考虑车辆随机停放的停车楼减震设计与可靠度分析

在停车楼的设计中通常将车辆荷载以活荷载的方式均匀分布到结构上,实际上受车辆随机停放的影响,停车楼结构整体质量中心偏移,一旦结构遭遇罕遇地震时,车辆的随机停放可能造成停车楼结构发生扭转破坏.本文在传统减震设计方法的基础上考虑车辆活荷载的随机性,并从可靠度的角度验算减震结构在大震作用下的倒塌概率.结果表明,相同的减震设计布...     

The Ramifications of the Centres: Quantised Function Algebras at Roots of Unity

This paper continues the study of quantised function algebrasO[G] of a semisimple group G at an lth root of unity . Thesealgebras were introduced by De Concini and Lyubashenko in 1994,and studied further by De Concini and Procesi and by Gordon,amongst others. Our main purpose here is to increase understandingof the finite-dimensional factor algebras O[G](g), for g G.We determine the representation type and block structure ofthese factors, and (for many g) describe them up to isomorphism.A series of parallel results is obtained for the quantised Borelalgebras and . 2000 Mathematical Subject Classification: 16W35,17B37.     

Poincaré inequalities and quasiconformal structure on the boundary of some hyperbolic buildings

In this paper we shall show that the boundary of the hyperbolic building considered by M. Bourdon admits Poincaré type inequalities. Then by using Heinonen-Koskela's work, we shall prove Loewner capacity estimates for some families of curves of and the fact that every quasiconformal homeomorphism is quasisymmetric. Therefore by these results, the answer to questions 19 and 20 of Heinonen and Semmes (Thirty-three YES or NO questions about mappings, measures and metrics, Conform Geom. Dyn. 1 (1997), 1-12) is NO.

     

On the Classification of Flag-Transitive c.c*- Geometries

Let ( G) be a flag-transitive c.c*-geometry whose point-stabilizer is not an affine group. We list all known examples and show that, if (, G) is a minimal unknown example, then G is an almost simple group and the commutator subgroup G is a simple group of Lie type.     

Sparse matrix multiplications for linear scaling electronic structure calculations in an atom-centered basis set using multiatom blocks

A sparse matrix multiplication scheme with multiatom blocks is reported, a tool that can be very useful for developing linear-scaling methods with atom-centered basis functions. Compared to conventional element-by-element sparse matrix multiplication schemes, efficiency is gained by the use of the highly optimized basic linear algebra subroutines (BLAS). However, some sparsity is lost in the multiatom blocking scheme because these matrix blocks will in general contain negligible elements. As a result, an optimal block size that minimizes the CPU time by balancing these two effects is recovered. In calculations on linear alkanes, polyglycines, estane polymers, and water clusters the optimal block size is found to be between 40 and 100 basis functions, where about 55-75% of the machine peak performance was achieved on an IBM RS6000 workstation. In these calculations, the blocked sparse matrix multiplications can be 10 times faster than a standard element-by-element sparse matrix package.     

A Difference Set in \left( {\mathbb{Z}/4\mathbb{Z}} \right)^3 \times \mathbb{Z}/5\mathbb{Z}

We present a (320, 88, 24)-difference set in , the existence of which was previously open. This new difference set improves a theorem of Davis-Jedwab with the removal of the exceptional case. It also enables us to state a theorem of Schmidt on Davis-Jedwab difference sets more neatly.     

On an asymptotic behavior of elements of order in irreducible representations of the classical algebraic groups with large enough highest weights

The behavior of the images of a fixed element of order in irreducible representations of a classical algebraic group in characteristic with highest weights large enough with respect to and this element is investigated. More precisely, let be a classical algebraic group of rank over an algebraically closed field of characteristic 2$">. Assume that an element of order is conjugate to that of an algebraic group of the same type and rank naturally embedded into . Next, an integer function on the set of dominant weights of and a constant that depend only upon , and a polynomial of degree one are defined. It is proved that the image of in the irreducible representation of with highest weight contains more than Jordan blocks of size if and are not too small and .

     

Preparation of both enantiomers of a synthon for novel nucleoside analogs by enzymatic desymmetrization of a meso-diol with a methylene cyclopropane skeleton

The enzymatic desymmetrization of methylenecyclopropane diol or its corresponding diacetate derivative, generated from a [2+1] cycloaddition between dioxepin and methylchlorocarbene, is described. After screening five commercial lipases, the two enantiomers of acetic acid 2-hydroxymethyl-3-methylene-cyclopropylmethyl ester are obtained in high yields and excellent enantioselectivities by using PFL or LPP in organic solvent. The stereostructure of the desymmetrization products was established by X-ray analysis. We also reported a new example with this non racemic chiral building block where the sign of optical rotation is dramatically solvent dependent and inverted. Using these enantiopure building blocks, a synthesis of novel nucleoside analogs is also presented.     

Two Chiral Building Blocks for the Stereocontrolled Synthesis of Anti-and Syn-1,3-Diols

During the last decade, chiral building blocks for 1, 3-diols of various configurations have been synthesized and applied widely in the total synthesis of natural polyene macrolide antibiotics1 and 1(, 25-dihydroxyvitamin D3 analogues2,3. The synthesis of the building block has attracted much interest in recent years. Herein, we report the synthesis of two chiral building blocks 1 and 2 in 8 steps and 7 steps respectively, starting from the readily available and inexpensive D (+)-xylose 3 as o…     

Open Chain Chiral Macrolide Building Blocks by Opening of Deoxygenated 1,6-Anhydrosugars with 1,3-Propanedithiol

Chiral building blocks for macrolides and related natural products are obtained from 1,6-anhydrosugars by conversion of the bicyclic acetals 2 or 12 into the open chain chiral 1,3-dithianes 6 and 13. Branched precursors can be obtained by opening of the ?erný epoxide 1 with the 1,3-dithiane anion to yield 7, followed by ring opening with 1,3-propanedithiol to the bis-1,3-dithiane 8.