116097 (2019)
Bogdana Borca et al.
ACS nano, 9(12), 12506-12512 (2015-11-19)
Single molecular switches are basic device elements in organic electronics. The pentacene analogue anthradithiophene (ADT) shows a fully reversible binary switching between different adsorption conformations on a metallic surface accompanied by a charge transfer. These transitions are activated locally in
Florence K Keane et al.
Cancer, 121(16), 2713-2719 (2015-05-01)
Radiotherapy (RT), short-course androgen deprivation therapy (ADT), and brachytherapy in various combinations are treatment options for patients with intermediate-risk prostate cancer (PC), but the question of which combination if any is necessary to minimize PC-specific mortality (PCSM) risk in patients

Articles

Optoelectronic devices such as light-emitting diodes (LEDs), solar cells, and light-emitting field effect transistors (FETs) that utilize organic materials as their light harvesting and/or charge transporting component have been the subject of much academic and commercial attention.

Intrinsically stretchable active layers for organic field-effect transistors (OFET) are discussed. Polymer structural modification & post-polymerization modifications are 2 methods to achieve this.

Solution-processed organic photovoltaic devices (OPVs) have emerged as a promising clean energy generating technology due to their ease of fabrication, potential to enable low-cost manufacturing via printing or coating techniques, and ability to be incorporated onto light weight, flexible substrates.

There is widespread demand for thin, lightweight, and flexible electronic devices such as displays, sensors, actuators, and radio-frequency identification tags (RFIDs). Flexibility is necessary for scalability, portability, and mechanical robustness.

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