Application of 1111-67-7, In heterogeneous catalysis, catalysts provide a surface to which reactants bind in a process of adsorption. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.In an article, once mentioned the application of 1111-67-7, Name is Cuprous thiocyanate, is a conventional compound.
The lamellar coordination polymer ?2[(CuSCN)2-(mu-1,10DT18C6)] (l,10DT18C6 = l,10-dithia-18-crown-6), in which staircase-like CuSCN double chains are bridged by thiacrown ether ligands, may be prepared in two triclinic modifications la and 1b by reaction of CuSCN with 1,10DT18C6 in respectively benzonitrile or water. Performing the reaction in acetonitrile in the presence of an equimolar quantity of KSCN leads, in contrast, to formation of the K+ ligating 2-dimensional thiocyanatocuprate(I) net ?2[{Cu2(SCN)3}-] of 2, half of whose Cu(I) atoms are connected by 1,10DT18C6 macrocycles. The potassium cations in ?2[{K(CH3CN)}{Cu2(SCN) 3(mu-l,10DT18C6)}] (2) are coordinated by all six potential donor atoms of a single thia crown ether in addition to a thiocyanate S and an acetonitrile N atom. Under similar conditions, reaction of Cul, NaSCN and 1,10DT18C6 affords ?2[{Na(CH3CN)2}{Cu 4I4(SCN)(mu-1,10DT18C6)}] (3), which contains distorted Cu4I4 cubes as characteristic molecular building units. These are bridged by thiocyanate and thiacrown ether ligands into corrugated Na+ ligating sheets. In the presence of divalent Ba2+ cations, charge compensation requirements lead to formation of discrete [Cu(SCN)3(1,10DT18C6-KS)]2- anions in ?2 [Ba{Cu(SCN)3(1,10DT18C6-KS)}] (4). WILEY-VCH Verlag GmbH, D-69451 Weinheim, 2001.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 1111-67-7, and how the biochemistry of the body works.Application of 1111-67-7
Reference：
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”