Halogen complexes thiocyanates

Pseudohalides of Se in which the role of halogen is played by cyanide, thiocyanate or selenocyanate are known and, in the case of Se are much more stable with respect to disproportionation than are the halides themselves. Examples are Se(CN)2, Se2(CN)2, Se(SeCN)2, Se(SCN)2, Se2(SCN)2. The selenocyanate ion SeCN is ambidentate like the thiocyanate ion, etc., p. 325), being capable of ligating to metal centres via either N or Se, as in the osmium(IV) complexes [OsCl5(NCSe)], [OsCl5(SeCN)], and trans-[OsCU(NCSe)(SeCN)]2-.920) Tellurium and polonium pseudohalogen analogues include Te(CN)2 and Po(CN)4 but have been much... 

Metal cyanides(and cyano complexes), 216 Metal derivatives of organofluorine compounds, 217 IV-Metal derivatives, 218 Metal dusts, 220 Metal fires, 222 Metal fulminates, 222 Metal halides, 222 Metal—halocarbon incidents, 225 Metal halogenates, 226 Metal hydrazides, 226 Metal hydrides, 226 Metal hypochlorites, 228 Metallurgical sample preparation, 228 Metal nitrates, 229 Metal nitrites, 231 Metal nitrophenoxides, 232 Metal non-metallides, 232 Metal oxalates, 233 Metal oxides, 234 Metal oxohalogenates, 236 Metal oxometallates, 236 Metal oxonon-metallates, 237 Metal perchlorates, 238 Metal peroxides, 239 Metal peroxomolybdates, 240 Metal phosphinates, 240 Metal phosphorus trisulfides, 240 Metal picramates, 241 Metal pnictides, 241 Metal polyhalohalogenates, 241 Metal pyruvate nitrophenylhydrazones, 241 Metals, 242 Metal salicylates, 243 Metal salts, 243 Metal sulfates, 244 Metal sulfides, 244 Metal thiocyanates, 246 Metathesis reactions, 246 Microwave oven heating, 246 Mild steel, 247 Milk powder, 248... 

By contrast, the catalytic site responsible for the halogenation, hydroxylation, and other (two-electron) oxygenation reactions has been better, although not completely, characterized by X-ray crystallography of CPO complexed with several substrates (such as iodide/bromide and cyclopentane-1,3-dione) and other compounds (such as carbon monoxide, thiocyanate, nitrate, acetate, formate and, in a ternary complex, with dimethylsulfoxide and cyanide) [88, 90]. The above substrates bind at the distal side of heme, and the corresponding structures were also useful to establish the mechanism of Compound I formation as discussed above [90]. 

Copper (Cu, at. mass 63.54) occurs in its compounds in the n, and less often in the I, oxidation state. The properties of copper(I) are similar to those of Ag, Au(I), and T1(I). Copper(I) forms sparingly soluble compounds with the halogens. In solution, copper(I) exists only in complexes, e.g., Cu(CN)2", CuCb", and Cu(NH3)2. Cupric hydroxide, Cu(OH)2, begins to precipitate at pH 5 and shows no amphoteric properties. Copper(II) forms ammine, chloride, tartrate, and EDTA complexes. As a result of oxidizing properties of Cu(ll), its cyanide complex is converted into copper(I) cyanide complex, and sparingly-soluble CuSCN is precipitated from Cu(II) thiocyanate. 

There are no examples of xenon bonded to sulfur or selenium and few for the halogens. The reported compounds involve the thiocyanate and selenocyanate ligands acting as pseudohalides, in the anions I(SCN)i and I(SeCN)2, for which IR and Raman spectra show the thiocyanate to have a linear S—I—S arrangement but give no definitive results for the selenocyanate, and two examples with more complex thio ligands for which crystal structures have been determined. 

Dinuclear ort/zo-metallated complexes consist of two ligands joined through a central bridge (Fig. 1). They have been widely studied, and several types of mesogenic, metal complexes derived from azobenzene, benzylideneaniline, benzalazine (imine) and phenylpyrimidine derivatives, with a wide variety of intermetallic bridges, such halogens, thiocyanates, carboxylates, have been reported [8, 9]. 

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