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25067-59-8

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25067-59-8 Usage

Chemical Properties

off-white crystalline powder

Uses

PVK:graphene oxide composite can be used as a hybrid film which can be coated on silica substrate for the fabrication of organic field effect transistors (OFETs). It can also form a nano-composite film with carbon nanospheres (CNS) which can be potentially used in supercapacitors and sensor based applications.

Preparation

N-Vinyl carbazole may be obtained from phenylhydrazine and cyclohexanone by the following route:The second step in this synthesis is an example of the Fischer indole synthesis. Carbazole also occurs in coal tar. Poly(vinyl carbazole) is produced by adiabatic bulk polymerization under nitrogen pressure using azobisisobutyronitrile and di-tert-butyl peroxide as initiators. Heating to 80-90°C causes an onset of polymerization and a rapid increase in temperature. After the maximum temperature has been reached the mass is cooled under pressure.Poly(vinyl carbazole) is a very brittle material with a high softening point (about 195°C Vicat). It is insoluble in most organic solvents except aromatic and chlorinated hydrocarbons and tetrahydrofuran. The polymer is difficult to mould, requiring high process temperatures, namely about 300°C for injection moulding and 250°C for compression moulding. More usually the material is cast as thin film from solution. The most significant property of poly(vinyl carbazole) is its high photoconductivity and this has resulted in widespread use of the polymer in electrostatic dry-copying machines. When an electrostatic charge is applied to the polymer in the dark it discharges to an equilibrium value but when the polymer is illuminated almost complete discharging occurs. This phenomenon is used to create a latent electrostatic image which is then developed by transferring the charge to the toner. Poly(vinyl carbazole) also has good electrical insulation characteristics which are maintained over a wide range of temperature and frequency. On account of these characteristics, the polymer has been used as a capacitor dielectric, but this application is now of minor importance.

Definition

ChEBI: A macromolecule composed of repeating 9-ethylcarbazole units.

General Description

Poly(9-vinylcarbazole) (PVK) is a conductive polymer which is mainly used as a hole transporting medium at high efficiencies with low driving voltage. It can also be used as an anode for hole injection and can act as an effective charge transferring gate by co-doping it with organic dyes.

Purification Methods

Precipitate it seven times from tetrahydrofuran with MeOH, with final freeze-drying from *benzene. Dry it under vacuum.

Check Digit Verification of cas no

The CAS Registry Mumber 25067-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,6 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25067-59:
(7*2)+(6*5)+(5*0)+(4*6)+(3*7)+(2*5)+(1*9)=108
108 % 10 = 8
So 25067-59-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H11N/c1-2-15-13-9-5-3-7-11(13)12-8-4-6-10-14(12)15/h2-10H,1H2

25067-59-8 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (P0656)  Poly(N-vinylcarbazole)  

  • 25067-59-8

  • 5g

  • 725.00CNY

  • Detail
  • TCI America

  • (P0656)  Poly(N-vinylcarbazole)  

  • 25067-59-8

  • 25g

  • 2,190.00CNY

  • Detail

25067-59-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name poly(vinylcarbazole) macromolecule

1.2 Other means of identification

Product number -
Other names Vinylcarbazole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:25067-59-8 SDS

25067-59-8Relevant articles and documents

Base-Mediated Site-Selective Hydroamination of Alkenes

Koh, Ming Joo,Lee, Boon Chong,Li, Ping,Zhang, Xiaoxiang

supporting information, (2021/12/29)

We present a base-mediated hydroamination protocol, using substoichiometric amounts of a hydrosilane and potassium tertbutoxide, that operates under mild conditions at 30 °C. Many aryl- and heteroatom-substituted olefins as well as arylamines are tolerated, affording the desired products with complete regioselectivity. Preliminary mechanistic investigations reveal a non-radical pathway for hydroamination. A sequential remote hydroamination strategy involving an initial Fe-catalysed olefin isomerisation followed by our base-mediated hydroamination was also developed to directly access-arylamines from terminal aliphatic alkenes.

Polymer, and mixture or formulation, and organic electronic device containing same, and monomer thereof

-

, (2020/11/23)

Disclosed are a polymer, and a mixture or a formulation and an organic electronic device containing same, and applications thereof, and further a monomer of which the polymer is made; the polymer comprises on its side chain a repeating structure unit E, characterizing in that its S1(E)?T1(E))≤0.35 eV or even less, which may allow the said polymer having thermally activated delayed fluorescence (TADF) property. Thus a TADF polymer suitable for printing processes is provided, thereby reducing OLED manufacturing costs.

Substrate-Controlled Regio- and Stereoselective Synthesis of (Z)- and (E)- N-Styrylated Carbazoles, Aza-carbazoles, and γ-Carbolines via Hydroamination of Alkynes

Garg, Vineeta,Kumar, Pradeep,Verma, Akhilesh K.

, p. 11686 - 11702 (2018/09/21)

We report herein the substrate-controlled regio- and stereoselective hydroamination of carbazoles, aza-carbazoles, and γ-carbolines with functionalized aromatic as well as aliphatic alkynes in a KOH/DMSO system in good yields. The electronic effect of the substrates governs the stereochemistry of the product. Electron-donating alkynes provided (Z)-stereoselective products, and electron-withdrawing alkynes provided (E)-stereoselective products. This approach also provides an easy route for the synthesis of mono- and bis-hydroaminated product. The deuterium-labeling studies were also conducted to support the mechanistic pathway.

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