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Atomfair 3,8-Dibromo-1,10-phenanthroline C12H6Br2N2

Description 3,8-Dibromo-1,10-phenanthroline (CAS No. 100125-12-0) is a high-purity brominated phenanthroline derivative with the molecular formula C12H6Br2N2. This heterocyclic aromatic compound features two bromine atoms at the 3 and 8 positions, enhancing its utility in coordination chemistry and material science applications. With a molecular weight of 338.00 g/mol, it is a versatile ligand for transition metal complexes, particularly in catalysis and photophysical studies. The compound is supplied as a crystalline solid with ??95% purity (HPLC), ensuring consistent performance in synthetic and analytical workflows. Ideal for researchers developing luminescent materials, electrochemical sensors, or supramolecular architectures.

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Description

Description

3,8-Dibromo-1,10-phenanthroline (CAS No. 100125-12-0) is a high-purity brominated phenanthroline derivative with the molecular formula C12H6Br2N2. This heterocyclic aromatic compound features two bromine atoms at the 3 and 8 positions, enhancing its utility in coordination chemistry and material science applications. With a molecular weight of 338.00 g/mol, it is a versatile ligand for transition metal complexes, particularly in catalysis and photophysical studies. The compound is supplied as a crystalline solid with ??95% purity (HPLC), ensuring consistent performance in synthetic and analytical workflows. Ideal for researchers developing luminescent materials, electrochemical sensors, or supramolecular architectures.

  • CAS No: 100125-12-0
  • Molecular Formula: C12H6Br2N2
  • Molecular Weight: 338.00
  • Exact Mass: 337.88772
  • Monoisotopic Mass: 335.88977
  • IUPAC Name: 3,8-dibromo-1,10-phenanthroline
  • SMILES: C1=CC2=CC(=CN=C2C3=NC=C(C=C31)Br)Br
  • Synonyms: 3,8-dibromo-1,10-phenanthroline, 100125-12-0, 845-981-3, 3,8-DIBROMOPHENANTHROLINE, 1,10-Phenanthroline, 3,8-dibromo-

Application

3,8-Dibromo-1,10-phenanthroline serves as a key building block for synthesizing photoactive metal-organic frameworks (MOFs) and coordination polymers. Its electron-withdrawing bromine substituents modify the electronic properties of phenanthroline-based ligands, enabling fine-tuning of emission spectra in luminescent materials. The compound is also employed in cross-coupling reactions (e.g., Suzuki-Miyaura) to construct extended ??-conjugated systems for organic electronics. In catalysis, it acts as a chelating agent for palladium and copper complexes in C-C bond-forming reactions.

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