Tetra(4-(4-pyridyl)phenyl)methane
CAS Number 1319736-15-6
Chemistry Building Blocks, Materials, MOF Ligands, Porous Organic FrameworksMetal Organic Frameworks (MOFs) Tetraphenylmethane Ligand
A rigid tetrahedral aromatic tecton ligand linker for MOFs in applications of chemisorption of iodine
Specifications | MSDS | Literature and Reviews
Tetra(4-(4-pyridyl)phenyl)methane (TPPM), is a rigid tetrahedral aromatic tecton which can be considered as the decoration of tetraphenylmethane with four p-substituted pyridyl rings. TPPM can act as hydrogen bond acceptor with its four nitrogen atoms forming N···H bondings. Meanwhile, due to the the presence of aromatic rings, TPPM can also give rise to π···π and C-H···π interactions as weak hydrogen bond donor.
Thermally stable network [Cu4I4(PPh3)4]-L, where L is TPPM, uniquely adsorbs iodine (I2) by chemisorption through I3− formation. The chemisorbed I2 readily desorbs above 380 K owing to the dynamic motion of the framework.
General Information
CAS Number | 1319736-15-6 |
Chemical Formula | C45H32N4 |
Full Name | Tetra(4-(4-pyridyl)phenyl)methane |
Molecular Weight | 628.76 g/mol |
Synonyms | TPPM, Tetrakis(4-(pyridin-4-yl)phenyl)methane |
Classification / Family | Tetraphenylmethane, MOF ligands, |
Chemical Structure
Product Details
Purity | >98% |
Melting Point | 323 °C (decomp) |
Appearance | White powder/crystal |
MSDS Documentation
Tetra(4-(4-pyridyl)phenyl)methane MSDS Sheet
Literature and Reviews
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Selective and Reversible Solvent Uptake in Tetra-4-(4-pyridyl)phenylmethane-based Supramolecular Organic Frameworks, D. Marchetti et al., Chem. Eur. J., 28, e202202977 (2022); DOI: 10.1002/chem.202202977.
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Kinetic Assembly of a Thermally Stable Porous Coordination Network Based on Labile CuI Units and the Visualization of I2 Sorption, H. Kitagawa et al., Angew. Chem., 125 (47), 12621-12625 (2013); DOI: 10.1002/ange.201306776.
- A tetrapyridine ligand with a rigid tetrahedral core forms metal–organic frameworks with PtS type architecture, Chem. Commun., 47, 8545–8547 (2011); DOI: 10.1039/c1cc12188j.