全文获取类型
收费全文 | 552篇 |
免费 | 10篇 |
国内免费 | 4篇 |
专业分类
化学 | 398篇 |
晶体学 | 4篇 |
力学 | 9篇 |
数学 | 27篇 |
物理学 | 128篇 |
出版年
2023年 | 2篇 |
2021年 | 5篇 |
2020年 | 4篇 |
2019年 | 7篇 |
2018年 | 4篇 |
2017年 | 4篇 |
2016年 | 11篇 |
2015年 | 10篇 |
2014年 | 10篇 |
2013年 | 26篇 |
2012年 | 25篇 |
2011年 | 33篇 |
2010年 | 16篇 |
2009年 | 18篇 |
2008年 | 26篇 |
2007年 | 38篇 |
2006年 | 35篇 |
2005年 | 39篇 |
2004年 | 24篇 |
2003年 | 25篇 |
2002年 | 23篇 |
2001年 | 18篇 |
2000年 | 17篇 |
1999年 | 14篇 |
1997年 | 3篇 |
1996年 | 2篇 |
1995年 | 9篇 |
1994年 | 8篇 |
1993年 | 5篇 |
1992年 | 8篇 |
1991年 | 6篇 |
1990年 | 6篇 |
1989年 | 2篇 |
1988年 | 6篇 |
1987年 | 8篇 |
1986年 | 6篇 |
1985年 | 6篇 |
1984年 | 9篇 |
1983年 | 4篇 |
1982年 | 2篇 |
1981年 | 3篇 |
1980年 | 3篇 |
1979年 | 6篇 |
1978年 | 4篇 |
1977年 | 6篇 |
1975年 | 3篇 |
1974年 | 5篇 |
1968年 | 2篇 |
1967年 | 2篇 |
1965年 | 2篇 |
排序方式: 共有566条查询结果,搜索用时 31 毫秒
1.
Hiroyuki Saimoto Tomoyuki Onitsuka Satoko Okabe Minoru Morimoto 《Tetrahedron letters》2004,45(48):8777-8780
Treatment of 1,3-dihydroxyacetone and acrolein with aqueous KOH gave a tetrahydrofuran derivative, 1,4-dihydroxy-3,7-dioxabicyclo[3.3.0]octane, in 80% yield. Similarly, 6-alkyl substituted 1,4-dihydroxy-3,7-dioxabicyclo[3.3.0]octanes were obtained by reaction of 1,3-dihydroxyacetone with various α,β-unsaturated aldehydes. In the cases of long chain alkenals, the reaction was effectively accelerated in the presence of organic co-solvent. On the other hand, the corresponding tricyclic products were synthesized by reaction of 1,3-dihydroxyacetone with cyclic enones, such as 2-cyclopentenone and 2-cyclohexenone. This method was successfully applied to the reaction of a tetrulose in the absence of any protecting groups. 相似文献
2.
T. Ishii M. Asai A. Makishima I. Hossain P. Kleinheinz M. Ogawa M. Matsuda S. Ichikawa 《The European Physical Journal A - Hadrons and Nuclei》2002,13(1-2):15-19
Nuclei in the neutron-rich Ni region have been studied by γ-ray spectroscopy. Gamma-rays emitted from isomers, with T
1/2 > 1 ns, produced in heavy-ion deep-inelastic collisions were measured with an isomer-scope. The nuclear structure of the
doubly magic 68Ni and its neighbor 69,71Cu is discussed on the basis of the shell model. Future experiments for more neutron-rich Ni nuclei are also viewed.
Received: 1 May 2001 / Accepted: 4 December 2001 相似文献
3.
