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61.
The morphological stability of sharp-edged silver nanoparticles is examined by the classical molecular dynamics (MD) simulations. The crystalline structure and the perfect fcc atom packing of a series of silver nanocubes (AgNC) of different sizes varying from 63 up to 1099 atoms are compared against quasi-spherical nanoparticles of the same sizes at temperature 303 K. Our MD simulations demonstrate that starting from the preformed perfect crystalline structures the cubic shape is preserved for AgNCs composed of 365–1099 atoms. Surprisingly, the rapid loss of the cubic shape morphology and transformation into the non-fcc-structure are found for smaller AgNCs composed of less than ~256 atoms. No such loss of the preformed crystalline structure is seen for quasi-spherical nanoparticles composed of 38–1007 atoms. The analysis of the temperature dependence and the binding energy of outermost Ag surface atoms suggests that the loss of the perfect cubic shape, rounding and smoothing of sharp edges and corners are driven by the tendency towards the increase in their coordination number. In addition, we revealed that AgNC1099 partially loses its sharp edges and corners in the aqueous environment; however, the polymer coating with poly(vinyl alcohol) (PVA) was able to preserve the well-defined cubic morphology. Finally, these results help improve the understanding of the role of surface capping agents in solution phase synthesis of Ag nanocubes. 相似文献
62.
The dynamics of the silver fir represent an important topic for researchers across Europe. Following its decline, which occurred in Europe after the last glaciation, the remaining relict areas became a very important laboratory for studying its conservation. The Central Apennine chain, particularly in Molise, represents one unique case where silver fir, Turkey oak and beech can be found within the same forest. This study focused on the forest structure of the Bosco Monteluponi where the closeness with Collemeluccio Man and Biosphere reserve has affected the diffusion of conifer within the forest. Consequently, the forest structure has shifted from even aged to uneven aged. The resulting complex forest structure offers new challenges for forest practitioners in the identification of silvicultural treatments, which identify and maintain the balance among the three species within the same forest. Particular importance was given to the silver fir natural regeneration in order to assess the forest suitability for conifer expansion. Results demonstrated that Monteluponi is strongly suitable for the in situ conservation of silver fir and offers a great opportunity for its diffusion. 相似文献
63.
南充雉鸡的巢址选择和春夏季栖息地选择 总被引:1,自引:0,他引:1
2006年3-6月,采用野外直接观察法和样方法,在四川省南充市太和白鹭自然保护区对雉鸡(Phasianus colchicus)的巢址选择和春夏季栖息地选择进行了研究。通过主成分分析和对比分析,巢址选择研究结果表明:雉鸡的巢都是选择在乔木盖度小、距水距离较近、草本高度和盖度都较大的白茅(Imperata cylindri-cal)干草丛中;影响雉鸡巢址选择的主要因子依次为:坡度、总盖度、乔木平均胸径、乔木盖度、郁闭度、距水距离、距路距离、灌木平均高度、巢周围干草比例、裸地面积、巢上方覆盖物厚、灌木盖度和巢所在草丛宽度等13个因子。春夏季栖息地选择研究结果表明:雉鸡在春夏季倾向于在植被总盖度大、坡度适中、乔木盖度适中、草本盖度和高度较大、灌木盖度较小、灌木高度较大、隐蔽度较大、距路距离较远和郁闭度较大等的生境栖息。 相似文献
64.
The synthesis, characterization, crystal structure, 1H NMR, spectrophotometric and conductometric studies of a new tetranuclear silver(I) complex of [1,3-di(2-methoxy)benzene]triazene are reported. Reaction of the ligand with silver acetate resulted in the formation of a tetranuclear cluster with a four-member Ag-Ag ring core, composed of four triazenide ligands and four metals. The results of studies of the stoichiometry and formation and of complex in tetrahydrofuran solution were found to be in support of its solid state structure. 相似文献
65.
雌核发育银鲫子代中微卫星特异序列分析 总被引:1,自引:0,他引:1
雌核发育个体的基因型基本上完全与母本相同,这是源于卵子发生过程中没有经过减数分裂.父本的遗传物质是在随机水平、亚基因组水平或基因组水平参与到子代的遗传重组过程,从而对长期突变积累的雌核发育生物基因组进行补偿,一直是遗传学家关注的问题.本文对雌核发育银鲫特异个体及父母本5个微卫星位点的扩增条带进行了克隆测序,相似性比对结果显示,特异个体所表现的父咎匾霥NA条带,序列结果与父本完全相同或相似(SCM4、SCM9、YJ5),并在某些位点上保留了母本的特异条带(YJ5),而个体本身特异的DNA条带与父母本的相似性均较高(SCM13).同时,所检测到的个体经越冬后查验为雌性个体,进一步进行同源繁育,研究变异条带在繁殖中的命运.连续2代的繁育检测结果表明,融合了父本特异性条带的银鲫个体在繁殖过程中仍行雌核发育的生殖方式,变异来的条带能够传递给子代,进一步证实同源雌核发育银鲫通过小概率两性融合事件丰富银鲫种群的遗传多样性[动物学报 53(3):537-544,2007]. 相似文献
66.
