Tris[4-(5-formyl-2-thienyl)phenyl]amine
CAS Number 883236-47-3
Carbaldehyde Monomers, COF Ligands, Materials, Monomers, Porous Organic FrameworksCovalent Organic Frameworks (COFs) Triphenylamine Ligand
Trigonal star shaped linker for covalent organic frameworks (COFs) in application of photocatalyst, OLEDs and organic solar cells
Specifications | MSDS | Literature and Reviews
Tris[4-(5-formyl-2-thienyl)phenyl]amine (TTA-TPA) is a derivative of triphenylamine with thiophene-2-carbaldehyde function groups at the positions that are opposite to the central nitrogen. Tris[4-(5-formyl-2-thienyl)phenyl]amine finds application in OLEDs, organic solar cells and covalent organic frameworks (COFs). With both triphenylamine core and extended thienyl groups, π-conjugated structures derived from tris[4-(5-formyl-2-thienyl)phenyl]amine is electron rich, serving as either hole transporting layer (HTL) or photoactive dyes for organic electronic devices. With three peripharal aldehyde end groups, it could form imine linkers with amines through Schiff base condensation reaction for the construction of COFs.
Bulk-heterojunction solar cell based on a solution-processable three-dimensional molecular architecture comprising tris[4-(5-formyl-2-thienyl)phenyl]amine and 1-(2-ethylhexyl)-4-methyl-2,6-dioxo-1,2,5,6-tetrahydropyridine-3-carbonitrile achieved device PCE of 4.76% with [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) as the acceptor.
MOF and COF ligands
Electron-rich ligand linker for cross-linked COF networks
Worldwide shipping
Quick and reliable shipping
High purity
>97% High purity
Facile reactions
Readily for polycondensation reactions to form imine linkages
General Information
CAS Number | 883236-47-3 |
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Chemical Formula | C33H21NO3S3 |
Full Name | Tris[4-(5-formyl-2-thienyl)phenyl]amine |
Molecular Weight | 423.51 g/mol |
Synonyms | TTA-TPA, TFTPA, 5,5',5''-(Nitrilotris(benzene-4,1-diyl))tris(thiophene-2-carbaldehyde) |
Classification / Family | Triphenylamine, Aldehydes, COF ligand |
Chemical Structure
Product Details
Purity | > 97% |
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Melting Point | Tm = 230 °C |
Appearance | Orange powder/crystals |
MSDS Documentation
Tris[4-(5-formyl-2-thienyl)phenyl]amine MSDS Sheet
Literature and Reviews
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Enhancing the efficiency of solution-processable bulk-heterojunction devices via a three-dimensional molecular architecture comprising triphenylamine and cyanopyridone, R. Hangarge et al., Dyes Pigm., 137, 126-134 (2017); DOI: 10.1016/j.dyepig.2016.10.008.
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Chiral Aggregates of Triphenylamine-Based Dyes for Depleting the Production of Hydrogen Peroxide in the Photochemical Water-Splitting Process, B. Adelizzi et al., Helv. Chim. Acta., e1900065 (2019); DOi: 10.1002/hlca.201900065.
- Peripheral group effects on the photophysical and photovoltaic properties of bulk-heterojunction type solar cells based on star-shaped conjugate molecules with triphenylamine core, Y. Kao et al., Mater. Chem. Phys., 163, 138-151 (2015); DOI: 10.1016/j.matchemphys.2015.07.024.