高功率可调谐连续NaCl：（F2^＋）H色心激光器

报道了掺硫和掺氧ＮａＣｌ：（Ｆ２＾＋）Ｈ色心激光器最新实验结果。最高输出功率分别达３Ｗ和４．８Ｗ。实验比较了掺硫及掺氧（Ｆ２＾＋）Ｈ心的热光稳定性。     

Vector Lattices on a Set of Two Generators

It is proved that the center of an automorphism group Aut(FVL2) of a free vector lattice FVL2 on a set of two free generators is isomorphic to a multiplicative group of positive reals. It is shown that the free vector lattice FVL2 has an isomorphic representation by continuous piecewise linear functions of the real line; as a consequence, the ideal lattice and the root system for rectifying ideals in FVL2 are amply described. Similar results are obtained for a free vector lattice FVL2 _Q 2 generated by two elements over a field of rational numbers.     

人性·人本·人化--人本管理的实质及其管理实现

管理理论的建构常常以某种人性假设为前提.对复杂人性本质的不同推定,决定着管理科学理论的不同走向.人本管理是一种有别于其他诸如"物本管理"、"资本管理"、"能本管理"等的管理理论,其不同之处或者说其进步性就在于它谋求对人的理解,即试图在对人性的种种假设中探寻"人"与人之"本"的内在逻辑,以建立一种"人为"与"为人"的柔性的管理规约.在我国特有的管理语境中,人本管理的本质与实现的理解是有其独特性的.在管理实践中,人不仅仅是手段,人本身也是目的.     

铜发光中心的分布和位错显微结构的关系

本文作者根据显著观测和发光光谱的测试结果表证实了在ＺｎＳ：Ｃｕ单晶中，蓝色铜发光中心及绿色铜发光中心的分布和位错线区域的横向与纵向的显著与纵向的显著结构有着固定的对应关系。     

Fe/Zn双金属氰化物催化剂催化环氧丙烷聚合的活性结构研究

以氯化锌、铁氰化钾（含有整合剂）的水溶液为原料，合成了铁锌双金属氰化物（DMC）催化剂。为获得高活性的DMC催化剂，需将叔丁醇 、多元醇螯合剂螯合至其结构中，用XRD、XPS等分析手段，对铁锌DMC催化剂的结构与活性进行分析表征。实验发现，DMC催化剂的晶体结构与螯合剂密切相关，螯合剂能显著降低DMC催化剂的结晶程度，从而提高DMC催化剂的活性。同时，氯化锌过量也有利于DMC催化剂活性的提高。并表征了相关DMC催化剂的活性中心。     

Ab initio calculations of small hydrides including electron correlation

Five different structures of CH₅ ⁺ and one structure of CH₅ ^– are calculated using a gaussian basis both in the SCF approximation and with the inclusion of electron correlation in the independent electron pair approximation (IEPA). While on SCF level the C _sstructure of CH₅ ⁺ has to lowest energy, the energy difference between the C _sand C _2vstructures becomes negligible if correlation is included. In contrast to this the approach of a proton to CH₄ at large and intermediate distances is most favorable towards a corner of the CH₄ tetrahedron which means a structure. The decomposition of CH₅ ⁺ into CH₃ ⁺ and H₂ requires 20kcal/mol on SCF level and 40 kcal/mol if correlation is included.     

FT-EPR Spectroscopic Study of Silicophosphate Glasses Derived from Gels

(100-x) mole% SiO₂-x mole% P₂O₅-glasses withx=1–9 have been prepared by the sol-gel process using tetraethylorthosilicate and triethylphosphate as precursors. The gels were fired at various temperatures up to 950°C and then exposed to γ-ray irradiation to induce paramagnetic centers. CW-EPR and FT-EPR Spectroscopies were employed at temperatures between 4 and 300 K in order to determine the resulting structures. The dried gels exhibited four types of O ₂ ⁻ -ions trapped in pores of different sizes. The gels fired atT=670°C exhibited theE’ ₁-center and non-bridging oxygen as a results of the fracture of the Si-O-Si bonds. At higher temperatures, the spectra of the POHC, POHC ^b ,E’, and CH ₃ ⁻ -centers have been detected that are a function ofx andT.     

