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1.
A self-consistent model of the development of dendrites and partial discharges in a dielectric solid under a variable voltage
is suggested. Dendrites originate at sites with the enhanced local field strength and also where the dielectric is broken
down under the action of partial discharges. The numerical simulation is used to quantitatively describe the space-time dynamics
of the dendrites and partial discharges in epoxy resin for the tip-plane electrode configuration. The simulated data are compared
with electrical measurements of partial discharges and with optical images of dendrite growth under the same conditions. 相似文献
2.
P. Schwab A. Kochemasov R. Kullmer D. Bäuerle 《Applied Physics A: Materials Science & Processing》1992,54(2):166-169
Pulsed-laser deposition of YBa2Cu3O7 in N2O permits lowering of the substrate temperature with respect to deposition in O2 atmosphere. Additional photodissociation of N2O near the substrate surface deteriorates the superconducting properties of deposited films.On leave from: Institute of Applied Physics of the Academy of Sciences of the USSR, SU-603600 Nishni Nowgorod, USSR 相似文献
3.
We describe a convergent synthesis of eight 1,3,5- and 1,2,4,5-substituted benzene derivatives with long rigid arms containing 4-pyridyl, 2,2'-bipyridyl, and 2,2'-bipyrimidyl termini, meant to be used as trigonal or tetragonal connectors for the construction of large molecular structures. The synthesis involved copper-free Pd-mediated coupling of terminal acetylenes to aryl halides. First, one of the termini of 1,3-diethynylbicyclo[1.1.1]pentane was coupled with a brominated aza heterocycle, and second, 3 equiv of the resulting extended arm were coupled with 1,3,5-triiodobenzene or 4 with 1,2,4,5-tetraiodobenzene. An improved large-scale synthesis for 1,3-diethynylbicyclo[1.1.1]pentane is described. The structures of two of the arms were determined by single-crystal X-ray analysis. Several long molecular rods with 4-pyridyl termini were obtained as byproducts, and a single-crystal X-ray structure is reported for the shortest of these. 相似文献
4.
Preparation and physical and chemical properties of 3-ethinyl-2,4-diformyl-pentandial (3 a) and its salts are described.3 a contains 2 malonaldehyde groups. Starting from3 a, 4H-pyranes, 4H-dihydropyridines, dipyrazoles, diisoxazoles, bisdiazepines and vinamidine derivates are obtained.
Mit 1 Abbildung 相似文献
Mit 1 Abbildung 相似文献
5.
Colour Effects in Oxidic and Other Mn2+ Compounds – the Ligand Field Spectra of Mixed Crystals MgO/MnO, CaO/MnO, and of MnAl2O4 The colour intensity and the shift of the hue is examined for mixed crystals Mg1?xMnxIIO and Mn1?yIICayO in dependence of the Mn2+-concentration and interpreted in terms of Mn2+? Mn2+ pair interactions and variations of the Mn? O bond length, respectively. The experimental band positions (sextet-quartet transitions) could be fitted quantitatively – also in case of Mn2+ in tetrahedral (MnAl2O4) and dodecahedral oxygen coordination (Mn3Al2Ge3O12, MnY2Mg2Ge3O12) – by means of crystal field calculations. The obtained ligand field parameters are discussed in comparison with data for octahedral Mn2+ ions with H2O, F? and Cl? as ligands. 相似文献
6.
Gallium-, Indium-Manganese-, and Thallium-Rhenium Carbonyl Compounds Compounds of type Na{Cl4?nM[Mn(CO)5]n} (M ? Ga, In; n = 1, 2, 3) were prepared by reaction of the Lewis acids MCl3 and NaMn(CO)5. Instead of the sodium salts were obtained the compounds (C3H7CO2)2InMn(CO)4L (Indium atom with the coordination number 5) from Indium(III) butyrate with two carboxylate groups bonded as chelate ligands and NaMn(CO)4L [L ? CO, P(C6H5)3] in the molar ratio 1:1. By reacting TlCl with NaRe(CO)5 i.r. spectroscopic measurements of the solution pointed out the intermediate product TlRe(CO)5, which was unstable against a disproportionation reaction into Tl and Tl[Re(CO)5]3. The last named compound delivered as a thermal decomposition product Re2(CO)8[μ-TlRe(CO)5]2. I.r. bands of the new compounds were assigned. 相似文献
7.
