全文获取类型
收费全文 | 822篇 |
免费 | 31篇 |
国内免费 | 2篇 |
专业分类
化学 | 652篇 |
晶体学 | 9篇 |
力学 | 3篇 |
综合类 | 1篇 |
数学 | 61篇 |
物理学 | 129篇 |
出版年
2024年 | 1篇 |
2023年 | 10篇 |
2022年 | 7篇 |
2021年 | 18篇 |
2020年 | 11篇 |
2019年 | 19篇 |
2018年 | 12篇 |
2017年 | 7篇 |
2016年 | 20篇 |
2015年 | 23篇 |
2014年 | 25篇 |
2013年 | 43篇 |
2012年 | 51篇 |
2011年 | 58篇 |
2010年 | 34篇 |
2009年 | 31篇 |
2008年 | 55篇 |
2007年 | 60篇 |
2006年 | 76篇 |
2005年 | 57篇 |
2004年 | 44篇 |
2003年 | 40篇 |
2002年 | 32篇 |
2001年 | 11篇 |
2000年 | 9篇 |
1999年 | 9篇 |
1998年 | 11篇 |
1997年 | 9篇 |
1996年 | 7篇 |
1995年 | 3篇 |
1994年 | 3篇 |
1993年 | 6篇 |
1992年 | 3篇 |
1991年 | 2篇 |
1990年 | 2篇 |
1988年 | 1篇 |
1985年 | 5篇 |
1984年 | 11篇 |
1983年 | 1篇 |
1982年 | 7篇 |
1981年 | 1篇 |
1980年 | 2篇 |
1979年 | 1篇 |
1977年 | 5篇 |
1976年 | 3篇 |
1975年 | 2篇 |
1974年 | 2篇 |
1973年 | 2篇 |
1972年 | 2篇 |
1970年 | 1篇 |
排序方式: 共有855条查询结果,搜索用时 15 毫秒
91.
92.
3-Chloro-2,5-dimethylpyrazine 1-oxide underwent cross-coupling with dialkylzinc reagents forming 3-alkyl-2,5-dimethylpyrazine 1-oxides. The reaction was realized by catalytic 1,3-bis(diphenylphosphino)-propane nickel(II) chloride and the optimum results were examined. 相似文献
93.
Tomoyuki Sekine Kunimitsu Uchinokura Mitsuru Izumi Etsuyuki Matsuura 《Solid State Communications》1984,52(4):379-383
The phase transition of the linear chain compound (NbSe4)3I was studied by Raman scattering. At 78 K three new peaks were observed at 73 cm?1, 205 cm?1 and 261 cm?1. The totally symmetric Raman peak at 73 cm?1 shows anomalous temperature dependence. The frequency decreases with increasing temperature, and at high temperatures an anticrossing occurs with another peak observed at about 58 cm?1. The Raman intensity decreases and the linewidth broadens remarkably as the temperature increases. These properties allow us to assign this peak to a soft phonon. This fact indicates clearly the existence of a structural phase transition of a displacive type below room temperature. 相似文献
94.
95.
Koichiro Fukuda Akira Moriyama Tomoyuki Iwata 《Journal of solid state chemistry》2005,178(6):2144-2151
The crystal structure of BaZr(PO4)2 at 298 K was determined from conventional X-ray powder diffraction data using direct methods, and it was further refined by the Rietveld method. The structure was monoclinic (space group C2/m, Z=2) with , , , β=93.086(1)° and . Final reliability indices were Rwp=8.21%, Rp=5.64% and RB=2.92%. The atom arrangement is similar to that of yavapaiite (KFe(SO4)2), however, these crystal structures differ distinctly in the coordination numbers of barium and potassium atoms; the former is tenfold coordinated, whereas the latter is sixfold coordinated. The powder specimens were also examined by high-temperature XRD and DTA to reveal the occurrence of a phase transition from monoclinic to orthorhombic at 732 K during heating. Upon cooling the reverse transition occurred at 710 K. The monoclinic crystal expanded almost one-dimensionally along [503] during the heating process. The orthorhombic phase also showed a tendency to expand one-dimensionally along the c-axis above 732 K. 相似文献
96.
Masaki Kita Tomoyuki Koyama Hiroshi Matsumoto Daisuke Uemura 《Tetrahedron letters》2005,46(49):8583-8585
The muricid gastropods genus Drupella are known to be voracious coral predator. Outbreaks of them have accelerated significant destruction on coral reefs, but its precise mechanism is poorly understood. Here, we describe the identification of montiporic acids C (1) and A (2) isolated from sea water extracts of the coral Montipora sp., which showed potent feeding-attractant activity toward D. cornus. 相似文献
97.
Mochida T Takazawa K Matsui H Takahashi M Takeda M Sato M Nishio Y Kajita K Mori H 《Inorganic chemistry》2005,44(23):8628-8641
Charge-transfer salts of branched-alkyl biferrocenes, (1',1' '-R2-1,1' '-biferrocene)[Ni(mnt)2] (1a, R = isopropyl; 2a, R = dineopentyl) and (1',1' '-R2-1,1' '-biferrocene)2[Co(mnt)2]2 (1b, R = isopropyl; 2b, R = dineopentyl), were prepared. Their valence states were investigated using X-ray crystallography and M?ssbauer spectroscopy. Complexes 1a and 1b show segregated-stack crystal structures that contain columns of acceptors, whereas structures of 2a and 2b, which contain bulky donors, are rather discrete. All of the complexes contain mixed-valent biferrocenium monocations. A two-step valence transition was found in complex 1a. The crystal contains two crystallographically independent cations: one undergoes valence localization below room temperature; the other undergoes valence localization below ca. 130 K. The former transition is derived from asymmetry of the crystal environment around the cation, whereas the latter one is caused by symmetry lowering coupled with a spin-Peierls transition (T(C) = 133.2 K) associated with the dimerization of the acceptors. This compound was found to exhibit a dielectric response based on valence tautomerization. Other complexes (1b, 2a, and 2b) show a valence-trapped state. In all complexes, charge localization was found to occur through local electrostatic interactions between the donor's cationic moiety and the acceptor's electronegative moieties. 相似文献
98.
99.
Akira Ishikawa Tomoyuki Ohno Shinji Sakano Yoshihiro Shiroishi 《Journal of magnetism and magnetic materials》1993,120(1-3):357-361
The magnetic properties and crystalline structure of Co alloy film deposited on a regularly corrugated substrate have been studied. Microscopic grooves are lithographically fabricated on InP substrates. In-plane anisotropy energy is 4–5×104J/m3. The magnetic anisotropy is affected by the crystallographic orientation and the microscopic shape of the corrugated Co alloy film. 相似文献
100.
Kishida I Koyama Y Kuwabara A Yamamoto T Oba F Tanaka I 《The journal of physical chemistry. B》2006,110(16):8258-8262
Migration of Li+ ions via the vacancy mechanism in LiX (X = F, Cl, Br, and I) with the rocksalt and hypothetical zinc blende structures and Li2X (X = O, S, Se, and Te) with the antifluorite structure has been investigated using first-principles projector augmented wave calculations with the generalized gradient approximation. The migration paths and energies, determined by the nudged-elastic-band method, are discussed on the basis of two idealized models: the rigid-sphere and charged-sphere models. The trajectories and energy profiles of the migration in these lithium compounds vary between these two models, depending on the anion species and crystal structure. The migration energies in LiX with both the rocksalt and hypothetical zinc blende structures show a tendency to decrease with increasing periodic number of the anion species in the periodic table. This is consistent with the widely accepted view that anion species with large ionic radii and high polarizabilities are favorable for good ionic conduction. In contrast, Li2O exhibits the lowest migration energy among Li2X compounds, although O is the smallest among the chalcogens, indicating that electrostatic attractive interactions play the dominant role in the inter-ion interactions in Li2O and, therefore, in the ion migration. 相似文献