The Stereochemistry of Complex Inorganic Compounds. XVIII. A New Method for the Preparation of Inorganic Complexes in their Optically Active Forms1

1955 ◽  
Vol 77 (21) ◽  
pp. 5480-5482 ◽  
Author(s):  
Basudeb Das Sarma ◽  
John C. Bailar
1978 ◽  
Vol 19 (39) ◽  
pp. 3741-3742 ◽  
Author(s):  
Toru Koizumi ◽  
Hiroko Amitani ◽  
Eiichi Yoshii
Keyword(s):  

1961 ◽  
Vol 39 (11) ◽  
pp. 2360-2370 ◽  
Author(s):  
Marvin J. Albinak ◽  
Dinesh C. Bhatnagar ◽  
Stanley Kirschner ◽  
Anthony J. Sonnessa

Considerable interest in the optical rotatory dispersion of asymmetric organic and inorganic compounds and its application to the elucidation of their structures has arisen in recent years. In order to study the effects of optically inactive ions on the rotatory dispersion of asymmetric complex ions, a series of salts was prepared of two active cations: levo cis-oxalato-bis(ethylenediamine)cobalt(III) and levo tris(ethylenediamine)chromium(III). Salts prepared included the fluoride, chloride, bromide, iodide, tetrafluoroborate, perchlorate, sulphate, and phosphate. In order to study this effect on an optically active anion, the lithium, sodium, potassium, rubidium, cesium, magnesium, calcium, and barium salts of dextro and levo tris(oxalato)rhodate(III) were also prepared. Rotatory dispersion curves and absorption spectra were obtained for all salts in water solution. A comparison of the curves within a series showed definite trends in changes of wavelength and intensity of maxima of rotation and absorption with changes in both the ionic charge/size ratio (ionic potential) and polarizability of the optically inactive ions.


1969 ◽  
Vol 47 (21) ◽  
pp. 4073-4076 ◽  
Author(s):  
K. G. Rutherford ◽  
J. L. H. Batiste ◽  
J. M. Prokipcak

A new method for the resolution of potentially optically active trityl alcohols is reported. Three trityl alcohols as pilot compounds were converted to hydracrylic acid derivatives. Esterification with diazo-methane was followed by degradation (reverse Michael reaction) to the original alcohols with sodium hydride. The resolution of phenyl-α-naphthyl-p-tolylcarbinol was effected conveniently by this route.


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