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71.
The Hamiltonian formulation of the usual complex quantum mechanics in the theory of generalized quantum dynamics is discussed.
After the total trace Lagrangian, total trace Hamiltonian and two kinds of Poisson brackets are introduced, both the equations
of motion of some total trace functionals which are expressed by total trace Poisson brackets and the equations of motion
of some operators which are expressed by the without-total-trace Poisson brackets are obtained. Then a set of basic equations
of motion of the usual complex quantum mechanics are obtained, which are also expressed by the Poisson brackets and total
trace Hamiltonian in the generalized quantum dynamics. The set of equations of motion are consistent with the corresponding
Heisenberg equations.
Project supported by Prof. T.D. Lee’s NNSC Grant, the National Natural Science Foundation of China, the Foundation of Ph.
D. Directing Programme of Chinese University, and the Chinese Academy of Sciences. 相似文献
72.
锌是人体必需的微量元素 ,也是金属酶的组成部分和酶的激活剂 ,目前已知有 80多种酶的活性与锌的存在有关 ,因此研究锌在生物分子 (如L 半胱胺酸 )自组装膜结构中的电化学行为 ,对于研究和了解生物体内生命物质的电子转移及生命现象的本质具有重要意义。本文研究Zn2 +在L 半胱氨酸自组装修饰金电极[1~3] ,Cys/SAM/Au上的电化学行为 ,建立了测定Zn2 +浓度的新方法 ,用于人体发样中痕量Zn2 +的测定 ,与目前所报道的锌的测定方法[4] 相比 ,具有快速、准确、灵敏度高等特点。1 实验部分1 1 仪器与试剂CHI660型电化学工作… 相似文献
73.
已有熔铁氨合成催化剂中添加稀土的报道.我们通过添加稀土得到了几种活性较高的催化剂,经进一步改进制备工艺(水浸处理后),活性又有所提高.本文利用XRD和AES等,对经水浸前后的含稀土催化剂的结构进行了测试,探讨了水浸后活性提高的原因. 相似文献
74.
Borohydride exchange resin-transition metal(Co,Ni,Cu,)compoundsystems reduced C=C double to C-C single bond in ethanol. 相似文献
75.
利用四氯合金酸和N-4-甲基苯基2-吡啶甲酰胺(HL)反应,合成得到了一种新的Au(Ⅲ)配合物:二氯(N-4-甲基苯基2-吡啶甲酰胺合金(Ⅲ)[Au(L-N,N′)Cl2]。并通过元素分析、红外光谱、核磁共振谱、质谱及X-射线单晶衍射对其进行了表征。结构分析表明,Au(Ⅲ)由二个氮原子和二个氯原子配位,呈平面四方形结构。质谱研究发现,该化合物与5′-单磷酸鸟苷(5′-GMP)反应生成[Au(L-N,N′)(5′-GMP)2]。 相似文献
76.
铁基超细粒子催化剂具有优良的F-T反应性能。本工作利用原位Mssbauer谱辅以XRD技术研究了含有钾助剂的F-T合成铁基超细粒子催化剂的结构与还原行为,考察了催化剂组成和第二金属组分(Mn,Zn,Mg)的影响。“纯”铁超细粒子催化剂在氢气中很容易经Fe_3O_4还原为零价铁。第二金属组分的引入,一方面阻碍了催化剂的还原,另一方面稳定了Fe~(2+)的存在而使其成为还原的主要中间相,这有利于反应条件下形成类尖晶石结构的活性相。对于Fe-Mn催化剂,上述效应随锰含量的增加而更趋显著。铁基超细粒子催化剂在氢气中的还原能力依“纯”Fe>Fe-Zn>Fe-Mn>Fe-Mg的顺序递减,这在一定程度上反映了铁与第二金属组分之间相互作用的强弱。 相似文献
77.
Fabrication of hexaphenylsilole nanowires and their morphology-tunable photoluminescence. 总被引:1,自引:0,他引:1
Liping Heng Jin Zhai Anjun Qin Yuqi Zhang Yongqiang Dong Ben Zhong Tang Lei Jiang 《Chemphyschem》2007,8(10):1513-1518
Immersion of nanoporous alumina membranes into saturated solutions of hexaphenylsilole with subsequent solvent evaporation affords aligned organic nanowires. The luminescent properties of the hexaphenylsilole nanowires can be manipulated by varying their morphologies, which were controlled by changing the channel sizes of the alumina templates. 相似文献
78.
Observation of a quadrupole plasmon mode for a colloidal solution of gold nanoprisms 总被引:3,自引:0,他引:3
Millstone JE Park S Shuford KL Qin L Schatz GC Mirkin CA 《Journal of the American Chemical Society》2005,127(15):5312-5313
The synthesis and optical properties of single crystalline gold nanoprisms have been investigated. A three-step mediated seed growth process in an aqueous solution generated gold nanoprisms with a relatively homogeneous size distribution. The purity of these nanostructures has allowed us to observe a weak quadrupole resonance in addition to a strong dipole resonance associated with these novel structures. The experimental optical spectra agree with discrete dipole approximation calculations that have been modeled from the dimensions of gold nanoprisms produced in this synthesis. 相似文献
79.
Qin W Baruah M Van der Auweraer M De Schryver FC Boens N 《The journal of physical chemistry. A》2005,109(33):7371-7384
The photophysical properties of seven new 8-(p-substituted)phenyl analogues of 4,4-difluoro-3,5-dimethyl-8-(aryl)-4-bora-3a,4a-diaza-s-indacene (derivatives of the well-known fluorophore BODIPY) in several solvents have been studied by means of absorption and steady-state and time-resolved fluorimetry. For each compound, the fluorescence quantum yield and lifetime are lower in solvents with higher polarity owing to an increase in the rate of nonradiative deactivation. Increasing the electron withdrawing strength of the p-substituent on the phenyl group in position 8 also leads to lower fluorescence quantum yields and lifetimes. When the p-substituent on the phenyl group in position 8 is a tertiary amine [8-(4-piperidinophenyl), 8-(4-N,N-dimethylaminophenyl), and 8-(4-morpholinophenyl)], the low quantum yields of these compounds in more polar solvents can be rationalized by the inversion of the energy levels of an apolar, highly fluorescent and a polar, nonfluorescent excited state, where charge transfer from the tertiary amine to the BODIPY unit occurs. These amine analogues can be protonated at low pH in aqueous solution. Fluorescence titrations yielded pK(a) values of their conjugate ammonium salts which are in agreement with the electron donating tendency of the amine group: piperidino (4.15) > dimethylamino (2.37) > morpholino (1.47), with the pK(a) values in parentheses. The rate constant of radiative deactivation (k(f)) is the same for all compounds in all solvents studied (k(f) = 1.4 x 10(8) s(-1)). 相似文献
80.
Zhang YL Qin WW Liu WS Tan MY Tang N 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2002,58(10):2153-2157
An amide-based open-chain crown ether ligand and its complexes with europium and terbium were synthesized. The complexes were characterized by elemental analysis, infrared spectra and conductivity. The europium and terbium ions were found to coordinate to the C=O oxygen atoms and pyridine nitrogen atoms. The fluorescence properties of these complexes in DMF and CH3OH/CHCl3 were studied. Under the excitation of UV light, these complexes exhibit characteristic fluorescence of europium and terbium ions. The solvent factors influencing the fluorescent intensity are discussed. 相似文献