Two-particle correlations in 360 GeV/cp p interactions

Two particle correlations of hadrons produced in 360 GeV/cpp interactions are investigated in the transverse plane and in rapidity. The data were obtained at the European hybrid spectrometer equipped with a rapid cycling bubble chamber. The observed transverse and rapidity correlations are compared with the one string LUND-and a two string dual parton-model. These models predict in general stronger correlations in the transverse plane and much weaker correlations in rapidity than found in the data. The LUND-FRITIOF-and multichain dual parton models provide a better reproduction of the data, although the agreement is not yet satisfactory. Only the UA5 cluster model GENCL shows agreement with the data.     

过氧化氢和磷酸对以亚磷酸作磷源合成SAPO-41和AlPO-41的影响

 考察了以亚磷酸作为磷源合成SAPO-41和AlPO-41时加入过氧化氢或磷酸对生成SAPO-41和AlPO-41的影响. 结果表明,向反应体系中加入过氧化氢或者使用磷酸部分替代亚磷酸,都能明显缩短SAPO-41和AlPO-41的晶化时间. 此外,使用混合磷源还能够降低模板剂的用量,获得小晶粒晶化产物.     

非线性项在零点和无穷远处非渐进增长的高维P-Laplacian半拟线性问题的全局分歧

本文将研究一般区域上高维p-Laplacian方程保号解的存在性:{u(x)=0,x∈ЭΩ,-div(φp(■u))=a(x)φp(u⁺+β(x)φp(u^-)+ra(x)f(u)),x∈Ω,其中Ω是R^N中一个有界且在其边界上光滑的区域,N≥2,1p-2s,a(x)∈C(Ω,(0,+∞)),u⁺=max{u,0},u^-=-min{u,0},a{x},β(x)∈C(Ω);f∈C(R,R)对于s>0,sf(s)>0成立.当f0■(0,∞)或f∞∈(0,∞)(其中f0=_|s|→0limf(s)/φp(s),f∞=_|s|→+∞limf(s)/φp(s)),且r≠0属于一定区间时,可以获得上述高维p-Laplacian方程保号解的存在性.我们用全局分歧技巧和连通序列集取极限的方法获得主要结果.     

Modification of the alumina surface with polyfunctional organic reagents

The sorption of polyfunctional organic reagents on the surface of alumina was studied. The optimum conditions of modification were found. A sorption mechanism was suggested. Sorption was found to depend on the structure of the modifier reagent. The sorption of iron(III) and cobalt(II) on alumina modified with nitroso-R-salt was studied.     

Synthesis and properties of phthalonitriles with an azo chromophore and related phthalocyanines

The 4-R-phenylazophenoxyphthalonitriles were synthesized by the reaction of 4-bromophthalonitrile with 4-R-phenylazophenols and were used to obtain tetra-R-phenylazophenoxyphthalocyanines and their metal complexes. The effect of substituents on the spectral and other properties of the synthesized compounds was established.     

Synthesis and Spectral-Luminescent Properties of Octa-substituted Aluminum Phthalocyanines Bearing Biphenyloxy Groups

Russian Journal of General Chemistry - Mixed-substituted aluminum phthalocyanines bearing biphenyloxy substituents and nitro groups or 1-benzotriazole moieties in the periphery were synthesized on...     

Thermodynamics of interactions of water-soluble porphyrins with RNA duplexes

We characterized the interactions of meso-tetrakis(4N-(2-hydroxyethyl)pyridinium-4-yl) porphyrin (TEtOHPyP4), meso-tetrakis(4N-allylpyridinium-4-yl) porphyrin (TAlPyP4), and meso-tetrakis(4N-metallylpyridinium-4-yl) porphyrin (TMetAlPyP4) with the poly(rA)poly(rU) and poly(rI)poly(rC) RNA duplexes between 18 and 45 degrees C by employing circular dichroism, light absorption, and fluorescence intensity spectroscopic measurements. Our results suggest that TEtOHPyP4 and TAlPyP4 intercalate into the poly(rA)poly(rU) and poly(rI)poly(rC) host duplexes, while TMetAlPyP4 associates with these RNA duplexes by forming outside-bound, self-stacked aggregates. We used our temperature-dependent absorption titration data to determine the binding constants and stoichiometry for each porphyrin-RNA binding event studied in this work. From the temperature dependences of the binding constants, we calculated the binding free energies, DeltaG(b), enthalpies, DeltaH(b), and entropies, DeltaS(b). For each RNA duplex, the binding enthalpy, DeltaH(b), is the most favorable for TEtOHPyP4 (an intercalator) followed by TAlPyP4 (an intercalator) and TMetAlPyP4 (an outside binder). On the other hand, for each duplex, external self-stacking of TMetAlPyP4 produces the most favorable change in entropy, DeltaS(b), followed by the intercalators TAlPyP4 and TEtOHPyP4. Thus, our results suggest that the thermodynamic profile of porphyrin-RNA binding may correlate with the binding mode. This correlation reflects the differential nature of molecular forces that stabilize/destabilize the two modes of binding-intercalation versus external self-stacking along the host duplex.     

产学研合作创新方式下政府补贴策略选择

创新补贴策略是政府鼓励企业创新的一种常见政策,考虑到企业内在的吸收能力与外部不同政府补贴策略方式的存在,本文以产学研合作创新方式为基础,通过建立三阶段博弈模型,利用模型解析与仿真分析讨论吸收能力与创新投入分配比例系数对政府补贴策略选择的影响。研究结果表明:无论政府采取哪一种补贴方式,均可以有效激励企业加大创新投入规模,并且企业的吸收能力与R&D投入、产量及社会福利均呈正相关关系;但是,吸收能力对利润及政府补贴的影响受限于补贴方式和企业的创新投入分配比例系数;此外,在创新产品补贴下,创新难度系数对政府补贴额度的影响并不明显,而创新产品补贴总体优于创新投入补贴。