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41.
LetX be ann-element set and letA and? be families of subsets ofX. We say thatA and? are crosst-intersecting if |A ∩ B| ≥ t holds for all A ∈A and for allB ∈ ?. Suppose thatA and ? are crosst-intersecting. This paper first proves a crosst-intersecting version of Harper's Theorem:
- There are two crosst-intersecting Hamming spheresA 0,? 0 with centerX such that |A| ≤ |A 0| and|?| ≤ |? 0| hold.
- Suppose thatt ≥ 2 and that the pair of integers (|A) is maximal with respect to direct product ordering among pairs of crosst-intersecting families. Then,A and? are Hamming spheres with centerX.
- Ifn + t = 2k ? 1 then |A| |?| ≤ max \(\left\{ {\left( {K_k^n + \left( {_{k - 1}^{n - 1} } \right)} \right)^2 ,K_k^n K_{k - 1}^n } \right\}\) holds, whereK l n is defined as \(\left( {_n^n } \right)\left( {_{n - 1}^n } \right) + \cdots + \left( {_l^n } \right).\)
- Ifn + t = 2k then |A| |? ≤ (K k n )2 holds.
42.
Z. M. Stadnik P. Griesbach P. Gütlich G. Stroink T. Kohara 《Hyperfine Interactions》1988,41(1):705-708
61Ni Mössbauer measurements have been performed at 4.2 K on spherical Ni particles with an average diameter of 100 and 30 Å, covered with a protective layer of SiO. Their spectra contain a surface component with a significantly reduced hyperfine magnetic field as compared with the field in the bulk. This result confirms recent theoretical predictions. 相似文献
43.
S Çak?r E Co?kunP Naumov E Biçer? Bulut H ?çbudakO Çak?r 《Journal of Molecular Structure》2002,608(1):101-107
Aspartame adduct of copper(II) chloride Cu(Asp)2Cl2·2H2O (Asp=aspartame) is synthesized and characterized by elemental analysis, FT IR, UV/vis, ESR spectroscopies, TG, DTG, DTA measurements and molecular mechanics calculations. Aqueous solution of the green solid absorbs strongly at 774 and 367 nm. According to the FT IR spectra, the aspartame moiety coordinates to the copper(II) ion via its carboxylate ends, whereas the ammonium terminal groups give rise to hydrogen bonding network with the water, the chloride ions or neighboring carboxylate groups. The results suggest tetragonally distorted octahedral environment of the copper ions. 相似文献
44.
4-Amino-3-hydroxybutyric acid was synthesized from allyl cyanide in four steps in an overall yield of 38%. Ultrasonically promoted epoxidation of allyl cyanide with m-chloroperoxybenzoic acid giving oxiranylacetonitrile was used as a key step. 相似文献
45.
《Tetrahedron: Asymmetry》2006,17(6):975-983
The inclusion complexes formed between two chiral N-imidazole derivatives and four cyclodextrins (α-, β-, γ-, and highly sulfated-β-CDs) were investigated by one- and two-dimensional 1H NMR. With the additional results of an ESI-MS study, a 1:1 stoichiometry was proven for all the complexes studied. The complexes were also characterized in terms of binding constants and the results were compared to those obtained by CD-EKC. An identical affinity order for the various CDs was obtained with both techniques. Furthermore, the affinity order for both enantiomers determined by their binding constants values is confirmed by the enantiomer migration orders previously determined by CD-EKC. The structural data obtained by the 2D-ROESY experiments allowed us to understand the interaction mechanisms and to propose, for different analyte structures, theoretical models of inclusion orientation in the CD cavity. These models are in accordance with our previous hypothesis based on the analyte structure–enantioseparation relationships and the thermodynamic parameters determined by CD-EKC. 相似文献
46.
Ryuzaburo Noda 《Graphs and Combinatorics》1986,2(1):277-282
It is shown that ifA is an orthogonal array (N, n, q, 3) achieving Rao's bound, thenA is either
- an orthogonal array (2n, n, 2, 3) withn ≡ 0 (mod 4), or
- an orthogonal array (q 3,q + 2,q, 3) withq even.