N. Hamamoto J. Jitsukawa C. Satoko 《The European Physical Journal D - Atomic, Molecular, Optical and Plasma Physics》2002,19(2):211-221
First-principle electronic structure calculations are carried out for MxC 60 q , where M = Li, Na, K and ( x , q ) = (1, 0),(1,±1),(2, 0),(3, - 1),(6, 0),(6, - 1),(12, 0) using the local density functional. The electric dipole moment for MC60 agrees with the experimental results. The calculated Mulliken charge indicates that the bonding of the alkali atom with C60 is mostly ionic except for lithium. The alkali atom prefers to make many bonds with the carbon atoms rather than a single bond with the neighbor carbon atom. The calculated adsorption energy suggest that the metal-metal bonding of sodiums and potassiums on C60 arises for more than the six valence electrons in the alkali atoms. The lithium-lithium bond is, on the other hand, not appeared for x ? 12. The difference in the most stable geometry between lithiums and the other alkali atoms on C60 comes from the covalent character of the lithium-carbon bond. 相似文献
4.
Rozics and Johnson's formula is examined and its inconsistency is pointed out. 相似文献
5.
6.
Y. Nagame M. Asai H. Haba K. Tsukada I. Nishinaka S. Goto A. Toyoshima K. Akiyama M. Sakama Y. L. Zhao S. Ichikawa H. Nakahara 《Physics of Atomic Nuclei》2003,66(6):1131-1136
The present status of heavy element nuclear chemistry research at JAERI (Japan Atomic Energy Research Institute) is reviewed. Production of the transactinide nuclei 261Rf and 262Db via the reactions of 248Cm(18O,5n) and 248Cm(19F, 5n), respectively, at the JAERI tandem accelerator is reported. Study of the aqueous chemistry of Rf is being carried out with a newly developed rapid ion-exchange separation apparatus. Anion-exchange behavior of Rf in acidic solution is briefly discussed. Recent experimental results on decay studies of neutron-deficient actinide nuclei using the gas-jet coupled JAERI-ISOL are given. We also discuss characteristics of nuclear deformation properties at scission in symmetric and asymmetric fission of actinides. Prospects for studies in the near future are briefly considered. 相似文献
7.
Esters of sulphur-containing 5- and 6-membered heterocycles, tetrahydro-3- and 4-thiopyranol and their 3- and 4-methyl, phenyl derivatives, and tetrahydro-2-thiophenemethanol, were synthesized. The solvolysis of β-thioesters in 80% aqueous acetone resulted in strong transannular S-participation and the products of solvolysis substantiated formation of bicyclic episulphonium ion intermediates. Such participation is considered to be present even in a tertiary system. On the other hand, γ-thioesters were solvolysed without any transannular S-participation, 相似文献
8.
9.
Akitomo Tachibana Yoshihiro Asai Shogo Ikeuchi Shigeru Ishikawa Tokio Yamabe 《Theoretical chemistry accounts》1990,78(1):1-9
Summary The vibronic character of this molecular device has been studied using isomorphic electron orbitals. The leading role of the softest vibrational mode for the electron transport process is stressed by the quantum mechanical treatment of the rearrangement operator. The theory was used to investigate the possible function of the soliton valve, which has been suggested as a switching tip. The electronic flexibility of the cyclopropenyl radical with respect to molecular vibrations, which is important for the function of the molecular device, is well characterized by the hardness and softness of the electron structure in terms of the orbital energy-occupation number correlation diagram. 相似文献
10.
A quantum chemical study of interchain hopping model of negatively charged solitons in polyacetylene
Akitomo Tachibana Shigeru Ishikawa Yoshihiro Asai Hideki Katagiri Tokio Yamabe 《International journal of quantum chemistry》1992,41(3):461-474
Phonon-assisted interchain hopping of negatively charged solitons in polyacetylene has been studied using a local chemical reaction model CH + CH4 → CH4 + CH. Quantum chemical characteristics of the electron transfer process have been analyzed in terms of the dynamic electron density and the mutual polarization moment. The CH stretching vibrational motion of CH4, which is a local model of the sp3 defect, has been found to play a significant role for the electron transfer. The excitation of the corresponding vibrational mode of the sp3 defect would promote the interchain hopping of the charged soliton. The electron transfer process has also been studied in terms of the “regional” density functional theory. It has been shown that the driving force of the electron transfer is represented by the regional chemical potentials. 相似文献