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161.
Weihua Zhang Judah Friese Kurt Ungar 《Journal of Radioanalytical and Nuclear Chemistry》2013,296(1):69-73
In this study, soil samples were collected at Canadian embassy in Tokyo (about 300 km from Fukushima) on 23 March and 23 May of 2011 for purposes of estimating concentrations of radionuclides in fallout, the total fallout inventory, the depth distribution of radionuclide of interest and the elevated ambient gamma dose-rate at this limited location. Some fission products and actinides were analyzed using gamma-ray spectrometry, alpha spectrometry and liquid scintillation counting. The elevated activity concentration levels of 131I, 132I, 134Cs, 137Cs, 136Cs, 132Te, 129mTe, 129Te, 140Ba and 140La were measured by the gamma-ray spectrometer in the first sample collected on 23 March. Two months after the accident, the 134Cs and 137Cs became only detectable nuclides. A mass relaxation depth of 3.0 g/cm2 was determined by the activities on the depth distribution of 137Cs in a soil core. The total fallout inventory was thus calculated as 225 kBq/m2 on March sampling date and 25 kBq/m2 on May sampling date. The ambient gamma dose-rates in the sampling area estimated by the fallout fission products inventory and 137Cs depth distribution ranged from 184 to 38 nGy/h. There was no detectable americium or plutonium in the soil samples by alpha spectrometry. Although 90Sr or 89Sr were detected supposedly as a result of this accident, it was less than the detection limit, which was about 0.4 Bq/kg in the soil samples. 相似文献
162.
Treatment of copper(I) chloride with R2Si(NLiPh)2 (R = Me, Ph) in thf led to the formation of the octanuclear cluster compounds [Cu8{(R2Si(NPh)2}4] [R = Me ( 1 ), Ph ( 2 ).] Compound 1 crystallizes in the tetragonal space group P4/n, with a = 1505.41(5) and c = 1911.32(7) pm. The X‐ray crystal structure determination revealed a cube shaped Cu8 cluster core with μ4 bridging Me2Si(NPh)22– ligands. The copper atoms display an almost linear coordination with Cu–N distances in the range of 191.1(3)–191.4(3) pm. The Cu–Cu distances are 265.7(1)–267.3(1) pm. Compound 2 forms monoclinic crystals, space group P21/n, with a = 1461.87(4), b = 2483.77(6), c = 2725.49(8) pm, β = 100.77(1)°. The cluster core of compound 2 consists formally of two mutually perpendicular arranged trigonal prisms, which share a common square face. Like in the case of compound 1 the square faces of the cluster core are capped by μ4 bridging Ph2Si(NPh)22– ligands. The copper atoms adopt a nearly linear N–Cu–N coordination with Cu–N distances of 190.0(4)–195.1(4) pm. The Cu–Cu distances are 252.3(1)–305.6(1) pm. 相似文献
163.
Soraia Meghdadi Mehdi Amirnasr Maryam Bagheri Fatemeh Ahmadi Najafabadi Kurt Mereiter Kurt Joß Schenk Fahimeh Ziaee 《Journal of the Iranian Chemical Society》2014,11(4):985-991
Nickel(II) and copper(II) complexes of two unsymmetrical tetradentate Schiff base ligands [Ni(Me-salabza)] (1), [Cu(Me-salabza)] (2) and [Ni(salabza)] (3), {H2salabza = N,N′-bis[(salicylidene)-2-aminobenzylamine] and H2Me-salabza = N,N′-bis[(methylsalicylidene)-2-aminobenzylamine]}, have been synthesized and characterized by elemental analysis and spectroscopic methods. The crystal structures of 2 and 3 complexes have been determined by single crystal X-ray diffraction. Both copper(II) and nickel(II) ions adopt a distorted square planar geometry in [Cu(Me-salabza)] and [Ni(salabza)] complexes. The cyclic voltammetric studies of these complexes in dichloromethane indicate the electronic effects of the methyl groups on redox potential. 相似文献
164.
