激光对红外系统的失效机理和破坏效应研究

根据红外光学系统的会聚特性,用光学增益方法分析了红外系统中各元件对应的光强分布,确定了位于焦面附近光学元件是激光破坏的易损部件,并提出了强激光对红外系统元件损伤,造成其探测、制导功能失效的硬破坏机理;由红外滤光片、探测器和信号处理电路与入射激光波长的光谱响应分析,提出了弱激光对红外系统干扰,导致其探测、制导功能在激光辐照一段时间内失效的软破坏机理;开展了激光辐照红外系统的失效验证实验,较好地解释了其失效的机理和效应。     

监管技术巨头：技术力量作为市场支配地位认定因素之再审视

如何有效规制技术巨头已然成为当前《反垄断法》修订的重要任务。技术力量虽然作为传统的市场支配地位认定要素,但长期以来呈现被虚置化的客观状态,致使技术巨头市场支配地位的认定难度增大,技术力量自身的传导效应被显著低估。数字技术对市场竞争的影响异于以往,其通过平台、数据、算法的数字市场三维结构框架影响生产与交易的全过程。技术与三维结构结合所形成的技术力量极为强大,超越了以控制价格为主的传统市场力量,结合社会与资本力量形成了更牢固的市场固化结构。在判断技术巨头的市场支配地位时,亟需发挥技术力量作为非价格型认定要素的重要作用。应当摒弃虚置技术力量作为市场支配地位认定要素的固有症结,提高技术力量在认定市场支配地位时所占权重,回归结构性视角,妥善防范技术巨头无序扩张。     

Füllstandsmessung mit Streustrahlungssonden

Es wird die Abhängigkeit der Impulsdichte vom Füllstand bei Meßanordnungen mit γ-Streustrahlungssonden verschiedener Länge untersucht. Verwendet werden die Nuklide ⁶⁰Co und ¹³⁷Cs. Ein nahezu linearer Anstieg der Impulsdichte mit dem Füllstand wird bei Füllgütern kleiner Ordnungszahl nur bei Sondenlängen L ≥ μ₀ ^?1.erzielt. Der Einfluß des Schüttwinkels und der Dichte des Füllgutes wird diskutiert.     

A System for Determination of Precise Isotopic Vapor Pressure Differences from —20 to 110 °C,including Temperature Control to 0·001 over that Range)

An experimental system for the precise measurement of small vapor pressure differences over the range —20 to 110°C is described.     

Über den Einfluß von Isotopieeffekten auf die Verbreitung der Isotope in der Natur

Die Isotopenzusammensetzung der chemischen Elemente in ihren natürlichen Vorkommen wird von kernphysikalischen Vorgängen, vom Einfall extraterrestrischer Materie und, namentlich bei den leichten Elementen (etwa bis zum Chlor), von kinetischen und thermodynamischen Isotopieeffekten beeinfluβt. Deshalb ist die Kenntnis der in der Natur wirkenden Isotopieeffekte eine entscheidende Voraussetzung für das Verständnis der Gesetzmäβigkeiten der Verbreitung der Isotope in der Natur und für die Anwendung dieser Gesetzmäβigkeiten als Mittel der geo- und kosmoswissenschaftlichen Forschung und der Umweltforschung [1].     

Electron radiation damage in copper in the high voltage electron microscope

The various factors influencing the nucleation of radiation damage in the HVEM are reviewed. A method for obtaining quantitative information from observations is given. The effect of reirradiation at room temperature on the damage formed at elevated temperatures is shown. This effect may give experimental information concerning the strain fields surrounding large dislocation loops.     

1H, 13C and 15N NMR spectral analysis of substituted 1,2,3,4‐tetrahydro‐pyrido[1,2‐a]pyrimidines

The NMR spectroscopic data of a series of thirty‐four 3‐acylpyrido[1,2‐a]pyrimidinium salts are analyzed, which were prepared as either perchlorates or chlorides. Methyl group substituted 3‐aroyltetrahydropyrido[1,2‐a]pyrimidines with the methyl substituent in positions 6, 8 and 9 as well as both in positions 6 and 8 were investigated bearing various aroyl substituents. Unequivocal assignment of all resonances was achieved via two‐dimensional ¹H,¹H‐COSY measurements, ¹H,¹³C and ¹H,¹⁵N HSQC as well as HMBC experiments, and important diagnostic CH and NH couplings in the heteroaromatic ring system are evaluated. The influence of the methyl substituents was analyzed on the proton, carbon and nitrogen shifts. A significant effect of the counter ion on some chemical shifts of the nuclei under discussion of the pyridopyrimidines is found, allowing the indirect detection of the anion, which is confirmed by direct measurement of the ³⁵Cl nucleus of the perchlorates. Copyright © 2013 John Wiley & Sons, Ltd.     

Coordination Chemistry of Gold Catalysts in Solution: A Detailed NMR Study

Coordination chemistry of gold catalysts bearing eight different ligands [L=PPh₃, JohnPhos (L2), Xphos (L3), DTBP, IMes, IPr, dppf, S‐tolBINAP (L8)] has been studied by NMR spectroscopy in solution at room temperature. Cationic or neutral mononuclear complexes LAuX (L=L2, L3, IMes, IPr; X=charged or neutral ligand) underwent simple ligand exchange without giving any higher coordinate complexes. For L2AuX the following ligand strength series was determined: MeOH?hex‐3‐yne <MeCN≈OTf^??Me₂S<2,6‐lutidine<4‐picoline<CF₃CO₂^?≈DMAP<TMTU<PPh₃<OH^?≈Cl^?. Some heteroligand complexes DTBPAuX exist in solution in equilibrium with the corresponding symmetrical species. Binuclear complexes dppf(AuOTf)₂ and S‐tolBINAP(AuOTf)₂ showed different behavior in exchange reactions with ligands depending on the ligand strength. Thus, PPh₃ causes abstraction of one gold atom to give mononuclear complexes LLAuPPh₃⁺ and (Ph₃P)_nAu⁺, but other N and S ligands give ordinary dicationic species LL(AuNu)₂²⁺. In reactions with different bases, LAu⁺ provided new oxonium ions whose chemistry was also studied: (DTBPAu)₃O⁺, (L2Au)₂OH⁺, (L2Au)₃O⁺, (L3Au)₂OH⁺, and (IMesAu)₂OH⁺. Ultimately, formation of gold hydroxide LAuOH (L=L2, L3, IMes) was studied. Ligand‐ or base‐assisted interconversions between (L2Au)₂OH⁺, (L2Au)₃O⁺, and L2AuOH are described. Reactions of dppf(AuOTf)₂ and S‐tolBINAP(AuOTf)₂ with bases provided more interesting oxonium ions, whose molecular composition was found to be [dppf(Au)₂]₃O₂²⁺, L8(Au)₂OH⁺, and [L8(Au)₂]₃O₂²⁺, but their exact structure was not established. Several reactions between different oxonium species were conducted to observe mixed heteroligand oxonium species. Reaction of L2AuNCMe⁺ with S^2? was studied; several new complexes with sulfide are described. For many reversible reactions the corresponding equilibrium constants were determined.