全文获取类型
收费全文 | 1387篇 |
免费 | 37篇 |
国内免费 | 2篇 |
专业分类
化学 | 1018篇 |
晶体学 | 18篇 |
力学 | 5篇 |
综合类 | 2篇 |
数学 | 104篇 |
物理学 | 279篇 |
出版年
2021年 | 6篇 |
2020年 | 11篇 |
2019年 | 11篇 |
2018年 | 18篇 |
2017年 | 10篇 |
2016年 | 22篇 |
2015年 | 23篇 |
2014年 | 17篇 |
2013年 | 70篇 |
2012年 | 46篇 |
2011年 | 65篇 |
2010年 | 24篇 |
2009年 | 45篇 |
2008年 | 89篇 |
2007年 | 59篇 |
2006年 | 67篇 |
2005年 | 75篇 |
2004年 | 63篇 |
2003年 | 57篇 |
2002年 | 55篇 |
2001年 | 23篇 |
2000年 | 33篇 |
1999年 | 11篇 |
1998年 | 16篇 |
1997年 | 21篇 |
1996年 | 27篇 |
1995年 | 21篇 |
1994年 | 19篇 |
1993年 | 19篇 |
1992年 | 12篇 |
1991年 | 11篇 |
1990年 | 20篇 |
1989年 | 16篇 |
1988年 | 25篇 |
1987年 | 20篇 |
1986年 | 18篇 |
1985年 | 24篇 |
1984年 | 24篇 |
1983年 | 14篇 |
1982年 | 20篇 |
1981年 | 22篇 |
1980年 | 15篇 |
1979年 | 20篇 |
1978年 | 20篇 |
1977年 | 18篇 |
1976年 | 27篇 |
1975年 | 17篇 |
1974年 | 9篇 |
1973年 | 13篇 |
1972年 | 5篇 |
排序方式: 共有1426条查询结果,搜索用时 250 毫秒
111.
Ohki Y Sunada Y Honda M Katada M Tatsumi K 《Journal of the American Chemical Society》2003,125(14):4052-4053
The [8Fe-7S] core of the P-clusters in nitrogenases is unique among the known [Fe-S] clusters which are essential to electron-transfer processes in nature. The [8Fe-7S] cluster has been thought unstable and to exist only in protein environments. We found that this unusual [8Fe-7S] structure can be self-assembled from the reaction of Fe(II) bis-amide, tetramethylthiourea, 2,4,6-triisopropylbenzenethiol, and elemental sulfur in a specific mole ratio. The structure of the complex isolated therefrom closely resembles that of the reduced form (PN) of the P-clusters, while the 6Fe(II)2Fe(III) oxidation state was manifested by the M?ssbauer study. 相似文献
112.
Nakamura E Yamanaka M Yoshikai N Mori S 《Angewandte Chemie (International ed. in English)》2001,40(10):1935-1938
113.
Suzuki S Tanaka R Takada K Inoue N Yashima Y Honda A Honda S 《Journal of chromatography. A》2001,910(2):319-329
A method for the analysis of the sialo-N-glycans in glycoproteins was established by the electrokinetic chromatography mode of capillary electrophoresis (CE) in sodium dodecyl sulfate (SDS) micelles as 1-phenyl-3-methyl-5-pyrazolone (PMP) derivatives, using sialo-N-glycans in fetuin as a model. Six major and some minor peaks were observed for the N-glycans in fetuin, which were well separated from each other using 50 mM phosphate buffer, pH 6.0, containing SDS to a concentration of 30 mM in an uncoated fused-silica capillary, and these peaks were assigned to sialo-N-glycans having either of the biantennary or β1-3/β1-4 linked galactose-containing complex type triantennary N-glycans as the basic structures, by an indirect method based on the assignment of the peaks in high-performance liquid chromatography separated in parallel with CE and peak collation between these two separation methods. The attaching position of the sialic acid residue was determined using the linkage preference of neuraminidase isozymes. The established system is considered to be useful for routine analysis of microheterogeneity of the carbohydrate moiety of this model glycoprotein from the following reasons: (1) the derivatization with PMP proceeds quantitatively under mild conditions without causing release of the sialic acid residue, (2) the derivatives can be sensitively detected by UV absorption, (3) the procedure is simple, rapid and reproducible. Preliminary results of N-glycan analysis for several other glycoproteins under these conditions are also presented. 相似文献
114.
