全文获取类型
收费全文 | 1162篇 |
免费 | 25篇 |
国内免费 | 2篇 |
专业分类
化学 | 815篇 |
晶体学 | 9篇 |
力学 | 10篇 |
数学 | 45篇 |
物理学 | 310篇 |
出版年
2022年 | 9篇 |
2021年 | 9篇 |
2020年 | 7篇 |
2019年 | 13篇 |
2018年 | 8篇 |
2017年 | 7篇 |
2016年 | 18篇 |
2015年 | 15篇 |
2014年 | 16篇 |
2013年 | 73篇 |
2012年 | 52篇 |
2011年 | 75篇 |
2010年 | 37篇 |
2009年 | 45篇 |
2008年 | 57篇 |
2007年 | 69篇 |
2006年 | 59篇 |
2005年 | 55篇 |
2004年 | 52篇 |
2003年 | 43篇 |
2002年 | 47篇 |
2001年 | 33篇 |
2000年 | 27篇 |
1999年 | 14篇 |
1998年 | 15篇 |
1997年 | 11篇 |
1996年 | 16篇 |
1995年 | 13篇 |
1994年 | 22篇 |
1993年 | 12篇 |
1992年 | 18篇 |
1991年 | 17篇 |
1990年 | 14篇 |
1989年 | 13篇 |
1988年 | 14篇 |
1987年 | 11篇 |
1986年 | 10篇 |
1985年 | 24篇 |
1984年 | 13篇 |
1983年 | 9篇 |
1982年 | 10篇 |
1981年 | 15篇 |
1980年 | 15篇 |
1979年 | 17篇 |
1978年 | 8篇 |
1977年 | 7篇 |
1976年 | 7篇 |
1975年 | 8篇 |
1973年 | 9篇 |
1972年 | 3篇 |
排序方式: 共有1189条查询结果,搜索用时 15 毫秒
31.
H. Kagetsu N. Shioyasu N. Fukunishi M. K. Kubo Y. Sakai T. Tominaga K. Nishiyama K. Nagamine 《Hyperfine Interactions》1994,84(1):517-520
We have carried out SR experiments on [Co(NH3)6]Cl3 and [Co(ND3)6]Cl3. At 293 K, all the muons implanted into the complexes were in the diamagnetic state. The observed Gaussian-type muon spin relaxation function proved that the internal magnetic field was caused by nuclear dipole moments of the atoms in the complexes. In addition, another exponential-type muon spin relaxation function was observed in [Co(ND3)6]Cl3 below 50 K. 相似文献
32.
33.
Transition of the radial electric field by electron cyclotron heating in the CHS heliotron/torsatron
34.
Yoshiyuki Oishi Shoichi Nakata Masa-Aki Kakimoto Yoshio Imai 《Journal of polymer science. Part A, Polymer chemistry》1992,30(10):2217-2221
New segmented aromatic poly(ether sulfone)-amide and poly(ether sulfone)-imide copolymers were synthesized by the chain extension of α,w-diamine-terminated poly(ether sulfone) oligomer with both aromatic dicarboxylic acid chlorides and tetracarboxylic dianhydrides, respectively. Crystallization of the poly(ether sulfone)unit was suppressed by the introduction of amide or imide linkage along the polymer backbone, giving amorphous copolymers that were +eadily soluble in various organic solvents. The copolymers had somewhat higher glass transition temperatures than the parent poly(ether sulfone). They afforded transparent and tough films by solution casting. © 1992 John Wiley & Sons, Inc. 相似文献
35.
Komatsu T Hayakawa S Tsuchida E Nishide H 《Chemical communications (Cambridge, England)》2003,(1):50-51
alpha-Cyclodextrin (alpha CD)-penetrating 2-methyl-1-phenethylimidazole coordinates to the zinc(II) and iron(II) complexes of meso-tetrakis[o-(N-methyl)pyridinium] porphyrinate, giving non-covalently linked alpha CD-porphyrin ensembles; the iron(II) complex can reversibly bind and release dioxygen in aqueous DMF solution. 相似文献
36.
Hosoya K Hira N Watabe Y Tanaka N Kubo T Kaya K 《Analytical and bioanalytical chemistry》2004,380(2):343-345
Thiacalix[4]arene (5,11,17,23-tetra-tert-butyl-25,26,27,28-tetrahydroxy-2,8,14,20-tetrathiacalix[4]arene) is an amphiphilic molecule comprising four p-tert-butylphenol-like groups ortho-linked by single sulfur atoms. This molecule has a high electron density area owing to the close proximity of the hydroxyl groups and sulfur atoms. We studied the applicability of this interesting compound as a selector for high-performance liquid chromatography (HPLC) thereby presumably exploiting this feature. Firstly, uniformly sized polymer particles were prepared by using a multi-step swelling and polymerization method with ethylene glycol dimethacrylate (EDMA) as a cross-linker. Methacrylic acid (MAA) was introduced onto the surface of the resulting polymer particles through a new modification method. Thiacalix[4]arene was chemically bonded through the MAA group by using 1,4-dibromobutane as a spacer to reduce steric hindrance around the MAA and the polymer particle itself. The performance of the prepared polymer-based thiacalix[4]arene-modified stationary phase was evaluated with HPLC. Specific chromatographic retention behavior was observed for catechol relative to positional isomers of xylene, cresol, and benzene-diol. Catecholamine and catechol showed specific chromatographic retention behavior. 相似文献
37.
