550566
2,2′-Bipyridine-4,4′-dicarboxylic acid
98%
Synonym(s):
2,2′-Bipyridyl-4,4′-dicarboxylic acid
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About This Item
Empirical Formula (Hill Notation):
C12H8N2O4
CAS Number:
Molecular Weight:
244.20
Beilstein:
212894
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
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Assay
98%
SMILES string
OC(=O)c1ccnc(c1)-c2cc(ccn2)C(O)=O
InChI
1S/C12H8N2O4/c15-11(16)7-1-3-13-9(5-7)10-6-8(12(17)18)2-4-14-10/h1-6H,(H,15,16)(H,17,18)
InChI key
FXPLCAKVOYHAJA-UHFFFAOYSA-N
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Application
- Enhanced catalysis of CO2 cycloaddition at ambient pressure through rational design of interpenetrating ZnII/LnIII heterometallic coordination polymers: This study highlights the use of 2,2′-bipyridine-4,4′-dicarboxylic acid in the synthesis of ZnII/LnIII coordination polymers, which exhibit enhanced catalytic performance for CO2 cycloaddition at ambient pressure (Chuasaard et al., 2024).
- Immobilization of a new copper (II) complex dye with multi-walled carbon nanotubes and functional simulation in dye-sensitized solar cell: This research describes the synthesis of a new ligand using 2,2′-bipyridine-4,4′-dicarboxylic acid combined with multiwalled carbon nanotubes for potential applications in dye-sensitized solar cells (Shahbaznejad et al., 2023).
- Impact of Anchoring Groups on the Photocatalytic Performance of Iridium (III) Complexes and Their Toxicological Analysis: The study investigates the photocatalytic performance and toxicological analysis of Iridium (III) complexes using 2,2′-bipyridine-4,4′-dicarboxylic acid as an anchoring unit (Yao et al., 2024).
- Phosphonate-based iron complex for a cost-effective and long cycling aqueous iron redox flow battery: This paper discusses the use of 2,2′-bipyridine-4,4′-dicarboxylic acid in the development of a high redox potential Fe-Dcbpy/CN catholyte for iron redox flow batteries (Nambafu et al., 2024).
- 2, 2′-bipyridine-4, 4′-dicarboxylic acid ligand engineered CsPbBr3 perovskite nanocrystals for enhanced photoluminescence quantum yield with stable display properties: This article explores the use of 2,2′-Bipyridine-4,4′-dicarboxylic acid to improve the optical properties of CsPbBr3 perovskite nanocrystals for display applications (Kumar et al., 2024).
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Bo Zheng et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(30), E3987-E3996 (2015-06-28)
New dyads consisting of a strongly absorbing Bodipy (dipyrromethene-BF2) dye and a platinum diimine dithiolate (PtN2S2) charge transfer (CT) chromophore have been synthesized and studied in the context of the light-driven generation of H2 from aqueous protons. In these dyads
Nathan R Rose et al.
Journal of medicinal chemistry, 51(22), 7053-7056 (2008-10-24)
The dynamic methylation of histone lysyl residues plays an important role in biology by regulating transcription, maintaining genomic integrity, and by contributing to epigenetic effects. Here we describe a variety of inhibitor scaffolds that inhibit the human 2-oxoglutarate-dependent JMJD2 subfamily
Xiang Huang et al.
The Analyst, 140(17), 6015-6024 (2015-07-21)
An efficient aptasensor was developed in which graphene oxide (GO) was employed as an indicator for both electrochemical impedance spectroscopy and electrochemiluminescence (ECL) signal generation. The aptasensor was fabricated by self-assembling the ECL probe of a thiolated adenosine triphosphate binding
Maxence Urbani et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(45), 16252-16265 (2015-09-12)
The detailed synthesis and characterization of four ruthenium(II) complexes [RuLL'(NCS)2 ] is reported, in which L represents a 2,2'-bipyridine ligand functionalized at the 4,4' positions with benzo[1,2-b:4,5-b']dithiophene derivatives (BDT) and L' is 2,2'-bipyridine-4,4'-dicarboxylic acid unit (dcbpy) (NCS=isothiocyanate). The reaction conditions
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