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81.
Let M(A) denote the comparison matrix of a square H-matrix A, that is, M(A) is an M-matrix. H-matrices such that their comparison matrices are nonsingular are well studied in the literature. In this paper, we study characterizations of H-matrices with either singular or nonsingular comparison matrices. The spectral radius of the Jacobi matrix of M(A) and the generalized diagonal dominance property are used in the characterizations. Finally, a classification of the set of general H-matrices is obtained. 相似文献
82.
J. Badier M. Bardadin-Otwinowska C. Bemporad U. Berthon H. Bienvenu J. Boucrot J. Bourotte G. Burgun O. Callot Ph. Charpentier A. M. Cnops M. Cohen F. Constantini M. Crozon D. Décamp P. Delpierre J. F. Detoeuf P. Espigat B. Gandois G. R. Giannini V. Hajjar M. Hansroul Y. Karyotakis P. Lariccia P. Le D? J. Mas A. Michelini G. C. Moneti M. Moniez E. Paré G. Rahal-Callot M. Rumpf O. Runolfsson A. Tilquin S. Weisz NA Collaboration 《Zeitschrift fur Physik C Particles and Fields》1986,31(3):341-347
Direct photon production has been studied by an experiment performed with the NA3 spectrometer at CERN, using incident negative and positive beams at 200 GeV/c interacting with an isoscalar Carbon target. Two different triggers have been used; one of them requires the photon conversion. The experiment is sensitive to direct photons produced with 3.0≦P T ≦6 GeV/c and center-of-mass rapidity ?0.4≦y *≦1.2. Inclusive cross sections are given for incident π± and protons, and compared with second order QCD predictions; finally an estimation of the gluon structure function of the nucleon is given. 相似文献
83.
Gheorghe R Kalisz M Clérac R Mathonière C Herson P Li Y Seuleiman M Lescouëzec R Lloret F Julve M 《Inorganic chemistry》2010,49(23):11045-11056
The heterometallic hexanuclear cyanide-bridged complex {[Mn(bpym)(H(2)O)](2)[Fe(HB(pz)(3))(CN)(3)](4)} (1), its C(15)N and D(2)O enriched forms {[Mn(bpym)(H(2)O)](2)[Fe(HB(pz)(3))(C(15)N)(3)](4)} (2) and {[Mn(bpym)(D(2)O)](2)[Fe(HB(pz)(3))(CN)(3)](4)} (3), and the hexanuclear derivative complex {[Mn(bpym)(H(2)O)](2)[Fe(B(pz)(4))(CN)(3)](4)}·4H(2)O (4) [bpym = 2,2'-bipyrimidine, HB(pz)(3)(-) = hydrotris(1-pyrazolyl)borate, B(pz)(4)(-) = tetra(1-pyrazolyl)borate] have been synthesized. Their structures have been determined through single-crystal X-ray crystallography at different temperatures. Whereas 3 and 4 maintain a discrete hexanuclear motif during the entire temperature range investigated (down to 95 K), 1 and 2 exhibit a thermally induced reversible single-crystal to single-crystal phase transition driven by a remarkable concerted rearrangement of hydrogen and cyanide coordination bonds. While hexanuclear complexes are observed in the high temperature phases (noted 1a and 2a) above 200 K, the low temperature phases are composed of one-dimensional coordination polymers noted 1b and 2b. The magnetic properties of the four compounds have been investigated in the 2-300 K range, and they reveal the occurrence of an overall antiferromagnetic behavior. The thermal dependence of the optical reflectivity and the FT-IR absorbance have been studied for 1 in the range 10-300 K and 130-300 K, respectively. A comparative analysis of the structural and electronic properties for 1-4 clearly underlines the major role of the intermolecular interactions in the topological and dimensional rearrangement observed during the structural phase transition. This result opens new perspectives in the design of cyanide-based switchable magnetic materials using coordination bonds rearrangements. 相似文献
84.
85.
86.