8.
R. L. Lichti K. H. Chow D. W. Cooke S. F. J. Cox E. A. Davis R. C. DuVarney T. L. Estle B. Hitti S. R. Kreitzman R. Macrae C. Schwab A. Singh 《Hyperfine Interactions》1994,86(1):711-716
Longitudinal-field muon-spin depolarization rates in high-purityGe and semiinsulatingGaAs are reported and compared to similar data for intrinsicSi. Depolarization onset temperatures provide a comparison of charge carrier concentrations leading to rapid charge exchange and a shift in the onset, for n-typeGaAs verifies anelectron process. The temperature dependence of the low-field rate constants imply more complicated dynamics inGe than observed earlier inSi. Features near 750K inGaAsTe appear consistent with dissociation of aMu-Te pair.This work was supported by the US National Science Foundation (DMR-8917639 [TLE, BH]), the Science and Engineering Research Council of the UK (EAD, AS, SFJC), the Robert A. Welch Foundation (D-1053 [RLL], and C-1048 [TLE]), and a NATO Collaborative Research Grant (RLL, SFJC, RCD, CS). We wish to thank D.A. Vanderwater of Hewlett Packard for providing theGaAsTe sample. 相似文献
9.
10.
Werner H Schwab P Bleuel E Mahr N Windmüller B Wolf J 《Chemistry (Weinheim an der Bergstrasse, Germany)》2000,6(24):4461-4470
A series of carbenerhodium(I) complexes of the general composition [(eta5-C5H5)Rh(=CRR')(L)] (2a-2i) with R = R'= aryl and L = SbiPr3 or PR3 has been prepared from the square-planar precursors trans-[RhCl(=CRR')(L)2] and NaC5H5 in excellent yields. Reaction of the triisopropylsibane derivative 2a. which contains a rather labile Rh-Sb bond, with CO, PMe3, and CNR (R = Me, CH2Ph, tBu) leads to the displacement of the SbiPr3 ligand and affords the substitution products [(eta5-C5H5)Rh(=CPh2)(L)] (3-7). In contrast, treatment of the triisopropylphosphane compound 2c with CO and CNtBu leads to the cleavage of the Rh=CPh2 bond and gives besides [(eta5-C5H5)Rh(PiPr3)(L)] (10, 12) by metal-assisted C-C coupling diphenylketene Ph2C=C=O (11) or the corresponding imine Ph2C=C=NtBu (13). While the reaction of 2a, c with C2H4 yields [(eta5-C5H5)Rh(C2H4)(L)] (14, 15) and the trisubstituted olefin Ph2C=CHCH3 (16), treatment of 2a, c with RN3 leads to the cleavage of both the Rh-EiPr3 and Rh=CPh2 bonds and gives the chelate complexes [(eta5-C5H5)Rh(kappa2-RNNNNR)] (19, 20). The substitution products 3 (L=CO) and 4 (L= PMe3) react with an equimolar amount of sulfur or selenium by addition of the chalcogen to the Rh=CPh2 bond to generate the complexes [(eta5-C5H5)Rh(kappa2-ECPh2)(L)] (21-24) with thio- or selenobenzophenone as ligand. Similarly, treatment of 3 with CuCl affords the unusual 1:2 adduct [(eta5-C5H5)(CO)Rh(mu-CPh2)(CuCl)2] (25), which reacts with NaC5H5 to form [(eta5-C5H5)(CO)Rh(muCPh2)Cu(eta5-C5H5)] (26). The molecular structures of 3 and 22 have been determined by X-ray crystallography. 相似文献