Binary structures silver

Recently, Silver and Bray (52) were able to differentiate and to estimate the relative proportions of three- and four-coordinated borons in binary borate glasses. This technique was thus adopted by the present author in order to ascertain the presence or absence of four-coordinated boron in liquid B203 (35). Glassy samples were quenched in liquid mercury from temperatures up to 1400°C but no four-coordinated boron was detected. (The lower limit of detectability was estimated to be about 2%.) Experiments were also carried out on liquid B203 up to 500°C but again no four-coordinated boron was found. It thus appeared that at least up to 500 or 600°C, the structural variation of liquid B203 with temperature is not primarily the result of a boron coordination change of from three to four. 

The binary system which is easiest to describe is the so-called ideal binary system . As you can tell from the inverted commas, such a system does not really exist, but there are systems which come very close. In an ideal system the components in the S and L phase are completely miscible. In order to be so in the S phase, the substances need to be isomorphous, i.e. possess the same crystal structure. This is often accompanied by an analogous chemical structure. Some examples of these systems are silver (Ag) / gold (Au) and sodium nitrate (NaN03) / calcium carbonate (CaC03). 

A wide range of structural motifs are found for the copper-triad xanthates, ranging from monomeric species to layer structures. This variety of structures can be ascribed to the flexible coordination modes adopted by the xanthate ligands in this group, in particular for the copper and silver xanthates. However, there is a dearth of binary xanthate structures with only two available for copper and one each for silver and gold. The paucity of data can be ascribed directly to the inability to obtain suitable crystals for structure determination. Phosphine adducts are known for all three elements of this group and in the case of both copper and silver, mixed-metal species are also known. 

The structure of the only binary xanthate structure of silver, that is, [Ag(S2COEt)]00, has only just recently become available (130). There is... 

The chemistry of gold is more diversified than that of silver. Six oxidation states, from -I to III and V, occur in its chemistry. Gold(-I) and Auv have no counterparts in the chemistry of silver. Solvated electrons in liquid ammonia can reduce gold to give the Au" ion which is stable in liquid ammonia (E° = -2.15 V). In the series of binary compounds MAu (M = Na, K, Rb, Cs), the metallic character decreases from Na to Cs. CsAu is a semiconductor with the CsCl structure and is best described as an ionic compound, Cs+Au . The electron affinity of gold (—222.7 kJ mol"1) is comparable to that of iodine (-295.3 kJ mol-1). Gold in the oxidation state -I is also found in the oxides (M+ Au O2 (M = Rb, Cs) these, too, have semiconducting properties.1... 

The -Alumina-related Structures.—Originally the compound )3-alumina was taken to be a binary aluminium oxide, but early Y-ray structure determinations and associated chemical analysis showed that the formula was approximately NaAlnOi7. Since then a number of isostructural compounds have been characterized in which sodium is replaced by other monovalent ions, particularly silver, and aluminium by other trivalent ions, notably gallium and iron. In addition, a number of other phases have been prepared which are structurally closely related to )8-alumina. Four principal structures are known, which are labelled / ", and P"". These can also be prepared with other monovalent cations replacing sodium, and some seem only to be formed when a few per cent of divalent cations, particularly magnesium, are present, so that they are, in fact, quaternary phases. The structure and stoicheiometry of these compounds has been summarized recently and we will only consider here those aspects relevant to the present topic. 

Dinuclear complexes were obtained by reacting some binary copper(I) and silver(I) homoleptic pyrazolate complexes with neutral ligands. The trimeric [Cu(dmpz)]3 (23) readily reacted with phen or RNC (R = cyclohexyl) to give the doubly bridged species [(phen)Cu(/i-dmpz)2Cu(phen)], 32, (49) or [(RNC)Cu(/t-dmpz)2Cu(RNC)], 33 (50). The dimeric nature of 32 was argued from its spectroscopic and chemical properties, while 33 was characterized by an X-ray crystal structure analysis (50). 

H.M. Lee, M. Ge, B.R. Sahu, P. Tarakeshwar, and K.S. Kim, Geometrical and electronic structures of gold, silver, and gold-silver binary clusters origins of ductility of gold and gold-silver alloy formation. J. Phys. Chem. B 107, 9994—10005, 2003. 

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