Application of the semilocalized approach to chemical reactivity of butadiene

The semilocalized approach to chemical reactivity (J. Mol. Struct. (Theochem) 588 (2002) 99; Int. J. Quant. Chem. 94 (2003) 302) is applied to study the addition reaction of an electrophile or nucleophile to the butadiene molecule. In accordance with the classical concept of the reaction center and its neighborhood (substituent), only one of the two H₂C=CH-fragments of butadiene is supposed to be under a direct attack of the reagent, whereas the remaining H₂C=CH-group is assumed to play the role of the substituent and thereby to participate in the process indirectly by exerting certain electron-donating or accepting effect upon the former group and/or the reagent. The main aim of the study consists in revealing the role of the H₂C=CH-substituent in the formation of the known higher reactivity of the terminal carbon atom of the attacked C=C-bond (as compared to the internal atom) irrespective of the nature of the reagent. To this end, we seek to obtain an explicit algebraic representation of the interdependence between the direction and the extent of the total influence of the H₂C=CH-substituent, on the one hand, and the nature of the reagent, on the other hand. The expressions for electron density and bond order redistributions among separate fragments of contacting molecules derived previously in the form of power series are shown to yield the above-anticipated representation. On this basis, it is demonstrated that the electron-donating effect of the initially occupied (bonding) orbital of the substituent and the electron-accepting effect of its initially vacant (antibonding) orbital upon the remaining fragments of the whole reacting system may be considered independently whatever the nature of the reagent. However, a strong interdependence is established between the actual relative extents of these two components of the total effect of the H₂C=CH-group and the electron-donating (accepting) properties of the reagent. Moreover, this group of atoms is shown to manifest itself as an electron-donating (accepting) substituent under influence of an electrophilic (nucleophilic) attack. Using this principal result of the paper, the actual reactivity of butadiene with respect to electrophile (nucleophile) is interpreted by invoking a model system of a substituted ethene containing a simple (one-orbital) electron-donating (accepting) substituent, and a terminal addition easily follows for both types of the reagent.     

STUDY ON 1-HEXENE POLYMERIZATION BASED ON ZIEGLER-NATTA CATALYSTS WITH DOPED SUPPORT

A series of Ti/Mg supported catalysts are prepared by using ball-milled mixtures of MgCl2-ethanol adducts and NaCl as supports, and 1-hexene polymerizations catalyzed by the novel catalysts are studied. It is found that the molecular weight distribution of poly(1-hexene) becomes apparently narrower when catalysts with doped supports are used, indicating that changing the structure of the support is an effective way to regulate the active center distribution of heterogeneous Ziegler-Natta catalyst.     

Effect of Thiourea on the Kinetics of the Hydrogen Evolution Reaction at Iron and the Transport of Hydrogen through a Steel Membrane in Solutions of C<Subscript>2</Subscript>H<Subscript>4</Subscript>(OH)<Subscript>2</Subscript>-H<Subscript>2</Subscript>O-HCl

The effect of thiourea (0.5–10 mM) on the kinetics of the hydrogen evolution reaction (HER) at iron and the hydrogen transport through a steel membrane out of ethylene glycol (containing 2 and 10 wt % H₂O) and aqueous solutions containing HCl (0.1–0.99 M) with a constant ionic strength equal to unity is studied in parallel experiments. The presence of 0.5 mM of thiourea in the solutions raises the overvoltage of hydrogen evolution, while a subsequent increase in its concentration does not effect the HER kinetics. The dependence of the flux of hydrogen diffusion through the membrane on the thiourea content passes through a maximum.