| Identification | More | [Name]
POLY(N-VINYLCARBAZOLE) | [CAS]
25067-59-8 | [Synonyms]
N-VINYLCARBAZOLE POLYMER
POLY(9-VINYLCARBAZOLE)
POLY(N-VINYLCARBAZOL)
POLY(N-VINYLCARBAZOLE)
POLYVINYL CARBAZOLE
9-ethenyl-9h-carbazolhomopolymer
9-vinylcarbazolehomopolymer
9-vinyl-carbazolpolymer
dh700
luvicanm150
luvicanm170
n-vinylcarbazolehomopolymer
tuvical210
POLY(9-VINYLCARBAZOLE), SECONDARY STANDA RD
Poly(N-vinylcarbazole), approx. M.W. 90,000
Poly(N-vinylcarbazole), secondary standard
M.N. 56,400
Poly(N-vinylcarbazole), secondary standard, M.W. 135,600
9-Vinyl-9H-carbazole
polyvinyl carbazole (PVK) | [Molecular Formula]
C42H33N3X2 | [MDL Number]
MFCD00134336 | [Molecular Weight]
579.73 | [MOL File]
25067-59-8.mol |
| Chemical Properties | Back Directory | [Appearance]
white to cream powder | [Melting point ]
>300 °C | [density ]
1.2 g/mL at 25 °C(lit.)
| [Tg]
227 | [refractive index ]
n20/D 1.683
| [form ]
powder
| [color ]
Off-white | [Stability:]
Stable. Incompatible with strong oxidizing agents. | [Thermal Conductivity]
0.155 W/(m·K) | [InChI]
1S/C14H11N/c1-2-15-13-9-5-3-7-11(13)12-8-4-6-10-14(12)15/h2-10H,1H2 | [InChIKey]
KKFHAJHLJHVUDM-UHFFFAOYSA-N | [SMILES]
[n]1(c2c(c3c1cccc3)cccc2)C=C | [CAS DataBase Reference]
25067-59-8(CAS DataBase Reference) | [EPA Substance Registry System]
25067-59-8(EPA Substance) |
| Safety Data | Back Directory | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
2
| [RTECS ]
FE6225480
| [TSCA ]
TSCA listed | [HS Code ]
29339900 | [Storage Class]
11 - Combustible Solids |
| Hazard Information | Back Directory | [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. | [Definition]
ChEBI: A macromolecule composed of repeating 9-ethylcarbazole units. | [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. | [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. | [Solubility in organics]
Benzene, chloroform, dichloromethane, dioxane, THF, toluene | [Purification Methods]
Precipitate it seven times from tetrahydrofuran with MeOH, with final freeze-drying from *benzene. Dry it under vacuum. |
|
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J & K SCIENTIFIC LTD. Gold
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https://www.jkchemical.com |
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Energy Chemical
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www.energy-chemical.com |
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T&W GROUP
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Sigma-Aldrich
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