全文获取类型
收费全文 | 2980篇 |
免费 | 552篇 |
国内免费 | 609篇 |
专业分类
化学 | 2516篇 |
晶体学 | 60篇 |
力学 | 160篇 |
综合类 | 14篇 |
数学 | 365篇 |
物理学 | 1026篇 |
出版年
2024年 | 13篇 |
2023年 | 51篇 |
2022年 | 79篇 |
2021年 | 93篇 |
2020年 | 147篇 |
2019年 | 142篇 |
2018年 | 113篇 |
2017年 | 94篇 |
2016年 | 148篇 |
2015年 | 159篇 |
2014年 | 145篇 |
2013年 | 227篇 |
2012年 | 221篇 |
2011年 | 242篇 |
2010年 | 223篇 |
2009年 | 251篇 |
2008年 | 254篇 |
2007年 | 237篇 |
2006年 | 179篇 |
2005年 | 179篇 |
2004年 | 133篇 |
2003年 | 124篇 |
2002年 | 151篇 |
2001年 | 137篇 |
2000年 | 59篇 |
1999年 | 69篇 |
1998年 | 40篇 |
1997年 | 18篇 |
1996年 | 30篇 |
1995年 | 32篇 |
1994年 | 21篇 |
1993年 | 23篇 |
1992年 | 22篇 |
1991年 | 26篇 |
1990年 | 17篇 |
1989年 | 10篇 |
1988年 | 3篇 |
1987年 | 8篇 |
1986年 | 4篇 |
1985年 | 7篇 |
1982年 | 1篇 |
1979年 | 3篇 |
1977年 | 3篇 |
1974年 | 1篇 |
1957年 | 1篇 |
1955年 | 1篇 |
排序方式: 共有4141条查询结果,搜索用时 31 毫秒
61.
Thermal treatment of Zn(NH3)(4)2+ precursor in ethanol solvent led to the formation of the tubular ZnO which exhibited strong ultraviolet photoluminescence around 385 nm at room temperature; TEM images showed the hollow tubules with approximately 450 nm in diameter and approximately 4 microns in length were built up by ZnO polycrystals. 相似文献
62.
Study on the Phase Diagram of CsCl-CeCl3-HCl(11%)-H2O System and the Properties of the Compounds 总被引:2,自引:0,他引:2
The equilibrium solubility of CsCl-CeCl3-HCl(11%)-H2O qua-ternary system at 25℃ has been determined by the physicchemical analysis method ,and the phase diagram was plotted, Two new double salts 3CsCl.CeCl3.3H2O and CsCl.CeCl3.4H2O obtained from the complicated system were identified and characterized by XRD,TG-DTA ,DSC,UV and fluorescence spectroscopy, Studies on the fluorescence excitation and emission show that 3CsCl.CeCl3.3H2O and CsCl.CeCl3.4H2O have upconversion luminescence of infrared-visible range,and the upconversion emission intensity increases with the increase of ratio of CeCl3 in CsCl. 相似文献
63.
64.
Quan Xiang WE Xia LIU Yan Ping SHI 《中国化学快报》2005,16(11):1477-1480
A novel dimeric eremophilane, ligulolide B, was isolated from the alcoholic extract of the whole plant of Ligularia virgaurea spp. oligocephala. The structure was elucidated by various spectroscopic methods including intensive 2D NMR techniques (^1H-^1H COSY, gHMQC, gHMBC and ^1H-^1H NOESY) and HR-ESI-MS. 相似文献
65.
A Novel Dihydroflavone from the Roots of Uvaria Macrophylla 总被引:1,自引:0,他引:1
A new dihydroflavone (1), named macrophyllol A, was isolated from the roots of Uvaria macrophylla. Its structure was elucidated on the basis of spectroscopic evidence. 相似文献
66.
