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A Comprehensive Treatise on Inorganic and Theoretical Chemistry

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284 INORGANIC AND THEORETICAL, CHEMISTRY<br />

platinite. The four-sided, prismatic crystals deliquesce in air, they melt at 100°<br />

slowly giving off 9£ mols. of water. L. F. Nils<strong>on</strong> could not prepare indium chloroplatinite.<br />

L. F. Nils<strong>on</strong> prepared thallous chloroplatinite, Tl2PtCl4, by mixing<br />

warm soln. of thallous sulphate <strong>and</strong> an alkali or amm<strong>on</strong>ium chloroplatinite. The<br />

salt is recrystallized from boiling water, <strong>and</strong> dried at 100°. The salt is sparingly<br />

soluble in boiling water. S. Meyer found the magnetic susceptibility at 20° to be<br />

—0-205 X 10~« mass unit.<br />

IJ. F. Nils<strong>on</strong> prepared cerous chloroplatinite, CeCl3.2PtCl2.10*5H2O, in thin,<br />

four-sided prisms which lose 15 mols. of water at 100° ; lanthanum chloroplatinite,<br />

2L.aCl3.3Pt012.18H2O, in thin, four-sided prisms, <strong>and</strong> also 2L.aCl3.3PtCl2.27H20,<br />

in prisms which lose 16 mols. of water at 100° ; didymium chloroplatinite,<br />

2.DiCl3.4PtCl2.2H2O, in prisms or plates which are deliquescent in air, <strong>and</strong><br />

2DiCI3.3PtCl2.18H20, in prismatic crystals ; erbium chloroplatinite, 2ErCl3.<br />

2PtCl2.27H2O, in dark red prisms, which lose 17 mols. of water at 100°, <strong>and</strong><br />

2ErCl3.3PtCIo.24H2O, in l<strong>on</strong>g, four-sided prisms, which lose 11 mols. of water at<br />

100°; yttrium chloroplatinite, 2YCl3.3PtCl2.24H20, in dark red, four-sided<br />

prisms, which melt at 100°, losing 10 mols. of water ; thorium chloroplatinite,<br />

2ThCl4.3PtCl2.24H2O, in rhombohedral crystals, which lose <strong>on</strong>e-fourth of their<br />

water of hydrati<strong>on</strong> at 100° without melting ; <strong>and</strong> zirc<strong>on</strong>yl chloroplatinite,<br />

ZrOCl2.PtCl2.8H2O, in quadratic prisms.<br />

R. J. Kane obtained greenish-brown, deliquescent crystals of stannous chloroplatinite,<br />

which are decomposed by water, <strong>and</strong> also a chloroplatinite with more<br />

tin. This salt forms a red soln. in water, <strong>and</strong> the salt is hydrolyzed. Gr. B. Buckt<strong>on</strong><br />

treated platinous tetramminochloride with an acid soln. of stannous chloride <strong>and</strong><br />

obtained stannous tetramminochloroplatinite, fPt(NH3)4]SnCl4, <strong>and</strong> likewise<br />

stannic tetramminochloroplatinite, LPt(NH3)4]SnCl6. C. Rudelius obtained a<br />

complex with propyl sulphide. J. Lang treated a soln. of lead nitrate or acetate<br />

with potassium chloroplatinite <strong>and</strong> obtained lead chloroplatinite, PbPtCl4, as<br />

a pale red, amorphous precipitate, which is decomposed slowly by boiling water.<br />

G. 13. Buckt<strong>on</strong> mixed soln. of platinous chloroplatinite <strong>and</strong> lead acetate, <strong>and</strong><br />

obtained four-sided plates of lead tetramminochloroplatinite, [Pb(NH3)4 JPtCl4,<br />

which are not decomposed at 170° ; <strong>and</strong> are insoluble in hydrochloric acid, <strong>and</strong> in<br />

alcohol.<br />

L. F. Nils<strong>on</strong> obtained chromic chloroplatinite, 2CrCl3.3PtCl2.18H20, by<br />

evaporating in vacuo the filtrate from a mixture of soln. of equimolar parts of<br />

violet chromic sulphate <strong>and</strong> barium chloroplatinite. The red deliquescent<br />

prisms lose water <strong>and</strong> hydrogen chloride at 100°. S. M. Jorgensen prepared<br />

chromic hydroxychlorohexamminochloroplatinite, [Cr2(NH3)0(OH)2Cl3 J2PtCl4.<br />

L. F. Nils<strong>on</strong> also obtained manganese chloroplatinite, MnPtCl4.6H2O, from<br />

barium chloroplatinite <strong>and</strong> manganese sulphate. The crystals lose 4 mols. of<br />

water at 100°. The crystals were examined by H. Topsoe <strong>and</strong> H. Christiansen.<br />

L. F. Nils<strong>on</strong> obtained ferrous chloroplatinite, FePtCl4.7H20, from the filtrate<br />

from a mixture of soln. of ferrous sulphate <strong>and</strong> barium chloroplatinite. The<br />

deliquescent, dark red prisms lose 5 mols. of water at 100°. According to<br />

G. B. Buckt<strong>on</strong>, ferrous salts do not unite with platinous tetramminochloride, <strong>and</strong><br />

ferric chloride transforms it into platinic dichlorotetramminochloride.<br />

Li. F. Nils<strong>on</strong> obtained cobalt chloroplatinite, CoPtCl4.6H2O, by evaporating,<br />

over sulphuric acid, a soln. of hydrochloroplatinous acid saturated with cobalt<br />

chloride. Crystals of cobalt chloroplatinate are first deposited, <strong>and</strong>" then crystals<br />

of the chloroplatinite in four-sided or six-sided plates which are deliquescent in<br />

moist air, <strong>and</strong> efflorescent in dry air. The salt loses 5 mols. of water at 100°.<br />

N. S. Kurnakoff prepared cobalt hexammitiochloroplatinite, [Co(NH3)6]PtCl4,<br />

in yellowish-red plates ; <strong>and</strong> also platinous tetramimnochlorocobaltite,<br />

[Pt(NH3)4]CoCl4, from a mixture of soln. of platinous tetramminochloride<br />

<strong>and</strong> cobalt chloride. The complexes cobaltous quaterpyridinochloroplatinite,<br />

Co Py4PtCl4, <strong>and</strong> cobaltous trisethylenediaminochloroplatinite, Co en2PtCl4, were

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