Kurt F. Hoffmann Dr. Anja Wiesner Dr. Simon Steinhauer Prof. Dr. Sebastian Riedel 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(57):e202201958
Preparation and characterization of the dimeric Lewis superacid [Al(OTeF5)3]2 and various solvent adducts is presented. The latter range from thermally stable adducts to highly reactive, weakly bound species. DFT calculations on the ligand affinity of these Lewis acids were performed in order to rank their remaining Lewis acidity. An experimental proof of the Lewis acidity is provided by the reaction of solvent-adducts of Al(OTeF5)3 with [PPh4][SbF6] and OPEt3, respectively. Furthermore, their reactivity towards chloride and pentafluoroorthotellurate salts as well as (CH3)3SiCl and (CH3)3SiF is shown. This includes the formation of the dianion [Al(OTeF5)5]2−. 相似文献
165.
Subhi A. Al-Jibori Rawaa A. Q. Al-Nassiry Ghassan H. H. Al-Jibori Kurt Merzweiler Christoph Wagner Harry Schmidt Sucharita Basak-Modi Graeme Hogarth 《Transition Metal Chemistry》2014,39(7):735-740
Reaction of Na2[PdCl4] with two equivalents of amino- or acetylamino-pyridines (LH) affords trans-[PdCl2-(LH)2] {LH = 2-amino-3-methylpyridine (2-ampyH), 3-aminopyridine (3-apyH), 2-acetylamino-3-methylpyridine (2-acmpyH), 3-acetylamino-pyridine (3-acpyH)}. An X-ray crystal structure of trans-[PdCl2(2-ampyH)2] shows that the 2-ampy-H ligands are coordinated in a monodentate fashion via the nitrogen atoms of the pyridine rings. Treatment of trans-[PdCl2(2-acmpyH)2] with NEt3 affords the cyclometalated complex, trans-[Pd(κ2-2-acmpy)2], the X-ray structure of which shows that the 2-acmpy ligand is coordinated to palladium in a bidentate fashion via the nitrogen atom of the pyridine ring and oxygen. Reaction of trans-[PdCl2(LH)2] with two equivalents of sodium saccharinate affords the bis(saccharinate) complexes, trans-[Pd(sac)2(LH)2], in which the saccharinate anions are coordinated via the amide nitrogen atom. 相似文献
166.
Six arsenic-containing β-D -ribofuranosides, including the naturally occurring (2′R)-dimethyl[1-O-(2′,3′-dihydroxypropyl)-5-deoxy-β-D -ribofuranos-5-yl]arsine oxide, were prepared in multi-step reactions from D -ribose and tetramethyldiarsine. The synthetic procedure uses the early substitution of the hydroxy group with bromine at C5, subsequent attachment of a chiral three-carbon aglycone at C1, and final delivery of arsenic at C5. The synthesis provides a viable route for the preparation of multigram quantities of the natural product. 相似文献
167.
168.
We perform Monte Carlo simulations of a lattice model for polymer melts, i. e., the bond fluctuation model in three dimensions. By using an energy parameter that prefers relatively long bonds, the model exhibits a glass transition at low temperatures, in close qualitative similarity to experiment. We modify this model by adding an attractive interaction of variable strength. We demonstrate that a small interaction strength has only a very small effect on the static properties of the melt. For a fixed strength of the potential, the chemical potential is measured by a modified particle-insertion method over a large range of temperatures and densities. The osmotic pressure is obtained by thermodynamic integration. In contrast to the original version our extended model exhibits a positive thermal expansion. 相似文献
169.
170.
We present results of computer simulations by the method of Brownian dynamics of polymeric brushes attached to impenetrable planes. For testing both model and method we have used one polymer brush attached to a repulsive plane and compare some results with Monte Carlo results of Lai and Binder on the bond fluctuation model. We have also studied two polymeric brushes attached to two parallel planes at different distances between planes, and investigate the interplay between the interpenetration of the brushes and the configurational properties of the grafted chains. 相似文献