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排序方式: 共有321条查询结果,搜索用时 62 毫秒
311.
We present the time-dependent holographic electron density theorem (TD-HEDT), which lays the foundation of time-dependent density-functional theory (TDDFT) for open electronic systems. For any finite electronic system, the TD-HEDT formally establishes a one-to-one correspondence between the electron density inside any finite subsystem and the time-dependent external potential. As a result, any electronic property of an open system in principle can be determined uniquely by the electron density function inside the open region. Implications of the TD-HEDT on the practicality of TDDFT are also discussed. 相似文献
312.
Yuangang Lu Cunlei Li Xuping Zhang Scott Yam 《Optics and Lasers in Engineering》2011,49(9-10):1111-1117
The thermal residual strain induced in the cabled optical fiber is a very important factor for evaluating the reliability of optical fiber cables. In order to determine the distributed thermal residual strain in cabled optical fiber, a measurement method based on Brillouin optical time-domain reflectometry (BOTDR) system is proposed in the article. Thermal characteristics of residual strain along cabled optical fibers are investigated theoretically and experimentally based on Brillouin frequency shift (BFS) detection. The thermal residual strain along the cabled fiber, if any, can be determined with a high spatial resolution that is equal to that of the BOTDR system and can be less than a few meters. A double-coated fiber in loose optical cable was used as the test cabled optical fiber, and the experimental results were in good agreement with those predicted from the theory. It has been found that the fiber residual strain increases linearly with decreasing temperature in the range from 50 to ?50 °C. 相似文献
313.
Tao Yu Daniel Ping‐Kuen Tsang Dr. Vonika Ka‐Man Au Dr. Wai Han Lam Dr. Mei‐Yee Chan Prof. Dr. Vivian Wing‐Wah Yam 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(40):13418-13427
A series of triarylamine‐containing tricarbonyl rhenium(I) complexes, [BrRe(CO)3(N^N)] (N^N=5,5′‐bis(N,N‐diaryl‐4‐[ethen‐1‐yl]‐aniline)‐2,2′‐bipyridine), has been designed and synthesized by introducing a rhenium(I) metal center into a donor‐π‐acceptor‐π‐donor structure. All of the complexes showed an intense broad structureless emission band in dichloromethane at around 680–708 nm, which originated from an excited state of intraligand charge transfer (3ILCT) character from the triarylamine to the bipyridine moiety. Upon introduction of the bulky and electron‐donating pentaphenylbenzene units attached to the aniline groups, the emission bands were found to be red shifted. The nanosecond transient absorption spectra of two selected complexes were studied, which were suggestive of the formation of an initial charge‐separated state. Computational studies have been performed to provide further insight into the origin of the absorption and emission. One of the rhenium(I) complexes has been utilized in the fabrication of organic light‐emitting diodes (OLEDs), representing the first example of the realization of deep red to near‐infrared rhenium(I)‐based OLEDs with an emission extending up to 800 nm. 相似文献
314.
Saturated Red‐Light‐Emitting Gold(III) Triphenylamine Dendrimers for Solution‐Processable Organic Light‐Emitting Devices 下载免费PDF全文
Man‐Chung Tang Dr. Carmen Ka‐Man Chan Dr. Daniel Ping‐Kuen Tsang Yi‐Chun Wong Dr. Maggie Mei‐Yee Chan Dr. Keith Man‐Chung Wong Prof. Vivian Wing‐Wah Yam 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(46):15233-15241
A novel isoquinoline‐containing C^N^C ligand and its phosphorescent triphenylamine‐based alkynylgold(III) dendrimers have been synthesized. These alkynylgold(III) dendrimers serve as phosphorescent dopants in the fabrication of efficient solution‐processable organic light‐emitting devices (OLEDs). The photophysical, electrochemical, and electroluminescence properties were studied. A saturated red emission with CIE coordinates of (0.64, 0.36) and a high EQE value of 3.62 % were achieved. Unlike other red‐light‐emitting iridium(III) dendrimers, a low turn‐on voltage of less than 3 V and a reduced efficiency roll‐off at high current densities were observed; this can be accounted for by the enhanced carrier transporting ability and the relatively short lifetimes in the high‐generation dendrimers. This class of alkynylgold(III) dendrimers are promising candidates as phosphorescent dopants in the fabrication of solution‐processable OLEDs. 相似文献
315.
316.
Noonan KJ Feldscher B Bates JI Kingsley JJ Yam M Gates DP 《Dalton transactions (Cambridge, England : 2003)》2008,(33):4451-4457
The chemical functionality of poly(methylenephosphine) n-Bu[MesP-CPh(2)](n)H () is examined in reactions with two isoelectronic species, namely BH(3) and CH(3)(+). The potential reactivity of polymer is modelled by examining the reactivity of molecular phosphines bearing similar substituents as the polymer. In particular, the phosphine-borane adducts Mes(Me)P(BH(3))-CPh(2)H () and Mes(Me)P(BH(3))-CPh(2)SiMe(2)H () are prepared from the reaction of BH(3).SMe(2) with Mes(Me)P-CPh(2)H () or Mes(Me)P-CPh(2)SiMe(2)H (), respectively. Treating with MeOTf affords the methylated model compound, [Mes(Me)(2)P-CPh(2)H]OTf (). X-Ray crystal structures are reported for each model compound. The reaction of n-Bu[MesP-CPh(2)](n)H (M(n) = 3.89 x 10(4), PDI = 1.34) with BH(3).SMe(2) affords the phosphine-borane polymer n-Bu[MesP(BH(3))-CPh(2)](n)H () (M(n) = 4.13 x 10(4), PDI = 1.26). In contrast, methylation of phosphine polymer gives n-Bu[MesP-CPh(2)](x)-/-[MesP(Me)-CPh(2)](y)H.(OTf)(y) () where approximately 50% of the phosphine moieties are methylated (from (31)P NMR). 相似文献
317.
Z Yin AY Tam KM Wong CH Tao B Li CT Poon L Wu VW Yam 《Dalton transactions (Cambridge, England : 2003)》2012,41(37):11340-11350
A series of BODIPY (4,4-difluoro-4-bora-3a,4a-diaza-s-indacene) derivatives containing ion- and pH-sensory units have been successfully designed and synthesized. One of the compounds was structurally characterized by X-ray crystallography. Owing to the presence of an ICT absorption band, one of the compounds was found to show pronounced solvatochromic behavior in different organic solvents. Their emission energies in various solvents show a linear dependence on the Lippert solvent parameter. The cation-binding properties of the complexes with different metal ions (alkali metal, alkaline earth metal and transition metal ions) have been studied using UV-vis and emission spectroscopies. A 1?:?1 complexation to metal ions (Li(+), Na(+), Mg(2+), Ba(2+), Zn(2+), Cd(2+)) was found for the compound with one azacrown moiety in acetonitrile while another one with two azacrown moieties was shown to form 1?:?2 complexes with Zn(2+) and Mg(2+) cations. Their stability constants have been determined by both UV-vis and emission spectrophotometric methods. By introducing triarylborane moieties into the meso position and the 2-position of the BODIPY skeleton, different electronic absorption spectral changes together with an emission diminution were observed in response to fluoride ions. Ditopic binding study of 5, which was functionalized with both azacrown and triarylborane moieties, showed emission enhancement in the presence of Mg(2+) and F(-). These findings suggest that these BODIPY derivatives are capable of serving as versatile colorimetric and luminescence probes for pH, cations and F(-). 相似文献
318.
Xuqiao Hu Hongyan Li Tiffany Ka-Yan Ip Yam Fung Cheung Mohamad Koohi-Moghadam Haibo Wang Xinming Yang Daniel N. Tritton Yuchuan Wang Yi Wang Runming Wang Kwan-Ming Ng Hua Naranmandura Eric Wai-Choi Tse Hongzhe Sun 《Chemical science》2021,12(32):10893
The mechanisms of action of arsenic trioxide (ATO), a clinically used drug for the treatment of acute promyelocytic leukemia (APL), have been actively studied mainly through characterization of individual putative protein targets. There appear to be no studies at a system level. Herein, we integrate metalloproteomics through a newly developed organoarsenic probe, As-AC (C20H17AsN4O3S2) with quantitative proteomics, allowing 37 arsenic binding and 250 arsenic regulated proteins to be identified in NB4, a human APL cell line. Bioinformatics analysis reveals that ATO disrupts multiple physiological processes, in particular, chaperone-related protein folding and cellular response to stress. Furthermore, we discover heat shock protein 60 (Hsp60) as a vital target of ATO. Through biophysical and cell-based assays, we demonstrate that ATO binds to Hsp60, leading to abolishment of Hsp60 refolding capability. Significantly, the binding of ATO to Hsp60 disrupts the formation of Hsp60-p53 and Hsp60-survivin complexes, resulting in degradation of p53 and survivin. This study provides significant insights into the mechanism of action of ATO at a systemic perspective, and serves as guidance for the rational design of metal-based anticancer drugs.A highly selective organoarsenic fluorescent probe As-AC and quantitative proteomics were employed to track arsenic-binding and regulating proteins in live leukemia cells. Hsp60 was validated as a new target of ATO. 相似文献
319.
William Alan Bertsche G. B. Andresen M. D. Ashkezari M. Baquero-Ruiz P. D. Bowe P. T. Carpenter E. Butler C. L. Cesar S. F. Chapman M. Charlton S. Eriksson J. Fajans T. Friesen M. C. Fujiwara D. R. Gill A. Gutierrez J. S. Hangst W. N. Hardy R. S. Hayano M. E. Hayden A. J. Humphries J. L. Hurt R. Hydomako S. Jonsell L. Kurchaninov N. Madsen S. Menary P. Nolan K. Olchanski A. Olin A. Povilus P. Pusa F. Robicheaux E. Sarid D. M. Silveira C. So J. W. Storey R. I. Thompson D. P. van der Werf J. S. Wurtele Y. Yamazaki 《Hyperfine Interactions》2012,212(1-3):61-67
In efforts to trap antihydrogen, a key problem is the vast disparity between the neutral trap energy scale ( $\sim\!50\,\upmu\mathrm{eV}$ ), and the energy scales associated with plasma confinement and space charge (~1 eV). In order to merge charged particle species for direct recombination, the larger energy scale must be overcome in a manner that minimizes the initial antihydrogen kinetic energy. This issue motivated the development of a novel injection technique utilizing the inherent nonlinear nature of particle oscillations in our traps. We demonstrated controllable excitation of the center-of-mass longitudinal motion of a thermal antiproton plasma using a swept-frequency autoresonant drive. When the plasma is cold, dense and highly collective in nature, we observe that the entire system behaves as a single-particle nonlinear oscillator, as predicted by a recent theory. In contrast, only a fraction of the antiprotons in a warm or tenuous plasma can be similarly excited. Antihydrogen was produced and trapped by using this technique to drive antiprotons into a positron plasma, thereby initiating atomic recombination. The nature of this injection overcomes some of the difficulties associated with matching the energies of the charged species used to produce antihydrogen. 相似文献
320.