456373
2,5-Dibromo-3-hexylthiophene
97%
Synonyme(s) :
2,5-Dibromo-3-hex-1-ylthiophene
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About This Item
Produits recommandés
Niveau de qualité
Pureté
97%
Indice de réfraction
n20/D 1.557 (lit.)
Densité
1.521 g/mL at 25 °C (lit.)
Température de stockage
2-8°C
Chaîne SMILES
CCCCCCc1cc(Br)sc1Br
InChI
1S/C10H14Br2S/c1-2-3-4-5-6-8-7-9(11)13-10(8)12/h7H,2-6H2,1H3
Clé InChI
NSYFIAVPXHGRSH-UHFFFAOYSA-N
Description générale
2,5-Dibromo-3-hexylthiophene is a 2,5 coupled conductive polymer with conjugated polythiophene based system, which has a controllable band gap.
Application
Conducting polymer precursor.
It can be used as a monomer with 5,5′-dibromo-3,3′-dihexyl-2,2′-bithiophene, which can synthesize regioregular-P3HT-regiosymmetric-P3HT (a diblock polymer) for organic electronics based applications. It can also be used in the synthesis of P3HT, which can be potentially used for photocatalytic applications.
Informations légales
Product of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
Code de la classe de stockage
10 - Combustible liquids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves
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Les clients ont également consulté
Charge Transport in Conjugated Polymers with Pendent Stable Radical Groups.
Chemistry of Materials (2018)
Sensors (Basel, Switzerland), 20(2) (2020-01-19)
In the present work, we report the use of regioregular poly(3-hexyltiophene) polymer (RR-P3HT) as a potential light-activated material for sensing the chemical nerve agent simulant dimethyl methylphosphonate (DMMP). The electrical response of thick films of RR-P3HT, deposited by spray-coating method
Evidence of Ni (0) complex diffusion during grignard metathesis polymerization of 2, 5-dibromo-3-hexylthiophene.
Macromolecules, 42(22), 8634-8639 (2009)
Uniform electroactive fibre-like micelle nanowires for organic electronics.
Nature Communications, 8(22), 15909-15909 (2017)
Nature communications, 8, 15909-15909 (2017-06-27)
Micelles formed by the self-assembly of block copolymers in selective solvents have attracted widespread attention and have uses in a wide variety of fields, whereas applications based on their electronic properties are virtually unexplored. Herein we describe studies of solution-processable
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