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2,4,5,6-tetrakis(carbazol-9-yl)-1,3-dicyanobenzene, >99%(HPLC), Sublimed

Catalog NumberACM1416881521-2

CAS Number1416881-52-1

CategoryOther Materials

2,4,5,6-tetrakis(carbazol-9-yl)-1,3-dicyanobenzene, >99%(HPLC), Sublimed
IUPAC Name
2,4,5,6-tetra(carbazol-9-yl)benzene-1,3-dicarbonitrile
Molecular Weight
788.9g/mol
Molecular Formula
C56H32N6
Canonical SMILES
C1=CC=C2C(=C1)C3=CC=CC=C3N2C4=C(C(=C(C(=C4C#N)N5C6=CC=CC=C6C7=CC=CC=C75)N8C9=CC=CC=C9C1=CC=CC=C18)N1C2=CC=CC=C2C2=CC=CC=C21)C#N
InChI
InChI=1S/C56H32N6/c57-33-43-53(59-45-25-9-1-17-35(45)36-18-2-10-26-46(36)59)44(34-58)55(61-49-29-13-5-21-39(49)40-22-6-14-30-50(40)61)56(62-51-31-15-7-23-41(51)42-24-8-16-32-52(42)62)54(43)60-47-27-11-3-19-37(47)38-20-4-12-28-48(38)60/h1-32H
InChI Key
PRWATGACIORDEL-UHFFFAOYSA-N
Application
2,4,5,6-Tetrakis(carbazol-9-yl)-1,3-dicyanobenzene, with a purity greater than 99% as determined by HPLC and available in sublimed form, is designed as an organic fluorescent dye. It functions primarily as a catalyst in photocatalysis reactions, leveraging its unique properties as a thermally activated delayed fluorescence (TADF) material. As a donor-acceptor fluorophore, it features carbazolyl groups as electron donors and a dicyanobenzene core as the electron acceptor. This structure endows the compound with an impressive redox window, high chemical stability, and a wide range of potential applications, particularly in organic transformations. It exhibits a remarkable emission peak at 507 nm in toluene with a photoluminescence quantum yield of 94.6%, making it a highly efficient photocatalyst for various chemical processes.
Complexity
1560
Covalently-Bonded Unit Count
1
Exact Mass
788.268845g/mol
Formal Charge
0
Heavy Atom Count
62
MeSH Entry Terms
1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene
Monoisotopic Mass
788.268845g/mol
Rotatable Bond Count
4
XLogP3
13.7
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