Metal tellurides bonding

More quantitatively, it appears to a first approximation that the unit cell contraction of a compound containing Mn2+, Co2+, Ni2+, or Fe2+, relative to the isomorphous Mg+2 compound, is a linear function of the Ax of the metal-ligand bond if we neglect selenides and tellurides. Inclusion of these more covalent compounds indicates a greater dependence on Ax. 

For example, no less than 12 different formula types are now known for the alkali metal tellurides MxTey [9, 10]. As the total bond order for Te-Te bonds and their opposite secondary Te---Te interactions must remain constant at 1.0, distances di/di will increase in logarithmic dependence on their individual bond order as d3/d4 shorten. Values of d-y/di can range from those of typical single bonds (269-287 pm [10]) to 304 + 9 pm for symmetrical and modestly distorted 3-center 4-electron interactions. 

The easily accessible ethynyl tellurolates were reacted with chloroiodomethane to give ethynyl chloromethyl tellurium, which, in turn, combined with an alkali metal telluride to form (ethynyltelluro)methanetellurolates. These compounds cyclized through intramolecular addition of the tellurolate to the C —C triple bond to 2/7-1,3-ditelluroles3,4... 

Ten /13-TePh ligands adopt an unsymmetrical pattern of one shorter , one longer and one intermediate Cu-Te bonding distances. These distances (2.552(3)-2.708(3) A) are, expectedly, shorter than their Ag-Te counterparts, and reflect the difference between the ionic radii of the two metals.This contraction of the metal-tellurium bonding distances is reflected in the overall size of the cluster frame. Thus, for comparison, the Te4 - Te7 distance is 12.29 A in 5 and 12.95 A in 3a similarly the telluride ligands Tel5-- Tel6 are 7.72 A apart in the copper complex whereas they are separated by 8.81 A in the silver cluster 3a. 

The fourth and final crystal structure type common in binary semiconductors is the rock salt structure, named after NaCl but occurring in many divalent metal oxides, sulfides, selenides, and tellurides. It consists of two atom types forming separate face-centered cubic lattices. The trend from WZ or ZB structures to the rock salt structure takes place as covalent bonds become increasingly ionic [24]. 

Two factors combine to lend a greater diversity in the stereochemistries exhibited by bivalent germanium, tin and lead compounds, the increased radius of Mn compared with that of Mw and the presence of a non-bonding pair of electrons. When the non-bonding pair of electrons occupies the isotropic valence level s orbital, as in, for example, the complex cations Pb[SC(NH2)2]6+ and Pb[antipyrine]6+, or when they are donated to conductance band levels, as in the binary tin and lead selenides or tellurides or the perovskite ternary phases CsMX3 (M = Sn, Pb X = Cl, Br, I), then the metal coordination is regular. However, in the majority of compounds an apparent vacancy in the coordination sphere of the metal is observed, which is usually ascribed to the presence of the non-bonding pair of electrons in a hybrid orbital and cited as evidence for a stereochemically active lone pair . 

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