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1.
本文对广义风险过程中的渐近方差作了非参数估计,得出并证明了两个定理,为广义风险过程中破产概率的区间估计作了理论准备. 相似文献
2.
Anthony W. Coleman C. Mitchell Means Simon G. Bott Jerry L. Atwood 《Journal of chemical crystallography》1990,20(2):199-201
[NBu4][Br3] interacts with C6H6 to form an air-stable liquid clathrate. The tribromide anion reacts with phenol to give para-bromophenol in>95% yield. The HBr which is generated in the reaction combines with the Br– anion to form [Br-H-Br]–. The latter forms the basis for a new liquid clathrate, [NBu4][Br-H-Br]·n C6H6. The parent salt, [NBu4][Br3], crystallizes in the monoclinic space group C2/c witha=12.983(5),b=10.380(7),c=16.222(6) Å,=93.93(3)°, andD
c
=1.47 g cm–3 forZ=4. The final R value is 0.068 based on 787 observed reflections. 相似文献
3.
4.
A novel two-dimensional coordination polymer containing infinite, coherently pitched single and triple helical motifs is formed by the self-assembly of Cd2+, succinate, water and a bipyridyl ligand. 相似文献
5.
6.
The crystal structure of iododimethyl(trimethylamine)aluminium has been determined from single-crystal X-ray diffraction data collected by counter methods. I(CH3)2Al · N(CH3)3 crystallizes in the othorhombic space group Pnma with cell dimensions a=12.59(1), b=10.75(1), c=7.58(1)å, and pcalc=1.58 g·cm?3 for Z=4. Least-squares refinement gave a final weighted R Value of 0.071 for 574 independet observed reflections. Each monomeric molecule lies on a crystallographic mirror plane with the trimethylamine and iododimethylaliminium groups in a staggered configuration about the aluminum nitrogen bond. 相似文献
7.
8.
Simon G. Bott Matthew Clark Joseph S. Thrasher Jerry L. Atwood 《Journal of chemical crystallography》1987,17(2):187-196
The X-ray structure of S-methyl(pentafluorosulfanyl)thiocarbamate, SF5NHC(O)SCH3, has been determined from three-dimensional diffractometer data and refined by full-matrix least-squares techniques. The crystals are monoclinic:P21/m,a=5.008 (5),b=7.811 (2),c=9.348 (4) Å, =99.08 (7)°, andZ=2; finalR=0.046 for 517 observed reflections. The structure comprises hydrogen-bonded (NHO) chains with the component monomers in thecis, cis-conformation, i.e., the arrangement of the nonhydrogen and nonfluorine atoms is nearly planar, the SF5 group and the O are in acis position with respect to the C-NH bond, and the O and the CH3 group are in acis position with respect to the C(O)-S bond. Theoretical methods including MNDO and molecular modeling were used to study the relative stabilities of the four possible conformations of SF5NHC(O)SCH3. 相似文献
9.
8,8"-Biflavonoidsareantw0rtantclass0fbiflavonoids.Asasystematicresearchofthe8,8"-biflav0noids,wehavepreviouslyreportedthestudyonthereactionof2'-hydroxychaloneswithl2-H2SO4-DMSOsystem.'InthispaPer,thesynthesisof5,5",7,7',-tetTameth0xy-8,8"-biflavonela2,4,4",7,7"-tetramethoxy-8,8"-biflavone1b',4',4",,5,5,',7,7"-hexamethoxy-8,8"-biflav0ne1c4and4,4"-dibenZyl0xy-5,5",7,7"-tetramothoxy-8,8"-biflavoneldisreported.ThesyntheticmethodisshownintheSchemebelow.2-Hydroxyacet0phenonescondensedwithsubsti… 相似文献
10.
Brandon D. ConleyBurl C. Yearwood Sean ParkinDavid A. Atwood 《Journal of fluorine chemistry》2002,115(2):155-160
The preparation and characterization of the ammonium hexafluorosilicate salts, 2[R]+ [SiF6]2− (where R=piperidinium (2), methylammonium (3), quinolinium (4), acridinium (5), 2,2,6,6-tetramethylpiperidinium (6), and propylammonium (7)) is described.The salts were prepared from the reaction of the corresponding alkylammonium fluoride with silica gel. The compounds were characterized by NMR, IR, mass spectrometry and in the case of 1 (piperidinium fluoride), 2-4 by X-ray crystallography. Compounds 1-3 crystallize in the orthorhombic crystal system (space groups Iba2, Fdd2, and Pnnm, respectively), with Z=8, 14, and 4, respectively. Compound 4 crystallizes in the triclinic space group P-1, with Z=2. Compounds 1-4 exhibit hydrogen bonding. 相似文献