The TG and DTA curves and diffractograms of powdered CeO2 samples irradiated with a CO2 laser beam with powers of 0.41–1.39 kW/cm2 are presented. The laser treatment induced structural changes and probably generation of a metastable phase. X-ray diffraction coupled with thermal analysis was used to establish the structural modifications in the irradiated samples after heating. 相似文献
The kinetics of the desilylation of the triorganosilyl derivatives of some biologically active heterocyclic bases and uridine were investigated by1H NMR spectroscopy. A correlation was established between the relative rates of desilylation and the steric environment of the silicon atom. In trials on locomotor activity and muscular tone, the effect on memory processes, and the Porsolt test it was found that tris(tert-butylmethylsilyl)barbituric acid has higher sedative activity than barbituric acid. In contrast to uridine, 5-O-tert-butyldimethylsilyluridine exhibits antitumor activity, suppressing the development of fibrosarcoma in human lungs (HT-1080) and fibroblasts in mice.For communication 4, see [1].Latvian Institute of Organic Synthesis, Riga, Latvia. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1253–1258, September, 1998. 相似文献
The N-(2-hydroxyethyl)-1, 2, 3, 4-tetrahydroquinoline, -isoquinoline, and -silaisoquinoline, and their trimethyland triethylsilyl derivatives and the corresponding methiodides were synthesized. The acute toxicity and psychotropic activity of the compounds synthesized were studied.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 793–799, June, 1996. Original article submitted April 25, 1996. 相似文献
n-Heptane-soluble “di-butylmagnesium” (I) (a commercially available material, prepared by addition of LiBus to MgBunCl, and subsequent addition of ca. 5% MgOct2n) has been found to be a useful starting material for obtaining numerous organic magnesium compounds. This is illustrated by its reaction with a number of protic compounds HA to give in good yields Mg(C5H5)2, Mg(C5H4Me)2, or the new compounds MgA2: IV (A = C5H4SiMe3), V [A = C5H3(SiMe3)2], VII (A = OC6H2Bu2t-2,6-Me-4), and X [A2 = N(SiMe3)C6H4N(SiMe3)-o(OEt2)]. The value of such compounds MgA2 as mild ligand transfer reagents is illustrated by the synthesis of Zr(C5H3X2)Cl3 (X = H or SiMe3). Compound X was isolated from OEt2 solution as the crystalline dimer with two o-(SiMe3)C6H4(SiMe3) ligands bridging two magnesium atoms and a terminal OEt2 ligand completing a distorted tetrahedral environment around each Mg. Some key parameters are: MgNt 1.997(7), MgNb 2.083(8), MgO 2.041(7) Å; OMgNt 112.1(3), OMgNb 119.7(3), and NtMgNb 118.5(3)°. 相似文献
Some cationic five coordinate complexes of formula [Os(CO)(NO)L2A]PF6 (L = tertiary phosphine, A = an acetylene) have been prepared by reaction of the appropriate acetylene with [Os(CO)(NO)L2(acetone)]PF6; the variable temperature 1H NMR spectra of some of these indicate that the coordinated π-acetylene undergoes fluxional behaviour. 相似文献