Platinum complex tellurium

Selenium occurs in the slimes as intermetallic compounds such as copper silver selenide [12040-91 -4], CuAgSe disilver selenide [1302-09-6], Ag2Se and Cu2 Se [20405-64-5], where x < 1. The primary purpose of slimes treatment is the recovery of the precious metals gold, silver, platinum, palladium, and rhodium. The recovery of selenium is a secondary concern. Because of the complexity and variabiUty of slimes composition throughout the world, a number of processes have been developed to recover both the precious metals and selenium. More recently, the emphasis has switched to the development of processes which result in early recovery of the higher value precious metals. Selenium and tellurium are released in the later stages. Processes in use at the primary copper refineries are described in detail elsewhere (25—44). 

The solution should be free from the following, which either interfere or lead to an unsatisfactory deposit silver, mercury, bismuth, selenium, tellurium, arsenic, antimony, tin, molybdenum, gold and the platinum metals, thiocyanate, chloride, oxidising agents such as oxides of nitrogen, or excessive amounts of iron(III), nitrate or nitric acid. Chloride ion is avoided because Cu( I) is stabilised as a chloro-complex and remains in solution to be re-oxidised at the anode unless hydrazinium chloride is added as depolariser. 

The aim of this chapter is to review the chemistry of chalcogenolates in the last 10 years. The more recent reviews in this field included chalcogenolates of the s-block elements,13,14 early transition metal thiolates,15 metal complexes with selenolate and tellurolate ligands,16 copper(I), lithium and magnesium thiolates,17 functionalized thiolate complexes,18 19 pentafluorobenzenethiolate platinum group compounds,20 tellurium derivatives,21 luminescent gold compounds,22 and complexes with lanthanide or actinide.23... 

The sulfide group forms a large number of complexes where it is in chelation with a different heteroatom. Among the common heteroatoms are N, P and As. These complexes are too numerous to list here, but individual complexes can be found from Table 9 or from refs. 1224 and 1667. It is also possible to synthesize compounds which will form bi-, tri- and tetra-dentate complexes to platinum(II), where sulfur, selenium and tellurium.are the only atoms which coordinate to the metal. A review of complexes formed from ligands of the type RS(CH2) SR has been recently published.1734 This article outlines the synthesis, reactions and spectroscopy of these complexes, and allows the complexes of platinum to be placed in context with those of other transition metals. 

A tellurium-containing borane without carbon atoms in the Te — B cage was obtained from B10H14 and sodium polytelluride. The telluraborane BioHjjTe was used for the preparation of cobalt, iron, platinum, rhodium, and iridium complexes, in which the TeBioHjo moiety served as the ligand. 

Class I. ELEMENTS. A. Metals. Cubic copper, silver, gold, iron, platinum, iridium. - Tetragonal tin. - Rhombohedral and Hexagonal arsenic, antimony, bismuth, tellurium, (Os, Ir). - B. Metalloids. Cubic diamond. - Hexagonal graphite. - Orthorhombic sulfur, iodine. - Monoclinic sulfur, selenium. - Class II. SULFIDES. - Class HI. HALIDES. -Class IV. OXIDES, divided into SIMPLE OXIDES and COMPLEX OXIDES, such as CARBONATES, PHOSPHATES, SILICATES, BORATES and SULFATES. 

Oxidative addition of other group 14 atom-tellurium bonds (Si-Te, Ge-Te, and Sn-Te) is also achieved (Eq. 3.47) [172]. Reactions of zero-valent platinum complex R(PEt3)3 with RTeMMcs (M = Se, Ge, Sn) at 25°C result in the formation of the tra 5 -Pt(TeR)(MMe2)(PEt3)2 within 10 min. 

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