全文获取类型
收费全文 | 1350篇 |
免费 | 39篇 |
国内免费 | 6篇 |
专业分类
化学 | 971篇 |
晶体学 | 22篇 |
力学 | 11篇 |
数学 | 84篇 |
物理学 | 307篇 |
出版年
2021年 | 11篇 |
2020年 | 18篇 |
2019年 | 19篇 |
2018年 | 13篇 |
2016年 | 24篇 |
2015年 | 26篇 |
2014年 | 33篇 |
2013年 | 38篇 |
2012年 | 71篇 |
2011年 | 65篇 |
2010年 | 45篇 |
2009年 | 40篇 |
2008年 | 82篇 |
2007年 | 59篇 |
2006年 | 76篇 |
2005年 | 59篇 |
2004年 | 47篇 |
2003年 | 58篇 |
2002年 | 46篇 |
2001年 | 38篇 |
2000年 | 27篇 |
1999年 | 25篇 |
1998年 | 11篇 |
1997年 | 16篇 |
1996年 | 16篇 |
1995年 | 22篇 |
1994年 | 30篇 |
1993年 | 18篇 |
1992年 | 25篇 |
1991年 | 23篇 |
1990年 | 21篇 |
1989年 | 16篇 |
1988年 | 13篇 |
1987年 | 13篇 |
1986年 | 21篇 |
1985年 | 25篇 |
1984年 | 19篇 |
1983年 | 12篇 |
1982年 | 8篇 |
1981年 | 9篇 |
1980年 | 12篇 |
1979年 | 10篇 |
1978年 | 9篇 |
1977年 | 15篇 |
1976年 | 18篇 |
1975年 | 12篇 |
1973年 | 8篇 |
1969年 | 8篇 |
1968年 | 8篇 |
1966年 | 8篇 |
排序方式: 共有1395条查询结果,搜索用时 15 毫秒
41.
A. Yokoyama S. Morimoto T. Inoue J. Sanada H. Araki T. Saito H. Baba S. Shibata A. Shinohara T. Muroyama Y. Ohkubo 《Journal of Radioanalytical and Nuclear Chemistry》1999,239(1):143-149
Target-like products, that is,191–200Au,185–200Pt, and183–195Ir, from197Au target bombarded with12C ions at the energies of 180, 230, and 400 MeV/u were measured by using off-line gamma-ray spectrometry combined with chemical
separation procedures. Spallation systematics by Rudstam reproduces well the measured cross sections for formation of platinum
and iridium isotopes. It was found that the cross sections of gold nuclides increase with increase of the incident energy
in the range studied and they are enhanced if compared with the reported proton-induced reaction of gold at a similar incident
energy. It is suggested that the electromagnetic dissociation process plays a role for production of such gold nuclides. 相似文献
42.
Hamao Watanabe Kazuaki Higuchi Tomoko Goto Tsutomu Muraoka Jun Inose Masaaki Kageyama Yasuko Iizuka Masakatsu Nozaki Yoichiro Nagai 《Journal of organometallic chemistry》1981,218(1):27-39
In the presence of a catalytic amount of sodium methoxide, sym-dimethoxytetramethyldisilane was converted into α,ω-dimethoxypermethylpolysilanes, MeO(SiMe2)nOMe where n ? 3, at room temperature. On the other hand, similar treatment of the disilane in THF solution gave cyclic polysilanes, (Me2Si)n where n = 5–7. Decomposition of the disilane in the presence of diphenylacetylene afforded a trisilacyclopentene derivative under similar conditions. This compound was obtained also by the reaction between α,ω-dimethoxypermethylpolysilanes and diphenylacetylene in the presence of sodium methoxide. These cyclic products most likely were formed via permethyl polysilyl anion intermediates derived from α,ω-dimethoxypermethylpolysilanes. Also, the formation of α,ω-dimethoxypermethylpolysilanes could be elucidated in terms of the mechanism involving the base-assisted, concerted nucleophilic substitution or stepwise substitution by silyl anions, rather than the successive dimethylsilylene (Me2Si:) insertion reaction. 相似文献
43.
