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Mercury pseudohalides

There is little evidence for the formation of soluble complexes in aqueous solutions of Hg1 halide and pseudohalide systems,12,32 but the mercury(I) halides themselves are well-known substances. X-ray studies on the dimercury(I) dihalides show that all these compounds possess... [Pg.1049]

The interaction of mercury(II) with nonlinear pseudohalide ions N(CN)I, ONC(CN)f and C(CN)3 in MeOH, MeCN, DMSO and Me Ac has been investigated potentiometrically.265... [Pg.1065]

The bromide and iodide, as well as pseudohalides see Pseudohalide) such as the thiocyanate and azide, all have the general formula Hg2X2. Mercury(I) bromide is a white solid that sublimes at 345 °C, while mercury(I) iodide is a yellow solid that sublimes at 140 °C. The crude iodide... [Pg.2588]

Addition of excess iodide to the insoluble Hgl2 results in the formation of soluble mercury iodo complex [Hgl3] , with a trigonal planar structure. The ion is solvated in water and converts to a tetrahedral structure. Further, addition of H leads to tetrahedral [Hg ] ". Reaction of iodide salts with Hg can be used to produce mercury iodo complexes. Other halide and pseudohalides also form [HgXj] and [HgX4] . The tetrahalo anions see Anion) are usually tetrahedral, while the trihalo ions readily add solvent molecules to form distorted tetrahedral or Trigonal Bipyramidal structures. [Pg.2591]

Mercury (II) is known to accelerate Ligand Substitution reactions of complexes of formula ML5X (M = Rh, Cr, Co, Ru L = H2O or NH3 X = bridging halide or pseudohalide), probably by forming an intermediate with a halide bridge between Hg and M. [Pg.2591]

As observed previously for soft donor ligands such as thioethers and phosphines, mercury(II) reacts with selenoethers and telluroethers to form complexes of the general type HgLX2, where X is a halide or pseudohalide. In addition, mercury (II) forms complexes with various Se-donor ligands such as diethylselenocarbamate and selenourea. [Pg.2594]

Stability constant measurements for the aqueous Zn -azide system indicate that four mononuclear complexes of moderate stability are formed, whereas for mercury, maximum coordination of only two azide ligands is observed. Complexation of Cd " in aqueous NOJ-NJ yields the mixed species [Cd(N03)(N3) ] ( = 1-4). Crystallographic structural determinations of A2Zn(Ns)4 (A = K or Cs) have been reported the former exhibits isolated Zn(Ns)4 tetrahedra with linear azide (N—N = 1.18 A). Thermal decomposition of the above compounds yields nitrogen and ZnsN2 as the main products. A new a modification of Zn(Na)2 has been obtained by the use of an ethereal solution of The compounds and ZnLC (M = Zn or Cd X = halide or pseudohalide L =... [Pg.5805]

MERCURY (Hg +) COORDINATION COMPOUNDS 56.Z3.1 Halide and Pseudohalide Ligands... [Pg.5920]

Mercury(n) is also an effective catalyst for pseudohalide leaving groups, for example thiocyanate. In this connection, recently determined equilibrium data for complex formation between cobalt(ra)-thiocyanate complexes and mercury(n) are of relevance. ... [Pg.154]


See other pages where Mercury pseudohalides is mentioned: [Pg.162]    [Pg.162]    [Pg.162]    [Pg.162]    [Pg.214]    [Pg.732]    [Pg.932]    [Pg.934]    [Pg.982]    [Pg.1084]    [Pg.3]    [Pg.1086]    [Pg.1101]    [Pg.214]    [Pg.440]    [Pg.208]    [Pg.2590]    [Pg.2591]    [Pg.1507]    [Pg.212]    [Pg.75]    [Pg.109]    [Pg.91]    [Pg.2589]    [Pg.2590]    [Pg.17]    [Pg.53]    [Pg.212]    [Pg.649]    [Pg.1732]    [Pg.1747]    [Pg.5855]    [Pg.5957]    [Pg.6050]    [Pg.437]    [Pg.164]   
See also in sourсe #XX -- [ Pg.1049 ]

See also in sourсe #XX -- [ Pg.5 , Pg.1049 ]




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Pseudohalide

Pseudohalides

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