134984-37-5

Basic information

• Product Name: 2,4,6-Tri(9H-carbazol-9-yl)-1,3,5-triazine
• Synonyms: 2,4,6-Tricarbazolo-1,3,5-triazine;2,4,6-Tricarbazolyl-1,3,5-triazine;2,4,6-Tris(carbazolyl)-1,3,5-triazine;2,4,6-Tri(9H-carbazol-9-yl)-1,3,5-triazine;2,4,6-Tri(9H-carbazol-9-yl)-1,3,5-triazine (purified by subliMation)
• CAS NO: 134984-37-5
• Molecular Formula: C39H24N6
• Molecular Weight: 576.64806
• Mol File: 134984-37-5.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,4,6-Tri(9H-carbazol-9-yl)-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-Tri(9H-carbazol-9-yl)-1,3,5-triazine(134984-37-5)
• EPA Substance Registry System: 2,4,6-Tri(9H-carbazol-9-yl)-1,3,5-triazine(134984-37-5)

Safety Data

• Hazardous Substances Data: 134984-37-5(Hazardous Substances Data)

Usage

Uses

Used in Environmental Applications:
2,4,6-Tri(9H-carbazol-9-yl)-1,3,5-triazine is used as a component in microporous polymers and polycarbazole networks for the selective adsorption and storage of CO2. This application is particularly relevant in the context of climate change and the need for innovative solutions to reduce greenhouse gas emissions. The compound's structure allows for efficient CO2 capture, making it a valuable material in the development of advanced carbon capture technologies.
Used in Chemical Industry:
In the chemical industry, 2,4,6-Tri(9H-carbazol-9-yl)-1,3,5-triazine can be utilized as a building block for the synthesis of more complex molecules and materials with tailored properties. Its unique structure and functional groups make it a promising candidate for the development of new polymers, dyes, and other specialty chemicals.
Used in Research and Development:
Due to its novel structure and potential applications, 2,4,6-Tri(9H-carbazol-9-yl)-1,3,5-triazine is also used as a subject of research and development in various scientific fields. Researchers may explore its properties, such as its electronic, optical, and thermal characteristics, to better understand its potential uses and to develop new applications for this compound.

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 86-74-8 9H-carbazole 

Relevant articles and documents

Gas uptake, molecular sensing and organocatalytic performances of a multifunctional carbazole-based conjugated microporous polymer

A multifunctional carbazole-based conjugated microporous polymer MFCMP-1 is successfully prepared by oxidative coupling polymerization using a single monomer and structurally characterized. A new three-dimensional π-conjugated polymer framework can be com

Carbazole-triazine based donor-acceptor porous organic frameworks for efficient visible-light photocatalytic aerobic oxidation reactions

We report the synthesis of a series of carbazole-triazine based donor-acceptor (D-A) POFs and their photocatalytic activities for aerobic oxidation reactions. The simultaneous introduction of a carbazole-based electron donor and a triazine-based electron acceptor in D-A POFs stabilizes the charge transfer state and enables an efficient triplet-triplet energy transfer to generate 1O2. Meanwhile, systematic variation of the D-A distance results in the tunable photoredox properties and consequently the efficiency for generation of reactive oxygen species (ROSs). Upon visible light excitation, all three D-A POFs exhibit excellent capability to promote three aerobic oxidations: sulfide oxidation, oxidative amine coupling, and Mannich reactions. This systematic study validates the design principle of D-A POFs as high-performance photo-oxidation catalysts with wide substrate scope and excellent stability and recyclability.