The number of pigments in single light-harvesting complexes (chlorosomes) were calculated by imaging single chlorosomes in a frozen buffer at cryogenic temperature with a confocal laser fluorescence microscope and pigment extraction. Chlorosomes were isolated from two types of green photosynthetic bacteria Chlorobium (Chl.) tepidum and Chloroflexus (Cfl.) aurantiacus and were individually imaged in the frozen medium. Each fluorescence spot observed mainly came from a single chlorosome and was ascribable to self-aggregates of bacteriochlorophyll (BChl) c molecules as core parts of chlorosomes. A three-dimensional distribution of fluorescence of single chlorosomes was analyzed, and the number of chlorosomes in a volume of 54,000 microm(3) was counted directly. On the basis of the results, averaged numbers of the BChl c molecules contained in a single chlorosome of Chl. tepidum and Cfl. aurantiacus were determined to be 1.4 x 10(5) and 9.6 x 10(4), respectively. The present numbers are almost comparable to those estimated by other methods (Martinez-Planells et al., Photosynth. Res. 2002, 71, 83 and Monta?o et al., Biophys. J. 2003, 85, 2560). 相似文献
44.
Naozumi Teramoto Toyoki MotoyamaRyutoku Yosomiya Mitsuhiro Shibata 《European Polymer Journal》2002,38(7):1365-1369
Amylose was etherified with 1-bromopropane in DMSO. The degree of substitution (DS) was varied by altering the feed ratio of 1-bromopropane. The structures of the products were characterized by IR and 1H-NMR spectroscopy. When the molar feed ratio of 1-bromopropane to hydroxyl groups of amylose was beyond 7.5, the hydroxyl groups were completely substituted with propyl ether groups. The etherified amylose with DS 1.9 showed a glass transition temperature (Tg), and that with DS 2.3 or 3.0 showed both Tg and melting temperature (Tm) (DS 3.0 means complete substitution). The etherification imparted melt processability and solubility in nonpolar organic solvent to amylose. 相似文献
45.
Yuki Shintani Taku Ohtomi Dr. Aya Shibata Dr. Yoshiaki Kitamura Koichiro M. Hirosawa Prof. Kenichi G. N. Suzuki Prof. Masato Ikeda 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(8):e202104421
Aqueous self-assembly of short peptides has attracted growing attention for the construction of supramolecular materials for various bioapplications. Herein, we describe how the thermolysin-assisted biocatalytic construction of a dipeptide hydrazide from an N-protected amino acid and an amino acid hydrazide leads to the formation of thermally stable supramolecular hydrogels. In addition, we demonstrate the post-assembly modification of the supramolecular architectures constructed in situ tethering hydrazide groups as a chemical handle by means of fluorescence imaging. 相似文献
46.
47.
48.
Takashi Uemura Nobuyuki Okuda Hiroya Kirmura Yasuko Okuda Yoshinobu Ueba Tuguru Shirakawa 《先进技术聚合物》1997,8(7):437-442
Electroluminescent(EL) devices have been fabricated using four different polymers with different glass transition temperatures (Tg) dispersed with N,N′-bis-(3-methylphenyl)-N,N′-diphenyl-1,1′-biphenyl-4,4′-diamine (TPD) as a hole transport layer and tris(8-hydroxyquinoline) aluminum (Alq3) as an emitting layer. It was found that the higher the Tg of the polymer, the longer the lifetime of the device. From observations of TPD-doped polymer films with optical microscope and atomic force microscope, dispersing TPD in the polymers was found to suppress the crystallization that causes the roughness of the film surface. It was also observed that the higher the Tg of the host polymers, the more difficult TPD crystallization was. The property of the EL device with polyethersulfone (PES) dispersed with TPD was also investigated. The lifetime of EL device with the TPD doped PES film was improved more than five times at a current density below 10 mA/cm2 compared with the device with a conventional TPD hole transport layer. © 1997 John Wiley & Sons, Ltd. 相似文献
49.
[reaction: see text]. Rhodium complex-catalyzed carbonylative alkene-alkyne coupling proceeds using aldehydes as a CO source. Cinnamaldehyde is the best CO donor, and various cyclopentenones were provided in high isolated yields by a solvent-free system. 相似文献
50.
Dithienylethenes with a novel photochromic performance 总被引:2,自引:0,他引:2
Dithienylethenes with low decoloration quantum yields and thermal reversibility at high temperature above 100 degrees C were prepared. Introduction of bulky alkoxy substituents at 2- and 2'-positions of the thiophene rings strongly suppressed the cycloreversion quantum yields. The quantum yields were lower than 10(-3), and the photogenerated color remained stable enough under room light. On the other hand, the bulky alkoxy substituent decreased the thermal stability of the colored closed-ring isomers at high temperature. The color of the dithienylethene with cyclohexyloxy substituents faded out in less than 1 min at 160 degrees C. 相似文献