The Ternary Systems Ferrous Chloride—Hydrogen Chloride—Water, Ferric Chloride—Ferrous Chloride—Water

1952 ◽  
Vol 74 (18) ◽  
pp. 4689-4691 ◽  
Author(s):  
Fred A. Schimmel
1982 ◽  
Vol 37 (6) ◽  
pp. 702-706 ◽  
Author(s):  
Helmut Entires

Abstract[Ni(C2H5N4O2)2] · HCl · H2O, C4H10N8NiO4 · HCl · H2O, forms triclinic crystals, Mr = 347.36, P1̄, a = 7.219(2), b = 7.316(1), c = 11.797(3) Å, α = 73.89(2), β = 86.37(2), γ = 85.71(2)°, V = 596 Å3 , Z = 2, dc = 1.93 Mgm-3 ; final Rw = 0.028 for 1957 reflections. The planar complex molecules form equidistant stacks along b, with the molecular planes inclined at ~29° to the stacking axis. Molecules of adjacent stacks are linked along a by an intermolecular H bridge coexistins with the usual intramolecular H bridges. The analogous Pt complex, C4H10N8O4Pt · HCl · H2O, Mr = 483.74, a = 6.480(4), b = 16.115(5), c = 12.194(9) Å, β = 101.27(4)°, V = 1249 Å3 , Z = 4, dc = 2.57 Mgm-3 , P21/a, crystallizes in a columnar structure with a Pt-Pt separation of ~a/2 ≈ 3.24 Å. Due to twinning, faking orthorhombic symmetry, a complete structure determination was not possible.


Author(s):  
E. Hirota ◽  
K. Kuchitsu ◽  
T. Steimle ◽  
J. Vogt ◽  
N. Vogt

The polymerizations of acrylonitrile, methacrylonitrile and styrene have been studied in NN -dimethylformamide solution at 60°C in the presence of ferric chloride. In each case the participating radicals enter into a termination reaction with the salt, with reduction of the latter to ferrous chloride. The rate constants of these reactions have been evaluated from kinetic observations; styryl radicals are much more reactive towards ferric chloride than either acrylonitrile or methacrylonitrile radicals. This is the expected order if the reactions are of the electron-transfer type. It is shown that estimation of the ferrous salt produced provides a useful practical method for determining the rate of chain starting. In the case of styrene, the reactivity of the radicals is so great that induction periods are observed, from which the rates of chain starting may also be deduced. A general treatment of retarded reactions under certain simple conditions is given and applied to the styrene polymerization.


2019 ◽  
Vol 15 (4) ◽  
pp. 2535-2547
Author(s):  
Eva Perlt ◽  
Sarah A. Berger ◽  
Anne-Marie Kelterer ◽  
Barbara Kirchner

Sign in / Sign up

Export Citation Format

Share Document