渐进多焦点镜片的逐点定向曲率补偿优化设计

提出一种利用逐点定向曲率补偿法对渐进多焦点镜片初始模型进行整体优化以减小周边散光区（俗称盲区）的优化设计方法。推导出自由曲面任意方向法曲率的计算公式、确定主曲率和主方向的方法,求出镜片初始模型上各点的曲率差和最大曲率方向、最小曲率方向,通过迭加由不同曲率、不同轴向微小柱面构成的自由曲面,来实现逐点定向曲率补偿,使镜片各点的曲率差适当减小,从而减小散光。给出具体优化步骤和一个优化设计实例,并进行实际加工制作与检测。对比优化前后的光焦度和散光度的面形分布图。结果表明,逐点定向曲率补偿法能有效减小渐进多焦点镜片初始模型的最大散光并明显扩大视远区清晰视觉范围。     

Trifluoroacetic anhydride—catalyzed conjugate addition of boronic acids to α,β-unsaturated ketones

The conjugate addition of boronic acids to α,β-unsaturated ketones catalyzed by acylating reagents has been explored. The results show that trifluoroacetic anhydride catalyzes the addition of vinylboronic acids under experimentally simple and metal-free conditions for a variety of substrates with good yields.     

An Analysis of Operational Conditions for the Double Addition Method of Determining Ions From Electromotive Forces of Ion-Selective Electrode Cells

Abstract

The working conditions for the double addition method of potentiometric determination of unknown concentrations C_K of ions from the electromotive forces of appropriate ion-selective electrode cells have been analyzed in terms of operational equations, standard concentrations for additions, volume ratios of second to first additions, etc. The best operational conditions for minimizing errors on C_X are discussed.     

ELECTRON SPIN RESONANCE OF γ -IRRADIATED COBALT(III) COMPLEXES; ELECTRONIC AND SPIN STATES OF HOT COBALT(II) IONS

Abstract

ESR investigation of the γ -ray irradiated Co(III) complexes have been carried out. The identification and the classification of the irradiation products on the basis of the ESR signal patterns, and the electronic and the spin states of the products are discussed.

Co(III) complexes are reduced by the γ irradiation into Co(II) complexes, where the produced Co(II) ions have low spin configurations, S = ½. Authors refer to these particular spin states as hot ions.     

Performance of the Continuous Addition of Reagent Technique in Fluorimetric Reaction-Rate Methods. Determination of Thiamine at the Nanomolar Level

Abstract

The potential of the continuous addition of reagent (CAR) technique, developed for reactions on the millisecond time scale, in fluorimetric reaction-rate methods, is evaluated. The approach was applied to the classical fast reaction involving the oxidation of thiamine to fluorescent thiochrome effected by potassium ferricyanide in basic solutions. Practical problems associated with this system were readily avoided by using the CAR technique. Several kinetic methods have been developed for the determination of thiamine; all are very sentitive (detection limit, 2. 5x10^?9 M) compared to other fluorimetric equilibrium and reaction-rate methods and are suitable for routine analyses (sample throughput, 100 h^?1).     

Synthesis of threo-β-aminoalcohols from aminoaldehydes via chelation-controlled additions. Total synthesis of l-threo sphingosine and safingol

Chelation-controlled addition of organocuprates to N-carbamoyl aminoaldehydes, prepared from functionalized amino acids, generated predominately the threo-β-amino alcohol derivatives through chelation with the carbamoyl moiety. The carbamate group is a stronger chelating group than other potentially good chelators, for example ethers, esters, thioethers, and gives good diastereoselectivity with cuprates. Thus addition of lithium divinylcuprate to the aldehyde generated from the serine derivative 25 in the presence of extra copper for chelation afforded the threo compound 26 in 83% yield. Cross-metathesis and cleavage of the protecting groups furnished l-threo sphingosine 21. In addition the lyso-sphingolipid protein kinase C inhibitor, safingol, 22, was prepared from commercially available O-benzyl N-BOC serine 28 in six steps and 56% overall yield by this method.     

Formation and manipulation of regular metallic nanoparticle arrays on bacterial surface layers: an advanced TEM study

The template-directed formation of regular nanoparticle arrays on two-dimensional crystalline protein layers after their treatment with metal salt complexes was studied by transmission electron microscopy. For these investigations, bacterial surface layers (S layers), recrystallized in vitro into sheets and tube-shaped protein crystals with typical dimensions in the micrometer range, were used as the template. As identified by electron holography and scanning force microscopy, the S-layer tubes form alternating double layers when deposited onto a solid substrate surface. Two distinct pathways for the metal particle formation at the templates have been found: the site-specific growth of metal clusters by chemical reduction of the metal salt complexes, and the electron-beam induced growth of nanoparticles in the transmission electron microscope. Both mechanisms lead to regular arrays with particle densities > 6×10¹¹ cm ^-2. Nanoparticle formation by electron exposure takes exclusively place in the flat-lying double-layered protein tubes, where a sufficient amount of metal complexes can be accumulated during sample preparation. Received 6 December 2000     

Facial Selectivity in the Nucleophilic Additions of endo-Tricyclo[5.2.1.0~(2,6)]deca-2(6),8-dien-3-one

The endo-tricyclo [5.2.1.02,6] decadienone system 1 has been used as a versatile synthon for the synthesis of a great variety of natural products1. The availability of both antipodes of 1 in enantiopure form2, and the ability to undergo [4+2] cycloreversion makes it useful for the enantioselective synthesis of naturally occurring cyclopentanoids with defined stereochemistry and chirality3. Starting from the 1,4 reduced Hertz ester 2, synthesis of the reactive and strained tricyclodecadienone 4…     

A Computational Study of the Combinatorial Addition of Oxygen to Buckminsterfullerene

All possible isomers of C₆₀O _x have been investigated for x=1, 2, and 3. The method used is a modified extended Hückel method. There is a single C₆₀O isomer, 8 unique C₆₀O₂ isomers, and 47 unique C₆₀O₃ isomers. It is found that a single C₆₀O₂ isomer is much more stable than the remaining 7 and that 3 C₆₀O₃ isomers are more stable than the remaining 44. A qualitative reason for these results is proposed. The results indicate that the three lowest-energy C₆₀O₃ isomers should exist in equilibrium at room temperature.