全文获取类型
收费全文 | 2541篇 |
免费 | 64篇 |
国内免费 | 9篇 |
专业分类
化学 | 1945篇 |
晶体学 | 21篇 |
力学 | 37篇 |
综合类 | 1篇 |
数学 | 112篇 |
物理学 | 498篇 |
出版年
2022年 | 12篇 |
2021年 | 17篇 |
2020年 | 18篇 |
2019年 | 25篇 |
2018年 | 17篇 |
2017年 | 12篇 |
2016年 | 35篇 |
2015年 | 44篇 |
2014年 | 46篇 |
2013年 | 115篇 |
2012年 | 101篇 |
2011年 | 144篇 |
2010年 | 80篇 |
2009年 | 58篇 |
2008年 | 148篇 |
2007年 | 181篇 |
2006年 | 147篇 |
2005年 | 159篇 |
2004年 | 127篇 |
2003年 | 125篇 |
2002年 | 124篇 |
2001年 | 64篇 |
2000年 | 62篇 |
1999年 | 36篇 |
1998年 | 21篇 |
1997年 | 20篇 |
1996年 | 26篇 |
1995年 | 17篇 |
1994年 | 34篇 |
1993年 | 27篇 |
1992年 | 31篇 |
1991年 | 30篇 |
1990年 | 26篇 |
1989年 | 18篇 |
1988年 | 25篇 |
1987年 | 32篇 |
1986年 | 26篇 |
1985年 | 46篇 |
1984年 | 29篇 |
1983年 | 17篇 |
1982年 | 25篇 |
1981年 | 18篇 |
1980年 | 18篇 |
1979年 | 23篇 |
1978年 | 27篇 |
1977年 | 23篇 |
1976年 | 24篇 |
1975年 | 25篇 |
1974年 | 22篇 |
1973年 | 20篇 |
排序方式: 共有2614条查询结果,搜索用时 15 毫秒
101.
The lattice image of the FeCr σ-phase was observed by high-resolution electron microscopy with the c axis of the tetragonal cell parallel to the incident beam. It was found that bright dots of the observed image correspond to the positions of atoms in the planes of the σ-phase structure. Sequence faults were found in the irregular part of the lattice image. The analysis of the faults shows that an extra plane of width is inserted into the regular structure and one side of the fault is slightly shifted parallel to the fault plane with respect to the other side, which is consistent with the model proposed by Frank and Kasper. A unit cell step of the sequence faults was found and a model of the step was proposed. 相似文献
102.
Shoichi Ikeda Gerald D. Fasman 《Journal of polymer science. Part A, Polymer chemistry》1970,8(4):991-1001
The absorption and fluorescence spectra of a detergent, polyoxyethylene octylphenyl ether, were measured in water at different concentrations. The absorption spectra had a peak at 275 mμ and a shoulder at 281 mμ. The spectra were independent of concentration below the critical micelle concentration, but the molar extinction coefficients of the peak and the shoulder increased with concentration above the critical micelle concentration. The critical micelle concentration value derived from the absorption data was in good agreement with those obtained by other methods. The fluorescence spectra of the detergent in water were independent of concentration in dilute solutions, if the intensities of the spectra were normalized at the peak at 302 mμ. At higher concentrations, a weak excimer band appeared at 345 mμ, whose intensity increased with concentration. The excimer band manifested itself at a concentration slightly lower than the critical micelle concentration. The main band decreased and the excimer band increased, as the temperature was raised. An excimer band was observed in the same region of the spectra for the pure detergent, either in the solid or liquid state. The equilibrium solid spectra exhibited a very strong excimer emission. It was concluded that the excimers were formed within micelles in the case of aqueous solutions. 相似文献
103.
Micelle size and shape of dodecyldimethylammonium bromide have been determined by measurement of light scattering from its aqueous NaBr solutions. In water and in the presence of NaBr up to 0.07 M, the Debye plots give straight lines with positive slopes, and spherical micelles having molecular weight less than 30 000 are formed. At higher NaBr concentrations, the Debye plots decrease with increasing micelle concentration, indicating the aggregation of the primary spherical micelles into larger secondary micelles. The molecular weight and the radius of gyration of the secondary micelles increase with increasing NaBr concentration, and the relation between molecular weight and radius of gyration suggests that they are rodlike and flexible. Linear logarithmic relations between micelle molecular weight and ionic strength hold for spherical and rodlike micelles, respectively, and the threshold concentration of NaBr for the sphere-rod transition is located at 0.07 M. The spherical micelle of dodecyldimethylammonium ions has a size more than 20 surfactant ions larger in NaBr solutions than in NaCl solutions, and their rodlike micelle has a shorter length in NaBr solutions than in NaCl solutions, when compared at an identical aggregation number, indicating 2 more surfactant ions in its cross-section. 相似文献
104.
H Ikeda Y Shimonishi M Ohmura K Kishimoto K Kosakai K Hamada H Ochi 《Radioisotopes》1990,39(11):487-492
Textural features for phantom images were extracted. Texture parameters which represent RI distribution--skew, energy, entropy and angular second moment were used. But, it was difficult to analyse the images using discriminant analysis for textural features, because textural features had statistical noise. Therefore fuzzy reasoning was adapted to analyse the images. Textural features for six kinds of images were showed using membership function. The possibility to the image was evaluated using the value of membership function on each images. Fuzzy reasoning could be done easily using max-min composition formula. The reasoning was found more suitable to analyse the images than discriminant analysis and will be considered useful for analysis of clinical scintigrams. 相似文献
105.
