Accéder au contenu
Merck
Toutes les photos(1)

Principaux documents

Voir toute la documentation

754080

Sigma-Aldrich

ADT

sublimed, 97%

Synonyme(s) :

Anthra[2,3-b:6,7-b′]dithiophene

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme
Toutes les photos(1)

About This Item

Formule empirique (notation de Hill) :
C18H10S2
Numéro CAS:
144413-58-1
Poids moléculaire :
290.40
Numéro MDL:
MFCD20257134
Code UNSPSC :
12352103
ID de substance PubChem :
329766397

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

Vous recherchez des produits similaires ? Visite Guide de comparaison des produits

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.[1][2]

Application

ADT can be used as a conducting polymer in the fabrication of organic field effect transistors (OFETs) and organic photovoltaics (OPVs).[3][4]

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302

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

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
MKBJ8009

Vous ne trouvez pas la bonne version ?

Si vous avez besoin d'une version particulière, vous pouvez rechercher un certificat spécifique par le numéro de lot.

Rechercher un(e) COA

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Isomerically pure anthra [2, 3-b: 6, 7-b?]-difuran (anti-ADF),-dithiophene (anti-ADT), and-diselenophene (anti-ADS): selective synthesis, electronic structures, and application to organic field-effect transistors
Nakano M, et al.
The Journal of Organic Chemistry, 77(18), 8099-8111 (2012)
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
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)
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)
Rashmi Gaur et al.
Scientific reports, 5, 13387-13387 (2015-08-26)
This study presents genome-wide discovery of SNPs through next generation sequencing of the genome of Cicer reticulatum. Mapping of the C. reticulatum sequenced reads onto the draft genome assembly of C. arietinum (desi chickpea) resulted in identification of 842,104 genomic
Afficher tous les articles scientifiques apparentés

Articles

Optoelectronic Devices with DPP-containing Molecules

Organic materials in optoelectronic devices like LEDs and solar cells are of significant academic and commercial interest.

Polymer Semiconductors for Intrinsically Stretchable Organic Transistors

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

Development of Small Molecule Donors for Solution-Processed Organic Solar Cells

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.

Organic Transistors for Biomedical Applications

Thin, lightweight, and flexible electronic devices meet widespread demand for scalable, portable, and robust technology.

Questions

Évaluations

Aucune valeur de notation

Filtres actifs

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique