Elastoplastic state of axisymmetrically loaded laminated bodies of revolution made of isotropic and orthotropic materials

Institute of Mechanics, Ukrainian Academy of Sciences, Kiev. Translated from Prikladnaya Mekhanika, Vol. 28, No. 1, pp. 31–39, January, 1992.     

Charm production in two-photon collisions: Calculation of the leading nonperturbative contribution in QCD

The leading nonperturbative contribution to the cross section of charm production in two-photon collisions is calculated in QCD. Operator expansion is used and the c-quark interaction with vacuum gluon condensate is taken into account. As a result, the moments of the charm contribution to the photon structure function are obtained. The moments with sufficiently high numbers turn out to be sensitive to the gluon condensate.     

Electrochemical reduction of 1,1-dihalo-2,2-disubstituted cyclopropanes

The electrochemical reduction of 1,1-dihalo-2-R-2-methylcyclopropanes was studied by polarography and preparative electrolysis. A mixture of stereoisomeric monoboro- and monochlorocyclopropanes was obtained with preparative yield of 60–70% in preparative electroreduction in methanol against a background of 0.1 M LiClO₄. In the case of bromine derivatives of cyclopropanes (except when R = CN) an effect was found on the part of the current density on the ratio of cis and trans isomers, which was interpreted as a change, in dependence on current density, of the contributions of the reactions of reduction of the starting compounds (S_N2 mechanism) and ionic pairs (S_N1 mechanism). The effect of the solvent (CHCl₃, DMF, DMSO, MeOH) and background salt (LiClO₄, Et₄NBr) on the ratio of stereoisomers is in agreement with this interpretation.A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Science Center, Russian Academy of Sciences, Kazan. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 9, pp. 2023–2032, September, 1992.     

Extended transverse-momentum analysis for intermediate-energy heavy-ion collisions

An extension of the transverse-momentum analysis of Danielewicz and Odyniec is proposed. This extension involves a consideration of baryonic p_T-distribution widths in and out of the reaction plane. Calculations within one- and two-fluid mean-field models show that such an analysis allows us to extract more information on the nuclear equation of state and stopping power than the conventional one does. Different criteria for selecting collision events (i.e. sorting them out according to impact parameters) are also examined. Selections according to the baryonic multiplicity in the midrapidity region and the transversal-to-longitudinal energy ratio are found to be suitable for this purpose.     

DISTRIBUTION OF THE（0，∞）ACCUMULATIVE LINES OF MEROMORPHIC FUNCTIONS

Suppose that f(z)is a meromorphic function of order λ（0<λ<+∞）and of lower order μ in the plane.Let ρ be a positive number such that μ≤ρ≤λ.(1)If f^(l)(z)(0≤l<+∞）has p(1≤p<+∞）finite nonzero deficient valnes αi(i=1,…，p)with deficiencies δ（αi,f^(l)),then f(z)has a (0,∞）accumulative line of order ≥ρin any angular domain whose vertex is at the origin and whose magnitude is larger than max(π/ρ，2π-4/ρ ∑i=1^p arcsin √δ（αi,f^(l))/2).(2)If f(z) has only p(0<p<+∞）（0,∞）,accumulative lines of order≥ρ：arg z=θk(0≤θ1<θ2<…<θp<2π，θp+1=θ1+2π）,then λ≤π/ω，where ω=min I≤k≤p(θk+1-θk),provided that f^(l)(z)(0≤l<+∞）has a finite nonzero deficient value.     

离子束引起的在Al／Cr双层薄膜界面处的原子混合

用600keV的Kr~ 离子轰击Al/Cr双层薄膜样品进行界面原子反应及相互混合的研究。实验样品是在单晶硅上蒸镀约500nm厚的铝膜,相继再蒸上所需厚度的铬膜而制成的。轰击剂量为2.0×10~(15)-2.5×10~(16)Kr~ /cm~2。用2.0MeVa粒子对轰击前后的样品进行了卢瑟福背散射(RBS)分析,发现界面处有明显的原子混合存在;当轰击剂量≥1.0×10~(16)Kr~ /cm~2时,RBS谱出现有明显的坪台,经拟合计算和x射线衍射(XRD)测量证实确有化合物Al_(13)Cr_2存在;还分别得到了原子混合量及混合效率与轰击剂量的关系;最后对界面处的原子混合机制进行了讨论。     

高压下氢化锂晶体中的离子间力与结合能公式的原子分子设计

本文提出一种利用材料Hugoniot数据研究高压下离子晶体中微观离子状态及其离子间排斥作用势的新方法。对氢化锂晶体进行研究时,我们得到Li~+和H~-离子之间排斥作用势函数,结果表明文献〔1〕中提出的离子压缩效应具有客观性。     

CX_2(NO_2)_2(X=H,F,C1)分子旋转势和构型稳定性的ab initio研究

本文用ab initio计算方法,采用STO-3G基组,对二硝基卤代甲烷CH_2(NO_2)_3(1),CF_2(NO_2)_2(2);CCl_2(NO_2)_2(3)等分子作了单点计算,研究其旋转势能.全构型优化研究了五个具有对称性构型的结构和稳定性,并作了理论分析和探讨.     

Phase-transfer catalysis in the chemistry of tetrazoles

In this review we discuss results obtained in the development of methods for the synthesis of tetrazoles and tetrazolium salts together with studies of alkylation, acylation, and imidoylation of tetrazole and 5-substituted tetrazoles under conditions of phase-transfer catalysis.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 754–761, June, 1992.