排序方式: 共有19条查询结果,搜索用时 15 毫秒
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D. Baldomir V. Pardo S. Blanco-Canosa D.I. Khomskii A. Piñeiro J.E. Arias 《Journal of magnetism and magnetic materials》2009,321(7):679-681
Electronic structure calculations were performed for ZnV2O4, a material close to a metal-insulator transition. Structural optimization leads to the formation of V-V dimers along the off-plane chains. A strong spin-lattice coupling is expected close to the transition to itinerancy. No orbital ordering is observed in such a structure, and the experimentally found magnetic structure is naturally explained. 相似文献
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S. Blanco-Canosa F. Rivadulla A. Pi?eiro V. Pardo D. Baldomir M.A. López-Quintela J. Rivas 《Journal of magnetism and magnetic materials》2010,322(9-12):1069-1071
We report high-pressure diffraction and magnetization measurements to demonstrate that the partial collapse of electronic gap at high-pressure insulator to metal transition reported in TiOCl (C. Kuntscher et al. Phys. Rev. B 74 184402 (2006).) corresponds to a Ti3+–Ti3+ dimerization at room temperature within the space group P21/m. The shortest Ti–Ti distance is comparable to that of the Ti metal, but a Peierls-like distortion prevents a metallic behaviour. 相似文献
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Simple Zeros of the Riemann Zeta-Function 总被引:1,自引:0,他引:1
Assuming the Riemann Hypothesis, Montgomery showed by meansof his pair correlation method that at least two-thirds of thezeros of Riemann's zeta-function are simple. Later he and Taylorimproved this to 67.25 percent and, more recently, Cheer andGoldston increased the percentage to 67.2753. Here we proveby a new method that if the Riemann and Generalized LindelöofHypotheses hold, then at least 70.3704 percent of the zerosare simple and at least 84.5679 percent are distinct. Our methoduses mean value estimates for various functions defined by Dirichletseries sampled at the zeros of the Riemann zeta-function. 1991Mathematics Subject Classification: 11M26. 相似文献
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This paper concerns a Markov operator T on a space L1, and aMarkov process P which defines a Markov operator on a spaceM of finite signed measures. For T, the paper presents necessaryand sufficient conditions for:
- a the existence of invariant probabilitydensities (IPDs)
- b the existence of strictly positive IPDs,and
- c the existence and uniqueness of IPDs.
- b the existence of strictly positive IPDs,and
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Delehanty JB Bradburne CE Susumu K Boeneman K Mei BC Farrell D Blanco-Canosa JB Dawson PE Mattoussi H Medintz IL 《Journal of the American Chemical Society》2011,133(27):10482-10489
Multicolor fluorescent labeling of both intra- and extracellular structures is a powerful technique for simultaneous monitoring of multiple complex biochemical processes. This approach remains extremely challenging, however, as it often necessitates the combinatorial use of numerous targeting probes (e.g., antibodies), multistep bioconjugation chemistries, different delivery strategies (e.g., electroporation or transfection reagents), cellular fixation coupled with membrane permeabilization, and complex spectral deconvolution. Here, we present a nanoparticle-based fluorescence labeling strategy for the multicolor labeling of distinct subcellular compartments within live cells without the need for antibody conjugation or cellular fixation/permeabilization. This multipronged approach incorporates an array of delivery strategies, which localize semiconductor quantum dots (QDs) to various subcellular structures. QD uptake is implemented in a spaciotemporal manner by staggering the delivery of QD-peptide composites and exploiting various innate (peptide-mediated endocytosis, peptide-membrane interaction, polymer-based transfection) along with physical (microinjection) cellular delivery modalities to live cells growing in culture over a 4 day period. Imaging of the different intracellular labels is simplified by the unique photophysical characteristics of the QDs in combination with Fo?rster resonance energy transfer sensitization, which allow for multiple spectral windows to be accessed with one excitation wavelength. Using this overall approach, QDs were targeted to both early and late endosomes, the cellular cytosol, and the plasma membrane in live cells, ultimately allowing for simultaneous five-color fluorescent imaging. 相似文献
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应用新发展的单一轨迹积分方法求解库仑加线性位的基态量子波函数,得到基态能量和波函数的一般解析表达式,并讨论了解的收敛性.应用此方法讨论了重夸克偶素系统. 相似文献
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Algar WR Wegner D Huston AL Blanco-Canosa JB Stewart MH Armstrong A Dawson PE Hildebrandt N Medintz IL 《Journal of the American Chemical Society》2012,134(3):1876-1891
The unique photophysical properties of semiconductor quantum dot (QD) bioconjugates offer many advantages for active sensing, imaging, and optical diagnostics. In particular, QDs have been widely adopted as either donors or acceptors in F?rster resonance energy transfer (FRET)-based assays and biosensors. Here, we expand their utility by demonstrating that QDs can function in a simultaneous role as acceptors and donors within time-gated FRET relays. To achieve this configuration, the QD was used as a central nanoplatform and coassembled with peptides or oligonucleotides that were labeled with either a long lifetime luminescent terbium(III) complex (Tb) or a fluorescent dye, Alexa Fluor 647 (A647). Within the FRET relay, the QD served as a critical intermediary where (1) an excited-state Tb donor transferred energy to the ground-state QD following a suitable microsecond delay and (2) the QD subsequently transferred that energy to an A647 acceptor. A detailed photophysical analysis was undertaken for each step of the FRET relay. The assembly of increasing ratios of Tb/QD was found to linearly increase the magnitude of the FRET-sensitized time-gated QD photoluminescence intensity. Importantly, the Tb was found to sensitize the subsequent QD-A647 donor-acceptor FRET pair without significantly affecting the intrinsic energy transfer efficiency within the second step in the relay. The utility of incorporating QDs into this type of time-gated energy transfer configuration was demonstrated in prototypical bioassays for monitoring protease activity and nucleic acid hybridization; the latter included a dual target format where each orthogonal FRET step transduced a separate binding event. Potential benefits of this time-gated FRET approach include: eliminating background fluorescence, accessing two approximately independent FRET mechanisms in a single QD-bioconjugate, and multiplexed biosensing based on spectrotemporal resolution of QD-FRET without requiring multiple colors of QD. 相似文献