全文获取类型
收费全文 | 76篇 |
免费 | 6篇 |
国内免费 | 1篇 |
专业分类
化学 | 40篇 |
力学 | 1篇 |
数学 | 19篇 |
物理学 | 23篇 |
出版年
2022年 | 1篇 |
2021年 | 2篇 |
2020年 | 4篇 |
2019年 | 2篇 |
2016年 | 2篇 |
2015年 | 3篇 |
2014年 | 3篇 |
2013年 | 1篇 |
2012年 | 1篇 |
2011年 | 1篇 |
2010年 | 2篇 |
2009年 | 1篇 |
2008年 | 2篇 |
2007年 | 7篇 |
2006年 | 2篇 |
2005年 | 4篇 |
2004年 | 5篇 |
2003年 | 2篇 |
2001年 | 2篇 |
2000年 | 1篇 |
1999年 | 1篇 |
1996年 | 2篇 |
1995年 | 3篇 |
1994年 | 2篇 |
1993年 | 4篇 |
1992年 | 4篇 |
1987年 | 1篇 |
1986年 | 1篇 |
1985年 | 2篇 |
1984年 | 3篇 |
1983年 | 1篇 |
1981年 | 1篇 |
1979年 | 2篇 |
1978年 | 2篇 |
1975年 | 2篇 |
1962年 | 1篇 |
1961年 | 1篇 |
1959年 | 1篇 |
1926年 | 1篇 |
排序方式: 共有83条查询结果,搜索用时 15 毫秒
1.
Plieger PG Ehler DS Duran BL Taylor TP John KD Keizer TS McCleskey TM Burrell AK Kampf JW Haase T Rasmussen PG Karr J 《Inorganic chemistry》2005,44(16):5761-5769
The ligand 4,5-dicarboxyimidazole (H(2)DCI) and its methyl derivative 1-methyl-4,5-dicarboxyimidazole (H(2)MDCI) have been shown to bind to Be(II) forming a zwitterionic species that has been structurally characterized. A new dicarboxyimidazole-based polymer has been prepared and its Be-binding properties have been studied using NMR ((1)H and (9)Be) and fluorescence spectroscopy; it represents a rare example of beryllium binding to a polymer. Models of the mononuclear and polymeric Be(II)-binding sites have been studied using density functional theory (DFT), and the (9)Be NMR chemical shifts of these model materials have been calculated for the purpose of direct comparison to experimentally observed values. Differences in the binding modes of the mononuclear and polymeric species are discussed. 相似文献
2.
3.
4.
5.
We report the operation of a 50 mW continuous-wave quantum cascade laser (QCL) in the 9.2 microm range, phase locked to a single-mode CO(2) laser with a tunable frequency offset. The wide free-running emission spectrum of the QCL (3-5 MHz) is strongly narrowed down to the kilohertz range, making it suitable for high-resolution molecular spectroscopy. 相似文献
6.
Phenothiazine–BODIPY–Fullerene Triads as Photosynthetic Reaction Center Models: Substitution and Solvent Polarity Effects on Photoinduced Charge Separation and Recombination 下载免费PDF全文
Chandra B. KC Gary N. Lim Dr. Vladimir N. Nesterov Prof. Dr. Paul A. Karr Prof. Dr. Francis D'Souza 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(51):17100-17112
Novel photosynthetic reaction center model compounds of the type donor2–donor1–acceptor, composed of phenothiazine, BF2‐chelated dipyrromethene (BODIPY), and fullerene, respectively, have been newly synthesized using multistep synthetic methods. X‐ray structures of three of the phenothiazine‐BODIPY intermediate compounds have been solved to visualize the substitution effect caused by the phenothiazine on the BODIPY macrocycle. Optical absorption and emission, computational, and differential pulse voltammetry studies were systematically performed to establish the molecular integrity of the triads. The N‐substituted phenothiazine was found to be easier to oxidize by 60 mV compared to the C‐substituted analogue. The geometry and electronic structures were obtained by B3LYP/6‐31G(dp) calculations (for H, B, N, and O) and B3LYP/6‐31G(df) calculations (for S) in vacuum, followed by a single‐point calculation in benzonitrile utilizing the polarizable continuum model (PCM). The HOMO?1, HOMO, and LUMO were, respectively, on the BODIPY, phenothiazine and fullerene entities, which agreed well with the site of electron transfer determined from electrochemical studies. The energy‐level diagram deduced from these data helped in elucidating the mechanistic details of the photochemical events. Excitation of BODIPY resulted in ultrafast electron transfer to produce PTZ–BODIPY.+–C60.?; subsequent hole shift resulted in PTZ.+–BODIPY–C60.? charge‐separated species. The return of the charge‐separated species was found to be solvent dependent. In nonpolar solvents the PTZ.+–BODIPY–C60.? species populated the 3C60* prior to returning to the ground state, while in polar solvent no such process was observed due to relative positioning of the energy levels. The 1BODIPY* generated radical ion‐pair in these triads persisted for few nanoseconds due to electron transfer/hole‐shift mechanism. 相似文献
7.
