## Abstrad -The diffusion coefficients of Cu(I), Ag(I) and Au(I) ions in molten KC1 were found to be 2.14 f 0.35, 2.03 f 0.08 and 2.2 x lo-' cma/s respectively by chronopotentiometry with a Pt indicator and Pt reference electrode. R&sum&-Les coefficients de diffusion respectifs des ions Cu(I), A&I
Raman spectra of copper(I), silver(I) and gold(I) cyanides in aqueous solutions of sodium thiosulphate
โ Scribed by Mahmoud A. El-Hinnawi; Lyle Peter; B. Meyer
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 705 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0377-0486
No coin nor oath required. For personal study only.
โฆ Synopsis
Systems of copper(I), silver(1) and gold(1) cyanides dissolved in aqueous solutions of sodium thiosulphate in different molar ratios have been studied by Raman Spectroscopy. CuCN dissolves completely in aqueous thiosulphate solution in a 1:3 CuCN to S,03'ratio, forming only mixed cyanothiosulphate species. No evidence was found for the formation of Cu (CN),-, Cu(CN);-or Cu(CN)2-. The mixed cyano copper complex was isolated as a white solid insoluble in water and most other solvents. The solid probably consists of a polymeric structure with bridging cyanide and thiosulphate. AgCN dissolves completely in aqueous thiosulphate solution in a 1 : I AgCN to S2032ratio, resulting in the formation of Ag(CN)2-and Ag(S20&-species. As the concentration of thiosulphate increases Ag(CN)2(Sz03)3-and Ag(CN)z(S,0,)25-are formed. There is strong evidence for the existence of bridging silver thiosulphate complex in solutions of low SzO;concentration. AuCN dissolves completely in aqueous thiosulphate solution in a 1 :2 AuCN to SZO3'ratio, forming Au(CN)~-, Au(CN) (S2O3)'and Au(S,O,);-.
No evidence was found for the formation of species of higher coordination number on increasing the concentration of S20J2--, which indicates that the linear two-coordinate gold complexes are the most stable.
๐ SIMILAR VOLUMES
Raman spectra of CHJ and CDJ in hexane, including absolute cross sections for CHJ, have been obtained using 266 nm excitation, on resonance with the directly dissociative 3Q0 state. Both isotopic species exhibit long vibrational progressions in the C-I stretch and its combination bands with the meth
## Abstract Full assignments of the ^1^H and ^13^C NMR spectra of spiramycin l in CDCl~3~ and buffered D~2~O were carried out unambiguously using a range of 1D and 2D NMR methods.
Excited-state absorption spectra are reported for the luminescent metal-ligand charge-transfer states of copper(l) complexes wth the hgands 2,9-dimethyl-and 2.9-dlphenyl-l,lO-phenanthroline. Excited-state lifetimes derived from transient absorbance decay, ground-state recovery or lummescence decay