全文获取类型
收费全文 | 1304篇 |
免费 | 57篇 |
国内免费 | 5篇 |
专业分类
化学 | 1021篇 |
晶体学 | 11篇 |
力学 | 9篇 |
数学 | 67篇 |
物理学 | 258篇 |
出版年
2023年 | 10篇 |
2022年 | 11篇 |
2021年 | 15篇 |
2020年 | 15篇 |
2019年 | 25篇 |
2018年 | 15篇 |
2017年 | 20篇 |
2016年 | 34篇 |
2015年 | 25篇 |
2014年 | 36篇 |
2013年 | 81篇 |
2012年 | 66篇 |
2011年 | 103篇 |
2010年 | 46篇 |
2009年 | 40篇 |
2008年 | 96篇 |
2007年 | 82篇 |
2006年 | 78篇 |
2005年 | 83篇 |
2004年 | 83篇 |
2003年 | 73篇 |
2002年 | 77篇 |
2001年 | 19篇 |
2000年 | 18篇 |
1999年 | 14篇 |
1998年 | 15篇 |
1997年 | 13篇 |
1996年 | 15篇 |
1995年 | 6篇 |
1994年 | 4篇 |
1993年 | 5篇 |
1991年 | 9篇 |
1990年 | 9篇 |
1989年 | 5篇 |
1988年 | 6篇 |
1986年 | 3篇 |
1985年 | 13篇 |
1984年 | 12篇 |
1982年 | 8篇 |
1981年 | 13篇 |
1980年 | 10篇 |
1979年 | 7篇 |
1978年 | 4篇 |
1977年 | 9篇 |
1976年 | 4篇 |
1975年 | 3篇 |
1974年 | 4篇 |
1973年 | 3篇 |
1972年 | 3篇 |
1964年 | 3篇 |
排序方式: 共有1366条查询结果,搜索用时 15 毫秒
41.
Masato Nagata 《Meccanica》2016,51(12):3015-3023
42.
Boon-Teck Heng Wan Ahmad Kamil Mahmood Teruo Shinomiya Nozomi Uchida Masato M. Ito 《Liquid crystals》2013,40(2):204-215
Two series of new Cu(II) complexes derived from the reaction of copper acetate with the non-linear 1,2,3-triazole-based Schiff bases have successfully been synthesised. The structures of the ligands and its complexes were elucidated by elemental analysis, FT-IR, 1H-NMR and UV–visible spectroscopic techniques. The differential scanning calorimetry and polarizing optical microscopy supported the anisotropic properties of uncoordinated ligands in which the focal conic fan-shaped texture and/or broken fan-shaped texture characteristics of respective SmA and SmC phases were recorded. However, not all of their corresponding Cu(II) complexes are mesogenic. Although the iodo-substituted ligands with even parity C10H29 to C14H33 are non-stable and exhibit SmA phase which is not reproducible, the ultimate Cu(II) complexes show exclusively stable SmA phase. This observation can be ascribed to the enhanced colinearity and molecular anisotropic by the presence of Cu-N and Cu-O coordination modes. On the other hand, the comparison studies show that different positions of ortho-hydroxyl group affect the mesomorphic and thermal behaviour of ligands and Cu(II) complexes. 相似文献
43.
