Application of 350-03-8, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 350-03-8, Name is 1-(Pyridin-3-yl)ethanone, SMILES is CC(C1=CC=CN=C1)=O, belongs to pyridine-derivatives compound. In a article, author is Al-Jibori, Subhi A., introduce new discover of the category.
Pd (II)- pyrrolidine dithiocarbamate complexes: Synthesis, spectroscopic studies and molecular structure of [Pd(PyDT)(ppy)]
Eight palladium(II) pyrrolidine dithiocarbamate complexes were prepared and fully characterized. Reactions of the dimeric cyclopalladated complexes, [Pd(ppy)(mu-Cl)](2) (ppyH= phenylpyridine) or [Pd(N-BAZ)(mu-Cl)](2) (N-BAZH = N,N-dimethylbenzylamine) with two moles equivalent of ammonium pyrrolidine dithiocarbamate NH4(PyDT) afford [Pd(PyDT)(ppy)] and [Pd(kappa(2)-PyDT)(N-BAZ)] in good yield (91 and 71 % respectively). A crystal structure of [Pd(PyDT)(ppy)] reveals that the PyDT ligand is bonded as a bidentate chelate. Reaction of trans-[PdCl2(DMSO)(2)] with sodium benzisothiazolinate (NaBit), followed by NH4(PyDT) afford Na[Pd(PyDT)(N-Bit)(2)]. Diphosphine adducts [Pd(PyDT)(2){Ph2P(CH2)(n)PPh2}] [n = 2-4 or (CH2)(n) = (C5H4)(2)Fe}, can be prepared in good yield upon addition of the diphosphine to [Pd(PyDT)(2)]. Reaction of trans-[PdCl2(PPh3)(2)] with sodium saccharinate (Nasac) followed by NH4(PyDT) afford trans-[Pd(PyDT)(N-sac)(PPh3)(2)]. The prepared complexes were characterized by elemental analysis, i.r., H-1, P-31 nmr spectroscopic data and conductivity measurements. (C) 2020 Published by Elsevier B.V.
Application of 350-03-8, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 350-03-8.
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem