Some scientific research about 147-85-3

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 147-85-3. Category: catalyst-ligand.

Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 147-85-3, Name is H-Pro-OH, molecular formula is C5H9NO2, belongs to catalyst-ligand compound. In a document, author is Kumari, Sheela, introduce the new discover, Category: catalyst-ligand.

Cu(i) based catalysts derived from bidentate ligands and studies on the effect of substituents for N-arylation of benzimidazoles and indoles

A family of Cu(i) complexes [Cu(L1-4)(Cl)(PPh3)] (C1-C4) were synthesized from bidentate ligands L-1-L-4 (where L-1 = (E)-2-(2-benzylidene-1-phenylhydrazinyl)pyridine, L-2 = (E)-N,N-dimethyl-4-((2-phenyl-2-(pyridin-2-yl)hydrazono)methyl)aniline, L-3 = (E)-2-(2-(4-chlorobenzylidene)-1-phenylhydrazinyl)pyridine and L-4 = (E)-2-(2-(4-nitrobenzylidene)-1-phenylhydrazinyl)pyridine) and characterized. The structure of complex C1 was authenticated by single-crystal X-ray diffraction. These complexes were utilised as catalysts for N-arylation of benzimidazoles and indoles. The effect of the substituents in the ligand frame of metal complexes were examined and the probable reaction pathway was scrutinized.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 147-85-3. Category: catalyst-ligand.

Reference:
Metal catalyst and ligand design,
,Ligand Template Strategies for Catalyst Encapsulation – NCBI