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131.
We show that the Ashtekar-Isham extension
of the configuration space of Yang-Mills theories
is (topologically and measure-theoretically) the projective limit of a family of finite dimensional spaces associated with arbitrary finite lattices.These results are then used to prove that
is contained in a zero measure subset of
with respect to the diffeomorphism invariant Ashtekar-Lewandowski measure on
. Much as in scalar field theory, this implies that states in the quantum theory associated with this measure can be realized as functions on the extended configuration space
. 相似文献
132.
The57Fe Mössbauer spectrum recorded from the material of composition Fe0.25NbTiP3O12 shows the presence of Fe2+ in a distribution of approximately octahedral type I sites within the channels of the NbTiP3O12 structure. A comparison of the results with those recorded from the material Fe0.33NbTiP3O12 demonstrates the existence of an upper limit to the occupation by the Fe2+ species of the type I sites. Lattice parameter measurements and57Fe Mössbauer spectroscopy show that treatment of Fe0.25NbTiP3O12 in air induces the migration of the incorporated iron from the channels to form macroscopic -Fe2O3. 相似文献
133.
José W. Maluf 《General Relativity and Gravitation》1996,28(11):1361-1376
In the teleparallel equivalent of general relativity the integral form of the Hamiltonian constraint contains explicitly theadm energy in the case of asymptotically flat space-times. We show that such expression of the constraint leads to a natural and straightforward construction of a Schrödinger equation for time-dependent physical states. The quantized Hamiltonian constraint is thus written as an energy eigenvalue equation. We further analyse the constraint equations in the case of a space-time endowed with a spherically symmetric geometry. We find the general functional form of the time-dependent solutions of the quantized Hamiltonian and vector constraints. 相似文献
134.
Beltrão EI Correia MT Figueredo-Silva J Coelho LC 《Applied biochemistry and biotechnology》1998,74(3):125-134
The phenomenon of altered carbohydrates in transformed cell surfaces has been studied through histochemical techniques using
lectins. Specific binding patterns to normal and transformed mammary tissues were evaluated by Isoform 1 fromCratylia mollis lectin (Cra Iso 1). Protocols using a direct method, incubation of Cra Iso I conjugated to peroxidase (Cra Iso 1-Per) with
mammary tissues, followed by diaminobenzidine and hydrogen peroxidase interaction, were performed. Neoplastic tissues, marked
by Cra Iso 1, showed a higher intensity of staining than normal ones, in comparison withCanavalia ensiformis lectin, Concanavalin A (Con A), conjugated to peroxidase (Con A-Per). The assay with Cra Iso 1 also indicated a possible
utilization of this lectin to characterize normal and transformed mammary cells. 相似文献
135.
Treatment of secondary aliphatic 2-bromoallylamines with an excess of an organolithium compound led to saturated amines in which the organic group of the organolithium compound is incorporated at the alpha carbon. On the other hand, the successive reaction of the former amines with BuLi and t-BuLi between -80 degrees C and rt gave 1,3-diamines or hexahydropyrimidines depending on the reaction time. The formation of these unexpected products involves initial generation of lithium propargylamides, which subsequently undergo cleavage of the C propargylic-C acetylenic bond induced by the organolithium present in each case in the reaction medium. A mechanism which takes into account all the different reaction products has been proposed and additionally supported by successful trapping of dilithium acetylide. 相似文献
136.
137.
Marco-Contelles J 《The Journal of organic chemistry》1996,61(22):7666-7670
The Pauson-Khand reaction on the carbohydrate derived precursors 1-6 is reported. We have described for the first time the cobalt-mediated cyclization of some O-branched chain 1,6-enynes in carbohydrate templates. The resulting bis-heteroannulated pyranosides 17-22 have been obtained in diastereomerically pure form, in moderate to good yield, and in one, simple synthetic operation. These enantiomerically pure, densely functionalized carbocycles are attractive advanced intermediates for the synthesis of complex natural products. 相似文献
138.
Junquera E Laynez J Menéndez M Sharma S Penadés S 《The Journal of organic chemistry》1996,61(20):6790-6798
Thermodynamic studies of the binding of a series of p-nitrophenyl glycosides (PNPGly) of varying stereochemistry to alpha-cyclodextrin (alpha-CD) were performed at three different temperatures (25, 35, and 42 degrees C) using a microcalorimetric technique. The system p-nitrophenol (PNP) at pH = 3 and alpha-CD was also studied for the sake of comparison. All these complexes were found to be enthalpy driven with a favorable enthalpic term clearly dominant over an unfavorable entropic term. A clear enthalpy-entropy compensation effect was observed at all the temperatures, with a slope close to unity (alpha = 1.02) and an intercept TDeltaS degrees (o) = 2.91 kcal mol(-)(1). This thermodynamic pattern is in agreement with those usually found for lectin-carbohydrate associations and for the binding processes of several host-guest systems. This pattern is explained in terms of the contribution of primarily two driving forces: the van der Waals interactions between the host and the guest, and the solvation/desolvation processes which accompany the association reaction. The presence of the carbohydrate molecule in the PNP ring causes a slight destabilization of the complex at 25 degrees C with respect to the alpha-CD-PNP (pH = 3) complex, although a different behavior has been observed depending on the axial/equatorial configuration of the glycoside and the temperature. This behavior is modulated by the stereochemistry of the glycoside. Differences were observed between the deoxy-derivatives (LAra and LFuc) and those derivatives with a hydroxymethyl group (Glc, Gal, Man). DeltaC(p) degrees values were obtained from the dependency of DeltaH degrees on temperature (=( partial differentialDeltaH degrees / partial differentialT)(p)). These values are small and negative except for alphaMan complex. For the latter complex, discrepancy between the calorimetric and the calculated van't Hoff enthalpies was observed. Parallels are drawn between the thermodynamics of our model and those proposed for carbohydrate-protein associations. 相似文献
139.
The conformational preferences of N-acetyl-N'-methyl-alpha-methyl-beta-L-aspartamide, which is the model compound for helical poly(beta-L-aspartate)s, have been determined by ab initio SCF-MO computations. Two driving patterns have been found for the existing 13 minimum energy conformations: (i) intramolecular hydrogen bonding interactions of both amide-amide and amide-ester type; and (ii) repulsive interactions between the four oxygen atoms contained in the molecule. Self-consistent reaction-field (SCRF) calculations based on the method proposed by Miertus, Scrocco, and Tomasi have been performed in order to evaluate the effect of the solvent on the conformational preferences of the compound subject of study. Water and carbon tetrachloride were the solvents chosen for this purpose, and results have been discussed and interpreted on the basis of their electronic structures. The conclusions drawn from this study are of assistance to understand some features of the conformational transitions experimentally found in poly(beta-L-aspartate)s. 相似文献
140.
The synthesis of tetracyclic polyhydroxyquinones 5a and 5b was achieved through a sequence involving two Diels-Alder reactions with 1-methoxy-1,3-cyclohexadiene: the first with 2-(p-tolylthio)naphthazarin and the second on the resulting tricyclic derivative previously transformed into a (p-tolylsulfinyl)naphthazarin. The success of this strategy stemmed from the efficient remote regiocontrol exerted by the thioether substituent in the first step. 相似文献