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51.
Let S be the class of all spaces, each of which is homeomorphic to a stationary subset of a regular uncountable cardinal (depending on the space). In this paper, we prove the following result: The product X×C of a monotonically normal space X and a compact space C is normal if and only if S×C is normal for each closed subspace S in X belonging to S. As a corollary, we obtain the following result: If the product of a monotonically normal space and a compact space is orthocompact, then it is normal.  相似文献   
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The UV, excitation, and luminescence spectra of tris(pivaloyltrifluoroacetonato)europium(III) ([Eu(pta)3]; Hpta=1,1,1‐trifluoro‐5,5‐dimethylhexane‐2,4‐dione=HA) were measured in the presence of bis(salicylidene)trimethylenediamine (H2saltn), bis[5‐(tert‐butyl)salicylidene]trimethylenediamine (H2(tBu)saltn), or bis(salicylidene)cyclohexane‐1,2‐diyldiamine (H2salchn), and the corresponding ZnII complexes [ZnB] (B=Schiff base). The excitation and luminescence spectra of the solution containing [Eu(pta)3] and [Zn(salchn)] exhibited much stronger intensities than those of solutions containing the other [ZnB] complexes. The introduction of a tBu group into the Schiff base was not effective in sensitizing the luminescence of [Eu(pta)3]. The luminescence spectrum of [ZnB] showed a band around 450 nm. The intensity decreased in the presence of [Eu(pta)3], reflecting complexation between [Eu(pta)3] and [ZnB]. On the basis of the change in intensity against the concentration of [ZnB], stability constants were determined for [Eu(pta)3Zn(saltn)], [Eu(pta)3Zn{(tBu)saltn}], and [Eu(pta)3Zn(salchn)] as 4.13, 4.9 and 5.56, respectively (log , where =[[Eu(pta)3ZnB]]([[Eu(pta)3]][[ZnB]])?1). The quantum yields of these binuclear complexes were determined as 0.15, 0.11, and 0.035, although [Eu(pta)3Zn(salchn)] revealed the strongest luminescence at 613 nm. The results of X‐ray diffraction analysis for [Eu(pta)3Zn(saltn)] showed that ZnII had a coordination number of five and was bridged with EuIII by three donor O‐atoms, i.e., two from the salicylidene moieties and one from the ketonato group pta.  相似文献   
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Thymopentin (TP5) is a synthetic pentapeptide fragment, which corresponds to position 32 - 36 of thymic polypeptide thymopoietin. Thymopoietin and TP5 display a variety of biological functions, including phenotypic differentiation of T cells and the regulation of immune systems. Previous chemical modification experiments suggested that there was an absolute requirement for N-terminal amino acids to maintain the biological activity of TP5. On the basis of this structure-activity relationship, we designed and synthesized the C-terminally 5-carboxyfluorescein-coupled TP5 (TP5-FAM) as a fluorescent probe for thymopoietin receptor. TP5-FAM could bind to the membrane of human lymphoid cell lines, MOLT-4 cells, in which the thymopoietin receptor is expressed. The binding is specific and saturable (K(d) = 33 microM). TP5 and human splenopentin are nearly equipotent inhibitors of TP5-FAM binding to the thymopoietin receptor, but porcine secretin did not show any significant inhibition of TP5-FAM binding to MOLT-4 cells. Thus, TP5-FAM is suggested to be a potent and biologically active ligand that would be useful for studying the binding and functional characteristics of the human thymopoietin receptor.  相似文献   
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ODMR measurements are combined with phosphorescence quantum yield data to show that deuterium isotope effects on the nonradiative decay rates of quinoxaline and dibenzoquinoxaline are spin sublevel-selective as well as position-dependent.  相似文献   
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The lifetimes of the blue fluorescence from a higher excited state are directly measured to be 80 ± 30 ps for cryptocyanine and 35 ± 15 ps for DTTC in methanolic solution. The relaxation processes associated with electronic excited states are discussed in the case of DTTC.  相似文献   
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