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211.
Yoshihiro Osamura 《Theoretical chemistry accounts》1989,76(2):113-124
Summary A new analytic second derivative expression of the electronic energy is derived for full configuration interaction (CI) wave functions. This formula is shown to be free from the derivative terms of both CI and MO coefficients. The second-order relationships between CI and MO coefficients for full CI wave functions are also presented. 相似文献
212.
导数阴极溶出方波伏安法测定卡那霉素注射液含量 总被引:2,自引:0,他引:2
研究了汞 卡那霉素络合物的电化学行为 ,并建立了导数阴极溶出方波伏安法测定卡那霉素注射液含量的方法。在 pH 4 .7的HOAc NaOAc缓冲溶液中 ,在约 0 .12 6V (vs.SCE)处出现一个汞 卡那霉素络合物的还原峰 ,卡那霉素的浓度在 0 .0 2~ 1.5mg·ml- 1之间与导数方波伏安图的峰高存在良好的线性关系 ,回归方程ip(10 - 4A) =3.6C(mg·ml- 1) + 0 .4 6 ,相关系数为 0 .992 0。方法简便、灵敏、准确 ,可用于卡那霉素注射液含量测定 相似文献
213.
氨-碘酸盐介质中白喉类毒素的平行催化氢波 总被引:6,自引:0,他引:6
在 0 .4mol/LNH3 NH4Cl (pH 8.3 1 )介质中 ,白喉类毒素 (DT)于 - 1 .89V(vs.SCE)处产生的极谱催化氢波可被碘酸钾进一步催化 ,峰电流明显增大 ,但峰电位不变 ,产生一种氢的新动力波 ,建议称其为平行催化氢波。在 0 .4mol/LNH3 NH4Cl(pH 8.3 1 ) - 5 .0× 1 0 - 3 mol/LKIO3介质中 ,DT平行催化氢波的二阶导数峰电流与其浓度在 0 .2 μg/mL~ 1 .0 μg/mL内呈线性关系 ,可用于生物制品中DT含量的测定。 相似文献
214.
镓-铬蓝黑R络合吸附波的研究及应用 总被引:3,自引:0,他引:3
在0.012mol/L HAc-0.10mol/L NaAc缓冲溶液中pH5.60,铬蓝黑R于-0.34V(vs.SCE)处有一极谱波P_1,加入Ga(Ⅲ),在-0.55V(vs.SCE)处产生一灵敏的极谱波P_2。i_p_2与Ga(Ⅲ)浓度在0.20~15.0μg/25ml范围内呈线性关系。试验表明,该极谱波属络合吸附波。本法用于测定铝箔、铅锌矿中微量镓,结果满意。 相似文献
215.
The antisymmetrized geminal power (AGP) and sequential product of geminals(SPG) functions, the basis functions with symplectic symmetry, are linearly combined to calculate the ground state of the LiH molecule. The calculation results show that the AGP or SPG function gives the same ground state results as the linear combination. 相似文献
216.
Luciana B.O. dos Santos 《Analytica chimica acta》2005,528(1):21-27
This paper describes the development of a sequential injection analysis method to automate the determination of atrazine by square wave voltammetry exploiting the concept of monosegmented flow analysis to perform in-line sample conditioning and standard addition. To perform these tasks, an 800 μL monosegment is formed, composed by 400 μL of sample and 400 μL of buffer/standard solution. To obtain an efficient homogenization, the sample solution is divided in five zones intercalated by four zones of the Britton-Robinson buffer (pH 2.0) in presence of appropriate concentration of NaNO3 and varying atrazine standard concentrations. This mixture zone is isolated from the carrier solution by two 100 μL air bubbles. After homogenization in an auxiliary reaction coil the mixture zone is injected toward the flow cell, which is adapted to the capillary of a hanging drop mercury electrode, at a flow rate of 50 μL s−1. After a suitable delay time, the potential is scanned from −0.5 to −1.2 V versus Ag/AgCl using a frequency of 300 Hz and pulse height of 25 mV. The linear dynamic range is observed for atrazine concentrations between 1.16 × 10−7 and 2.32 × 10−6 mol L−1, obeying the linear equation ip = (−6.91 ± 0.07) × 108[atrazine] + (4 ± 8), with r2 = 0.9996, for which the slope is given in nA L mol−1. The detection and quantification limits of the method are 2.1 × 10−8 and 7.0 × 10−8 mol L−1, respectively. The sampling frequency is 37 h−1, when the standard addition protocol is followed. This frequency can be increased to 42 h−1 if the protocol to obtain in-line calibration curve is used for quantification. The method was applied for determination of atrazine in spiked river water samples and its accuracy was evaluated by comparison with the batch standard addition approach, which revealed that there is no evidence of statistically significant differences between the two methods. 相似文献
217.
Winfried Mientus Hans-Georg Bartel Werner Haberditzl Hans-Joachim Spitzer 《Monatshefte für Chemie / Chemical Monthly》1980,111(3):597-606
A normalization of the wave functions by means of the theoretical exact Multiple-Scattering-(MS)-formalism is discussed within the framework of the SCF-X-SW-method. For the atomic and extramolecular regions the integrals of normalization can be easily determined and the results can be described by the corresponding electronic charges. The calculation of the integral of the interatomic region is problematic. The needful volume integration is only necessary to theGreen's functions of the wave functions and can be solved by means of the residual theory. The further analytical calculation of the surface integrals leads to a complicated formalism which can be numerically evaluated. 相似文献
218.
A. D. Smirnov 《Journal of Structural Chemistry》2003,44(5):757-762
The vibrational, rotational, and centrifugal constants have been calculated for the ground electronic states of KRb and RbCs molecules. The calculation is performed using the semiempirical potential curves constructed in a wide range of internuclear distances. The estimated spectroscopic constants are compared with experimental data. 相似文献
219.
本文提出了铀(Ⅵ)-5-Br-PADAP-磺基水杨酸三元配合物的极谱配位吸附波。在pH为7.5-8.2的醋酸、三乙醇胺、乙醇底液中,该波的峰电位在-0.6855V(vs.SCE)。在1.00×10-7-1.00×10-5mol·dm-3范围内,铀(Ⅵ)浓度与峰电流呈线性关系。对极谱波的电流、电位性质进行了研究,测定了配合物的组成、表观稳定常数和离解及生成速率常数。 相似文献
220.
槲皮素伏安行为及其稀土络合物极谱催化氢波研究 总被引:7,自引:0,他引:7
在乙醇量小于5%的水溶液中,于pH1.5至4.5,4.2至9.5分别得到槲皮素的两个还原波,均为羰基两电子还原.前者为其分子的强吸附波,后者为一价阴离子的波.在pH6.1附近的醋酸盐缓冲底液中,可获得槲皮素与Tb(Ⅲ)、Dy(Ⅲ)、Ho(Ⅲ)、Er(Ⅲ)、Tm(Ⅲ)、Yb(Ⅲ)、Lu(Ⅲ)和Y(Ⅲ)等重稀土离子络合物的双重表面催化氢波.络合物被诱导吸附,组成为(REL_2)L_吸.Sc(Ⅲ)与槲皮素形成单一表面催化氢波,其组成为(ScL)L_吸. 相似文献