Yang Jie Wu Shou Quan Huo Li Yang Chen Xia Du 《Journal of organometallic chemistry》1995,490(1-2):249-254
Three series of cyclomercurated ferrocenylimines (2-chloromercurio-ferrocenylimines) have been studied using 13C NMR spectroscopy. Good to excellent linear relationships have been found to exist between the chemical shifts of the carbon atoms in the ferrocenyl moiety and normal Hammett substituent constants σm and σp. The δ values of the iminyl carbon atoms show excellent linear correlations with the σ values. In three series of the ferrocenes, the sensitivity of the carbon atoms to the substituent effect is different, which is discussed in terms of the twist angle between the N-phenyl ring and the C---C=N---C plane. The relative sensitivity of the chemical shifts on different positions in ferrocenyl moiety to the substituent effect has also been presented. 相似文献
67.
Ping ZHENG Wei Lin SUN Zhi Quan SHEN 《中国化学快报》2005,16(10):1413-1416
N-2-Thiazolylacrylamide (NTA) was polymerized by a radical route to obtain the polymer in good yield. The polymer with a pendent heterocyclic group is soluble in common organic solvents, which allow to prepare the corresponding metal complexes with higher loads easily. FTIR, ^1H NMR, elemental analysis, and energy-dispersive X-Ray spectroscopy (EDX) were applied to characterize these materials. The magnetic behavior of Fe(Ⅱ) and Nd(Ⅲ) complexes of poly(N-2-thiazolylacrylamide) was examined by a PPMS-9T magnetometer, exhibiting the characteristics of a soft ferromagnet. It is found that the Nd(Ⅲ) complex has an extremely high relative saturation magnetization of 35 emu/g. 相似文献
68.
QuanZhenHUANG GongZhenCHENG HaiBoZHANG SongTaoDING XiaoBingYANG XiaoHaiZHOU GaoYongZHANG 《中国化学快报》2005,16(4):497-500
The Q-band position of tin-centered 5, 9, 14, 18, 23, 27, 32, 36-octabutoxy 2, 3-phthalocyanine(SnNc(OBu)8) exhibits dramatic red-shift as mixed with SnCl2 in CH2Cl2. 相似文献
69.
Jiang Ke QIN Xian Zhang BU Yu Fang WANG Zhi Yun DU Xing Yuan WANG Zhi Shu HUANG Lin MA Lin Kun AN Lian Quan GU 《中国化学快报》2005,16(11):1451-1454
The reactions of tanshinone IIA with aromatic aldehydes have been investigated and several 2, T-(substituted arylmethylene) bis (1,6,6-trimethyl-6,7,8,9-tetrahydrophenanthro[1,2-b]- furan- 10, 11-dione) derivatives were obtained, 相似文献
70.
The 1205 classical isomers of fullerene C58, as well as one quasi-fullerene C58 isomer with a heptagonal ring (labeled as Cs:hept) have been investigated by the quantum chemical methods PM3, HCTH/3-21G, and B3LYP/6-31G(d). Isomer C3v:0001, which has the lowest number of adjacent pentagons, is predicted to be the most stable isomer, but the quasi-fullerene isomer Cs:hept is only 2.50 kcal mol-1 higher in energy. Systematic investigations of the electronic properties of C3v:0001 and Cs:hept find that the C3v:0001 isomer has high vertical electron affinity (3.19 eV). The nucleus-independent chemical shifts (NICS) value at the center of Cs:hept (-5.1 ppm) is more negative than that of C60 (-2.8 ppm). The NICS value at the center of the heptagonal ring in Cs:hept (-2.5 ppm) indicates weakly aromatic character. In contrast, the C58(6-) and C58(8-) ions of the C3v:0001 and Cs:hept geometries possess large aromatic character, with NICS values between -14.0 and -26.2 ppm. To clarify the thermodynamic stabilities of C58 isomers at different temperatures, the entropy contributions are taken into account on the basis of the Gibbs energy at the B3LYP/6-31G(d) level. The C3v:0001 isomer prevails in a wide range of temperatures, and the Cs:hept isomer is also an important component around 2800 K. The IR spectra of C58 isomers are simulated to facilitate experimental identification of different isomers. In addition, the electronic spectra and the second-order hyperpolarizabilities are predicted by ZINDO and the sum-over-states model. The static second-order hyperpolarizability of the C3v:0001 isomer is 96.5 % larger than that of C60, and its second-order hyperpolarizabilities at external field frequencies are at least nine times larger than those of C60. 相似文献