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991.
L. Lozzi M. Passacantando P. Picozzi S. Santucci M. De Crescenzi 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1991,20(1):387-390
The electronic structure of small chromium clusters deposited by evaporation onto clean polycrystalline graphite has been studied by means of Auger, X-ray Photoemission (XPS) and Electron Energy Loss (EELS) spectroscopies. The XPS results show an increase in the binding energy of both core levels and valence band reducing the cluster size. The EELS measurements show a variation of the intensity ratio of L3-to-L2 ionization core edges. We interpret this change as due to different redistribution, within the clusterd-band, of the empty states above the Fermi level. As a consequence the XPS results may also be attributed to sizeable change of the electronic structure of the small clusters. 相似文献
992.
The systematic preparation of partially fluorinated pentafluorosulfur alkanes containing no additional halogens is reported. Thus, the indirect addition of “HF” (via KF/formamide) to SF5CH=CF2, SF5CFCF2, and SF5C(CF3)CF2 produces SF5CH(in2)CF3, SF5CHFCF3, and SF5C(CF3)2H respectively. The monohydryl-pentafluorosulfur-F- alkanes react readily with S2O6F2 to form the corresponding fluorosulfates by oxidative displacement of hydrogen, while the dihydryl derivative undergoes cleavage to produce F-acetyl fluoride. Efforts to convert some of the new materials to the important but unknown pentafluorosulfur “ketone,” SF5C(O)CF3, were unsuccessful. 相似文献
993.
A. Van Baalen C.J. Groenenboom H.J. De Liefde Meijer 《Journal of organometallic chemistry》1974,74(2):245-253
The synthesis and the properties of the complexes Cp2TaCl2, Cp2M(allyl), Cp2M(1-methylallyl) and Cp2M(2-methylallyl) with M Nb, Ta are described. The complex Cp2TaCl2 has one unpaired electron per tantalum atom, while the allyl complexes are diamagnetic. The IR and PMR spectra indicate that the allyl group is π-bonded to the metal. The mass spectra of the complexes are discussed; the thermal stability of the Cp2Nb- and Cp2Ta-(allyl) complexes was investigated by differential thermal analysis. The properties of the niobium and tantalum complexes are compared with those of the corresponding titanium complexes. 相似文献
994.
The quantum yields of thecis trans andtrans cis Hg 6(3P1) photosensitized isomerizations of 1,3-pentadiene at 100 Torr and 22°C are 0.54±0.02 and 0.42±0.02, respectively. The steady state ratio ([trans]/[cis])ss is 1.27±0.05 which is almost identical with the ratio of the quantum yields, (ct)/(tc)=1.29±0.10. Thecistrans isomerization is suggested as a useful actinometer for mercury sensitized reactions.
Hg 6(3P1) 1,3- 100 22°C 0,54±0,02 0,42±0,02, . ([]/[]) 1,27±0,05, ( )/( )=1,29±0,10. , .相似文献
995.
A. Zwijnenburg H.O. Van Oven C.J. Groenenboom H.J. De Liefde Meijer 《Journal of organometallic chemistry》1975,94(1):23-27
(Cyclopentadienyl)(1-methylallyl)(butadiene)titanium, C13H18Ti, has been obtained from the reaction between (C5H5)TiCl3 or (C5H5)TiCl2 and 1-methylallylmagnesium bromide in ether. The brown compound is diamagnetic and thermally stable, but very sensitive to oxygen. The nature of the new compound has been elucidated from its reaction with bromine and by IR, 1H and 13C NMR, and mass spectral analysis. 相似文献
996.
997.
998.
Arie van Der Kaaden Johan Haverkamp Jaap J. Boon Jan W. De Leeuw 《Journal of Analytical and Applied Pyrolysis》1983,5(3):199-220
Inorganic additives, viz. Na2CO3, NaOH, HCl, ZnC2, NaH2PO4, Na2HPO4, NaCl. MgSO4 and sea salt, to the pyrolysis matrix change the pyrolysis-mass spectrum of amylose significantly. Carbonyl compounds, acids and their lactones, furans, pyranones anhydrosugars and aromatic substances are found in different ratios under the various conditions, as determined by pyrolysis-gas chromatography-mass spectrometry (Py-GC-MS).Carbonyl compounds, acids and lactones are released from alkaline and neutral matrices. Furans and anhydrohexoses are particularly formed under neutral and acidic conditions. Pyranones are specific for phosphate matrices. Unsaturated hydrocarbons and aromatic substances arise from strongly alkaline or dehydrating matrices. Degradation pathways are proposed for various compound categories.The results of pyrolysis-mass spectrometry and Py-GC-MS are highly compatible. 相似文献
999.
Summary The addition of appropriate concentrations of an organic amine and an alkylsulphonate to the mobile phase in reversed-phase, ion-pair liquid chromatography can introduce unique selectivity in to the chromatographic system allowing separation of complex mixtures of basic, acidic and neutral compounds. As an example, the methodology for a specific stability-indicating determination of propantheline bromide, a quaternary ammonium anticholinergic agent, on several reversedphase stationary phases, was developed. The retention mechanism was studied and it was concluded that both ion-interaction processes and ion-exchange processes were involved in the separation technique developed with two counterions of opposite charge in the eluent. 相似文献
1000.
The molecular structure of 1,1-dimethyl-3-phenylpyrazolium-5-oxide has been determined by a single crystal x-ray diffraction study. The crystals are monoclinic, space group P21/a, with unit cell dimensions a = 12.630 (5) Å, b = 6.644 (1) Å, c = 12.486 (5) Å, β = 99.17 (2)°. The final R value was 0.049 for 2930 reflections. The bond lengths and angles suggest that a significant contribution to the structure is made by a resonance form in which one of the ring bonds does not exist. No close intermolecular approaches were found. 相似文献