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A Comprehensive Treatise on Inorganic and Theoretical Chemistry

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298 INORGANIC AND THEORETICAL, CHEMISTRY<br />

nitrate. W. Peters showed that anhydrous platinic chloride takes up 6 mols. of<br />

dry amm<strong>on</strong>ia, <strong>and</strong> that the resulting hexammine in vacuo loses a mol. of amm<strong>on</strong>ia.<br />

R. Silberberger found that the presence of platinum salts in dil. soln. does not affect<br />

the precipitati<strong>on</strong> of barium sulphate by the additi<strong>on</strong> of barium chloride ; in c<strong>on</strong>e,<br />

soln. some platinic salt may be adsorbed by the precipitated barium sulphate.<br />

H. Vohl, <strong>and</strong> W. Knop observed that in acidic soln. platinum salts give a precipitate<br />

of platinous sulphide when they are treated with a soln. of sodium thiosulphate—<br />

particularly with warm soln. ; <strong>and</strong> P. Schottl<strong>and</strong>er, <strong>and</strong> P. Jochum, that in<br />

amm<strong>on</strong>iacal soln., a complex platinous alkali thiosulphate is formed. M. C. Lea<br />

observed that with an amm<strong>on</strong>iacal soln. of sodium thiosulphate, amm<strong>on</strong>ium<br />

chloroplatinate is first precipitated, <strong>and</strong> then, with heating, the soln. becomes<br />

yellow, then colourless, <strong>and</strong> finally wine-red. C. Langlois observed that trithi<strong>on</strong>ic<br />

acid gives a black precipitate ; M. C. Lea, that tetrathi<strong>on</strong>ic acid forms a wine-red<br />

soln. ; F. Raschig, that sulphaminic acid produces no change in a soln. of hydrochloroplatinic<br />

acid ; <strong>and</strong> J. A. Palmer, that amm<strong>on</strong>ium thiocarb<strong>on</strong>ate in<br />

amm<strong>on</strong>iacal soln. al<strong>on</strong>g with amm<strong>on</strong>ium chloride, gives a precipitate soluble in<br />

excess. H. Rose, M. Delepine, <strong>and</strong> G. <strong>and</strong> W. van Dam noted that with amm<strong>on</strong>ia<br />

a precipitate of amm<strong>on</strong>ium chloroplatinate is formed in soln. of platinic chloride,<br />

<strong>and</strong> that the precipitate is soluble in excess when heated ; the precipitate is attacked<br />

by chlorine ; 3Cl2+ (NH4)2PtCJ6 ^PtCl4+8HCl+N2. H. St. C. Deville <strong>and</strong><br />

J. S. Stas, S. M. Jorgensen, <strong>and</strong> S. A. Nort<strong>on</strong> observed that amm<strong>on</strong>ium chloride<br />

slowly forms a precipitate with the aq. soln. at ordinary temp, or when heated.<br />

T. Curtius <strong>and</strong> II. Schulz represented the reacti<strong>on</strong> with hydrazine : 2PtCl4<br />

+N2H4.H20===2PtCl2+4HCl+N2+H20. E. Knoevenagel <strong>and</strong> E. Ebler found<br />

that hydrazine gives a precipitate in an amm<strong>on</strong>iacal or feebly acidic soln. <strong>and</strong><br />

hydroxylamine gives an incomplete precipitati<strong>on</strong> in amm<strong>on</strong>iacal soln. N. Tarugi<br />

studied the reacti<strong>on</strong> with hydroxylamine ; <strong>and</strong> F. Reitzenstein observed that<br />

hydroxylamine gives no precipitate with a cyanide soln. H. Rose found that<br />

potassium nitrite precipitates potassium chloroplatinate from soln. of platinic<br />

chloride, <strong>and</strong> that boiling the soln. produces no further change. H. Precht,<br />

H. D. Rogers <strong>and</strong> M. H. Boye observed that a soln. of platinum in aqua regia<br />

c<strong>on</strong>taining an excess of nitric acid furnishes platinic tetrachlorobisdinitrosylchloride,<br />

[Pt(NOCl)2Cl4]—R. Weber recommended fuming nitric acid, <strong>and</strong> gave<br />

the formula PtCl4.N2O3Cl2.H2O. S. M. Jorgensen obtained it by passing the<br />

vapours from aqua regia into a c<strong>on</strong>e. soln. of hydrochloroplatinic acid, <strong>and</strong> drying<br />

the crystals at 100° ; <strong>and</strong> J. J. Sudborough, by the acti<strong>on</strong> of nitrosyl chloride <strong>on</strong><br />

platinum at 100°. S. M. Jorgensen said that the yellowish-brown crystalline powder<br />

c<strong>on</strong>tains cubic forms. No water is lost at 100°, but str<strong>on</strong>ger heating decomposes<br />

the salt leaving platinum behind. The crystals are very deliquescent, <strong>and</strong> freely<br />

soluble in "water. The salt decomposes in aq. soln. E. Baudrim<strong>on</strong>t prepared a<br />

complex with phosphorus pentachloride, namely, platinic tetrachlorodiphosphorichloride,<br />

[Pt(PCl5)2C14]. R. Bottger observed that phosphorus, at ordinary temp.,<br />

does not decompose soln. of platinum salts, but A. C. Christomanos observed that<br />

a soln. of phosphorus in ether or benzene gives a precipitate with soln. of platinic<br />

chloride. R. Bottger observed that phosphine does not give a precipitate with<br />

soln. of platinic salt ; <strong>on</strong> the c<strong>on</strong>trary, P. Kulisch found that with platinic chloride<br />

soln., phosphine gives a lem<strong>on</strong>-yellow precipitate which so<strong>on</strong> becomes darker,<br />

<strong>and</strong> finally, dark brown. R. Engel said that some platinous hypophosphite is<br />

formed. G. Oddo found that anhydrous platinic chloride is soluble in phosphoryl<br />

chloride. L. Vanino, A. Gutbier, <strong>and</strong> A. Gutbier <strong>and</strong> G. Hofmeier observed that<br />

hypophosphorus acid does not precipitate platinum. M. C. Lea, <strong>and</strong> A. Atterberg<br />

said that with hypophosphites platinic chloride is reduced to platinous chloride<br />

<strong>and</strong>, added A. Sieverts <strong>and</strong> M. Major, the metal is not formed in hot or cold or in<br />

acidified soln. but with very dil. -soln. of potassium chloroplatinite, <strong>and</strong> a large<br />

excess (1 : 120) of a warm soln. of sodium hypophosphite. A. Sieverts <strong>and</strong> E. Peters<br />

observed that a yellowish-brown colloidal soln. of platinum is formed. A. Rosen-

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