排序方式: 共有37条查询结果,搜索用时 31 毫秒
1.
D. A. Johnson A. G. Maddock M. Taylor 《Journal of Radioanalytical and Nuclear Chemistry》1987,119(1):43-50
When anhydrous EuCl3, GdCl3, DyCl3 or Eu2O3 are irradiated with fast neutrons and then dissolved in dilute hydrochloric acid, small amounts of reducing species, believed to be divalent lanthanide cations, are revealed. The amount produced increases with the thermodynamic stability of the Ln2+ species /Eu>Dy>Gd>/. 相似文献
2.
A procedure for the simultaneous assay of clebopride and its major metabolite N-desbenzylclebopride in plasma has been developed. The method utilizes capillary gas chromatography-negative-ion chemical ionization mass spectrometry with selected-ion monitoring of characteristic ions. Employing 2-ethoxy analogues as internal standards, the benzamides were extracted from basified plasma using dichloromethane. Subsequent reaction with heptafluorobutyric anhydride produced volatile mono- and diheptafluorobutyryl derivatives of clebopride and N-desbenzylclebopride, respectively. The methane negative-ion mass spectra of these derivatives exhibited intense high-mass ions ideal for specific quantitation of low levels in biological fluids. Using this procedure the recovery of the drug and metabolite from human plasma was found to be 84.4 +/- 1.5% (n = 3) and 77.4 +/- 4.7% (n = 3), respectively, at 0.5 ng/ml. Measurement of both compounds down to 0.10 ng/ml with a coefficient of variation of less than 10.5% is described. Plasma levels are reported in four volunteers up to 24 h following oral administration of 1 mg of clebopride malate salt. 相似文献
3.
E. Ianovici M. Kosinski P. Lerch A. G. Maddock 《Journal of Radioanalytical and Nuclear Chemistry》1981,64(1-2):315-326
The photochemical decomposition of (NH4)2TcCl6 in dilute HCl, HClO4 and H2SO4 solutions has been studied. Electrophoresis and spectrophotometry were used to identify TcCl 6 2? , TcCl5 (H2O)?, cationic and uncharged species and TcO 4 ? . The yield of each species as a function of the time of uv irradiation was determined. The TcCl 6 2? , yield decreases to zero after 50 h of irradiation. The TcCl5(H2O)?, cationic and uncharged species and TcO 4 ? are formed in different proportions in the three acids. After 120 h of irradiation of the HCl solution the principal Tc species was the cationic one (≈70%) followed by the uncharged species (≈24%). In HClO4 solution the cationic species (≈70%) was followed by TcO 4 ? , but in H2SO4 solution the uncharged species amounts to ≈90%. 相似文献
4.
Dr. Marzia Dell'Aera Dr. Filippo Maria Perna Dr. Paola Vitale Dr. Angela Altomare Prof. Alessandro Palmieri Dr. Lewis C. H. Maddock Leonie J. Bole Dr. Alan R. Kennedy Prof. Eva Hevia Prof. Vito Capriati 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(40):8742-8748
We report the first transition metal catalyst- and ligand-free conjugate addition of lithium tetraorganozincates (R4ZnLi2) to nitroolefins. Displaying enhanced nucleophilicity combined with unique chemoselectivity and functional group tolerance, homoleptic aliphatic and aromatic R4ZnLi2 provide access to valuable nitroalkanes in up to 98 % yield under mild conditions (0 °C) and short reaction time (30 min). This is particularly remarkable when employing β-nitroacrylates and β-nitroenones, where despite the presence of other electrophilic groups, selective 1,4 addition to the C=C is preferred. Structural and spectroscopic studies confirmed the formation of tetraorganozincate species in solution, the nature of which has been a long debated issue, and allowed to unveil the key role played by donor additives on the aggregation and structure of these reagents. Thus, while chelating N,N,N’,N’-tetramethylethylenediamine (TMEDA) and (R,R)-N,N,N’,N’-tetramethyl-1,2-diaminocyclohexane (TMCDA) favour the formation of contacted-ion pair zincates, macrocyclic Lewis donor 12-crown-4 triggers an immediate disproportionation process of Et4ZnLi2 into equimolar amounts of solvent-separated Et3ZnLi and EtLi. 相似文献
5.
