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61.
Volker Eberhardt 《manuscripta mathematica》1974,12(1):47-65
This paper contains a detailed study of those locally convex spaces E-which we call GN-spaces-for which the following closed graph theorem holds: Every closed linear map from E to any normed linear space is continuous. In the first two sections we establish some characterisations and permanence-properties of these spaces. The main result reads as follows: Every separated GN-space is isomorphic to a barrelled subspace of some ωd?d′, and conversely. Then we determine those GN-spaces which are (DF)-spaces, Schwartz-spaces or nuclear spaces. Finally we show that neither the strong dual nor the tensor product of GN-spaces are GN-spaces. 相似文献
62.
63.
Summary Second drawing of monoaxially drawn PP and PET films perpendicular to the first drawing direction has been investigated. At low draw ratios structural systems having an angle of 45° with regard to the second draw direction are formed. By increasing the draw ratio the structures rotate into the new preferred direction. The results lead to the impression that the structural transformations do not turn out molecule by molecule, but domain by domain.
Zusammenfassung Die Zweitverstreckung monoaxial verstreckter PP- und PET-Folien senkrecht zur Erstverstreckrichtung wird untersucht. Bei kleinen Verstreckgraden bilden sich Struktursysteme unter 45° zur Zweitverstreckrichtung; bei weiterer Verdehnung drehen sich die Strukturen in die Vorzugsrichtung. Die Ergebnisse vermitteln den Eindruck, daß die Strukturänderung nicht Molekül für Molekül, sondern Bereich für Bereich abläuft.
With 10 figures and 2 tables 相似文献
64.
J. L. Eberhardt R. E. Horstman P. C. Zalm H. A. Doubt G. Van Middelkoop 《Hyperfine Interactions》1977,3(1):195-212
Nuclear spin precessions due to the transient magnetic field in polarized Fe have been measured as a function of the initial velocity of28Si ions in the first-excited nuclear state. The transient field was found to increase linearly with the ion velocityv in the regionv/c=0.006–0.049. This is in contrast to the Lindhard and Winther model, which requires an inverse proportionality with ion velocity. Reanalysis of an earlier measurement on30Si(2
1
+
) with the linear velocity dependence yields a reduced value for theg-factor ofg=0.37±0.12. Other available velocity-dependent data for22Ne,56Fe and196Pt are consistent with a linear velocity dependence and suggest in addition a linear dependence on the nuclear charge Z of the moving ion. The increase of the transient field with recoil velocity can be explained semi-quantitatively by the capture of polarized Fe electrons into 1s and 2s vacancies in the moving ion. The velocity-dependent data and other discrepancies from the Lindhard and Winther model for16N,18O and very recently, for12C are also discussed in terms of the proposed microscopic model. 相似文献
65.
66.
Maul J Strachnov I Eberhardt K Karpuk S Passler G Trautmann N Wendt K Huber G 《Analytical and bioanalytical chemistry》2006,386(1):109-118
A combined setup for spatially resolved mass analysis of trace amounts of elements and macromolecules is presented. Using
a MALDI-TOF mass spectrometer, a laser spectroscopic setup for resonant ionization of neutral atoms has been implemented.
This allows for an efficient and selective detection of trace elements by means of resonance ionization mass spectrometry
(RIMS). The instrumental scheme is described, and methodological developments are presented. In a first application pure,
laser desorption/ionization with TOF-MS was used to measure mass distributions of cosmic nanodiamonds. For further applications
regarding the spatially resolved ultra-trace analysis of elements in solid samples, an implanted target was used to characterize
both laser desorption/ionization and laser desorption/resonance ionization for the detection of trace elements within. A perspective
of the setup is given and future investigations are outlined. 相似文献
67.
68.
