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The intermolecular Pauson-Khand reaction between norbornene and dicobalt carbonyl complexes of phenylacetylene substituted with chiral phosphorus ligands has been investigated. High yields (?98%) and enantiomeric excesses of up to 56% have been observed. 相似文献
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A. Muntasar D. Le Roux G. Denes 《Journal of Radioanalytical and Nuclear Chemistry》1995,190(2):431-437
In divalent tin halides, when the halogen is small and highly electronegative (F, Cl), the tin valence orbitals are hybridized, the tin(II) non-bonded electron pair is located on one of the hybrid orbitals, and the resulting large electric field gradient gives a large quadrupole splitting. The reaction of barium chloride and tin difluoride in aqueous solutions, for large BaCl2.2H2O/SnF2 ratios (>10) results in the precipitation of a white powdered material, which is identified by X-ray diffraction to be BaCIF. However, Tin-119 Mossbauer spectroscopy shows the material contains a fairly large amount of divalent tin in the Sn2+ ionic form, with unhybridized orbitals, like in SnCl2. Using X-ray diffraction, we have established that Sn2+ ions substitute 15% of the Ba2+ ions at random, and chemical analysis shows the material has the formula Ba5.66SnCl7.30F6.04 and thus is enriched in chlorine. 相似文献
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Alem N Yazyev OV Kisielowski C Denes P Dahmen U Hartel P Haider M Bischoff M Jiang B Louie SG Zettl A 《Physical review letters》2011,106(12):126102
Crystalline systems often lower their energy by atom displacements from regular high-symmetry lattice sites. We demonstrate that such symmetry lowering distortions can be visualized by ultrahigh resolution transmission electron microscopy even at single point defects. Experimental investigation of structural distortions at the monovacancy defects in suspended bilayers of hexagonal boron nitride (h-BN) accompanied by first-principles calculations reveals a characteristic charge-induced pm symmetry configuration of boron vacancies. This symmetry breaking is caused by interlayer bond reconstruction across the bilayer h-BN at the negatively charged boron vacancy defects and results in local membrane bending at the defect site. This study confirms that boron vacancies are dominantly present in the h-BN membrane. 相似文献
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The rate of oxidation of SnF2 in aqueous solutions has been studied by redox titrations and Mössbauer spectroscopy on frozen solutions versus the acidity of the solutions and versus time. Tin(II) oxidizes in aqueous solutions; however, the rate of oxidation is much slower than previously reported. Redox titrations show that the amount of tetravalent tin increases continuously with time. Oxygen dissolved in water seems to be the oxidizing species. The oxidation rate is faster in acidic solutions. Mössbauer spectroscopy on frozen solutions shows the slow formation of tetravalent tin; it also indicates that divalent tin in aqueous solutions is similar to that observed in solid SnF2, except that one water molecule coordinates tin. 相似文献
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Chlorides, nitrates and sulfates of M (M=Mn, Fe, Co, Ni and Zn) were dissolved in aqueous solutions of SnF2 at M/Sn molar ratios of 0.5 to 3. No HF was used. The solutions were allowed to evaporate in air. Very small amounts of hexagonally shaped crystals of unknown materials were obtained for M=Mn, Co, Ni and Zn. Fe did not yield this phase. X-ray powder diffraction gives identical patterns for the four materials, which are therefore most likely isostructural, and showed that the products are not MSn2F6·6H2O or MSnF6·6H2O. Tin-119 Mössbauer spectroscopy gives a single line at negative isomer shift, characteristic of [Sn(IV)F6]2– ions. 相似文献
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Nonlinear Dynamics - Multistability is an area of interest in robotics and locomotion because the ability to achieve multiple configurations or generate multiple gaits allows a single robotic or... 相似文献
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G. Denes 《Fresenius' Journal of Analytical Chemistry》1927,71(7):247
Ohne Zusammenfassung 相似文献
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Stability of self-assembled monolayers on titanium and gold 总被引:1,自引:0,他引:1
Mani G Johnson DM Marton D Dougherty VL Feldman MD Patel D Ayon AA Agrawal CM 《Langmuir : the ACS journal of surfaces and colloids》2008,24(13):6774-6784
Methyl- and hydroxyl-terminated phosphonic acid self-assembled monolayers (SAMs) were coated on Ti from aqueous solution. Dodecyl phosphate and dodecyltrichlorosilane SAMs were also coated on Ti using solution-phase deposition. The stability of SAMs on Ti was investigated in Tris-buffered saline (TBS) at 37 degrees C using X-ray photoelectron spectroscopy, contact angle goniometry, and atomic force microscopy. For comparison purposes, a hydroxyl-terminated thiol SAM was coated on Au, and its stability was also investigated under similar conditions. In TBS, a significant proportion of phosphonic acid or phosphate molecules were desorbed from the Ti surface within 1 day, while the trichlorosilane SAM on Ti or thiol SAM on Au was stable for up to 7 days under similar conditions. The stability of hydroxyl-terminated phosphonic acid SAM coated Ti and thiol SAM coated Au was investigated in ambient air and ultraviolet (UV) light. In ambient air, the phosphonic acid SAM on Ti was stable for up to 14 days, while the thiol SAM on Au was not stable for 1 day. Under UV-radiation exposure, the alkyl chains of the phosphonic acid SAM were decomposed, leaving only the phosphonate groups on the Ti surface after 12 h. Under similar conditions, decomposition of alkyl chains of the thiol SAM was observed on the Au surface accompanied by oxidation of thiolates. 相似文献