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81.
82.
Fernandez E Ford WT Qi N Read AL Smith JG Camporesi T De Sangro R Marini A Peruzzi I Piccolo M Ronga F Blume HT Hurst RB Venuti JP Wald HB Weinstein R Band HR Gettner MW Goderre GP Meyer OA Moromisato JH Shambroom WD Sleeman JC von Goeler E Ash WW Chadwick GB Clearwater SH Coombes RW Kaye HS Lau KH Leedy RE Lynch HL Messner RL Moss LJ Muller F Nelson HN Ritson DM Rosenberg LJ Wiser DE Zdarko RW Groom DE Lee H Delfino MC Heltsley BK Johnson JR Lavine TL Maruyama T Prepost R 《Physical review letters》1985,54(15):1620-1623
83.
A. Bähring E. Meyer I. V. Hertel H. Schmidt 《Zeitschrift für Physik A Hadrons and Nuclei》1985,320(1):141-149
Pronounced polarization effects have been observed in inelastic collisions of laser state-prepared Na*(3p,M L) with Na+ leading to Na*(3d) for the energy rangeE CM=20–45 eV. Using linearly polarized light the dependence of the inelastic process on the alignment of the electronic charge cloud of the Na*(3p) prior to the collision has been measured. In studies with left and right hand circularly polarized light the angular momentum transferred in the collision process has been determined. The results are compared with similar data for the 3p→3s deexitation process studied previously [6]. The density matrix of the Na*(3p) state has been evaluated with respect to the collisional excitation to Na*(3d). Semiclassical calculations based on the coupled channel impact parameter approximation using pseudopotentials [7] and nonadiabatic rotational coupling elements for the Na 2 * system [12] have been performed. The agreement with the experimental results is good, in particular for the higher collision energies. 相似文献
84.
85.
Colourless single crystals of [Hg(OH)](NO3)(H2O) were obtained by slow evaporation of an aqueous solution of Hg(NO3)2 and Bi(NO3)3. The crystal structure (orthorhombic, Pbca, Z = 8, a = 943.2(2), b = 697.6(1), c = 1349.0(2) pm, R1(all) = 0.0780) contains [Hg(OH)] = …OH–Hg–OH–Hg… zig zag chains (O–Hg–O angle: 168°, Hg–O–Hg angle: 112°, Hg–OH distance: 212 pm) to which one water molecule is attached loosely. The [Hg(OH)](H2O) chains are connected via bis‐monodentate‐bridging nitrate ions to corrugated layers that are stacked in the [001] direction. Hg2+ has an effective 2+2+2(+1) coordination. 相似文献
86.
87.
Non-racemic, planar chiral 1, 2-disubstituted [Cr(η6-arene)(CO)3] complexes were obtained via external chiral ligand-controlled nucleophilic addition of alkyl-, vinyl-, and aryllithium reagents to monosubstituted complexes followed by an endo-hydride abstraction with trityl cation. The reactions with [Cr(CO)3(η6-phenyloxazoline)], [Cr(CO)3(η6-phenylmethaneimine)], and [Cr(CO)3 (η6-phenylmethanenydrazone)] took place with complete ortho-selectivity and a high degree of enantioselectivity (up to 98% ee). 相似文献
88.
The alkali phosphides of 1.2-bis-phosphinobenzene, and 1-alkyl-derivatives react with (Me2N)2COEt+BF4? to give the title compounds with dicoordinated phosphorus. The structure is proved by their nmr spectra. 相似文献
89.
Friedrich Bossert Horst Meyer Egbert Wehinger 《Angewandte Chemie (International ed. in English)》1981,20(9):762-769
The aryldihydropyridines first prepared by Hantzsch almost 100 years ago have recently been found to be highly effective calcium antagonists with suitable pharmacological profiles. An illustrative example is dimethyl-l,4-dihydro-2,6-dimethyl-4-(o-nitrophenyl)pyridine-3,5-dicarboxylate (Nifedipine) which is already employed therapeutically. This substance lowers the frequency of attack of angina pectoris and reduces blood pressure. The discovery of the therapeutic activity of this class of substances initiated renewed investigation of the Hantzsch condensation and the synthesis of numerous 4-aryldihydropyridines and related compounds. Qualitative and quantitative structure/activity relationships of these substances can be deduced from their biological data. 相似文献
90.
Parac-Vogt TN Pacco A Nockemann P Laurent S Muller RN Wickleder M Meyer G Vander Elst L Binnemans K 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,12(1):204-210
Proton nuclear magnetic relaxation dispersion (NMRD) profiles were recorded between 0.24 mT and 1.4 T for lanthanum(III)- and gadolinium(III)-containing [15]metallacrown-5 complexes derived from alpha-aminohydroxamic acids and with copper(II) as the ring metal. The influence of the different R-groups on the proton relaxivity was investigated, and a linear relationship between the relaxivity and the molecular mass of the metallacrown complex was found. The selectivity of the metallacrown complexes was tested by transmetalation experiments with zinc(II) ions. The crystal structure of the copper [15]metallacrown-5 gadolinium complex with glycine hydroximate ligands is reported. 相似文献