首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   495篇
  免费   4篇
化学   387篇
力学   10篇
数学   35篇
物理学   67篇
  2022年   11篇
  2021年   6篇
  2020年   8篇
  2019年   6篇
  2018年   3篇
  2017年   8篇
  2016年   9篇
  2015年   4篇
  2014年   14篇
  2013年   26篇
  2012年   10篇
  2011年   18篇
  2010年   8篇
  2009年   11篇
  2008年   23篇
  2007年   24篇
  2006年   21篇
  2005年   16篇
  2004年   15篇
  2003年   12篇
  2002年   19篇
  2001年   26篇
  2000年   13篇
  1999年   14篇
  1998年   8篇
  1997年   9篇
  1996年   5篇
  1995年   3篇
  1994年   5篇
  1993年   6篇
  1992年   14篇
  1991年   8篇
  1990年   12篇
  1989年   5篇
  1988年   6篇
  1987年   8篇
  1986年   6篇
  1985年   7篇
  1984年   4篇
  1983年   3篇
  1982年   5篇
  1981年   4篇
  1980年   8篇
  1979年   5篇
  1978年   6篇
  1977年   6篇
  1976年   5篇
  1973年   7篇
  1967年   4篇
  1966年   4篇
排序方式: 共有499条查询结果,搜索用时 31 毫秒
41.
42.
43.
Optics and Spectroscopy - We found that the long-wavelength absorption band of the laser dye IR 1061 and its analogue with an unsubstituted polymethine chain is strongly broadened and decreases in...  相似文献   
44.
The heterospin mixed-ligand complex [Ni6(OH)4Piv4(hfac)4(NIT-Ph)2] (1) (NIT-Ph is 4,4,5,5-tetramethyl-2-phenyl-4,5-dihydro-1H-imidazol-1-oxyl 3-oxide, hfac is hexafluoroacetylacetonate, and Piv is pivalate) was synthesized. The method for the synthesis of complex 1 is based on the replacement of acetone molecules in the hexanuclear complex containing the hexafluoroacetylacetonate and pivalate ligands [Ni6(OH)4Piv4(hfac)4(Me2CO)4] by NIT-Ph molecules. Two monodentate NIT-Ph molecules replace four acetone molecules, because the coordination of the O atom of the nitroxide group results in the blocking of one of the positions in the coordination environment of NiII the access to which is hindered by the phenyl ring of NIT-Ph. As a result, these ions are in a square-pyramidal environment unusual of NiII. In the low-temperature range, the dependence of the magnetization of 1 on the magnetic field is described by the Brillouin function. The reaction of [Ni6Piv4(hfac)4(OH)4(Me2CO)4] with the nitronyl nitroxide radicals 4,4,5,5-tetramethyl-2-(4-pyridyl)-4,5-dihydro-1H-imidazol-1-oxyl 3-oxide (NIT-p-Py) or 4,4,5,5-tetramethyl-2-(1-methyl-1H-imidazol-5-yl)-4,5-dihydro-1H-imidazol-1-oxyl 3-oxide (NIT-Iz) containing the pyridine or 1-methylimidazol-5-yl substituent, respectively, in the side chain is accompanied by the decomposition of the polynuclear fragment and affords the mononuclear complexes Ni(hfac)2(NIT-p-Py)2 and Ni(hfac)2(NIT-Iz)2, respectively. The reaction of 4,4,5,5-tetramethyl-2-(1-methyl-1H-imidazol-5-yl)-4,5-dihyd-ro-1H-imidazol-1-oxyl (Im-Iz), which is the imine analog of NIT-Iz, with [Ni6Piv4(hfac)4(OH)4(Me2CO)4] afforded the decanuclear complex [Ni10(OH)8Piv4(hfac)8(Im-Iz)2(H2O)6]. The molecular and crystal structures of all heterospin compounds were determined, and the magnetic properties of all compounds were investigated in the 2–300 K temperature range.  相似文献   
45.
We study a one-dimensional system of two parabolic loaded equations of a special kind and a one-dimensional composite-type system of a special kind. Both systems are considered with Cauchy data. We obtain sufficient conditions for the existence of a solution in the class of bounded smooth functions. The method of splitting on the differential level (the weak approximation method) is used in the proof.  相似文献   
46.
U.v spectra study of phosphacgclic compounds with tetracoordinated ring phosphorus atom has been an object of a rather limited number of WOZkS. There are only few works on U.V. absorption spectra of cyclic phosphonitriles which reveal a specifio character of their Π-electronic structure1; besides, there are some data on a significant low - frequency shifting of the electronic spectrum of 1.1 - diphenylphos-phabemene against that of benzene2. This communication presents an analyisis of the experimental findings on electronic absorption spectra of a Wide variety of substituted phospha-pyrimidines, PhP, (1,2,6 - phosphadiazines) for elucidating the nature of the observed absorption ban and for studying electronic distribution as well as separate characteristics of the php moLecules in the ground and excited states.  相似文献   
47.
48.
49.
A theoretical analysis is presented of the change in the momentum of a three-level atom due to its interaction with counterpropagating laser pulses that overlap in time. The two lower energy states of the atom are metastable; i.e., a lambda-type configuration of atomic levels is considered. The cases of two and four counterpropagating pulses having different carrier frequencies are considered. In the case of adiabatic atom-field interaction, it is shown that the atom’s momentum can change by an integer multiple of the photon momentum and the corresponding standard deviation is small as compared to the photon momentum squared.  相似文献   
50.
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号