Dye laser pulse shortening and stabilization by Q-switching

The properties of passive Q-switched short-cavity dye lasers (SCDL) and passive Q-switched distributed-feedback dye lasers (DFDL) are investigated theoretically by using rate-equation models. The calculations, in agreement with experimental results, predict a significant decrease of the pulse energy fluctuation and the pulse duration of both the SCDL and DFDL, when passive Q-switching is used.     

How many atoms can be defined by boxes?

We study the functionb(n, d), the maximal number of atoms defined byn d-dimensional boxes, i.e. parallelopipeds in thed-dimensional Euclidean space with sides parallel to the coordinate axes. We characterize extremal interval families definingb(n, 1)=2n-1 atoms and we show thatb(n, 2)=2n ²-6n+7. We prove that for everyd, exists and . Moreover, we obtainb*(3)=8/9.     

在-170℃到+20℃温度范围内Sb-Cs光阴極的光效应对温度的依赖关系

本文研究了在-170℃到+20℃温度范围内,Sb-Cs光阶极的光效应对温度的依赖关系。在极限波长附近,当温度下降时,发现灵敏度单纯地下降。在短波的地方,灵敏度在一个宽的温度范围内与温度无关;只有到极低温度时,灵敏度才很快下降。     

关于透明光阴極的反射

强度为I_0的一束光射到一个光阴极上,只有光强度(1-γ)I_0起了产生光电效应,而入射光强度的其余部分γI_0则被反射,以是而不起作用。 蒸发喷塗在玻璃面上的一个光阴极,它的灵敏度(即每单位光强度所产生的光电流)依存于光阴极本身对于光强度(1-γ)I_O的量子效率(即光电子数与被吸收的光量子数之比),同时也依存于阴极和玻璃面的反射系数。如何增强量子效率的问题在文献[1]中已有广泛的讨论。在这篇论文里,我们将从实验的角度来研究关系于光阴极     

Oxidative self-decomposition of the nickel(III) complex of glycylglycyl-L-histidylglycine

Self-decomposition of the nickel(III) doubly deprotonated peptide complex of Gly2HisGly occurs by base-assisted oxidation of the peptide. At < or =p[H+] 7.0, the major pathway is a four-electron oxidation (via 4 Ni(III) complexes) at the alpha carbon of the N-terminal glycyl residue. The product of this oxidation is oxamylglycylhistidylglycine, which hydrolyzes to yield ammonia and oxalylglycylhistidylglycine. Both of these peptide products decompose to give isocyanatoacetylhistidylglycine. A small amount (2%) of oxidative decarboxylation also is observed. In another major pathway above p[H+] 7.0, two Ni(III)-peptide complexes coordinate via an oxo bridge in the axial positions to form a reactive dimer species. This dimer generates two Ni(II)-peptide radical intermediates that cross-link at the alpha carbons of the N-terminal glycyl residues. In 0.13 mM Ni(III)-peptide at p[H+] 10.3, this pathway accounts for 60% of the reaction. The cross-linked peptide is subject to oxidation via atmospheric O2, where the 2,3-diaminobutanedioic acid is converted to a 2,3-diaminobutenedioic acid. The products observed at 相似文献   

Ramsey numbers for local colorings

The concept of a localk-coloring of a graphG is introduced and the corresponding localk-Ramsey numberr _loc ^k (G) is considered. A localk-coloring ofG is a coloring of its edges in such a way that the edges incident to any vertex ofG are colored with at mostk colors. The numberr _loc ^k (G) is the minimumm for whichK _m contains a monochromatic copy ofG for every localk-coloring ofK _m . The numberr _loc ^k (G) is a natural generalization of the usual Ramsey numberr ^k (G) defined for usualk-colorings. The results reflect the relationship betweenr ^k (G) andr _loc ^k (G) for certain classes of graphs.This research was done while under an IREX grant.     

Nickel(III) oxidation of its glycylglycylhistamine complex

The doubly-deprotonated Ni(III) complex of Gly(2)Ha (where Ha is histamine) undergoes base-assisted oxidative self-decomposition of the peptide. At 相似文献   

Cold neutron facility for prompt gamma-neutron activation analysis

The restart of the recently upgraded research reactor in Budapest is foreseen at the end of this year. A number of fast, thermal and cold neutron beams will serve for research, industrial and educational activities. One of the cold neutron guide end positions will be utilized for neutron capture prompt gamma-ray activation analysis (PGAA). Further development of the PGAA method as well as new applications in environmental research, biology and medicine are planned.     

Correlation between biological activity and energies of electronic transitions in benzodiazepines. Negative ion mass spectrometry and ultraviolet absorption spectroscopy study of some derivatives

A correlation between the energies of electronic singlet transitions in benzodiazepines and their biological activity, which was revealed earlier by means of negative ion mass spectrometry with resonance electron capture, has been verified with a UV absorption spectroscopy investigation. Also, it has been noted that the energies of electronic singlet transitions in benzodiazepines are close in value to the ionization energies of atoms Cs, Rb, K, Na, Li and Tl, the cations of which are known to play an important role in nerve cell excitation processes. Copyright 1999 John Wiley & Sons, Ltd.