Laura Parejo Dr. Mahdi Chaari Sara Santiago Dr. Gonzalo Guirado Prof. Francesc Teixidor Dr. Rosario Núñez Dr. Jordi Hernando 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(1):270-280
Icosahedral metallacarboranes are θ-shaped anionic molecules in which two icosahedra share one vertex that is a metal center. The most remarkable of these compounds is the anionic cobalt-based metallacarborane [Co(C2B9H11)2]−, whose oxidation-reduction processes occur via an outer sphere electron process. This, along with its low density negative charge, makes [Co(C2B9H11)2]− very appealing to participate in electron-transfer processes. In this work, [Co(C2B9H11)2]− is tethered to a perylenediimide dye to produce the first examples of switchable luminescent molecules and materials based on metallacarboranes. In particular, the electronic communication of [Co(C2B9H11)2]− with the appended chromophore unit in these compounds can be regulated upon application of redox stimuli, which allows the reversible modulation of the emitted fluorescence. As such, they behave as electrochemically-controlled fluorescent molecular switches in solution, which surpass the performance of previous systems based on conjugates of perylendiimides with ferrocene. Remarkably, they can form gels by treatment with appropriate mixtures of organic solvents, which result from the self-assembly of the cobaltabisdicarbollide-perylendiimide conjugates into 1D nanostructures. The interplay between dye π-stacking and metallacarborane electronic and steric interactions ultimately governs the supramolecular arrangement in these materials, which for one of the compounds prepared allows preserving the luminescent behavior in the gel state. 相似文献
87.
88.
Francesc Planas-Vilanova 《manuscripta mathematica》1995,87(1):349-357
For a given idealI of a commutative ringA, B=A/I, the vanishing of the second André-Quillen (co)homology functorH
2
(A, B, δ) is characterized in terms of the canonical homomorphism α:S(I)→R(I) from the symmetric algebra of the idealI onto its Rees algebra. This is done by introducing a Koszul complex that characterizes commutative graded algebras which
are symmetric algebras.
This article was processed by the author using the LATEX style filecljour1 from Springer-Verlag. 相似文献
This article was processed by the author using the LATEX style filecljour1 from Springer-Verlag. 相似文献
89.
The notion of automorphism is an essential tool to capture the meaning of any mathematical structure. We apply this idea to cooperative games and obtain two interesting characterizations of the automorphisms of such a game: the one, in the complete case, as the permutations of players which preserve the (classical) Shapley value; the other, for the general case, as the permutations preservingall weighted Shapley values.Carreras' research supported by project UPV 036321-HA186/92 of the Basque Country University. Owen's research supported by the National Science Foundation, Grant DMS-9116416. This collaboration was made possible by the Polytechnic University of Catalonia, which sponsored Owen's visit to Terrassa. 相似文献
90.
Metal poly(vinyl acetates) polymers were obtained by radical polymerization with azodiisobutyronitrile. The thermal stabilities of the metal polymers (M-PVAC) have been studied by thermogravimetry (TG) between 25 and 550°C under nitrogen flow. The decomposition temperature was obtained from the maximum of the first derivative from TG curve. The kinetic parameters of the thermal decomposition were determined by the Arrhenius equation. All these polymers degrade mainly in a single step with a very small second step, probably via a complex reaction. The kinetic data thus obtained show that the thermostabilities decrease in the order: Sb-PVAc~Ge-PVAc>Bi-PVAc~Cd-PCAc>Ag-PVAc~PVAc>Zn-PVAc> Au-PVAc>In-PVAc>Sn-PVAc>Ga-PVAc>Pd-PVAc. Again, the thermal stability is dependent upon the metal incorporated in the backbone polymer. They loose weight after 320°C. The order of reaction from the thermal decomposition of these metal polymers was found to be ?0.5 for the first step and 0 for the second. The pre-exponential factor, the reaction order and the activation energy of the decomposition for metal (PVAc) have been determined in most of them. 相似文献