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101.
We consider a renewal jump–diffusion process, more specifically a renewal insurance risk model with investments in a stock whose price is modeled by a geometric Brownian motion. Using Laplace transforms and regular variation theory, we introduce a transparent and unifying analytic method for investigating the asymptotic behavior of ruin probabilities and related quantities, in models with light- or heavy-tailed jumps, whenever the distribution of the time between jumps has rational Laplace transform.  相似文献   
102.
Ten novel and stable free radicals of nitronyl-, imino-nitroxide and hydrazyl type compounds were synthesized and their physico-chemical properties investigated. UV-Vis and ESR spectroscopic data, as well as the lipophilicities and specific hydrophobic areas of the compounds are compiled. The reaction of these radical compounds with nitric oxide and nitrogen dioxide was also investigated. The radicals synthesized, show selectivity in their reaction with these nitric oxides, depending on their structure (nitronyl-nitroxide radicals react with NO, while hydrazyl radicals react with NO2). The processes are easily monitored by UV-Vis or ESR spectroscopy.  相似文献   
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We prove a result on the transfer of essentiality of extensions of modules over subnormalizing extensions of rings, then apply it to look at the semiprimeness of Hopf-Galois extensions, in particular that of crossed products.

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4-Chloro-7-nitrobenzofurazan reacts by nucleophilic substitution with phenoxide anions derived from estriol (2c), ethynylestradiol (2d), phenol (3e), guaiacol (3f), 2,6-dimethoxyphenol (3g), eugenol (3h), isoeugenol (3i), the cytostatic Etoposide (4), and Reichardt’s betaine (5) in the presence of crown ethers affording the corresponding 4-aryloxy-7-nitrobenzofurazan derivatives 6c, 6d, 7e-7i, 8, and 9. The structure of these compounds was confirmed by NMR spectra. Hydrophobicity/hydrophilicity parameters were investigated by reverse phase thin-layer chromatography.  相似文献   
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The interplay between the chemical structure of the precursors, internal organization in the end materials and dye retention was investigated for composites (ormosils) doped with rhodamine B. Besides formulations with triethoxysilanes (RTES) only, we synthesized as well organic–inorganic hybrids with addition of titanium isopropoxide (TIP) and maleic anhydride (MA). The organic (R) functionality of RTES was changed from methyl (MeTES), to phenyl (PTES) and octyl (OTES). Atomic force microscopy and electron microscopy, coupled with thermogravimetric analysis prove that hydrophobicity increase stimulates the transition of film structure: from well-defined, compact particles (for MeTES), to a mixture of porous particles and non-granular material (for MeTES/PTES), with extreme results observed for octyl-based composites. For this latter, the apparent homogeneity comes from cluster-like organization, where the primary entities are pseudo—granules produced by hydrophobic interactions of oligomeric siloxanes. Controlling the composition and gelation procedure resulted in doped composites with good optical transparency and rhodamine B fluorescence emission bands at around 580 nm. Dye transport inside the inorganic structure is not facilitated when: (a) the particles have a compact (nonporous) inner structure and (b) the recipe does not contain the TIP/MA combination. For silica-based films, the dye is located in the macropores (between the granules) of the material and could be easy removed by washing with acetone. On the contrary, using TIP/MA changes not only the internal composition of the granular-like material (by creating a microporous titania-rich outer-shell of the particles) but also the affinity of the Rh-B to permeate and reside inside these new structures.  相似文献   
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