Texter J Ziemer P Rhoades S Clemans D 《Journal of industrial microbiology & biotechnology》2007,34(8):571-575
A much studied oil-soluble surfactant, bis[2-ethylhexyl]sulfosuccinate, sodium salt, was ion exchanged into the silver ion
form and dissolved into microemulsions of immiscible polyurethane step monomers. Coating and curing of these microemulsions
produced polyurethane coatings that exhibit bactericidal activity against representative Gram negative bacteria. After 24 h
exposure, 0.006–0.012% weight Ag relative to coating weight (0.0013–0.0025 μmol Ag/cm2) results in the three-log reduction in Escherichia coli. A slightly higher level of 0.031% weight Ag relative to coating weight (0.006 μmol Ag/cm2) killed all of the E. coli after 12 h exposure. Similar results were obtained for Pseudomonas aeruginosa. Since the double-tail surfactant anion promotes reverse micelle formation in many different kinds of oils and solvents,
it appears an excellent vector for incorporating low and effective amounts of silver ion into many industrial, hospital, and
household coating formulations. 相似文献
67.
Varelius J 《Bioethics》2007,21(3):140-149
In a recent issue of this journal, David Silver and Gerald Dworkin discuss the physicians' role in execution by lethal injection. Dworkin concludes that discussion by stating that, at that point, he is unable to think of an acceptable set of moral principles to support the view that it is illegitimate for physicians to participate in execution by lethal injection that would not rule out certain other plausible moral judgements, namely that euthanasia is under certain conditions legitimate and that organ-donation surgery is sometimes permissible. This article draws attention to some problems in the views of Silver and Dworkin and suggests moral principles which support the three moral views just mentioned. 相似文献
68.
Mariana Dennehy Susana H. Tarulli Sandra D. Mandolesi Gustavo A. Echeverría Eduardo E. Castellano 《Inorganica chimica acta》2007,360(10):3169-3181
The title compounds, for short Ag6(tsac)6 (1) and [Cu4(tsac)4(MeCN)2] · 2MeCN (2), were prepared by the reaction of thiosaccharin with Ag(I) or Cu(II) salts in different solvents. The new complexes were characterized by FT-IR, Raman, UV-Vis and NMR spectroscopy. Their crystal and molecular structures were determined by X-ray diffraction methods. The structures were solved from 1621 (1) and 7080 (2) reflections with I > 2σ(I) and refined to agreement R1-factors of 0.0261 (1) and 0.0456 (2). Ag6(tsac)6 molecule derives from the clustering of six Ag(tsac) moieties related to each other through the crystallographic 3-bar (S6) symmetry operations of the space group. This results in a highly regular molecular structure where the silver atoms are at the corners of an octahedral core slightly compressed along one of its three-fold axis [inter-metallic Ag?Ag contacts of 3.1723(4) and 3.1556(4) Å]. The six thiosaccharinate ligands bridge neighboring Ag atoms along the C3-axis through Ag-N bonds [d(Ag-N) = 2.285(2) Å] at one end and bifurcated Ag-S(thione)-Ag bonds [Ag-S distances of 2.4861(7) and 2.5014(8) Å] at the other end. In contrast, the 2 compound is arranged in the lattice as an irregular tetrameric copper complex [Cu4(tsac)4(MeCN)2] where the metals show different environments. Two copper ions are four-fold coordinated to three tsac ions through the N-atom of one tsac [Cu-N distances of 2.112(3) and 2.064(3) Å] and the thione sulfur atom of the other two [Cu-S distances in the range from 2.284(1) to 2.358(1) Å] and to a MeCN solvent molecule [Cu-N distances of 1.983(4) and 2.052(3) Å]. The other two copper ions are in three-fold environment, one trans-coordinated to two tsac ions [Cu-N distances of 1.912(3) and 1.920(3) Å] and to the thione S-atom of a third ligand [d(Cu-S) = 2.531(1) Å], the other one to the thione sulfur atom of three tsac ligands [Cu-S distances in the range from 2.229(1) to 2.334(1) Å]. The clustering renders the metals to short distances from each other, the shorter Cu?Cu distance being 2.6033(7) Å, as to presume the existence of weak inter-metallic interaction within the cluster. 相似文献
69.
A tetrameric [Ag(μ-3,5-tBu2pz)]4 · CH2Cl2 (1 · CH2Cl2) has been prepared and structurally characterized. The four Ag-atoms are in an approximate rhombic arrangement with pyrazolato bridges alternating on either side of the Ag4-plane. A 1H NMR study shows partial decomposition of 1 to the mononuclear [Ag(3,5-tBu2pzH)2]+ in solution. 相似文献
70.
Ya-Qiong Gong Jiu-Tong Chen Ming-Yan Wu You-Gui Huang Fei-Long Jiang 《Inorganica chimica acta》2007,360(7):2207-2214
Two new 2D coordination polymers, [Ag4(μ-4,4′-bpp)3(1,3-bdc)2]n · 2nH2O (1) and [Ag(μ-4,4′-bpp)2ClO4]n(2) (4,4′-bpp = 2,2′-bis(4-pyridylmethyleneoxy)-1,1′-biphenylene; 1,3-bdc = 1,3-benzenedicarboxylate) have been synthesized using three-layer diffusion methods. Single-crystal X-ray analyses reveal that they are both extended grid networks of the (4,4) topology. In complex 1, a chain built by Ag(I) centers with T-shaped and linear geometries is further connected by the interesting ligand-unsupported Ag?Ag interactions as well as the conjugated π systems to form an interdigitated 2-D coordination network. The corrugated (4,4) sheets of 2 are packed in the ab planes and stacked along the c direction with the anions occupying the gaps in the squares. 相似文献