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51.
52.
A study was carried out on the composition and nature of the stabilizing additive on the activity of nickel-containing composites
based on zirconia in the methane steam conversion. The methane conversions were 91–99% on Ni/ZrO2(Y, Sc, Ce) at 700–800 °C. 相似文献
53.
54.
将酞菁锰(MnPc)掺入阳离子表面活性剂双十二烷基二甲基溴化铵(DDAB)的氯仿溶液,并涂布于热解石墨电极表面,待氯仿挥发后即制得MnPc-DDAB薄膜电极。循环伏安实验表明,在KBr溶液中,该薄膜电极有两对还原氧化峰,第一对峰的Epc1=-0.27V,Epa1=0.01V;第二对峰的Epc2=-0.76V,Epa2=-0.62V(vs.SCE)。本文着重探讨了第二对峰的电化学行为,估计了该体系的电荷传递扩散系数Dct和表观非均相电极反应速率常数K0′等电化学参数,并可将该薄膜电极用于催化三氯乙酸的电化学还原。 相似文献
55.
56.
过渡金属酞等配合物(MPC)用手均相液相氧化中作催化剂已有不少报导,象许多均相催化剂一样,MPC用于均相反应存在着难于从反应体系中分离出来的问题.把均相配合物催化剂固载在无机氧化物如硅股或有机高分子载体上是解决这一问题的一种方法.我们曾尝试把MP。固载在分子筛载体和硅胶载体上,并用ESR研究其对O2的活化作用[1,2].本文报导MPc通过共价键键联固载在SiO2上,并研究其对O2的活化作用.1实验部分1.1试剂HSIC13为日本东京化成株式会社产品,二级试剂·发烟硫酸(SO。质量分数大于20%)为分析纯试剂.PCl5为化学纯试… 相似文献
57.
Cycloaddition of carbon dioxdie and propylene oxide to propylene carbonate catalyzed by tetra-tert-butyl metal phthalocyanine in the presence of tributylamine(TBA) shows higher yield than catalyzed by unsubstituted metal phthalocyanine.Comparing different catalysts of diverse metals,(t-Bu)4PcMg is more active than (t-Bu)PcFe ,But(t-Bu)4PcCo and (t-Bu)4PcNi only have low catalytic activities towards the reaction.Moreover,the yield will increase as the temperature increases. 相似文献
58.
Elisa Brivio Alessandro Ceriotti Roberto Della Pergola Luigi Garlaschelli Mario Manassero Mirella Sansoni 《Journal of Cluster Science》1995,6(2):271-287
Redox condensation of [Ru3H(CO)11]- with Ni(CO)4, in tetrahydrofuran solution, under a nitrogen atmosphere, yields the tetranuclear anion [NiRuH(CO)11)-. Subsequent deprotonation with Bu'OK in acetonitrile solution leads to the formation of the related dianion. Both anions have been characterized by spectroscopic techniques, elemental analysis and single crystal X-ray diffraction. [PPh4][NiRu3H(CO)12] crystallizes in the triclinic space group PI with unit cell dimensionsof a = 11.842(2) Å,b = 12.335(3) Å, c = 13.3080) Å,a = 91.89(2)°, = 93.35(1)°,y = 96.41(2)°, Z = 2, V= 1926.9(7) Å'. The NiRu3, metal core of the molecule defines a distorted tetrahedron with nine terminal and three edge bridging carbonyl groups. The hydrido ligand was located by difference Fourier techniques and was found to bridge the NiRu2 basal triangle at a distance of 0.88(6) A from this plane. Selected average distances and angles are: Ru-Ru = 2.839 Å, Ru-Ni = 2.640 Å, Ru-C, = 1.910 A,Ru-C
b
= 2.084 Å, Ni-C
b
= 2.022 Å, Ru-H = 1.77 Å, C-0, = 1.135 Å, C-O
b
= 1.159 Å, M-C-O, = 176.3°,M-C--O
b
= 139.3°;other distances are: Ni-C1 = l.758(7) Å, Ni-H= 1.85(7) Å. [NEt4]2[NiRu3(CO)12] crystallizes in the orthorhombic space group Pnma (no. 62) with unit cell dimensions ofa=20.247(5) Å,b = 15.038(4)Å,c = 12.079(3) Å, Z=4, V=3678(2) A'. The molecule contains a tetrahedral NiRu3 core with eight terminal and four edge bridging carbon monoxide groups which bridge the three Ni-Ru and one Ru-Ru bond. Average distances and angles are: Ru -Ru =2.3050A Ru-Ni 2.648 Å, Ru-C
t
= 1.878 Å, Ru-C
b
2.045 Å, Ni-C
b
= 2.055 Å, C-O
t
= 1.145 Å, C-01,=1.157 Å, M-C-O,= 176.9°, M-C-O
b
= 138.6°; other distance is: Ni-C
t
= 1.754(10) Å,t = terminal,b = bridging. 相似文献
59.
This is the first report on the determination of proteins with tetra-substituted sulphonated aluminum phthalocyanine (AlS4Pc) by resonance light-scattering (RLS). At pH 3.0, the weak RLS of AlS4Pc can be enhanced by the addition of proteins. Based on this, a novel quantitative method has been developed for the determination of proteins in aqueous solutions. Under optimal conditions, the linear ranges of the calibration curves were 0.050–2.0 μg ml−1 for both human serum albumin (HSA) and human r-IgG. The detection limits were 12.7 ng ml−1 for HSA and 16.1 ng ml−1 for human r-IgG. The method has been applied to the analysis of total protein in human serum samples collected from the hospital and the results were in good agreement with those reported by the hospital, which indicates that the method presented here is not only sensitive, simple, but also reliable and suitable for practical applications. 相似文献
60.
A nickel catalyst was nodeled with ligand L^2,[NH=CH-CH=CH-0]^-,which should have potential use as a syndiotactic plyolefin catalyst,and the reaction mechanism was studied by theoretical calculations using the density functinal method at the B3LYP/LANL2MB level.The mechanism involves the formation of the intermediate [NiL^2Me]^ ,in which the metal occupies a T-shaped geometry.This intermediate has two possible structures with the methyl group trans either to the oxygen or to the nitrogen atom of L^2.The results show that both structures can lead to the desired product via similar reaction paths,A and B.Thus,the polymerization could be considered as taking place either with the alkyl group occupying the position trans to the Ni-0 or trans to the Ni-N bond in the catalyst.The polymerization process thus favors the catalysis of syndiotactic polyolefins.The syndiotactic synthesis effects could also be enhanced by varations in the ligand substituents.From energy considerations,we can conclude that it is more favorable for the methyl ttrans-O position to form a complex than to occupy the trans-N position.From bond length considerations,it is also more favoured for ethene to occupy the trans-O position than to occupy the trans-N position. 相似文献