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Phosphorus-antimony bonds

The ylides have been classified on the basis of the heteroalom covalently bonded to the carbanion. Accordingly, they can be differentiated into nitrogen ylide (Scheme 2), sulfur ylide Scheme 3, phosphorus ylide Scheme 4, arsenic ylide Scheme 5, antimony ylide (Scheme 6), bismuth ylide (Scheme 7) and thallium ylide (Scheme 8). [Pg.373]

Phosphorus, arsenic, antimony and bismuth multiply bonded systems with low coordination number — their role as complex ligands. O. J. Scherer, Angew. Chem., Int. Ed. Engl., 1984, 24, 924 (85). [Pg.69]

A mixture of monolauryl phosphate sodium salt and triethylamine in H20 was treated with glycidol at 80°C for 8 h to give 98% lauryl 2,3-dihydro-xypropyl phosphate sodium salt [304]. Dyeing aids for polyester fibers exist of triethanolamine salts of ethoxylated phenol-styrene adduct phosphate esters [294], Fatty ethanolamide phosphate surfactant are obtained from the reaction of fatty alcohols and fatty ethanolamides with phosphorus pentoxide and neutralization of the product [295]. A double bond in the alkyl group of phosphoric acid esters alter the properties of the molecule. Diethylethanolamine salt of oleyl phosphate is effectively used as a dispersant for antimony oxide in a mixture of xylene-type solvent and water. The composition is useful as an additive for preventing functional deterioration of fluid catalytic cracking catalysts for heavy petroleum fractions. When it was allowed to stand at room temperature for 1 month it shows almost no precipitation [241]. [Pg.615]

The magnetic criterion is particularly valuable because it provides a basis for differentiating sharply between essentially ionic and essentially electron-pair bonds Experimental data have as yet been obtained for only a few of the interesting compounds, but these indicate that oxides and fluorides of most metals are ionic. Electron-pair bonds are formed by most of the transition elements with sulfur, selenium, tellurium, phosphorus, arsenic and antimony, as in the sulfide minerals (pyrite, molybdenite, skutterudite, etc.). The halogens other than fluorine form electron-pair bonds with metals of the palladium and platinum groups and sometimes, but not always, with iron-group metals. [Pg.313]

Two modifications are known for polonium. At room temperature a-polonium is stable it has a cubic-primitive structure, every atom having an exact octahedral coordination (Fig. 2.4, p. 7). This is a rather unusual structure, but it also occurs for phosphorus and antimony at high pressures. At 54 °C a-Po is converted to /3-Po. The phase transition involves a compression in the direction of one of the body diagonals of the cubic-primitive unit cell, and the result is a rhombohedral lattice. The bond angles are 98.2°. [Pg.107]

Many of the properties of the group 15 element diheteroferrocences are very similar to ferrocenes and other metallocenes. It seems justified to regard the diheteroferrocenes as perturbed ferrocenes just as we regard the group 15 heterobenzenes as perturbed benzenes. Thus, it is very clear that the elements phosphorus, arsenic, antimony, and bismuth can take part in 7r-bonding in a manner similar to carbon. [Pg.351]

The synthesis of stable complexes with transition metal-phosphorus triple bonds is of fundamental importance and opens a novel chapter of a special field of coordination chemistry. The synthesis of analogous complexes with ligands of the heavier homologues like arsenic has partially been carried out [6], while for antimony and bismuth, the elusive M=Sb and M=Bi systems have now moved within reach. Moreover, the experimental and theoretical... [Pg.20]


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