Miwa Kubo 《Tetrahedron letters》2006,47(12):1927-1931
We synthesized a peptidocalix[4]arene library consisting of 1000 members that was suitable for peptide recognition in aqueous media. Some peptidocalix[4]arenes in the library were host molecules for guest peptides. Electrostatic interaction between the host and guest molecules was the most important factor for binding in aqueous media. 相似文献
38.
A case of giant internal carotid ophthalmic aneurysm was presented. In order to clarify whether the patient could tolerate carotid occlusion, a balloon clamping test was performed. before surgery. The cerebral blood flow was measured using early imaging by single photon emission computed tomography (SPECT) with N-isopropyl-(iodine-123)-p-iodoamphetamine (123I-IMP). When the balloon clamping test was performed the tracer was injected, and scanning was performed 35 minutes after removing the catheter. This tracer enabled a "memory of blood flow" during temporary ischemia to determine the character of quick diffusion and slow wash out, that could not be performed by other methods of cerebral blood flow measurement. SPECT with 123I-IMP can simplify the measurement of cerebral blood flow during the balloon clamping test. 相似文献
39.
Ai Suzuki Parasuraman Selvam Tomonori Kusagaya Seiichi Takami Momoji Kubo Akira Imamura Akira Miyamoto 《International journal of quantum chemistry》2005,102(3):318-327
The decomposition reaction dynamics of 2,3,4,4′,5‐penta‐chlorinated biphenyl (2,3,4,4′,5‐PeCB), 3,3′,4,4′,5‐penta‐chlorinated biphenyl (3,3′,4,4′,5‐PeCB), and 2,3,7,8‐tetra‐chlorinated dibenzo‐p‐dioxin (2,3,7,8‐TCDD) was clarified for the first time at atomic and electronic levels, using our novel tight‐binding quantum chemical molecular dynamics method with first‐principles parameterization. The calculation speed of our new method is over 5000 times faster than that of the conventional first‐principles molecular dynamics method. We confirmed that the structure, energy, and electronic states of the above molecules calculated by our new method are quantitatively consistent with those by first‐principles calculations. After the confirmation of our methodology, we investigated the decomposition reaction dynamics of the above molecules and the calculated dynamic behaviors indicate that the oxidation of the 2,3,4,4′,5‐PeCB, 3,3′,4,4′,5‐PeCB, and 2,3,7,8‐TCDD proceeds through an epoxide intermediate, which is in good agreement with the previous experimental reports and consistent with our static density functional theory calculations. These results proved that our new tight‐binding quantum chemical molecular dynamics method with first‐principles parameterization is an effective tool to clarify the chemical reaction dynamics at reaction temperatures. © 2004 Wiley Periodicals, Inc. Int J Quantum Chem, 2005 相似文献
40.
Nomura S Itoh T Nakasho H Uno T Kubo M Sada K Inoue K Miyata M 《Journal of the American Chemical Society》2004,126(7):2035-2041
Highly conjugated monomers, 7,7,8,8-tetrakis(alkoxycarbonyl)quinodimethanes (methoxy (1a), ethoxy (1b), isopropoxy (1c), benzyloxy (1d), chloroethoxy (1e), and bromoethoxy (1f)), were synthesized. Recrystallizations of 1a, 1c, 1e, and 1f yielded two crystal forms (prisms (1a-A) and needles (1a-B), needles (1c-A) and plates (1c-B), prisms (1e-A) and plates (1e-B), and prisms (1f-A) and needles (1f-B)), which have different molecular packing modes by X-ray crystal structure analysis, indicating that the crystals are polymorphic. In the photopolymerizations of these monomer crystals in the solid state, 1a-A, 1e-A, and 1f-A polymerized topochemically to give crystalline polymers. For their thermal polymerizations in the solid state, in addition to 1a-A, 1e-A, and 1f-A, 1e-B and 1f-B polymerized, but polymers formed from the 1e-B and 1f-B were amorphous. The packing of quinodimethane molecules in the crystals was defined by four kinds of parameters, stacking distance (d(s)), the distance between the reacting exomethylene carbon atoms (d(cc)), the angles formed between the stacking axis and longer axis of the monomer molecule (theta(1)), and the shorter axis of the monomer molecule (theta(2)), and then the polymerization reactivity of these quinodimethanes in the solid state was discussed on the basis of these parameters. 相似文献