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951.
通过使用含时量子波包方法,对HF分子该类型的布居转移动力学进行了研究. 提出双Σ型激光控制方案,用于控制布居从|v=16>能级向|v=0>能级进行转移. 该方案的第一步是将布居从|v=16>经过中间能级|v=11>向|v=7>转移,第二步是将布居从|v=7>经过中间能级|v=3>向|v=0>转移. 在每一个步骤中,三个振动能级在两束重叠的激光脉冲作用下形成一个Σ型的布居转移路径. 通过优化激光的强度、频率和延迟时间,得到了最大的布居转移效率. 计算并比较了正序脉冲和反序脉冲两种情况,在这两种情况下,布居都可以超过90%从|v=16>能级向|v=0>能级进行转移. 相似文献
952.
扩散过程中弱相干光场的退相干 总被引:1,自引:0,他引:1
研究了扩散过程中弱相干光场量子特性的演化.利用正规乘积、反正规乘积和Weyl编序算符内的积分技术,采用热纠缠态表象求解密度矩阵主方程,利用Kraus算符给出扩散过程中密度算符解的表达式,导出初态为弱相干态的量子态密度算符演化规律.讨论了扩散对光场压缩效应和反聚束效应的影响.结果表明:随着扩散过程的进行,弱相干场压缩深度和压缩范围均在减小;扩散初期光场呈反聚束效应,扩散时间大于一定值后反聚束效应消失. 相似文献
953.
In this paper we characterize the Schatten p class membership of Toeplitz operators with positive measure symbols acting on generalized Fock spaces for the full range 0<p<∞. 相似文献
954.
Comparison of the 13C (C = N) chemical shifts of substituted N‐(phenyl‐ethylene)‐anilines and substituted N‐(benzylidene)‐anilines
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Comparison of 13C NMR of C = N bond chemical shifts δC(C = N) in substituted N‐(phenyl‐ethylene)‐anilines XArC(Me) = NArY (XPEAYs) with that in substituted N‐(benzylidene)‐anilines XArCH = NArY (XBAYs) was carried out. The δC(C = N) of 61 samples of XPEAYs were measured, and the substituent effect on their δC(C = N) were investigated. The results show the factors affecting the δC(C = N) of XPEAYs are quite different from that of XBAYs. A penta‐parameter correlation equation was obtained for the 61 compounds, which has correlation coefficient 0.9922 and standard error 0.12 ppm. The result indicates that, in XPEAYs, the inductive effects of substituents X and Y are major factors affecting the δC(C = N), while the conjugative effect of them have very little effect on the δC(C = N) and can be ignored. The substituent‐specific cross‐interaction effects between X and Y and between Me of C = N bond and substituent Y are important factors affecting the δC(C = N). Also, the excited‐state substituent parameter of substitute Y has certain contribution to the δC(C = N). Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
955.
Yb3+ doped phosphor of Gd2O3 (Gd2O3:Yb3+) have been prepared by solid state reaction method. The structure and the particle size have been determined by X-ray powder diffraction measurements. The average particle size of the phosphor is in between 35 and 50 nm. The particle size and structure of the phosphor was further confirmed by TEM analysis. The visible and NIR luminescence spectra were recorded under the 980 nm laser excitation. The visible upconversion luminescence of Yb3+ ion was due to cooperative luminescence and the presence of rare earth impurity ions. The cooperative upconversion and NIR luminescence spectra as a function of Yb3+ ion concentration were measured and the emission intensity variation with Yb3+ ion concentration was discussed. Yb3+ energy migration quenched the cooperative luminescence of Gd2O3:Yb3+ phosphor with doping level over 5%, while the NIR emission luminescence continuously increases with increasing Yb3+ ion concentration. 相似文献
956.
The interband and intraband radiation from the n-InGaAs/GaAs heterostructures with the double and triple tunnel coupled and selectively doped quantum wells (QWs), which is appeared under the lateral electric field and in the presence of hole injection from the anode contact, has been investigated. A steep increase of the interband radiation intensity was found at the fields of E≥1.7 kV/cm. This effect should be related to the big lifetime of the injected charge carriers (~10−6 s) which exceeds by three orders of magnitude the lifetime in the similar bulk direct-band semiconductor. Its reason lies in spatial separation of the injected holes and electrons between coupled wells, firstly, by the built-in transverse electric field between wells and, secondly, due to the real-space transfer of carriers heated by the lateral electric field from the wide well to the narrow δ-doped one. Furthermore, an increase of the carrier concentration due to injection leads to an increase of that transition intensity and, consequently, to an intensity increase of the radiative intersubband transitions of carriers in QWs which results in a steep intensity increase of the far (50–120 µm) infrared radiation. 相似文献
957.
958.
采用密度泛函理论计算方法模拟了简单钴卟啉过氧中间体PCo-O2与环己烷C6H12的作用,分析了反应路径中各驻点能量和反应过渡态分子构型。研究结果表明,PCo-O2向底物环己烷夺氢的反应可以延正方向进行,二线态PCo-O2更具反应活性,反应过程中Co-O键得到加强,O-O键被削弱。依据理论计算结果,探讨了四苯基钴卟啉催化环己烷氧化生成环己醇和环己酮的反应机理,指出反应延Lyons高价金属氧代物机理生成环己醇,而反应循环中产生的烷基自由基可以延烷基过氧化过渡金属配合物反应机理进行生成环己酮。 相似文献
959.
Giuseppe Gattuso Sebastiano Pappalardo Melchiorre F. Parisi Ilenia Pisagatti 《Supramolecular chemistry》2014,26(7-8):597-600
The molecular recognition in water of neurotransmitter monoamine and trace amine hydrochlorides by p-tert-butylcalix[5]-arene 1 – bearing 4-sulphonatobutoxy groups at the lower rim – has been investigated. According to 1H NMR measurements, the hydrophobic cavity of receptor 1 best binds tyramine hydrochloride, Ka = 5370 ± 870 M? 1. 相似文献
960.
In this study, alleviation of ion suppression effect in sonic spray ionization mass spectrometry (SSI‐MS) was investigated. Ion suppression effect was firstly compared between electrospray ionization (ESI) and conventional SSI, and more severe ion suppression effect was observed with SSI. Ion suppression effect of SSI was also found difficult to be alleviated by simply optimizing major parameters. Alternatively, we found that with the assistance of an alternating current (AC) voltage with low amplitude, the ion suppression effect was greatly alleviated (comparable with conventional ESI). That AC voltage was applied outside the SSI spray tip, and no direct contact between the electrode and spray solution was necessary. Besides the alleviation of the ion suppression effect, this newly‐developed method, termed as induced electrosonic spray ionization (IESSI), appeared to preserve similar charge state distribution with SSI for protonated cytochrome c, hemoglobin, and bradykinin. IESSI could also obtain significantly improved ion intensities (~1000‐fold over conventional SSI). In addition, tolerance of concentrated salts for IESSI‐MS was investigated through the analysis of cytochrome c in the presence of concentrated sodium chloride (NaCl) or ammonium acetate (NH4OAc). Copyright © 2014 John Wiley & Sons, Ltd. 相似文献