Synthesis, structural and spectral features of CH-Acids: Amides of 2,4-dinitrophenylcyanoacetic acid and their ammonium salts

New N-methylmorpholinium and triethylammonium salts of 2,4-dinitrophenylcyanoacetic acid were obtained. Their electronic and spatial structure was studied by IR, NMR spectroscopy (including two-dimensional correlation spectra HMQC and HMBC), as well as by XRD analysis.     

The spin-wave resonance spectrum and the structure of cermet Fe - SiO films

The results of electron-microscopic investigation of the structure and spin-wave resonance of thin ferromagnetic Fe_100-x(SiO)_x films are presented in the paper. The correlation radii of fluctuations of the exchange interaction parameter are determined from the analysis of the experimental results of spin-wave resonance. These radii are compared with characteristic sizes of the structural clusters in the films.     

Structure and conformational flexibility of hexamethyldiperoxacyclononane

3,3,6,6,9,9-Hexamethyl-1,2,4,5-tetraoxacyclononane, one of the most thermally stable organic peroxides, has been studied by X-ray structural analysis. Possible conformations of this compound have been calculated by the molecular mechanics method.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 110–112, January, 1995.     

Germanium carboxylates: the first X‐ray diffraction study of germanium(II) dicarboxylate and germanium(IV) tetracarboxylate

Germanium(II) dipropionate (1) has been synthesized and its crystal structure, as well as that of germanium(IV) tetrapropionate (2), has been determined. By contrast to monomeric 2 with monodentate propionate ligands, compound 1 is associated, forming a cyclotetramer [Ge(O₂CEt)₂]₄ (1a) via intermolecular dative C?O → Ge interactions. Copyright © 2005 John Wiley & Sons, Ltd.     

Chemical Modification of Plant Alkaloids. III. X-Ray Diffraction and NMR Studies of the Structure of 1,3-Dimethyl-5-arylmethyl-5-cytisylmethylbarbituric Acids

The three-dimensional structure of 1,3-dimethyl-5-(4-allyloxybenzyl)-5-cytisylmethylbarbituric acid was found by x-ray structure analysis. A conformation with proximal cytisine and 2,4,6-trioxopyrimidine moieties was observed. Analogous structures for other synthesized 1,3-dimethyl-5-arylmethyl-5-cytisylmethylbarbituric acids and their 2-thio analogs were proved and the intramolecular effects caused by mutual magnetic shielding of spatially proximal groups were studied using PMR.