Dr. Lewis C. H. Maddock Rebekka Morton Dr. Alan R. Kennedy Prof. Dr. Eva Hevia 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(61):15181-15187
Alkali-metal ferrates containing amide groups have emerged as regioselective bases capable of promoting Fe−H exchanges of aromatic substrates. Advancing this area of heterobimetallic chemistry, a new series of sodium ferrates is introduced incorporating the bulky arylsilyl amido ligand N(SiMe3)(Dipp) (Dipp=2,6-iPr2-C6H3). Influenced by the large steric demands imposed by this amide, transamination of [NaFe(HMDS)3] (HMDS=N(SiMe3)2) with an excess of HN(SiMe3)(Dipp) led to the isolation of heteroleptic [Na(HMDS)2Fe{N(SiMe3)Dipp}]∞ ( 1 ) resulting from the exchange of just one HMDS group. An alternative co-complexation approach, combining the homometallic metal amides [NaN(SiMe3)Dipp] and [Fe{N(SiMe3)Dipp}2] induces lateral metallation of one Me arm from the SiMe3 group in the iron amide furnishing tetrameric [NaFe{N(SiCH2Me2)Dipp}{N(SiMe3)Dipp}]4 ( 2 ). Reactivity studies support that this deprotonation is driven by the steric incompatibility of the single metal amides rather than the basic capability of the sodium reagent. Displaying synergistic reactivity, heteroleptic sodium ferrate 1 can selectively promote ferration of pentafluorobenzene using one of its HMDS arms to give heterotrileptic [Na{N(SiMe3)Dipp}(HMDS)Fe(C6F5)]∞ ( 4 ). Attempts to deprotonate less activated pyridine led to the isolation of NaHMDS and heteroleptic Fe(II) amide [(py)Fe{N(SiMe3)Dipp}(HMDS)] ( 5 ), resulting from an alternative redistribution process which is favoured by the Lewis donor ability of this substrate. 相似文献
6.
The electron scavenging properties of aqueous solutions of two series of solutes are investigated, using the positron as a probe. For a better interpretation of the data, both lifetime spectroscopy and the Doppler broadening of annihilation line shape technique are used. All solutes inhibit the positronium (Ps) formation, by the scavenging of electrons. The first series consists of the halate ions, that should follow the Hunt linear relation between the rate constant for reaction with the solvated electrons, k(e?aq+S), and that for its precursor(s), 1/C37. The Ps inhibition constants, k, are 0.14, 1.44 and 3.45 M?1 for ClO?3, BrO?3 and IO?3, respectively. This sequence is quantitatively consistent with that of the respective k(e?eq+S). The second series includes the SeO=4, Te(OH)6 and BrO?4 species, and the Ps inhibition constants are 5.62, 10.5 and 14.3 M?1 respectively. These values are much higher than expected from the k(e?aq+S) constants, on basis of the Hunt relation, in agreement with previous results from pulse radiolysis experimets. 相似文献
7.
Zachary Maddock 《Monatshefte für Mathematik》2010,121(3):167-186
The Takagi function τ(x) is a continuous non-differentiable function on the unit interval defined by Takagi in 1903. This paper studies level sets
L(y) = {x : τ(x) = y} of the Takagi function and bounds their Minkowski dimensions and Hausdorff dimensions above by 0.668. There exist level
sets with Minkowski dimension 1/2. The method of proof involves a multiscale analysis that relies upon the self-similarity
of τ(x) up to affine shifts. 相似文献
8.
Self-injection length in La0.7Ca0.3MnO3-YBa2Cu3O7-δ ferromagnet-superconductor multilayer thin films
We have carried out extensive studies on the self-injection problem in barrierless heterojunctions between La0.7Ca0.3MnO3 (LCMO) and YBa2Cu3O7-δ (YBCO) thin films. The heterojunctions were formed in situ by sequentially growing LCMO and YBCO films on 〈100〉 LaAlO3 (LAO) substrate using a pulsed laser deposition (PLD) system. YBCO micro-bridges with 64 μm width were patterned both on
the LAO (control) and LCMO side of the substrate. Critical current, I
c, was measured at 77 K on both the control side as well as the LCMO side for different YBCO film thickness. It was observed
that while the control side showed a J
c of ∼ 2 × 106 A/cm2, the LCMO side showed about half the value for the same thickness (1800 ?). The difference in J
c indicates that a certain thickness of YBCO has become ‘effectively’ normal due to self-injection. From the measurement of
J
c at two different thicknesses (1800 ? and 1500 ?) of YBCO films both on the LAO as well as the LCMO side, the value of self-injection
length (at 77 K) was estimated to be ∼ 900 ?. To the authors’ best knowledge, this is the first time that self-injection length
has been quantified. A control experiment carried out with LaNiO3 deposited by PLD on YBCO did not show any evidence of self-injection. 相似文献
9.
The inhibition ofpositronium formation and the quenching reactions of positronium in aqueous solutions of AgCIO4, Cd(C104)2 and AgOOC-CF3 have been studied using the positron lifetime spectroscopy. The variations of the lifetimes of ortho-positronium (0-Ps) wiLls the concentration of the solute in water reveal peculiar features, attributed to the formation of complex ions. 相似文献
10.
J. Ch. Abbe G. Duplatre A. G. Maddock A. Haessler 《Journal of Radioanalytical and Nuclear Chemistry》1980,55(1):25-33
The formation of positronium in various solvents and the inhibition and enhancement of positronium formation by a wide variety
of solutes are discussed. The studies contribute to the investigation of localisation processes in liquids. 相似文献