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von Neumann’s inequality in matrix theory refers to the fact that the Frobenius scalar product of two matrices is less than or equal to the scalar product of the respective singular values. Moreover, equality can only happen if the two matrices share a joint set of singular vectors, and this latter part is hard to find in the literature. We extend these facts to the separable Hilbert space setting, and provide a self-contained proof of the “latter part”.  相似文献   
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Molecular Diversity - Hypertension is a medical condition that affects millions of people worldwide. Despite the high efficacy of the current antihypertensive drugs, they are associated with...  相似文献   
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A practical access to alkyl- and aryl-substituted (E)-2-(azidomethyl)alkenoates and related azido compounds from the corresponding allylic bromides in aqueous acetone is described. An alternative method to obtain the starting bromides based on heterogeneous catalysis under mild conditions was also investigated.  相似文献   
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In the first part of the paper we establish the existence of a boundary trace for positive solutions of the equation ?Δu + g(x, u) = 0 in a smooth domain Ω ? ?N, for a general class of positive nonlinearities. This class includes every space independent, monotone increasing g which satisfies the Keller‐Osserman condition as well as degenerate nonlinearities gα,q of the form gα,q (x, u) = d(x, ?Ω)α |u|q?1 u, with α > ?2 and q > 1. The boundary trace is given by a positive regular Borel measure which may blow up on compact sets. In the second part we concentrate on the family of nonlinearities {gα,q}, determine the critical value of the exponent q (for fixed α > ?2) and discuss (a) positive solutions with an isolated singularity, for subcritical nonlinearities and (b) the boundary value problem for ?Δu + gα,q (x, u) = 0 with boundary data given by a positive regular Borel measure (possibly unbounded). We show that, in the subcritical case, the problem possesses a unique solution for every such measure. © 2003 Wiley Periodicals, Inc.  相似文献   
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Poly(pyridine ether)s were prepared in two ways: the polycondensation of silylated 1,1,1‐tris(4‐hydroxyphenyl)ethane (THPE) with 2,6‐difluoropyridine (method A) and the polycondensation of free THPE with 2,6‐dichloropyridine (method B). With method A, the THPE/difluoropyridine feed ratio was varied from 1.0:1.0 to 1.0:1.6. Cycles, bicycles, and multicycles were the main reaction products, and crosslinking was never observed. When ideal stoichiometry was used exclusively, multicycles free of functional groups were obtained. These multicycles were detectable in matrix‐assisted laser desorption/ionization time‐of‐flight (MALDI‐TOF) mass spectra up to B38C76 with a mass of approximately 32,000 Da. With method B, the reaction conditions were varied at a fixed feed ratio to achieve an optimum for the preparation of multicyclic polyethers, but because of the lower reactivity of 2,6‐dichloropyridine, a quantitative conversion was not achieved. The reaction products were characterized with MALDI‐TOF mass spectrometry, viscosity measurements, and size exclusion chromatography. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5725–5735, 2004  相似文献   
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