基于液晶体的大错位量散斑相移技术研究

系统地分析了大错位量散斑干涉术测量离面位移的原理,并结合晶体光学理论详细分析液晶体的相移过程．同时从理论上剖析了沃拉斯顿棱镜的错位机理,从而构造出一种新的基于液晶体实现大错位量散斑相移技术的测试系统。采用该检测系统对结构实体混凝土在不同养护时间情况下的力学行为进行测试研究。实验结果揭示：随着养护时间的增加,混凝土结构的力学性能指标也相应增加,但在养护21天后,混凝土结构材料的弹性模量和结构强度都达到某一稳定值(即标准试样在同等养护条件下的实验室测量值)。并且也发现该技术使用方便,检测时受环境的影响小,可以实现现场在线原位实时无损检测,并能够得到非常真实的检测结果,从而可以实现更精确的定量计算。     

Alkene Carboarylation through Catalyst-Free,Visible Light-Mediated Smiles Rearrangement

A light-mediated Truce–Smiles arylative rearrangement is described that proceeds in the absence of any photocatalyst. The protocol creates two C−C bonds from simple starting materials, with the installation of an aryl ring and a difluoroacetate moiety across unactivated alkenes. The reaction proceeds via a radical mechanism, utilizing a light-mediated reduction of ethyl bromodifluoroacetate by N,N,N′,N′-tetramethylethylenediamine (TMEDA) to set up intermolecular addition to an unactivated alkene, followed by Truce–Smiles rearrangement.     

Generation and Reactivity of a One-Electron-Oxidized Manganese(V) Imido Complex with a Tetraamido Macrocyclic Ligand

The synthesis and X-ray structure of a new manganese(V) mesitylimido complex with a tetraamido macrocyclic ligand (TAML), [Mn^V(TAML)(N-Mes)]⁻ ( 1 ), are reported. Compound 1 is oxidized by [(p-BrC₆H₄)₃N ]^+.[SbCl₆]⁻ and the resulting Mn^VI species readily undergoes H-atom transfer and nitrene transfer reactions.     

Regularized gap functions and error bounds for split mixed vector quasivariational inequality problems

In this paper, we consider a class of split mixed vector quasivariational inequality problems in real Hilbert spaces and establish new gap functions by using the method of the nonlinear scalarization function. Further, we obtain some error bounds for the underlying split mixed vector quasivariational inequality problems in terms of regularized gap functions. Finally, we give some examples to illustrate our results. The results obtained in this paper are new.     

Cyclic orbifolds of lattice vertex operator algebras having group-like fusions

Letters in Mathematical Physics - Let L be an even (positive definite) lattice and $$gin O(L)$$. In this article, we prove that the orbifold vertex operator algebra $$V_{L}^{{hat{g}}}$$ has...     

Mass spectrometry combined with affinity probes for the identification of CP4 EPSPS in genetically modified soybeans

Sample preparation methods used for genetically modified organisms (GMOs) analysis are often time consuming, require extensive manual manipulation, and result in limited amounts of purified protein, which may complicate the detection of low‐abundance GM protein. A robust sample pretreatment method prior to mass spectrometry (MS) detection of the transgenic protein (5‐enolpyruvylshikimate‐3‐phosphate synthase [CP4 EPSPS]) present in Roundup Ready soya is investigated. Liquid chromatography‐multiple reaction monitoring tandem MS (nano LC‐MS/MS‐MRM) was used for the detection and quantification of CP4 EPSPS. Gold nanoparticles (AuNPs) and concanavalin A (Con A)‐immobilized Sepharose 4B were used as selective probes for the separation of the major storage proteins in soybeans. AuNPs that enable the capture of cysteine‐containing proteins were used to reduce the complexity of the crude extract of GM soya. Con A‐sepharose was used for the affinity capture of β‐conglycinin and other glycoproteins of soya prior to enzymatic digestion. The methods enabled the detection of unique peptides of CP4 EPSPS at a level as low as 0.5% of GM soya in MRM mode. Stable‐isotope dimethyl labeling was further applied to the quantification of GM soya. Both probes exhibited high selectivity and efficiency for the affinity capture of storage proteins, leading to the quantitative detection at 0.5% GM soya, which is a level below the current European Union's threshold for food labeling. The square correlation coefficients were greater than 0.99. The approach for sample preparation is very simple without the need for time‐consuming protein prefractionation or separation procedures and thus presents a significant improvement over existing methods for the analysis of the GM soya protein.