Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 144750-52-7, Name is Methyl 2-(2-chlorophenyl)-2-(4,5-dihydrothieno[2,3-c]pyridin-6(7H)-yl)acetate hydrochloride, SMILES is O=C(OC)C(C1=CC=CC=C1Cl)N2CCC(C=CS3)=C3C2.[H]Cl, belongs to pyridine-derivatives compound. In a document, author is Richburg, Chase S., introduce the new discover, Recommanded Product: 144750-52-7.
Influence of Pyridine on the Multielectron Redox Cycle of Nickel Diethyldithiocarbamate
Two-electron (2e(-))-transfer reactions for monometallic complexes of first-row transition metals are uncommon because of the tendency of these metals to proceed through sequential one-electron (1e(-))-transfer pathways. For this chemistry to be observed, structural changes upon electron transfer are often needed to shift the 1e(-) redox potentials to a condition of potential inversion where 2e(-) transfer becomes favorable. Nickel(II) dithiocarbamate complexes take advantage of these conditions to drive 2e(-) oxidation from Ni-II to Ni-IV. Here, we have studied the electrochemistry of Ni-II(dtc)(2), where dtc(-) is N,N-diethyldithiocarbamate in an acetonitrile solvent as a function of the scan rate and added pyridine to gain further insight into the mechanism for its 2e(-) oxidation to [Ni-IV (dtc)(3)](+). The scan rate dependence revealed evidence for an ECE mechanism in which the chemical step constituted ligand exchange between [Ni-III(dtc)(2)](+) and Ni-II(dtc)(2). A pseudo-first-order rate constant for this reaction of 34 s(-1) was obtained at 1 mM Ni-II(dtc)(2). The addition of pyridine to the electrolyte solution showed pronounced changes to the cyclic voltammetry (CV) that were consistent with the formation of a pyridine-bound Ni-III complex, [Ni-III(dtc)(2)(py)(2)](+), which was stable at high scan rates but decomposed to [Ni-IV(dtc)(3)]+ at low scan rates. The observed decomposition rate constant was well modeled with two parallel decay pathways, one through the dipyridine [Ni-III(dtc)(2)(py)(2)](+) and another through a monopyridine [Ni-III(dtc)(2)(py](+). Overall, these data point to a mechanism for oxidation from Ni-II(dtc)(2) to [Ni-IV(dtc)(3)] + that proceeds through an undercoordinated [Ni-III(dtc)(2)](+) complex, which can be trapped on the time scale of CV experiments using pyridine ligands. These studies provide insight into how we may be able to control 1e(-) versus 2e(-) redox chemistry using the coordination environment and nickel oxidation state.
The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 144750-52-7 is helpful to your research. Recommanded Product: 144750-52-7.
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem