全文获取类型
收费全文 | 148篇 |
免费 | 17篇 |
国内免费 | 20篇 |
专业分类
化学 | 90篇 |
晶体学 | 7篇 |
力学 | 2篇 |
数学 | 16篇 |
物理学 | 70篇 |
出版年
2022年 | 1篇 |
2021年 | 1篇 |
2020年 | 4篇 |
2019年 | 1篇 |
2018年 | 1篇 |
2017年 | 2篇 |
2016年 | 6篇 |
2015年 | 1篇 |
2013年 | 6篇 |
2012年 | 14篇 |
2011年 | 7篇 |
2010年 | 5篇 |
2009年 | 6篇 |
2008年 | 7篇 |
2007年 | 6篇 |
2006年 | 8篇 |
2005年 | 4篇 |
2004年 | 10篇 |
2003年 | 10篇 |
2002年 | 11篇 |
2001年 | 7篇 |
2000年 | 11篇 |
1999年 | 4篇 |
1998年 | 2篇 |
1997年 | 3篇 |
1996年 | 1篇 |
1995年 | 1篇 |
1994年 | 2篇 |
1993年 | 1篇 |
1992年 | 1篇 |
1991年 | 4篇 |
1990年 | 2篇 |
1989年 | 4篇 |
1988年 | 2篇 |
1987年 | 1篇 |
1986年 | 1篇 |
1985年 | 2篇 |
1984年 | 2篇 |
1983年 | 2篇 |
1982年 | 4篇 |
1981年 | 4篇 |
1980年 | 1篇 |
1979年 | 2篇 |
1978年 | 2篇 |
1976年 | 3篇 |
1975年 | 2篇 |
1970年 | 1篇 |
1943年 | 1篇 |
1939年 | 1篇 |
排序方式: 共有185条查询结果,搜索用时 15 毫秒
71.
Shawn R. Hitchcock Ryan A. Davis Daniel M. Richmond Delvis D. Dore Stephanie L. Kuschel Jeremy F. Vaughn Jesse A. Wolfe Christopher G. Hamaker David M. Casper Jarvis Dingle 《Journal of heterocyclic chemistry》2008,45(5):1265-1274
72.
The effect of the molecular organization of lipid components on the properties of the bilayer membrane has been a topic of increasing interest. Several experimental and theoretical studies have suggested that cholesterol is not randomly distributed in the fluid-state lipid bilayer but forms nanoscale domains. Several cholesterol-enriched nanodomain structures have been proposed, including rafts, regular or maze arrays, complexes, and superlattices. At present, the molecular mechanisms by which lipid composition influences the formation and stability of lipid nanodomains remain unclear. In this study, we have used molecular dynamics (MD) simulations to investigate the effects of the molecular organization of cholesterol--superlattice versus random--on the structure of and interactions between lipids and water in lipid bilayers of cholesterol and 1-palmitoyl-2-oleoylphosphatidylcholine (cholesterol/POPC) at a fixed cholesterol mole fraction of 0.40. On the basis of four independent replicates of 200-ns MD simulations for a superlattice or random bilayer, statistically significant differences were observed in the lipid structural parameters, area per lipid, density profile, and acyl chain order profile, as well as the hydrogen bonding between various pairs (POPC and water, cholesterol and water, and POPC and cholesterol). The time evolution of the radial distribution of the cholesterol hydroxy oxygen suggests that the lateral distribution of cholesterol in the superlattice bilayer is more stable than that in the random bilayer. Furthermore, the results indicate that a relatively long simulation time, more than 100 ns, is required for these two-component bilayers to reach equilibrium and that this time is influenced by the initial lateral distribution of lipid components. 相似文献
73.
利用全量子理论的方法,研究了存在相位退相干时多光子T-C模型中两个二能级原子与二项式光场相互作用系统中两原子的布居数反转。讨论了相位退相干系数、二项式光场系数、最大光子数、跃迁光子数对原子布居数反转的影响。结果表明:相位退相干减少了原子布居数反转的振幅、破坏了原子的量子特性。改变跃迁光子数,可以改变原子间布居数反转演化周期及演化强度。当二项式光场的最大光子数增大时,原子布居差的崩塌-回复现象就会逐渐消失。相位退相干因子不变时, 二项式光场从相干态过渡到数态过程中,原子布居的振荡频率由大变小,周期性的崩塌与回复现象逐渐消失。 相似文献
74.
We investigate the thermoelectric properties of GaN with p-and n-type doping by the first principles calculation and the semi-classical Boltzmann theory. We find that the power factors (S2σof p-type GaN (-3500 W/mK2) is about twice that of the n-type (-1750 W/mK2), which indicates the thermoelectric properties of p-type GaN would be better. Thermal conductivity of GaN crystal decreases rapidly as the temperature increases, but it is still too large for thermoelectric applications. The figure of merit (ZT) estimated at 1500 K is 0.134 for p-type GaN crystal and 0.062 for the n-type. 相似文献
75.
Madden C Vaughn MD Díez-Pérez I Brown KA King PW Gust D Moore AL Moore TA 《Journal of the American Chemical Society》2012,134(3):1577-1582
Hydrogenases catalyze the interconversion of protons and hydrogen according to the reversible reaction: 2H(+) + 2e(-) ? H(2) while using only the earth-abundant metals nickel and/or iron for catalysis. Due to their high activity for proton reduction and the technological significance of the H(+)/H(2) half reaction, it is important to characterize the catalytic activity of [FeFe]-hydrogenases using both biochemical and electrochemical techniques. Following a detailed electrochemical and photoelectrochemical study of an [FeFe]-hydrogenase from Clostridium acetobutylicum (CaHydA), we now report electrochemical and single-molecule imaging studies carried out on a catalytically active hydrogenase preparation. The enzyme CaHydA, a homologue (70% identity) of the [FeFe]-hydrogenase from Clostridium pasteurianum , CpI, was adsorbed to a negatively charged, self-assembled monolayer (SAM) for investigation by electrochemical scanning tunneling microscopy (EC-STM) techniques and macroscopic electrochemical measurements. The EC-STM imaging revealed uniform surface coverage with sufficient stability to undergo repeated scanning with a STM tip as well as other electrochemical investigations. Cyclic voltammetry yielded a characteristic cathodic hydrogen production signal when the potential was scanned sufficiently negative. The direct observation of the single enzyme distribution on the Au-SAM surface coupled with macroscopic electrochemical measurements obtained from the same electrode allowed the evaluation of a turnover frequency (TOF) as a function of potential for single [FeFe]-hydrogenase molecules. 相似文献
76.
Kim CH Axup JY Dubrovska A Kazane SA Hutchins BA Wold ED Smider VV Schultz PG 《Journal of the American Chemical Society》2012,134(24):9918-9921
Bispecific antibodies were constructed using genetically encoded unnatural amino acids with orthogonal chemical reactivity. A two-step process afforded homogeneous products in excellent yield. Using this approach, we synthesized an anti-HER2/anti-CD3 bispecific antibody, which efficiently cross-linked HER2+ cells and CD3+ cells. In vitro effector-cell mediated cytotoxicity was observed at picomolar concentrations. 相似文献
77.
QCD PERTURBATION THEORY AND NUCLEI (1) THE ENERGY SHIFTS OF HADRENS AND HADRONS MASS DIFFERENCE MASS DIFFERENCE
下载免费PDF全文
![点击此处可从《中国物理C(英文版)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
QCD perturbation theory for confined quarks and gluons (inhadrons) is discussed.Based on the equivalent potential for the quark-gluon interaction derived, the energyshifts of hadrons and hadron mass difference in MIT bag (cavity) model and correcpond-ing approximation of the w. f. with Gassian form are calculated. 相似文献
78.
In the framework of density functional theory (DFT), the electronic excitations and nonlinear optical (NLO) properties of six binuclear transition metal cluster anions with the formula of [Ch2M-(μ-Ch)2-M'CN]^2- (M = Mo, W; Ch = S, Se; M' = Cu, Ag) have been systemically investigated at both cases of gas phase and DMF solution. The obtained electronic absorption spectra reveal that the element replacements of metals M and ligands Ch have significant influence on the absorptions, especially on the low-lying ones. In addition, the transitions of μ-Ch→M are dominant for the low-lying excitations, whereas the transitions of M'→M as well as Ch→M are mainly responsible for the higher excitations. The calculated molecular first and second hyperpolarizabilities present the remarkable element substitution and solvent effects. The analyses show that the transitions involving μ-Ch→M charge transfer make the critical contributions to the first hyperpolarizability t, and that the charge transfers from the moieties of MCh4 to M'CN as well as those of μ-Ch→M and M'→M are responsible for the second hyperpolarizability y. Moreover, the introduction of solvent leads to the results that the transitions within the moieties of MCh4 and M'CN make larger contributions to the hyperpolarizability, especially to γ. 相似文献
79.
Michael T. Vaughn 《Zeitschrift fur Physik C Particles and Fields》1982,13(2):139-146
Renormalization group constraints on the behavior of Yukawa and scalar quartic couplings in unified gauge theories are examined. Yukawa couplings are generally asymptotically free whenever the gauge couplings are, but scalar quartic couplings can be asymptotically free only for simple scalar multiplets in large groups with large fermion content. The infrared behavior of Yukawa and scalar quartic couplings implied by the renormalization group equations has interesting and phenomenologically useful consequences: infrared fixed points (or quasifixed points) lead to bounds on masses of fermions and scalars, while scalar quartic couplings can be driven out of the domain of positivity of the classical potential, with possible implications for patterns of symmetry breaking. 相似文献
80.
James M. Boncella Shu-Yu S. Wang Daniel D. Vanderlende R. Leigh Huff Khalil A. Abboud William M. Vaughn 《Journal of organometallic chemistry》1997,530(1-2):59-70
The complex W(NPh)Cl2[o-(NSiMe3)2C6H4] 3 was synthesized from PhN = WCl4 · OEt2 and N,N′-(Li2[o-(NSiMe3)2C6H4] and reacts with Lewis bases to form the adducts W(NPh)Cl2[o-(NSiMe3)2C6H4](L) (L = PMe3, THF, 3-picoline, tBuNC, MeCN) 4a–e. Crystals of 4a are triclinic, space group P1¯, with a = 9.562(1), b = 10.277(1), c = 14.920(2) Å, = 82.15(1), β = 80.18(1), γ = 80.41(1)°, and Z = 2. The structure was solved by the heavy atom method and refined to R = 0.0408 for 4224 observed (I > 2σ(I)) reflections. The dialkyl complexes W(NPh)R2[o-(NSiMe3)2C6H4] (R = Me, Et, CH2Ph, CH2CMe3, CH2CMe2Ph) 5–9 are formed through subsequent reactions of 3 with the corresponding Grignard reagent. Crystals of complex 5 are monoclinic, space group P2(1)/n, with a = 10.3545(2), b = 17.9669(1), c = 13.3168(1) Å, β = 103.826(1)°, and Z = 4. The structure of complex 5 was solved by direct methods in SHELXTL5 and refined to R = 0.0247 for 4572 observed reflections. Compound 5 has a square pyramidal geometry in which the imido ligand occupies the apical position and reacts with PMe3 to form the adduct W(NPh)Me2[o-(NSiMe3)2C6H4](PMe3) 5a. Crystals of complex 5a are monoclinic, space group C2/m, with a = 13.5336(1), b = 14.4291(1), c = 15.3785(1) Å, β = 110.365(1)°, and Z = 4. The structure of compound 5a was solved by direct methods in shelxtl5 and refined to R = 0.0272 for 3057 observed reflections. Crystals of the bis-neopentyl complex 8 are monoclinic, space group P2(1)/n, with a = 10.6992(4), b = 18.3144(7), c = 16.0726(6) Å, β = 92.042(1)°, and Z = 4. The structure of 8 was solved by direct methods in shelxtl5 and refined to R = 0.0261 for 5881 observed reflections. Complex 8 has a trigonal bipyramidal geometry with both neopentyl groups and one amido nitrogen in the equatorial plane. 相似文献