We have developed a miniature double-pass cylindrical mirror electron energy analyzer (DPCMA) with an outer diameter of 26 mm. The DPCMA consists of a shield for the electric field, inner and outer cylinders, two pinholes with a diameter of 2.0 mm, and an electron multiplier. By assembling the DPCMA in a coaxially symmetric mirror electron energy analyzer (ASMA) coaxially and confocally we developed an analyzer for Auger photoelectron coincidence spectroscopy (APECS). The performance was estimated by measuring the Si-LVV-Auger Si-1s-photoelectron coincidence spectra of clean Si(1 1 1). The electron-energy resolution of the DPCMA was estimated to be E/ΔE = 20. This value is better than that of the miniature single-pass CMA (E/ΔE = 12) that was used in the previous APECS analyzer. 相似文献
115.
T. Honda T. Oi T. Ossaka T. Nozaki H. Kakihana 《Journal of Radioanalytical and Nuclear Chemistry》1989,130(1):81-97
Hot spring water and crater lake water samples were analyzed for their rare earth elements: (REE's) by neutron activation method, which, in the irradiation, sample preparation, incorporated a coprecipitation process in which aluminium was used as a collector. Ten REE's, La, Ce, Sm, Eu, Gd, Tb, Dy, Tm, Yb and Lu, were consequently detected and determined at the ppb level with satisfactory precision. It was shown that the aluminium coprecipitation is effective in enhancing concentrations of the REE's and reducing the amounts of interfering nuclides before neutron irradiation. 相似文献
116.
117.
Mutsumi Tashiro Pradeep K. Pujari Shu Seki Yoshihide Honda Shigehiro Nishijima Seiichi Tagawa 《Radiation Physics and Chemistry》2000,58(5-6):587-592
Temperature dependence of positron annihilation lifetime spectra of polysilanes such as, poly(methyl-n-propylsilane) (PMPrS) and poly(di-n-hexylsilane) (PDHS) has been investigated. The τ3 in PMPrS is seen to increase monotonically around the solid–liquid transition temperature. The transition temperature and free volume are observed to depend on the molecular weight and/or packing of the backbones. For PDHS, a sharp change in τ3 and I3 is seen at the solid–solid transition temperature. Free volume radius probability density functions, above and below the transition temperature, are presented in PMPrS and PDHS. Positron studies are complimented by conventional thermal analysis studies. 相似文献
118.
M. Yamaga T. Inoue S. Yabashi M. Honda J.-P. R. Wells K. Shimamura 《辐射效应与固体损伤》2013,168(6-12):977-982
Electron paramagnetic resonance (EPR) spectra of Ce 3+ in LiLuF 4 (LLF) and LiSr 0.8 Ca 0.2 AlF 6 (LSCAF) observed at low temperatures (<20 v K) show that the Ce 3+ centers have tetragonal and pseudo-trigonal symmetry with ( g , g )=(2.751, 1.467) and (2.14, 0.80), respectively. The EPR lines of Ce 3+ in LSCAF are inhomogeneously broadened by different Ce 3+ configurations which correspond to the random occupation of the second nearest neighbor cation sites by Ca 2+ and Sr 2+ and/or charge compensators. These EPR results indicate that the Ce 3+ centers in LLF and LSCAF are associated with substitution of Ce 3+ for Lu 3+ with eight-fold coordination and Sr 2+ /Ca 2+ with six-fold coordination, respectively. Fourier transform infrared absorption has been used to measure transitions between the 2 F 5/2 ground state and the 2 F 7/2 multiplet of Ce 3+ in LLF at 10 v K. The optical absorption and luminescence of Ce 3+ :LLF and Ce 3+ :LSCAF in the UV range are strongly polarized. The energy levels and polarization dependence of the optical transitions can be accounted for in terms of the crystal field potential experienced by the Ce 3+ ions under the action of the different point group symmetries. 相似文献
119.
We prove that any mapping class on a compact oriented surface with non-empty boundary can be made pseudo-Anosov and right-veering
after a sequence of positive stabilizations.
相似文献
120.
The sensor for adenosine-5′-triphosphate (ATP) is based on H+-ATPase immobilized via a polyvinylbutyral resin on a pH-sensitive field effect transistor. A linear relationship was obtained between the initial rate of change of the differential gate output voltage and the logarithm of the ATP concentration over the range 0.2–1.0 mM ATP. The optimum pH was 9.0 at 40°C but pH 7.0 was preferred for routine measurements. Only slight responses were obtained for 1 mM glucose, creatinine or urea. The ATP-sensing system exhibited a response to 1 mM ATP for at least 18 days. 相似文献