广义风险过程中渐近方差的非参数估计

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．     

3,3,6,6-四甲基-9-邻氯苯基-1,8-二氧代-3,4,5,6,7,9-六氧化氧杂蒽的合成和晶体结构

标题化合物C23H25对O3Cl是由邻氯苯甲醛与5，5-二甲基1，3-环己二酮在N，N-二甲基甲酸腹中反应而得。结构通过单晶X-射线衍射法确定，其晶体属于单科晶系，空间群=1632。晶体结构用直接法解出，使用全矩阵最小二乘法对原子参数进行修正，最后的偏离因子为R=0．054，Rw一0．063。在晶体结构中，吡喃环与苯环之间的两面角为92．43°。     

Neutron interactions with germanium isotopes and amorphous and crystalline GeO2

Coherent neutron scattering lengths and total cross sections have been measured on elemental and oxide samples of ordinary Ge and of isotopically enriched substances. From the experimental results the following values were obtained:

the coherent scattering lengths (in fm) of the bound atoms Ge(8.185±0.020);⁷⁰Ge(10.0±0.1);⁷²Ge(8.51±0.10);⁷³Ge(5.02±0.04);⁷⁴Ge(7.58±0.10) and⁷⁶Ge(8.2 ±1.5);

the absorption cross sections at 0.0253 eV (in barn) for Ge(2.20±0.04);⁷⁰Ge(2.9±0.2);⁷²Ge(0.8±0.2);⁷³Ge(14.4±0.4) and⁷⁴Ge(0.4±0.2);

the free cross sections for epithermal neutrons and the zero energy scattering cross sections.

On the basis of this data, the isotopic- and spin-incoherent cross sections and thes-wave resonance contributions to the coherent scattering lengths have been determined and discussed. Transmission measurements at 0.57 meV on amorphous and crystalline GeO₂ yielded for the amorphous sample an inelastic cross section eight times larger than for the crystalline samples. This effect corresponds to a clearly higher density of low energy states in the amorphous than in the crystalline substances.     

Total Synthesis of Several 8, 8",-Biflavones

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…     

Interaction of slow neutrons with nuclides of scandium,titanium, vanadium and manganese

Total cross section measurements at various neutron energies were performed on metallic and oxide samples of natural Sc, Ti, V, and Mn. By means of the Christiansen filter technique the coherent scattering lengths were determined on natural and isotopically enriched samples of Ti-, V-, and Mn-compounds. From the measured values we deduced the following data:

? the absorption cross sections (at 0.0253 eV in barn) of^natTi (6.43±0.06) and of^natV (5.06±0.04);

? the bound coherent scattering lengths (in fm) of^natTi (?3.370±0.013),⁴⁶Ti (4.72±0.05),⁴⁷Ti (3.53±0.07),⁴⁸Ti (?5.86±0.02),⁴⁹Ti (0.98±0.05),⁵⁰Ti (5.88±0.10),^natV (?0.443±0.014), and Mn (?3.750±0.018);

? the free potential radii (in fm) of Sc (3.60 ±0.10),⁴⁶Ti (3.50±0.10),⁴⁷Ti (3.60±0.10),⁴⁸Ti (3.90±0.10),⁴⁹Ti (4.10 ±0.15),⁵⁰Ti (4.50±0.15),⁵¹V (5.20±0.20), and Mn (6.50±20).

On the basis of the well known resonance parameters in combination with new fits of bound levels the spin state scattering lengths, the spin incoherence, and the obtained potential radii are discussed. Total cross section calculations were performed by multi-level formalism and are compared with the measurements.     

高效液相色谱氮杂冠醚键合固定相的合成及性能研究

我们曾用γ－氯丙基键合硅胶（ＣＰＳ），在氢化钠（ＮａＨ）作用下合成了３－（氮杂－１８－冠－６）丙基键合固定相（ＢＣＰ）［１］．该固定相对碱基、核苷酸、硝基苯酚等有较好的分离选择性，但由于ＮａＨ对硅胶基质腐蚀作用较大，导致ＢＣＰ柱效及渗透性较低．本文采...     

Interaction of neutrons with zinc and its isotopes

Coherent neutron scattering lengths and total cross sections have been measured for elemental Zn,Zn-compounds and on isotopicly enriched samples for neutron energies from 0.5 meV up to 143 keV using different techniques. From the experimental data the following quantities were obtained:

the coherent scattering lengths (b in fm) of Zn (5.689±0.014);⁶⁴Zn (5.23±0.04);⁶⁶Zn (5.98±0.05);⁶⁷Zn (7.58±0.08;b ₊=9.4±0.5/5.8±0.5;b _?=5.0±0.7/10.1±0.7);⁶⁸Zn (6.04 ±0.03);

the potential scattering radii (R′ in fm) of Zn (6.2±0.2),⁶⁴Zn (6.0±0.3) and⁶⁶Zn (6.2 ±0.3);

the absorption cross sections (σ _γ at 0.025 eV in barn) of Zn (1.11±0.02);⁶⁴Zn (1.1 ±0.1) and⁶⁶Zn (0.62±0.06).

Derived quantities are the “zero energy” scattering cross sections (σ ₀ in barn) for Zn (4.128±0.010) and⁶⁷Zn (7.8±0.3) and the incoherent bound cross sections of Zn (0.061 ±0.023) and⁶⁷Zn (0.6±0.4). In the epithermal region the Zn-cross section can be described by introduction of two strong bound levels of⁶⁷Zn+n for which estimated parameters are given.     

2,4,6-三硝基苯酚改性锆铝复合氧化物固定相分离富勒烯的色谱性能研究

制备了用于分离C60和C70的2，4，6－三硝基苯酚改性锆铝复合氧化物高效液相色谱固定相，考察了流动相中甲苯的含量、柱温及流速对C60和C70分离的影响，同时比较了酸腐蚀前后锆铝复合氧化物基质对分离的影响，结果表明，2，4，6－三硝基苯酚改性酸腐蚀后锆铝复合氧化物填料对富勒烯表现出较强的分离能力，具有作为富勒烯制备分离的潜力。     

酸性化合物在十二胺-N,N-二亚甲基膦酸改性氧化锆固定相上的分离

酸性化合物在十二胺-N; N-二亚甲基膦酸改性氧化锆固定相上的分离;氧化锆;色谱固定相;十二胺-N; N-二亚甲基膦酸     

Highly Enantioselective Phenylacetylene Addition to Benzaldehyde Catalyzed by Chiral Tridentate Ligand

Development of new or improved methods for the asymmetric preparation of chiral propargylic alcohols has gained considerable significance during the past years because they are useful building blocks for the synthesis of many biologically active compounds and natural products.[1] A series of chiral tridentate ligands were conveniently synthesized from amino acids with good yields (Scheme 1).[2] A preliminary study of the enantioselective alkynylation of benzaldehyde catalyzed by this chiral tridentate ligand was carried out and up to 83% ee of chiral propargyl alcohols was obtained (Table 1 ). A further investigation of the tridentate ligand is currently underway.