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Katharina Habermann Lutz Habermann Paul Rosenthal 《Calculus of Variations and Partial Differential Equations》2007,30(2):137-152
A Yang–Mills theory in a purely symplectic framework is developed. The corresponding Euler–Lagrange equations are derived
and first integrals are given. We relate the results to the work of Bourgeois and Cahen on preferred symplectic connections. 相似文献
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CHLOROFLUOROCARBONS AND OZONE 总被引:2,自引:0,他引:2
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A central problem that arises in evolutionary biology is that of displaying partitions of subsets of a finite set X on a tree whose vertices are partially labelled with the elements of X. Such a tree is called an X-tree and, for a collection of partitions of subsets of X, characterisations for the existence and uniqueness of an X-tree that displays have been previously given in terms of chordal graphs. In this paper, we obtain two closely related characterisations also in terms of chordal graphs. The first describes when identifies an X-tree, and the second describes when a compatible subset of is of maximum size. 相似文献
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According to the theory of superselection sectors of Doplicher, Haag, and Roberts, field operators which make transitions between different superselection sectors—i.e. different irreducible representations of the observable algebra—are to be constructed by adjoining localized endomorphisms to the algebra of local observables. We find the relevant endomorphisms of the chiral algebra of observables in the minimal conformal model with central chargec=1/2 (Ising model). We show by explicit and elementary construction how they determine a representation of the braid groupB
which is associated with a Temperley-Lieb-Jones algebra. We recover fusion rules, and compute the quantum dimensions of the superselection sectors. We exhibit a field algebra which is quantum group covariant and acts in the Hilbert space of physical states. It obeys local braid relations in an appropriate weak sense. 相似文献
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Böcking T Kilian KA Hanley T Ilyas S Gaus K Gal M Gooding JJ 《Langmuir : the ACS journal of surfaces and colloids》2005,21(23):10522-10529
Surface modification with oligo(ethylene oxide) functionalized monolayers terminated with reactive headgroups constitutes a powerful strategy to provide specific coupling of biomolecules with simultaneous protection from nonspecific adsorption on surfaces for the preparation of biorecognition interfaces. To date, oligo(ethylene oxide) functionalized monolayer-forming molecules which can be activated for attachment of biomolecules but which can selectively form monolayers onto hydrogen terminated silicon have yet to be developed. Here, self-assembled monolayers (SAMs) containing tetra(ethylene oxide) moieties protected with tert-butyl dimethylsilyl groups were formed by thermal hydrosilylation of alkenes with single-crystal Si(111)-H. The protection group was used to avoid side reactions with the hydride terminated silicon surface. Monolayer formation was carried out using solutions of the alkene in the high-boiling-point solvent 1,3,5-triethylbenzene. The protecting group was removed under very mild acidic conditions to yield a free hydroxyl functionality, a convenient surface moiety for coupling of biological entities via carbamate bond formation. The chemical composition and structure of the monolayers before and after deprotection were characterized by X-ray photoelectron spectroscopy (XPS) and X-ray reflectometry. To demonstrate the utility of this surface for covalent modification, two reagents were compared and contrasted for their ability to activate the surface hydroxyl groups for coupling of free amines, carbonyl diimidazole (CDI), and disuccinimidyl carbonate (DSC). Analysis of XP spectra before and after activation by CDI or DSC, and after subsequent reaction with glycine, provided quantitative information on the extent of activation and overall coupling efficiencies. CDI activated surfaces gave poor coupling yields under various conditions, whereas DSC mediated activation followed by aminolysis at neutral pH was found to be an efficient method for the immobilization of amines on tetra(ethylene oxide) modified surfaces. 相似文献