Poly(9-vinylcarbazole) - Approx Mw 90000 , CAS No.25067-59-8

CAS: 25067-59-8 Cat. No.: P121309

GRADE & PURITY Approx Mw 90000

Synonyms

NSC406868 | NSC-406868 | 9-Vinylcarbazole, 98% | DTXSID4022155 | Vinylcarbazole | UNII-D629AMY6F9 | N-Vinylcarbazole | AI3-08510 | SCHEMBL36244 | CARBAZOLE, 9-VINYL- | AM84449 | NSC 406868 | N-Vinyl carbazole | N-Vinylkarbazol | 9-Ethenyl-9H-carbazole | 9

Storage

Room temperature

Shipped In

Normal

Descripción general

Poly(9-vinylcarbazole) (PVK) is a conjugated polymer with hydrophobic properties. PVK films have a glass transition temperature (Tg) of 200°C and are mainly used as hole transport materials for semiconductor application.

Specifications

Sinónimos

NSC406868 | NSC-406868 | 9-Vinylcarbazole, 98% | DTXSID4022155 | Vinylcarbazole | UNII-D629AMY6F9 | N-Vinylcarbazole | AI3-08510 | SCHEMBL36244 | CARBAZOLE, 9-VINYL- | AM84449 | NSC 406868 | N-Vinyl carbazole | N-Vinylkarbazol | 9-Ethenyl-9H-carbazole | 9

Especificaciones y pureza

Approx Mw 90000

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Nombres e identificadores

• Sonrisas canónicas: C=CN1C2=CC=CC=C2C3=CC=CC=C31
• IUPAC Name: 9-ethenylcarbazole
• InChIKey: KKFHAJHLJHVUDM-UHFFFAOYSA-N
• INCHI: 1S/C14H11N/c1-2-15-13-9-5-3-7-11(13)12-8-4-6-10-14(12)15/h2-10H,1H2
• Isómeros SMILES: C=CN1C2=CC=CC=C2C3=CC=CC=C31
• WGK Alemania: 2
• RTECS: FE6225480
• Reaxy-Rn: 132988
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=132988&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Indoles and derivatives
      • Subclass Carbazoles

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Indoles and derivatives
• Subclass: Carbazoles
• Intermediate Tree Nodes: Not available
• Direct Parent: Carbazoles
• Alternative Parents: Indoles Substituted pyrroles Benzenoids Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Carbazole - Indole - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as carbazoles. These are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Solubilidad: soluble in benzene，chloroform，dichloromethane，dioxane，THF，toluene.
• Índice de refracción: 1.683
• Punto de fusión (°C): >300°C
• Peso molecular: 193.240 g/mol
• XLogP3: 3.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 193.089 Da
• Monoisotopic Mass: 193.089 Da
• Topological Polar Surface Area: 4.900 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 226.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Haoyue Zhang, Yuru Tang, Chen Chen, Meiqin Xiao, Jonghee Yang, Wei Zhang, Chaochao Qin, Ting Xiang, Long Xu, Ping Chen.  (2023)  Enhanced Charging/Discharging Process in Perovskite Active Light Source for High-Speed Visible-Light Communication.  Advanced Optical Materials,      [PMID:] [10.1002/adom.202303051]

2. Yanyan Wu, Fang Yuan, Feifei Fu, Chenxing Liu, Bo Jiao, Fanghui Zhang, Zhaoxin Wu.  (2021)  Enhanced performance of spectra stable blue perovskite light-emitting diodes through Poly(9-vinylcarbazole) interlayer incorporation.  ORGANIC ELECTRONICS,      [PMID:] [10.1016/j.orgel.2021.106259]

3. Zheng Chao, Xiang Xu.  (2019)  Spectroscopic Study of Aggregation of Carbazole Units.  JOURNAL OF FLUORESCENCE,  29  (6): (1343-1348).  [PMID:31720948] [10.1007/s10895-019-02457-2]

4. Man Li, Xin Li, Ying-Feng Han.  (2025)  Achieving a Record Photoluminescence Quantum Yield in Green Light-Emitting Carbon-Centered Radicals with Nanosecond Emission Lifetimes.  ADVANCED MATERIALS,      [PMID:40109129] [10.1002/adma.202418324]

5. Bo Chen, He Liu, Jonghee Yang, Mahshid Ahmadi, Qi Chen, Ni Yin, Shitong Zhang, Meiqin Xiao, Haoyue Zhang, Long Xu, Ping Chen.  (2024)  Coordination of Thermally Activated Delayed Fluorescent Molecules for Efficient and Stable Perovskite Light-Emitting Diodes.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202402522]

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7. Rui Qi, Wenfei Shen, Rui Xu, Zengkun Li, Zaixin Long, Yao Wang, Qinglin Tang, Matt J. Kipper, Ketul Popat, Laurence A. Belfiore, Jianguo Tang.  (2024)  Excellent Electroluminescent Property of Eu3+-Induced Polystyrene-co-poly(acrylic acid) Aggregates (EIPAs) in Polymeric Light-Emitting Diodes.  ACS Applied Materials & Interfaces,      [PMID:38978456] [10.1021/acsami.4c06466]

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