Absorption spectra arising from the interaction between aromatic hydrocarbons and aliphatic amines

Absorption spectra arising from the interaction between various aromatic hydrocarbons and aliphatic amines have been newly observed in the ultraviolet region by the technique of adsorption, and interpreted as being due to transitions to the charge-transfer Franck-Condon states which may correspond electronically to the fluorescent charge-transfer states observed recently in solutions. No charge-transfer fluorescence was observed in the present system. The formation of the fluorescent charge-transfer states seems to be prevented because of the rigid spatial configurations between adsorbed molecules.     

Kristallstrukturbestimmung von NaHC2O4 · H2O

NaHC₂O₄ · H₂O crystallizes in space group P 1 with a₀ = 6,51, b₀ = 6,66, c₀ = 5,70 Å, α₀ = 95,0°, β₀ = 109,8°, γ₀ = 74,9° and Z = 2. The structure was solved by direct methods. The refinement was carried out with 679 reflections to R₁ = 7,7%. The angle between the O? C? O planes is 12,6°.     

Reaction of perfluoroisobutylene with potassium thiocyanate

Conclusions The authors obtained perfluoroisobutenyl isothiocyanate by reacting perfluoroisobutylene with potassium thiocyanate, and studied some of its properties.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1176–1178, May, 1969.     

Die Auswertung von γ-Spektren mit Programmen

Modern activation analysis requires the application of efficient data processing for the evaluation of theγ-spectra of samples containing several radionuclides, especially if preceding radiochemical separations are to be largely or completely eliminated. The essential aspects of two programs for quantitative determinations and qualitative identifications are described. These programs are based on the least squares analysis of the total spectrum and the search, arrangement and processing of the photopeaks. With respect to their details the programs are adapted for application on the computer IBM-360/75.     

Radiation Effects on Concentrated Potassium Hexacyanoferrate(III) Solutions

The neutron irradiated potassium hexacyanoferrate(III) solutions were analyzed for Fe(CN)₆^4?, Fe(CN)₆^3?, and Prussian blue. The retention values (1.1%) were constant throughout the pH and concentration ranges studied, and did not change with the length of irradiation. The complex behavior of the radiochemical yield of the Fe(CN)₆^4? and Prussian blue was attributed to the competition of the various reactions involved in the irradiation.     

Massenspektrometrie isomerer Diazaphenanthrene—I

The mass spectra of five diazaphenanthrenes formed by photochemical cyclodehydrogenation of styryl diazines are investigated. It is shown that fragmentation of these compounds starts almost exclusively at the heterocyclic part of the molecule and proceeds by competitive α-cleavage. From the intensity ratios of the ions [M ? H˙]⁺, [M ? HCN]⁺˙, [M ? N₂]⁺˙ and [M ? 2 HCN]⁺˙ generated in this way, each isomer can unequivocally be identified.     

Die Kristallstruktur von Li2SnO3

Li₂SnO₃ crystallises monoclinic, C, with a = 5.295, b = 9.184, c = 10.032 Å and β = 100.13°; Z = 8. The positions of Sn were obtained from PATTERSON maps and the positions of O and Li by FOURIER difference method. Parameters were refined by least squares-method [1462 reflexes (h 01)–(h 71); R = 10.5%]. The average distances of Li? O are 2.07 Å, and 2.20 Å for Sn? O. The Li₂SnO₃ structure can be derived from the NaCl type: in a cubic closest packing of oxygen 2/3 of the octahedral holes are occupied by lithium and 1/3 by tin.