Dr. Luis Martín-Gomis Sairaman Seetharaman David Herrero Prof. Dr. Paul A. Karr Prof. Dr. Fernando Fernández-Lázaro Prof. Dr. Francis D'Souza Prof. Dr. Ángela Sastre-Santos 《Chemphyschem》2020,21(20):2254-2262
The effect of donor-acceptor distance in controlling the rate of electron transfer in axially linked silicon phthalocyanine-C60 dyads has been investigated. For this, two C60-SiPc-C60 dyads, 1 and 2 , varying in their donor-acceptor distance, have been newly synthesized and characterized. In the case of C60-SiPc-C60 1 where the SiPc and C60 are separated by a phenyl spacer, faster electron transfer was observed with kcs equal to 2.7×109 s−1 in benzonitrile. However, in the case of C60-SiPc-C60 2 , where SiPc and C60 are separated by a biphenyl spacer, a slower electron transfer rate constant, kcs=9.1×108 s−1, was recorded. The addition of an extra phenyl spacer in 2 increased the donor-acceptor distance by ∼4.3 Å, and consequently, slowed down the electron transfer rate constant by a factor of ∼3.7. The charge separated state lasted over 3 ns, monitoring time window of our femtosecond transient spectrometer. Complimentary nanosecond transient absorption studies revealed formation of 3SiPc* as the end product and suggested the final lifetime of the charge separated state to be in the 3–20 ns range. Energy level diagrams established to comprehend these mechanistic details indicated that the comparatively high-energy SiPc.+-C60.− charge separated states (1.57 eV) populated the low-lying 3SiPc* (1.26 eV) prior returning to the ground state. 相似文献
8.
Alan F. Karr 《Operations Research Letters》1984,3(2):59-63
Since 1975 there has developed a powerful and sophisticated theory of statistical inference for point processes known as the ‘martingale method’. Because it is based on deep and in many cases technical results in the (French) general theory of stochastic processes, it has remained inaccessible to many who might usefully apply it. Yet the fundamental ideas (as opposed to the details, which can be formidable) are not hopelessly arcane; our purposes here are to describe the theory in a manner that reveals its underlying conceptual simplicity (although oversimplified, (6) below is the essential idea), to illustrate it with three examples, and to give some points of entry into the complex and now rather extensive literature. This is not a guide to application, much less even an incomplete development of the theory, but merely (so to speak) a silhoutte. 相似文献
9.
Messin G Karr JP Baas A Khitrova G Houdré R Stanley RP Oesterle U Giacobino E 《Physical review letters》2001,87(12):127403
We present novel experimental results demonstrating the coherence properties of the nonlinear emission from semiconductor microcavities in the strong coupling regime, recently interpreted by parametric polariton four-wave mixing. We use a geometry corresponding to degenerate four-wave mixing. In addition to the predicted threshold dependence of the emission on the pump power and spectral blueshift, we observe a phase dependence of the amplification which is a signature of a coherent polariton wave mixing process. 相似文献
10.
We demonstrate a novel kind of polariton four wave mixing oscillation. Two pump polaritons scatter towards final states that emit two beams of equal intensity, separated both spatially and in polarization with respect to the pumps. The measurement of the intensity fluctuations of the emitted light demonstrates that the final states are strongly correlated. 相似文献