Manganese complex bismuth

Treatment of 5-thioxo-4,5-dihydro-3,4-dimethyl-l,2,4-triazole with sodium tetrahydroborate at 210 °C provides the new N3S3-donor tripod ligand Tt as its sodium complex salt [Na(H20)6] [Na(Tt)2]. Bailey also describes some Tt bismuth(III), tin(IV) and manganese complexes, which illustrated the flexible Tt offering a combination of the properties ot the Tp and Tm ligands.163... 

Rubidium metal alloys with the other alkaU metals, the alkaline-earth metals, antimony, bismuth, gold, and mercury. Rubidium forms double haUde salts with antimony, bismuth, cadmium, cobalt, copper, iron, lead, manganese, mercury, nickel, thorium, and 2iac. These complexes are generally water iasoluble and not hygroscopic. The soluble mbidium compounds are acetate, bromide, carbonate, chloride, chromate, fluoride, formate, hydroxide, iodide. 

Although trialkyl- and triarylbismuthines are much weaker donors than the corresponding phosphoms, arsenic, and antimony compounds, they have nevertheless been employed to a considerable extent as ligands in transition metal complexes. The metals coordinated to the bismuth in these complexes include chromium (72—77), cobalt (78,79), iridium (80), iron (77,81,82), manganese (83,84), molybdenum (72,75—77,85—89), nickel (75,79,90,91), niobium (92), rhodium (93,94), silver (95—97), tungsten (72,75—77,87,89), uranium (98), and vanadium (99). The coordination compounds formed from tertiary bismuthines are less stable than those formed from tertiary phosphines, arsines, or stibines. 

H. 8-Hydroxyquinaldine (XI). The reactions of 8-hydroxyquinaldine are, in general, similar to 8-hydroxyquinoline described under (C) above, but unlike the latter it does not produce an insoluble complex with aluminium. In acetic acid-acetate solution precipitates are formed with bismuth, cadmium, copper, iron(II) and iron(III), chromium, manganese, nickel, silver, zinc, titanium (Ti02 + ), molybdate, tungstate, and vanadate. The same ions are precipitated in ammoniacal solution with the exception of molybdate, tungstate, and vanadate, but with the addition of lead, calcium, strontium, and magnesium aluminium is not precipitated, but tartrate must be added to prevent the separation of aluminium hydroxide. 

If solvent extraction is carried out in the presence of cyanide, the zinc group of metals (Zn, Cd, Hg) is complexed and they will not extract. Addition of citrate complexes the elements of the ammonia group (Fe, Al, etc.) so that their hydroxides will not precipitate. The precipitation of the alkaline earth phosphates can be prevented by the addition of hexametaphosphate (Jl). Under these conditions, Bi(III), TI(I), and Sn(II) interfere in alkaline solution. The bismuth can be removed by preextraction at pH 3. Alternatively, if a positive lead test is found, bismuth could be ruled out or confirmed by back-extracting at pH 3. If bismuth is present, it will remain in the organic layer while lead will go into the aqueous phase. Extraction of thallium can be prevented by extracting the lead at pH 6.0-6.4 with chloroform. Or the thallium can be back-extracted at this pH this requires much closer control of the pH. The oxidation of dithizone by air is catalyzed by the presence of significant amounts of manganese (II). 

Lead is reported to be almost imique in not forming compounds of this tA pe, basic lead nitrate and chloride being the principal products formed when aqueous hexamethylenetetramine solutions are reacted with lead nitrate and lead chloride, respectively - . Complexes are reported ivith salts of lithium, sodium, potassium, copper,. silver, gold, magnesium, calcium, strontium, barium, zinc, cadmium, mercury, aluminum, titanium, lanthanum, cerium, neodymium, yttrium, erbium, thorium, tin, antimcnj, bismuth, chromium, molybdenum, tungsten, uranium, manganese, iron, cobalt, nickel, platinum, and palladium -... 

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