A transference theorem for hermite expansions

A transference theorem for multipliers of Hermite expansions is proved. The result allows to transfer weightedL ²(ℝ ⁿ ) estimates from lower to higher dimensions. Research of the author supported by grant BFM2003-06335-603-03 of the D.G.I..     

ON OPTIMAL ENVIRONMENTAL TAXATION AND ENFORCEMENT: INFORMATION,MONITORING AND EFFICIENCY

ABSTRACT. The purpose of the paper is to contribute to the narrowing of the distance between formal theory and practical environmental policy design. We formulate a general and comprehensive theoretical model in order to take into account the different informational and technological problems which characterize the definition and implementation of environmental taxes in a second best world where there also are distortionary taxes. Having formalized these problems, we present a general model which allows us to discuss the existence of efficient and implementable environmental quality objectives and policy instruments, and to analyze many particular cases.     

Spatial Carrier Bi-frequency Fourier Transform Profilometry for the 3-D Shape Measurement of Object with Discontinuous Height Steps

1 IntroductionProjecting a single frequency lfringe pattern upon an Object and observing itsdeformation from a different view angle has been a common method for various threedimensional shape measurement techniques. An autpmatic analysis of the fringepatterns is normally carried out either by the FOurier transform method[IJ or by phasestepping['] of the fringe patterns. HOWever, these techniques have a disadvantage ofprincipal importance, the so-called indetedrinaCy tO a factor Of Zap, or …     

Crystal Structure and Thermodynamic Study of Ephedrine Hydrochloride C10H16NOCI（s）

The crystal structure of ephedrine hydrochloride was determined by means of X-ray crystallography.The crystal system of the compound is monoclinic,and the space group is P21.Unit cell parameters are a=0.7308(6) nm,b=0.6124(5) nm,and c=1.2618(11) nm;α=90°,β=102°,and γ=90°;Z=2.Low-temperature heat capacities of the title compound were measured with an improved precision automated adiabatic calorimeter over a temperature range from 77 K to 396 K.A polynomial equation of the heat capacities as a function of temperature in the temperature region was fitted by the least-squares.Based on the fitted polynomial equation,the smoothed heat capacities and thermodynamic functions of the compound relative to the standard reference temperature 298.15 K were calculated and tabulated at the intervals of 5 K.     

梯度磁场中薄膜厚度梯度的形成机理

借助于基片下方放置的磁铁，在溅射的放电空间中引入了纵向的梯度磁场，辉光放电时，其外貌发生了显著的收缩，由此沉积的薄膜在平面内存在明显的厚度梯度，用磁场中带电粒子的运动理论解释了此种薄膜的形成机制。     

UV Photolysis of a Re(I) Macromolecule, [(4-vinylpyridine)2(4-vinylpyridineRe(C0)3(1,10-phenanthroline)+]200: Addition of C-centered Radicals to Coordinated CO

Abstract

Proteins that bind preferentially to specific recognition sites on DNA also bind more weakly to nonspecific DNA. We have studied both specific and non-specific binding of the EcoRI and BamHI restriction endonucleases, and determined enthalpic and entropic contributions to binding free energy (ΔG°_bind) using both the van't Hoff method and isothermal titration calorimetry. Specific binding is characterized by a strongly negative ΔC°_p and can be either enthalpy-driven or entropy-driven, depending on temperature. Nonspecific binding has ΔC°_p ≈ 0 and is enthalpy-driven. A strongly negative ΔC°_p is the ?thermodynamic signature’ of site-specific binding, because it reflects the characteristics of a tight complementary recognition interface: the burial of previously hydrated nonpolar surface and restriction of configurational-vibrational freedoms of protein, DNA, and water molecules trapped at the protein-DNA interface. These factors are absent in nonspecific complexes. We probed the contributions to ΔC°_p by varying the sequence context surrounding the recognition site. As ΔG°_bind improves, ΔC°_p' ΔH° and ΔS° all become more negative, and there is a linear correlation between ΔH° and ΔS° (enthalpy-entropy compensation). Because these context variations do not change the protein-base or protein-phosphate contacts, the hydrophobic contribution or the number of trapped water molecules at the interface, we conclude that a better sequence context improves the ?goodness of fit’ in the interface and and thus increases the magnitude of the negative configurational-vibrational contribution to ΔC°_p.