Decrypt The Mystery Of 14389-12-9

There are many compounds similar to this compound(14389-12-9)Computed Properties of C6H5N5. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 14389-12-9, is researched, Molecular C6H5N5, about Solvent-dependent luminescent Cu(I) framework based on 5-(4-pyridyl)tetrazole, the main research direction is crystal structure copper pyridyltetrazole coordination polymer; copper pyridyltetrazole coordination polymer ethanol solvate preparation; luminescence copper pyridyltetrazole coordination polymer solvent dependent; solvent copper pyridyltetrazole coordination polymer fluorescence; framework polymer copper pyridyltetrazole nitrogen surface adsorption pore size.Computed Properties of C6H5N5.

A new Cu(I) coordination compound, Cu4(L)4·2EtOH (1), has been obtained from the solvothermal reaction of CuBr, 5-(4-pyridyl) tetrazole (HL), EtOH and NH3·H2O. The structure determination revealed that 1 has a 2D network, where each Cu(I) atom adopts a trigonal coordination mode. The 2D networks stacked in an ABAB sequence through the π-π interaction to form a 3D supramol. framework, giving a 1D channel along the b-axis. The TGA and powder XRD measurements revealed that the framework is stable after removal of the guest mols. Gas (N2) adsorption measurement was carried out for the framework and showed that N2 mols. cannot diffuse into the micropore and that only surface adsorption occurred. The photoluminescent study showed that compound 1 displays an interesting solvent-dependent luminescence.

There are many compounds similar to this compound(14389-12-9)Computed Properties of C6H5N5. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

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