Properties and Exciting Facts About 2-(1H-1,2,4-Triazol-3-yl)pyridine

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Related Products of 23195-62-2, you can also check out more blogs about23195-62-2

Related Products of 23195-62-2, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 23195-62-2, Name is 2-(1H-1,2,4-Triazol-3-yl)pyridine, molecular formula is C7H6N4. In a Article,once mentioned of 23195-62-2

A new copper coordination polymer [Cu2I(C7H5N4)2]n (1) with the 3-(pyridin-2-yl)- 1,2,4-triazole (Hpt) and copper iodide was synthesized. It crystallizes in the triclinic space group P1 with a = 8.6380(9), b = 9.2434(9), c = 11.8588(12) A, alpha = 99.5890(10), beta = 109.0990(10)o, gamma = 105.2800(10)o, V = 829.25(15) A3, Dc = 2.180 g/cm3, Z = 2, F(000) = 522, GOOF = 1.046, the final R = 0.0245 and wR = 0.0598. The crystal structure shows that two copper ions are bridged by two mu2-n1:n0-3-(pyridin-2-yl)-1,2,4-triazole anions and two iodide ions. The coordination environments of the Cu ion are Cu(1)N5 and Cu(2)N2I2, giving distorted square pyramidal geometry and trigon pyramid geometry. The magnetic and fluorescent properties of 1 were studied.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Related Products of 23195-62-2, you can also check out more blogs about23195-62-2

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