New Advances in Chemical Research, April 2021. Related Products of 23814-12-2, The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. 23814-12-2, Name is 1H-Benzo[d][1,2,3]triazole-5-carboxylic acid, SMILES is O=C(C1=CC=C(NN=N2)C2=C1)O, belongs to naphthyridine compound. In a article, author is Matveeva, A. G., introduce new discover of the category.
The reaction of 2-phosphorylalkyl-substituted 1,8-naphthyridines, viz., 2-[2-(diphenylphosphoryl)propan-2-yl]-1,8-naphthyridine (L (1) ) and 2-[2-(diphenylphosphoryl)ethyl]-1,8-naph-thyridine (L (2) ), with lanthanide nitrates (Nd, Eu, or Lu) afforded complexes with the metal-to-ligand molar ratio of 1: 1 and 1: 2. Based on the IR and Raman spectroscopic data, it was found that the coordination of the ligands L (1) and L (2) in all complexes occurs through the P=O group and the nitrogen atoms of the naphthyridine moiety.
Related Products of 23814-12-2, Consequently, the presence of a catalyst will permit a system to reach equilibrium more quickly, but it has no effect on the position of the equilibrium as reflected in the value of its equilibrium constant.I hope my blog about 23814-12-2 is helpful to your research.
Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem