Synthetic Route 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 Neumann, Tristan, introduce new discover of the category.
Crystal structure of pyridinium tetraisothiocyanatodipyridinechromium(III) pyridine monosolvate
In the crystal structure of the title compound, (C5H6N)[Cr(NCS)(4)(C5H5 N)(2)]center dot-C5H5N, the Cr-III ions are octahedrally coordinated by four N-bonding thiocyanate anions and two pyridine ligands into discrete negatively charged complexes, with the Cr-III ion, as well as the two pyridine ligands, located on crystallographic mirror planes. The mean planes of the two pyridine ligands are rotated with respect to each other by 90 degrees. Charge balance is achieved by one protonated pyridine molecule that is hydrogen bonded to one additional pyridine solvent molecule, with both located on crystallographic mirror planes and again rotated by exactly 90 degrees. The pyridinium H atom was refined as disordered between both pyridine N atoms in a 70:30 ratio, leading to a linear N-H center dot center dot center dot N hydrogen bond. In the crystal, discrete complexes are linked by weak C-H center dot center dot center dot S hydrogen bonds into chains that are connected by additional C-H center dot center dot center dot S hydrogen bonding via the pyridinium cations and solvent molecules into layers and finally into a three-dimensional network.
Synthetic Route 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