Square‐Planar Ruthenium(II) Complexes: Control of Spin State by Pincer Ligand Functionalization
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Dr. Bjorn Askevold Dr. Marat M. Khusniyarov Dr. Wolfgang Kroener Dr. Klaus Gieb Prof. Paul Müller Dr. Eberhardt Herdtweck Dr. Frank W. Heinemann Dr. Martin Diefenbach Prof. Max C. Holthausen Veacheslav Vieru Prof. Liviu F. Chibotaru Prof. Sven Schneider 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(2):579-589
Functionalization of the PNP pincer ligand backbone allows for a comparison of the dialkyl amido, vinyl alkyl amido, and divinyl amido ruthenium(II) pincer complex series [RuCl{N(CH2CH2PtBu2)2}], [RuCl{N(CHCHPtBu2)(CH2CH2PtBu2)}], and [RuCl{N(CHCHPtBu2)2}], in which the ruthenium(II) ions are in the extremely rare square‐planar coordination geometry. Whereas the dialkylamido complex adopts an electronic singlet (S=0) ground state and energetically low‐lying triplet (S=1) state, the vinyl alkyl amido and the divinyl amido complexes exhibit unusual triplet (S=1) ground states as confirmed by experimental and computational examination. However, essentially non‐magnetic ground states arise for the two intermediate‐spin complexes owing to unusually large zero‐field splitting (D>+200 cm?1). The change in ground state electronic configuration is attributed to tailored pincer ligand‐to‐metal π‐donation within the PNP ligand series. 相似文献
69.
Liu Q Meermann C Görlitzer HW Runte O Herdtweck E Sirsch P Törnroos KW Anwander R 《Dalton transactions (Cambridge, England : 2003)》2008,(44):6170-6178
Complexes (Salpren(tBu,tBu))Y[N(SiHMe2)2](thf) and (SALEN(tBu,tBu))La[N(SiHMe2)2](thf) (SALEN(tBu,tBu) = Salcyc(tBu,tBu) and Salpren(tBu,tBu)) were prepared from Ln[N(SiHMe2)2]3(thf)2 and H2SALEN(tBu,tBu). The yttrium complex was characterized by X-ray crystallography revealing intrinsic solid-state structural features: the metal centre is displaced by 1.05 angstroms from the [N2O2] least squares plane of a highly bent Salpren(tBu,tBu) ligand (angle(Ph,Ph) dihedral angle of 80.4(1) degrees ) and is coordinated asymmetrically by the silylamide ligand exhibiting one significant Y---(HSi) beta-agostic interaction (Y-N1-Si1, 106.90(9) degrees; Y---Si1, 3.2317(6) angstroms). Complexes (SALEN(tBu,tBu))Ln[N(SiHMe2)2](thf)n (n = 1, Sc; n = 2, Y, La) react with ammonium tetraphenylborate to form the ion pairs [(SALEN(tBu,tBu))Ln(thf)n][BPh4]. The cationisation was proven by X-ray crystal structure analyses of [(Salpren(tBu,tBu))Sc(thf)2][B(C6H5)4].2(thf) and [(Salpren(tBu,tBu))Ln(thf)3][B(C6H5)4].4(thf) (Ln = Y, La), showing an octahedral and pentagonal-bipyramidal coordination geometry, respectively. 相似文献
70.
Aziz EF Eisebitt S Eberhardt W Cwiklik L Jungwirth P 《The journal of physical chemistry. B》2008,112(4):1262-1266
We probe the local electronic structure at solvated Na+ ions in 1 M aqueous NaCl solutions as a function of pH. A dramatic change in the Na+ white line intensity in X-ray absorption is observed for high pH values, reflecting a changing local electronic structure at the Na+ ions when OH- is present. Given the relative abundance of sodium and hydroxide ions, we conclude that one OH- affects at least 2.4+/-0.6 Na+ ions in an electronically noticeable way at pH 13. From the experimental data we infer that spatially extended clusters or networks incorporating Na+ and OH- can exist in the electrolyte solution. The experimental data are complemented by molecular dynamics simulations, which indicate the presence of structured clusters incorporating Na+, OH-, and solvent molecules. 相似文献