全文获取类型
收费全文 | 358篇 |
免费 | 6篇 |
专业分类
化学 | 292篇 |
晶体学 | 2篇 |
力学 | 1篇 |
数学 | 13篇 |
物理学 | 56篇 |
出版年
2020年 | 3篇 |
2019年 | 1篇 |
2016年 | 4篇 |
2015年 | 2篇 |
2014年 | 9篇 |
2013年 | 11篇 |
2012年 | 30篇 |
2011年 | 33篇 |
2010年 | 12篇 |
2009年 | 8篇 |
2008年 | 25篇 |
2007年 | 13篇 |
2006年 | 19篇 |
2005年 | 26篇 |
2004年 | 28篇 |
2003年 | 29篇 |
2002年 | 29篇 |
2001年 | 7篇 |
2000年 | 4篇 |
1999年 | 1篇 |
1998年 | 1篇 |
1997年 | 3篇 |
1996年 | 7篇 |
1995年 | 4篇 |
1994年 | 2篇 |
1991年 | 1篇 |
1990年 | 2篇 |
1988年 | 2篇 |
1987年 | 1篇 |
1986年 | 2篇 |
1985年 | 7篇 |
1984年 | 2篇 |
1982年 | 6篇 |
1981年 | 1篇 |
1980年 | 1篇 |
1979年 | 4篇 |
1977年 | 3篇 |
1976年 | 3篇 |
1975年 | 3篇 |
1973年 | 1篇 |
1970年 | 1篇 |
1969年 | 2篇 |
1968年 | 1篇 |
1964年 | 1篇 |
1960年 | 1篇 |
1959年 | 2篇 |
1956年 | 3篇 |
1955年 | 2篇 |
1954年 | 1篇 |
排序方式: 共有364条查询结果,搜索用时 15 毫秒
1.
2.
The structure of senecicannabine(), a new mcrocyclic pyrrolizidine alkaloid isolated from , has been established by chemical study and X-ray analysis. 相似文献
3.
Matsumoto T Kamada Y Sugimoto T Tada T Noguchi S Nakazumi H Shiro M Yoshino H Murata K 《Inorganic chemistry》2003,42(17):5192-5201
Two donor molecules newly synthesized, dimethylthio- and ethylenedithio-tetrathiafulvalenothioquinone-1,3-diselenolemethides (1 and 2), were used to prepare their charge-transfer (CT) salts with a magnetic FeBr(4)(-) counteranion. For 1, a low electrical conducting 1:1 salt (1.FeBr(4)) was obtained, in which molecules of 1 are tightly dimerized in a one-dimensional (1D) stacking column. On the other hand, 2 gave a 2:1 salt (2(2).FeBr(4)) as two different kinds of plate crystals (I and II). Both I and II possess similar stacking structures of molecules of 2 in each 1D column with a half-cut pipelike structure along the c axis. However, for I, the stacking columns are aligned in the same direction along the a and b axes, while for II they are in the same direction along the a axis, but in the reverse direction along the b axis, resulting in the difference in the relative arrangement of molecules of 2 and FeBr(4)(-) ions between the two crystals. The room-temperature electrical conductivities of the single crystals of I and II were 13.6 and 12.7 S cm(-)(1), respectively. The electrical conducting behavior in I was metallic above 170 K but changed to be semiconducting with a very small activation energy of 7.0 meV in the temperature range 4-170 K. In contrast, II showed the semiconducting behavior in the whole temperature range 77-285 K. The corresponding nonmagnetic GaBr(4)(-) salts with almost the same crystal structure as I and II showed definitively different electrical conducting properties in the metal to semiconductor transition temperature in I as well as in the magnitude of activation energy in the semiconducting region of I and II. The interaction between the d spins of FeBr(4)(-) ions was weak and antiferromagnetic in both I and II, but the magnitude of the spin interaction was unexpectedly larger compared with that in the FeBr(4)(-) salt of the corresponding sulfur derivative of 2 with closer contact between the neighboring FeBr(4)(-) ions. These electrical conducting and magnetic results suggest a significant interaction between the conducting pi electrons and the d spins of FeBr(4)(-) ions located near the columns or layers. 相似文献
4.
Chiral β-dimethylaminoalkylphosphines were prepared starting with amino acids, (S)-alanine, (S)-phenylalanine, (R)-phenylglycine, (S)-valine, and (R)-tert-leucine. The chiral phosphines were found to be highly efficient ligands for a nickel catalyzed asymmetric Grignard cross-coupling reaction (38~94% optical yield). 相似文献
5.
Ester on treatment with sodium salt of sulfone or sulfoxide afforded 2-substituted 1,3-bis(trimethylsily)propene in good yield, from which cyclopentane and cyclohexane derivatives bearing a trimethylsilyl group in the molecules were synthesized. 相似文献
6.
The state of an arsenic layer electrodeposited at various potentials on platinum electrodes has been examined electrochemically. The relation between the state and the electrocatalytic activity for hydrogen evolution has been investigated. The number of vacant sites have been found to increase with lowering of the deposition potential. The activity has been found to depend not on the amount of deposited arsenic but on the number of vacant sites. The difference in the effects of arsenic and of copper on hydrogen evolution is pointed out. This is attributed to the difference in the affinity of the ad-atoms for hydrogen. 相似文献
7.
Hydrogen evolution on a platinum electrode decays against Xpt with the deposition of Sn ad-atoms and Pb ad-atoms in the same way as it decays with that of Ge ad-atoms, in which all of these ad-atoms occupy two platinum sites. In general the decay depends on the number of sites occupied by an atom of the ad-atom species.The potential ranges for oxygen adsorption by Sn ad-atoms and Pb ad-atoms are 0.45 to 1.24 V and 0.48 to 0.77 V, respectively, but the oxygen adsorbed by the latter ad-atoms is very small in amount. 相似文献
8.
Sugimoto H Harihara M Shiro M Sugimoto K Tanaka K Miyake H Tsukube H 《Inorganic chemistry》2005,44(18):6386-6392
The cis-dioxo-molybdenum(VI) complexes, [MoO2(L(H))2]2- (1b), [MoO2(L(S))(2)]2- (2b), and [MoO2(L(O))2]2- (3b) (L(H) = cyclohexene-1,2-dithiolate, L(S) = 2,3-dihydro-2H-thiopyran-4,5-dithiolate, and L(O) = 2,3-dihydro-2H-pyran-4,5-dithiolate), with new aliphatic dithiolene ligands were prepared and investigated by infrared (IR) and UV-vis spectroscopic and electrochemical methods. The mono-oxo-molybdenum(IV) complexes, [MoO(L(H))2]2- (1a), [MoO(L(S))2]2- (2a), and [MoO(L(O))2]2- (3a), were further characterized by X-ray crystal structural determinations. The IR and resonance Raman spectroscopic studies suggested that these cis-dioxo molybdenum(VI) complexes (1b-3b) had weaker Mo=O bonds than the common Mo(VI)O2 complexes. Complexes 1b-3b also exhibited strong absorption bands in the visible regions assigned as charge-transfer bands from the dithiolene ligands to the cis-MoO2 cores. Because the oxygen atoms of the cis-Mo(VI)O2 cores are relatively nucleophilic, these complexes were unstable in protic solvents and protonation might occur to produce Mo(VI)O(OH), as observed with the oxidized state of arsenite oxidase. 相似文献
9.
12-Hydroxymethyltetrahydroabietic acid has been homopolymerized by melt condensation and homopolyester has been obtained. Vinyl 12-hydroxymethyltetrahydroabietate has been prepared from 12-hydroxymethyltetrahydroabietic acid by vinyl interchange procedure with vinyl acetate, and has been homopolymerized, copolymerized with vinyl chloride, vinyl acetate, and terpolymerized with styrene and acrylonitrile. The acrylate ester of 12-hydroxymethyltetrahydroabietic acid also has been prepared from 12-hydroxymethyltetrahydroabietic acid and acrylyl chloride. The acrylate thus obtained has been homopolymerized and copolymerized with vinyl chloride and vinyl acetate. Polymers thus obtained have been characterized. 相似文献
10.
K. Katagiri T. Shimizue Y. Akatsu H. Ishiguro 《Journal of Radioanalytical and Nuclear Chemistry》1997,226(1-2):23-27
Transfer parameters for dose assessment such as deposition velocity (V
g), fraction of directly deposited on plants to the edible parts (r) and transfer factors (B
iv) have been evaluated. Deposition velocity under drying and wet conditions was evaluated about 0.8 cm/s. Fraction of directly deposited on plants and transfer factors in plants showed a lognormal distribution. Geometric means of fraction of deposited in rice, leafy vegetable and grass were <9·10–3, 0.2 and about 9·10–2, respectively. Geometric mean of the transfer factor in leafy vegetable was about 3·10–2. These results were compared with the parameters given in the US NRC Regulatory Guide and previous literature values. The results showed that the fraction of directly deposited on plants were smaller than the recommended value in the NRC Regulatory Guide. They also showed that the deposition velocity and transfer factors were almost similar to the results reported in the literature. 相似文献