Extended knowledge of 14389-12-9

Compound(14389-12-9)Electric Literature of C6H5N5 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5-(4-Pyridyl)-1H-tetrazole), if you are interested, you can check out my other related articles.

Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Australian Journal of Chemistry called Laser-Based Formation of Copper Nanoparticles in Aqueous Solution: Optical Properties, Particle Size Distributions, and Formation Kinetics*, Author is Mulder, Ashley J.; Tilbury, Rhys D.; Wright, Phillip J.; Becker, Thomas; Massi, Massimiliano; Buntine, Mark A., which mentions a compound: 14389-12-9, SMILESS is C1(C2=NN=NN2)=CC=NC=C1, Molecular C6H5N5, Electric Literature of C6H5N5.

The authors explore the formation kinetics, optical absorption spectra, and particle size distributions of copper nanoparticles (CuNPs) formed by direct laser ablation from the bulk metal via a process the authors refer to as Laser Ablation Synthesis in Solution (LASiS). Comparisons are made between CuNPs formed in pure water vs. those formed in the presence of 1×10-4 M solutions of the N-donor ligands 4,4′-bipyridine (4,4’Bipy) and 1H-5-(4-pyridyl)tetrazole (T-4Py). CuNPs formed in pure water and in the presence of 4,4’Bipy display similar UV-visible absorption spectra and very similar particle size distributions. In comparison, CuNPs formed in the presence of T-4Py display significantly different absorption properties, with the surface plasmon resonance transition blue-shifted by ∼55nm, and a much smaller and narrower particle size distribution compared with the former samples. Based on previous literature reports, it is possible to ascribe these differences to differences in the CuNP surface oxidation states for samples prepared in the presence of T-4Py. However, an anal. of the formation kinetics of all three samples indicates near-identical behavior.

Compound(14389-12-9)Electric Literature of C6H5N5 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5-(4-Pyridyl)-1H-tetrazole), if you are interested, you can check out my other related articles.

Reference:
Chiral nitrogen ligands in late transition metal-catalysed asymmetric synthesis—I. Addressing the problem of ligand lability in rhodium-catalysed hydrosilations,
Nitrogen-Containing Ligands for Asymmetric Homogeneous and Heterogeneous Catalysis