Related Products of 1111-67-7, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps. In an article, authors is Trivedi, Manoj, once mentioned the application of Related Products of 1111-67-7, Name is Cuprous thiocyanate,molecular formula is CCuNS, is a conventional compound.
The reaction of copper(I) salts CuX (X = Cl, Br, I, CN, SCN), [Cu(CH3CN)4]PF6 with 1-diphenylphosphino-1?-di-tert-butylphosphinoferrocene (dppdtbpf) in 1:1 M ratio in DCM-MeOH (50:50 V/V) at room temperature afforded mono and binuclear compounds having formula [Cu2(mu-Cl)2(kappa2-P,P-dppdtbpf)2] (1), [Cu2(mu-Br)2(kappa2-P,P-dppdtbpf)2] (2) [Cu2(mu-I)2(kappa2-P,P-dppdtbpf)2] (3), [Cu2(mu-CN)2(kappa2-P,P-dppdtbpf)2] (4), [Cu2(mu2-SCN)2(kappa2-P,P-dppdtbpf)2] (5), and [Cu(kappa2-P,P-dppdtbpf)(CH3CN)2]PF6 (6). Reacting palladium(II) complex [Pd(C6H5CN)2Cl2] with dppdtbpf gave mononuclear compound [Pd(kappa2-P,P-dppdtbpf)Cl2] (7). The reaction of dppdtbpf with sulfur powder under reflux in chloroform afforded a ferrocene diphosphine disulfide dppSdtbpSf (8). All of the synthesized compounds were characterized by elemental analyses, IR, 1H and 31P NMR, ESI-MS and electronic absorption spectroscopy. Molecular structures for the compounds 5, 6, 7 and 8 were determined crystallographically. Compound 5 exists as centrosymmetric dimer in which the two copper atoms are bonded to two dppdtbpf ligands and two bridging thiocyanate groups in mu2-manner. In cationic compound 6, the copper atom is coordinated to one dppdtbpf ligand in kappa2-manner and two acetonitrile molecules, whereas in 7, the palladium(II) adopted cis square-planar geometry by coordinating to one dppdtbpf ligand in kappa2-manner and two chlorine atoms. Compound 8 revealed a sandwiched structure with both phosphine groups sulfurized. The electrochemical properties of 1-6 were studied by cyclic voltammetry. Compounds 1-6 exhibited moderately weak to strong luminescence properties, however compounds 7 and 8 are non-emissive in the solution state.
Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Related Products of 1111-67-7, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about Related Products of 1111-67-7
Reference：
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”