3,3'-Dihydroxy-[1,1'-biphenyl]-4,4'-dicarbaldehyde
CAS Number 14969-32-5
Chemistry Building Blocks, COF Ligands, Materials, Porous Organic Frameworks
Covalent organic frameworks (COFs) biphenyl ligand
used for the synthesis of Schiff base COFs and metal-COF complexes serve as porous materials and electrocatalysts
Specifications | MSDS | Literature and Reviews
3,3'-Dihydroxy-[1,1'-biphenyl]-4,4'-dicarbaldehyde (CAS number 14969-32-5) contains two salicylaldehydes connected at the 4,4'-positions. 3,3'-Dihydroxy-[1,1'-biphenyl]-4,4'-dicarbaldehyde is commonly used to synthesise Schiff base COF with amine derivatives. Additionally, salen-COFs can be prepared by using ethylenediamine in the synthesis. Salen-COFs feature salen (salicylaldehyde and enthylenediamine) linkages within the COF networks, which provide tetradentate sites for coordinating with metal centres in various applications.
A COF based on 3,3'-dihydroxy-[1,1'-biphenyl]-4,4'-dicarbaldehyde and porphyrin is applied for electrocatalytic oxygen evolution reactions. This bimetallic two-dimensional COF exhibits remarkable turnover frequency value up to 26.19 s−1 at an overpotential of 500 mV.
Duo functionality
Enabling post-functionalisation
High Purity
>98% Purity
Worldwide shipping
Quick and reliable shipping
MOF and COF ligands
Aldehyde and hydroxy ligand for cross-linked COF networks
General Information
CAS Number | 14969-32-5 |
Chemical Formula | C14H10O4 |
Full Name | 3,3'-Dihydroxy-4,4'-biphenyldicarbaldehyde |
Molecular Weight | 242.23 g/mol |
Synonyms | 3,3'-Dihydroxy-[1,1'-biphenyl]-4,4'-dicarboxaldehyde, DHBD, BDP, 3,3'-Dihydroxybiphenyl-4,4'-dicarbaldehyde |
Classification / Family | COFs, Metal-COF complexes, CMPs, Salen COFs, Schiff base COFs, Electrocatalysts |
Chemical Structure
Product Details
Purity | 98% |
Melting Point | N/A |
Appearance | Light brown powder |
MSDS Documentation
3,3'-Dihydroxy-[1,1'-biphenyl]-4,4'-dicarbaldehyde MSDS Sheet
Literature and Reviews
- A three-dimensional luminescent covalent organic framework for rapid, selective, and reversible uranium detection and extraction, W.-R. Cui et al., Sep. Purif. Technol., 306, 122726 (2023); DOI: 10.1016/j.seppur.2022.122726.
- Spatial well-defined bimetallic two-dimensional polymers with single-layer thickness for electrocatalytic oxygen evolution reaction, D. Fa et al., Angew. Chem. Int. Ed., 61, e202207845 (2022); DOI: 10.1002/anie.202207845.
- The excited-state intramolecular proton transfer properties of three imine-linked two-dimensional porous organic polymers, P. Jagadesan et al., J. Mater. Chem. C, 5, 5676–5679 (2022); DOI: 10.1039/C7TC00123A.