Stereoselective analysis of flecainide enantiomers using reversed‐phase liquid chromatography for assessing CYP2D6 activity 下载免费PDF全文
Kosuke Doki Yukio Sekiguchi Keisuke Kuga Kazutaka Aonuma Yukinao Kohda Masato Homma 《Biomedical chromatography : BMC》2014,28(9):1193-1198
Stereoselective analyses of flecainide enantiomers were performed using reversed‐phase high‐performance liquid chromatography (HPLC) equipped with a polysaccharide‐based chiral column (Chiralpak AS‐RH) and fluorescence detector. Excitation and emission wavelengths were set at 300 and 370 nm, respectively. Flecainide enantiomers in serum and urine were extracted using diethyl ether. The mobile phase solution, comprising 0.1 m potassium hexafluorophosphate and acetonitrile (65:35, v/v), was pumped at a flow rate of 0.5 mL/min. The recoveries of flecainide enantiomers were greater than 94%, with the coefficients of variation (CVs) <6%. The calibration curves of flecainide enantiomers in serum and urine were linear in the concentration range 5–500 ng/mL and 0.75–15 µg/mL (r > 0.999), respectively. CVs in intra‐day and inter‐day assays were 1.8–5.8 and 3.4–7.5%, respectively. In a pharmacokinetic study, the ratios of (S)‐ to (R)‐flecainide (S/R ratio) in the area under the curve and the amount of flecainide enantiomers excreted in urine were lower in a subject carrying CYP2D6*10/*10 than in subjects carrying CYP2D6*1/*2. The S/R ratio of trough serum flecainide concentration ranged from 0.79 to 1.16 in patients receiving oral flecainide. The present HPLC method can be used to assess hepatic flecainide metabolism in a pharmacokinetic study and therapeutic drug monitoring. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
44.
We generalize the author’s formula (2011) on weighted counting of inversions on permutations to one on alternating sign matrices. The proof is based on the sequential construction of alternating sign matrices from the unit matrix which essentially follows from the earlier work of Lascoux-Schützenberger (1996).
相似文献45.
Type I (α-) and II cleavages are two of the best known photochemical processes of alkanone.2 Extensive and intensive investigations have been done on both types of reactions in order to clarify the influence of structural changes on the reactivity, specificity, and efficiency of photoreactions of alkanones.3 The type I cleavage of medium-ring alkanones is believed to produce a radical pair, the fate of which will be determined by the ready formation of transition states for transfer of Ha, Hb, and recyclization. We now wish to report 相似文献
46.
47.
48.
Highly selective acylation of the alcoholic hydroxy group can be achieved with (hydroxyalkyl)phenols carrying both alcoholic and phenolic hydroxyls by the use of the most common acylating agents, acid chlorides, under microwave irradiation. 相似文献
49.
Ryohei Yamakado Shin-ichi Matsuoka Masato Suzuki Koji Takagi Kosuke Katagiri Isao Azumaya 《Tetrahedron》2013,69(5):1516-1520
m-Calix[3]amide bearing three pyrenes (1a) was prepared by the condensation reaction of 3-nonylaminobenzoic acid derivative using Ph3PCl2. Pyrenyl groups were found to be aligned in the screw-like fashion by m-calix[3]amide as confirmed by the X-ray crystallography. Aromatic proton signals observed at the up-field region in the 1H NMR spectrum at low temperature indicated that pyrenyl groups in 1a are aligned in close proximity in THF solution. UV–vis absorption and fluorescence emission spectra did not show marked peak shift nor concentration fluorescence quenching compared with reference compounds implying no significant electronic interaction between pyrenyl groups. These results can be explained by the steric effect of the m-calix[3]amide platform. On the other hand, an excimer emission was observed for m-calix[3]amide having a flexible spacer between pyrene and m-calix[3]amide (1b). 相似文献
50.
Yew-Hong Ooi Chun-Chieh Han Hong-Cheu Lin Kenji Kubo Masato M. Ito 《Liquid crystals》2013,40(4):516-527
A series of symmetrical trimeric liquid crystalline compounds of which the molecular structure with a central core of 1,3,5-benzene attached by three rod-like mesogenic Schiff base moieties via the propylene spacers and ether linkages has successfully been synthesised and characterised by infra red and nuclear magnetic resonance spectroscopic techniques. All the star-shaped compounds in this series exhibit predominantly SmC phase except the analogue possessing terminal C8H17 group. It is apparent that the members with even parity from C10H21 to C16H33 show enantiotropic SmC phase while the member with longest terminal chain of C18H37 is inclined to monotropic smectogen. The X-ray diffraction measurements reveal that the tilted smectic layer structures of the SmC phase are confirmed to have an obvious sharp peak at small angles of 2θ ~ 1.03°–1.48° with d-spacing values of 4.01–4.58 nm, which are corresponding to tilt angles of ~48° in the SmC phase. 相似文献