47.
Sevim?Hamamci Veysel?T.?YilmazEmail author William?T.?A.?Harrison 《Structural chemistry》2005,16(4):379-383
The first silver(I) complex of saccharinate (sac) with pyridine (py), [Ag(sac)(py)]n has been synthesized and characterized by elemental analysis, IR spectroscopy and single crystal X-ray diffractometry. The complex crystallizes in chiral, trigonal space group P3121 (No. 152) with unit cell parameters of a = 11.2605(2) Å, c = 17.3300(4) Å, V = 1903.02(6) Å3 and Z = 6. [Ag(sac)(py)]n contains monomeric [Ag(sac)(py)] units linked into infinite helices by way of Ag⋅sAg interactions [d(Ag⋅sAg) = 2.909(2) and 2.985(1) Å]. The distorted square-planar environment of Ag is completed by an N-bonded sac [Ag—N = 2.084(2) Å] and a py molecule [Ag—N = 2.116(2) Å]. The Nsac—Ag—Npy angle is 173.85(10)∘. The one-dimensional chains are crosslinked by C—H⋅sO interactions involving the carbonyl and sulfonyl O atoms of sac and aromatic-ring hydrogen atoms of both sac and py. The thermal stability of the title complex was investigated using thermogravimetry and differential thermal analysis in a static atmosphere of air. The first decomposition stage between 90 and 160∘C corresponds to removal of the py molecule in a single stage, while the degradation of the sac moiety occurs at two stages in the temperature range 370–515∘C, giving an end product of metallic Ag. 相似文献
48.
《Journal of organometallic chemistry》2005,690(24-25):6096-6100
The easy cycloaddition of ureas with alkynyl alkoxy biscarbene complexes afforded, in fairly good yields, new biscarbene uracil analogs. X-ray structural data is reported for the dimethyluracil biscarbene complex. By changing the reaction conditions, a new non symmetric complex was obtained whose reaction with ethylenediamine afforded a new tetrakis amino carbene complex. 相似文献
49.
The rectifying junction characteristics of the organic compound pyronine-B film on a p-type Si substrate has been studied. The pyronine-B has been sublimed on the top of p-Si surface. The barrier height and ideality factor values of 0.79±0.04 and 1.13±0.06 eV for this structure have been obtained from the forward bias current-voltage (I-V) characteristics. From the low capacitance-frequency (C-f) characteristics as well as conductance-frequency (G-f) characteristics, the energy distribution of the interface states and their relaxation time have been determined in the energy range of (0.53−Ev)-(0.79−Ev) eV taking into account the forward bias I-V data. The interface state density Nss ranges from 4.93×1010 cm−2 eV−1 in (0.79−Ev) eV to 3.67×1013 cm−2 eV−1 in (0.53−Ev) eV. Furthermore, the relaxation ranges from 3.80×10−3 s in (0.53−Ev) eV to 4.21×10−4 s in (0.79−Ev) eV. It has been seen that the interface state density has an exponential rise with bias from the midgap towards the top of the valence band. The relaxation time shows a slow exponential rise with bias from the top of the valence band towards the midgap. 相似文献
50.
High-resolution 17O NMR spectra have been collected for crystalline samples of lanthanum new phase, La3Si8N11O4. In conjunction with previously published 29Si and 15N spectra obtained for this phase, and in the light of the high-quality crystal structure data reported recently, a more detailed interpretation of the NMR spectra is presented than was possible in previous studies. The non-bridging oxygens in the structure are responsible for the single sharp peak seen in the 17O spectrum at 188 ppm; the remaining oxygens, occupying bridging sites shared with nitrogen, show up only weakly on the 17O spectrum as a broad diffuse band centered around zero ppm. The peak at −57.3 ppm on the 29Si spectrum is believed to correspond to an overlap of [SiN4] and [SiON3] environments, with the −68.2 ppm peak corresponding to an [SiO2N2] environment. 相似文献