Nambu H Hata K Matsugi M Kita Y 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(2):719-727
The combination of the water-soluble radical initiator, 2,2'-azobis[2-(2-imidazolin-2-yl)propane] dihydrochloride (VA-044) and the surfactant, cetyltrimethyl-ammonium bromide (CTAB), was found to be the most suitable condition for the effective and direct synthesis of useful active thioesters (pentafluorophenyl thioesters) in water. In addition, the direct amidation of aldehydes was achieved by the addition of the amines to the thioesterification reaction mixture in water. 相似文献
106.
T Yotsuyanagi N Ohta T Futo S Ito D N Chen K Ikeda 《Chemical & pharmaceutical bulletin》1991,39(11):3003-3006
Irreversible bindings of cis-diamminedichloroplatinum(II) (cis-DDP) to human serum albumin (HSA) were investigated in a pH 7.4 buffer containing 0.1 M NaCl at various molar ratios (cis-DDP/HSA) up to 60 over a 14 d period (37 degrees C). The metal binding seemed to reach a plateau when incubated at less than 10 times excess of cis-DDP. As the molar ratio increased, the reaction rate was relatively fast within the first day, followed by a moderate increase in the metal binding. When incubated at 60 times excess of cis-DDP, the metal bound as much as 20 mol per mol of HSA in 14 d. Fluorescence quenching of the metal-bound protein suggested that the tryptophan residue was gradually exposed to a hydrophilic environment as the metal binding increased. Furthermore, cis-DDP cleaved disulfide bonds at the ratio of 1 mol of disulfide bond per 5.3 mol of the metal binding. It was therefore suggested that the metal binding also occurred at several sites other than the disulfide bond. Warfarin binding to the metal-bound protein, examined by fluorescence changes, also decreased with increasing metal binding or cleavage of the disulfide bonds. Thus, cis-DDP bound to multiple sites in addition to the lone sulfhydryl group (Cys-34), suggesting that massive conformational changes of the protein took place. 相似文献
107.
Yasumitsu Tamura Yasuyoshi Miki Yoshinori Nishikawa Masazumi Ikeda 《Journal of heterocyclic chemistry》1976,13(2):317-320
N-Aminophenanthridinium salt reacted with dimethyl acetylenedicarboxylate in the presence of potassium carbonate to give a 3,3a-dihydropyrazolo[1,5-f]phenanthridine but with mono-substituted acetylenes (ethyl propiolate and benzoylacetylene) it produced aromatized pyrazolo-[1,5-f]phenanthridines (XII and XIII). The reaction of the N-benzoylimine with di-substituted acetylenes (dimethyl acetylenedicarboxylate and methyl phenylpropiolate) and mono-substituted acetylenes (ethyl propiolate and benzoylacetylene) yielded 1,3a-dihydropyrazolo[1,5-f]phenanthridines and the aromatized products (XII and XIII), respectively. 相似文献
108.
Tezuka Y 《Chemical record (New York, N.Y.)》2005,5(1):17-26
A collection of recent developments in topological polymer chemistry is presented. First, topological isomerism occurring on randomly coiled, flexible polymer molecules having cyclic and linear structures is discussed. Second, an electrostatic self-assembly and covalent fixation strategy has been developed for the synthesis of polymeric topological isomers. These isomers have double cyclic, manacle-, and theta-shaped constructions, and are prepared by using either linear or star telechelic polymer precursors having moderately strained cyclic ammonium salt groups, which carry multifunctional carboxylate counteranions. A technique of reversed-phase chromatography (RPC) is demonstrated as an effective means to separate polymers with different topologies, especially polymeric topological isomers. A further extension of topological polymer chemistry has been observed by dynamic selection from electrostatic polymer self-assembly to enable the effective formation of tadpole-shaped, cyclic-linear hybrid topologies. 相似文献
109.
Akai S Kawashita N Satoh H Wada Y Kakiguchi K Kuriwaki I Kita Y 《Organic letters》2004,6(21):3793-3796
[reaction: see text] The reactions of (phenylsulfinyl)furans or -thiophenes with carbon nucleophiles in the presence of trifluoroacetic anhydride allowed the nucleophilic installation of carbon functional groups on the furan and thiophene nuclei with complete regioselectivity. 相似文献
110.
Matsuura K Hibino M Ikeda T Yamada Y Kobayashi K 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(2):352-359
We describe herein the relationship between the spatial arrangement of self-organized galactose clusters and lectin recognition. beta-Galactose-modified deoxyuridine phosphoramidite was synthesized and applied to solid-phase synthesis to provide 18-, 20-, and 22-mers of site-specifically galactosylated oligodeoxynucleotides (Gal-ODNs). These Gal-ODNs were self-organized through hybridization with the corresponding 18-, 20-, and 22-mers of half-sliding complementary ODNs (hsc-ODNs) to give periodic galactoside clusters. The self-organization of ODNs was confirmed by size exclusion chromatography and gel electrophoresis. The binding of the Gal-clusters to the FITC-labeled RCA(120) lectin was analyzed by monitoring the change in fluorescence intensity. The assembly of 20-mer Gal-ODN with the 20-mer hsc-ODN was strongly and cooperatively recognized by the lectin. The 18-mer assembly was bound more weakly and less cooperatively, and the 22-mer assembly was minimally bound to the lectin. RCA(120) lectin recognized not only the density of galactoside residues, but also the spatial arrangement. The size of the Gal cluster was estimated from the association constant of Gal-ODN with hsc-ODN. The relationship between lectin-recognition and Gal-cluster size is also discussed. 相似文献