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1.
Affects of microwave bandwidth on the high-charge-states of ion beams extracted from a conventional minimum-B-geometry ECR ion source are first demonstrated. The high-charge-state intensities, produced with broadband microwave radiation are observed to be factors ?2 than those produced with narrow bandwidth microwave radiation at the same power level. 相似文献
2.
Dilation theorems for Banach space valued stochastic processes and operator valued positive definite kernels are considered. It is shown, e.g., that a Banach space valued stochastic process X can be dilated to another process Y, if and only if the covariance kernel of Y is a majorant of the covariance kernel of X. Positive definite operator kernels having majorants of certain special type are characterized. 相似文献
3.
Planar reconstruction patterns at the zigzag and armchair edges of graphene were investigated with density-functional theory. It was unexpectedly found that the zigzag edge is metastable and a planar reconstruction spontaneously takes place at room temperature. The reconstruction changes electronic structure and self-passivates the edge with respect to adsorption of atomic hydrogen from a molecular atmosphere. 相似文献
4.
Glyoxal bis(amidinohydrazone) (GBG) and several analogs thereof are compounds of considerable pharmacological interest, and a variety of HPLC and MECC methods have been developed for their analysis. In these methods, detection is invariably based on the strong UV absorption of the compound. Yet, almost nothing has been known of their UV and VIS spectral properties. In the present paper the UV and VIS Spectroscopy of GBG has been studied in several solvent systems (water, 0. 03 M aqueous sodium acetate buffer, 0. 1 inM aqueous NaOH and dimethylsulfoxide). In the case of solutions in bare water, the shape of the UV spectrum depends drastically on concentration, probably because of changes in the species distribution of GBG as a function of concentration. The spectrum comprises one maximum at ca. 200 nm, and between ca. 250 nin and 400 nm an absorption region with distinctly higher absorbance. In the case of aqueous sodium acetate as well as NaOH solutions, one strong maximum can be detected (at ca. 285–288 nm and 332–337 nm, respectively). In both cases, the maximum occurs at constant wavelength, being independent of concentration. In dimethylsulfoxide, the spectrum of GBG contains an absorption band at distinctly higher wavelengths (λmax 354 nm) than in any one of the aqueous solvents studied, indicating that solvent effects are considerable in the UV spectrum of GBG. In no case, distinct absorption could be detected at wavelengths higher than 400 nm. The results indicate that if aqueous media are used as elements in HPLC analyses of bis(amidinohydrazones) or as solvents in direct UV analysis, they must be buffered. 相似文献
5.
González Cabrera D Koivisto BD Leigh DA 《Chemical communications (Cambridge, England)》2007,(41):4218-4220
A series of mono- and bis-metallated [2]rotaxanes has been prepared using a CuAAC 'click' protocol that is compatible with metal-coordinated building blocks and ligands; the methodology provides a general means for appending a metal ion or complex to an organic scaffold via Cu(I)-catalysed 'click' chemistry, even when the molecule contains redox-active or kinetically labile metals or vacant ligand sites. 相似文献
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8.
Wagemaker M Kearley GJ Van Well AA Mutka H Mulder FM 《Journal of the American Chemical Society》2003,125(3):840-848
Intercalation of Li in TiO2 anatase results in a phase separation in a Li-poor and a Li-rich phase. The local lithium configuration in the coexisting crystallographic phases is resolved by detailed analysis of neutron diffraction data. In each of the phases, two distinct positions within the octahedral interstices are found, with a temperature-dependent occupancy. A combination of quasi-elastic neutron scattering and force field molecular dynamics simulations shows that Li is hopping on a picosecond time scale between the two sites in the octahedral interstices. The results also suggest a specific Li arrangement along the crystallographic a direction, albeit without long range order. It is likely that multiple discrete Li sites within a distorted oxygen octahedron occur not only in intercalated TiO2 anatase but also in other (transition metal) oxides. 相似文献
9.
Williams DH Davies NL Koivisto JJ 《Journal of the American Chemical Society》2004,126(43):14267-14272
Two models (A and B) have been proposed to account for decreased downfield chemical shifts of a proton bound by noncovalent interactions at a ligand/antibiotic interface as the number of ligand/antibiotic interactions is decreased. In model A, the proton involved in the noncovalent bond suffers a smaller downfield shift because the bond is, with a relatively large probability, broken, and not because it is longer. In model B, the proton involved in the noncovalent bond suffers a smaller downfield shift because the bond is longer, and not because it is, with a relatively large probability, broken. We show that model A cannot account for the chemical shift changes. Model B accounts for the process of positively cooperative binding, in which noncovalent bonds are reduced in length and thereby increase the stability of the organized state. 相似文献
10.
We report on the electronic structure of Ge(9)[Si(SiMe(3))(3)](3)(-). Systematic density functional theory analysis of the electronic shell structure of the cluster and its derivatives reveals that the Ge(9)[Si(SiMe(3))(3)](3)(-) and its neutral counterpart have electronic shells that can be explained using the superatom model. The ligand-core interaction of these complexes is distinctly different from previously identified gold, gallium, and aluminium superatom complexes, indicating an electron-donating rather than electron-withdrawing ligand. We modify the electron-counting rule for this case and introduce a simple picture for superatom and superantiatom complexes. Discussions comparing shell models, Zintl clusters, the superhalogen Al(13) and superatom complexes to Ge(9)[Si(SiMe(3))(3)](3)(-) are presented. 相似文献