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231.
Leoni S Matsuo M Bracco A Benzoni G Blasi N Camera F Grassi C Million B Paleni A Pignanelli M Vigezzi E Wieland O Døssing T Herskind B Hagemann GB Wilson J Maj A Kmiecik M Lo Bianco G Petrache CM Castoldi M Zucchiati A De Angelis G Napoli D Bednarczyk P Curien D 《Physical review letters》2004,93(2):022501
The gamma decay in the quasicontinuum from selected configurations of the rotational nucleus 163Er has been measured with the EUROBALL array. A new analysis technique has allowed for the first time to directly measure the compound and rotational damping widths Gamma (micro) and Gamma (rot). Values of Gamma (micro) approximately 20 keV and Gamma (rot) approximately 200 keV are obtained in the spin region I approximately 30-40 variant Planck's over 2pi, in good agreement with microscopic cranked shell model calculations. A dependence of Gamma (micro) and Gamma (rot) on the K-quantum number of the nuclear states is also presented. 相似文献
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Methyl hydrodisulfide and methyl deuterodisulfide have been prepared in a four-step synthesis. These compounds have been characterized spectroscopically including microwave spectra. 相似文献
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R. Pucci M. Baldo G. Giansiracusa A. Grassi G. Piccitto 《Solid State Communications》1984,52(12):1025-1027
Extensive many-body calculations of the ground state properties of hydrogen chemisorbed on all 3d, 4d and 5d transition metal surfaces are performed. The trends of the location Ep of the discrete level under the bottom of the d-band are presented. It is found that, on going to the right of the series, Ep approaches the bottom of the d-band, eventually merges in it and detaches again from it for the last elements of the series. 相似文献
238.
Recently the Navier-Stokes equations have been derived from the duality with the black branes in 5AdS. The zero modes of black branes are reinterpreted as dynamical degrees of freedom of a conformal fluid on the boundary of 5AdS. Here, we derive the corrections to the Navier-Stokes equations due to fermionic zero modes of the black branes. We study only the contributions due to bilinears in the fermionic zero modes in the first order of the parameter expansion. The need of a superextension of the fluid dynamics is a consequence of the full AdS/CFT correspondence and yet to be investigated. 相似文献
239.
The coordination behavior and reactivity of the phenol-substituted bis(pyrazolyl)methane ligands, (3,5-(t)Bu(2)-2-phenol)bis(3,5-Me(2)-pyrazol-1-yl)methane (L1-H) and 2-phenol-bis(3,5-Me(2)-pyrazol-1-yl)methane (L2-H) have been investigated in the metal complexes (L1-H)CoCl(2) (1), (L1-H)ZnCl(2) (2), (L3)CuCl(2) (3), (L2)(2)Co(2)Cl(2) (4) (L2-H)ZnCl(2) (5), and (L2-H)CuCl(2)·H(2)O (6). The mononuclear tetrahedral cobalt complex 1 was isolated and fully characterized by X-ray single crystal diffraction and (1)H NMR spectroscopy and relaxometry. The neutral L1-H is κ(2)-coordinated to the metal center whereas the not coordinated hydroxy-phenyl group is involved in extended intermolecular hydrogen bonds. Aerobic oxidation of L1-H was observed in the reaction of this ligand with CuCl(2) to yield the para-quinone derivative L3 (L3 = 2-(t)Bu-6-(bis(3,5-Me(2)-pyrazol-1-yl)methyl)cyclohexa-2,5-diene-1,4-dione). Upon oxidation L3 resulted κ(2)-coordinated to the tetrahedral Cu(II) metal center, affording 3. The reaction of L2-H with CoCl(2)·6H(2)O produced the elimination of 1 equiv of hydrochloric acid and the formation of the binuclear complex 4 in which one cobalt is in an octahedral environment featuring two κ(3)-coordinated deprotonated ligands whereas the second cobalt center is detected in tetrahedral coordination geometry, bound to the octahedral cobalt via two phenoxo bridging moieties. Interestingly L2-H, (3-(t)Bu-2-phenol)bis(3,5-Me(2)-pyrazol-1-yl)methane (L4-H), or (5-(t)Bu-2-phenol)bis(3,5-Me(2)-pyrazol-1-yl)methane (L5-H) were not oxidized in the reaction with CuCl(2). The reaction of the ligand L2-H with ZnCl(2) and CuCl(2)·2H(2)O yielded the κ(2)-coordinated tetrahedral complex 5 and the square planar complex 6, respectively. The application of the cobalt complex 1 as molecular dosimeter for H(2)S was explored and compared to that of the zinc analogue 2. Density functional theory (DFT) calculations and NMR experiments to assess the possible mechanisms of H(2)S detection by both 1 and 2 are also described. 相似文献
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