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111.
本文着重研究了自还原性胺钨盐的性质及其氢还原,发现,将自还原与一般氢还原适当结合,可以高效率地制备比表面积大于20m~2/g的极细、超细钨粉。对自还原的本性及该类钨盐在制取极细、超细钨粉方面的应用前景进行了讨论。 相似文献
112.
Frank Langhans Stefan Kiefer Carsten Hartmann Toni Markurt Tobias Schulz Christo Guguschev Martin Naumann Sandro Kollowa Andrea Dittmar Jürgen Wollweber Matthias Bickermann 《Crystal Research and Technology》2016,51(2):129-136
In order to evaluate the possible involvement of crucible materials in the growth of AlN bulk crystals grown by physical vapor transport, we applied growth conditions with a high vertical thermal gradient and hence high supersaturation of aluminum vapor. Under these conditions, precipitates formed causing diffuse grayish substructures at the initial growth interface and in the crystal body, decorating dislocations. Electron microscopy studies revealed that the precipitates are elongated, single‐phase particles with sizes of 50–500 nm of commensurate structure, oriented along the <110> direction. Chemical analysis of the precipitates showed tungsten as well as carbon and oxygen. The lattice parameters of the precipitates are in close agreement to hexagonal tungsten hemicarbide (W2C). The possible transport from the tungsten parts and its conversion into tungsten hemicarbide precipitates is discussed. We thus conclude that the W2C precipitates may contribute to the decoration of dislocations, even in growth with moderate thermal gradients. 相似文献
113.
Beatriz Baeza Prof. Luis Casarrubios Prof. Miguel A. Sierra 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(4):1429-1435
Alkynylamino Cr0 and W0 Fischer carbenes undergo a CuAAC reaction with a diverse range of di‐, tri‐, and tetra‐azides to produce polymetallic chromium(0) and tungsten(0) (Fischer)‐carbene complexes in good‐to‐excellent yields. This method is simple, versatile, and is suitable for the preparation of a diverse range of structures with a high level of symmetry. Moreover, the resulting polymetallic carbene complexes are suitable partners for the peripheral functionalization of the metal nuclei, whilst retaining the metal fragment. This fact has been demonstrated in a simultaneous Pauson–Khand reaction, which, in some cases, allows for the generation of four bicyclic [5,5] rings on the periphery of a tetrametallic molecule in a process that involves the formation of 12 new C? C bonds, with four simultaneous CO‐insertion processes. The electrochemistry of the polymetallic Fischer carbenes show completely independent behavior for each nucleus, as well as an anomalous observation of the reversible oxidation of the allyl substituents, which has not been reported before in this class of chemistry. 相似文献
114.
为研究玻璃及玻璃/钨复合材料药型罩射流与靶板间的反应及其对破甲性能的影响,对两种材料射流侵彻后的45钢靶分别进行组织和性能测试分析.结果表明:玻璃药型罩适合在较大炸高条件下使用,而玻璃/钨药型罩适合在小炸高条件下使用.侵彻过程中玻璃射流与钢靶之间不发生反应,而玻璃/钨与钢靶之间发生反应生成了Fe-W相,使得射流能量部分横向耗散.玻璃及玻璃/钨射流在侵彻钢靶的过程中均会引起弹孔表面发生马氏体相变,且随着侵彻的深入,相变区域宽度呈增加的趋势. 相似文献
115.
Satoshi Kaneco Kensuke Hayashi Hideyuki Katsumata Tohru Suzuki 《International journal of environmental analytical chemistry》2013,93(13):1381-1388
A preconcentration method by adsorption of cadmium on a niobium wire was developed for the environmental waters, followed by electrothermal atomic absorption spectrometry with a tungsten tube atomizer. After the preconcentration, the niobium wire was directly inserted into the tungsten tube atomizer. In the preconcentration (adsorption) process of cadmium, the optimal immersing time was 60?s. The effects of large amounts of concomitants on the preconcentration of cadmium were evaluated. When 103–104 fold excess of matrix elements existed in aqueous solution at pH 4 and 9, the cadmium response was profoundly affected by the matrix elements. However, the cadmium absorption signal was not significantly influenced at pH 7. Therefore, pH 7 was selected for the application into the real environmental samples. Under the optimal conditions, the detection limit (3S/N) for cadmium by the niobium wire preconcentration method was 7.0?pg?mL?1 and the relative standard deviation was 6.8%. The method with preconcentration on a niobium wire was applied to the determination of cadmium in water and proved to be sensitive, simple and convenient. Because this preconcentration method can be utilized in the in situ treatment of trace cadmium in environmental water samples, it was unnecessary to carry the water samples to the analytical work place. The technique was shown to be useful for the determination of cadmium in environmental water samples at 0.1–1?µg?L?1 levels. 相似文献
116.
Takashi Yoshimoto Prof. Dr. Hisako Hashimoto Dr. Nozomi Takagi Prof. Dr. Shigeyoshi Sakaki Naoki Hayakawa Dr. Tsukasa Matsuo Prof. Dr. Hiromi Tobita 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(15):3795-3798
A tungsten silylyne complex having a W≡Si triple bond reacted with two molecules of aldehydes at room temperature to give W−Si−O−C four-membered metallacycles by [2+2] cycloaddition and subsequent formyl hydrogen transfer from one aldehyde molecule to another. Upon heating to 70 °C, the four-membered metallacycles underwent metathesis-like fragmentation cleanly to afford carbyne complexes and “silanoic esters,” in a manner similar to that of metallacyclobutadiene, an intermediate of alkyne metathesis reactions, and dimerization of the latter products gave 1,3-cyclodisiloxanes. The “silanoic ester” was also trapped by pivalaldehyde to give a [2+2] cycloaddition product in high yield. 相似文献
117.
Xin‐Bao Han Zhi‐Ming Zhang Zhi‐Shu Wang Huan Zhang Hui Duan En‐Bo Wang 《ChemInform》2012,43(22):no-no
K2NaH2 [BW12O40]·12H2O, prepared by the conventional aqueous method, is characterized by single crystal XRD and IR spectroscopy. 相似文献
118.
《Journal of Coordination Chemistry》2012,65(3-4):349-357
Abstract Reactions of HBr with trans-[W(N2)2(dppe)PPh2Me)2] (1) (dppe = Ph2CH2CH2PPh2) result in protonation of coordinated N2 but no formation of ammonia or hydrazine. The tungsten-containing product depends upon the reaction conditions: (i) in MeOH, the product formed is [WBr(NNH2) (dppe)(PPh2Me)2]HBr2 (2) which converts to the hydride, [WBr2(H)(NNH2(dppe)(PPh2Me)](Br(3), with loss of phosphine in THF or CH2Cl2, (ii) in THF or CH2Cl2, the hydride (3) is formed directly. Reaction of 2 with Na2CO3 in MeOH results in the loss of HBr and the formation of the diazenido complex [WBr(NNH)(dppe)(PPh2Me)2] which reacts further with Na2CO3 in benzene under N2 to lose HBr and form a mixture of 1 and trans-[W(N2)(dppe)2]. The reaction of 1 with aqueous HF forms [WF(NNH2)(dppe)(PPh2Me)2]BF4. The X-ray photoelectron spectra of trans-[M(N2)2 (dppe)2], [MBr(NNH2)(dppe)2Br (M = Mo, W), [WCl(NNH2)(dppe)2]Cl, [WCl(N)(dppe)2]Cl and [WCl(NH) (dppe)2] are reported. In all of these complexes, nitrogen is in a highly reduced form. 相似文献
119.
以HZSM-5(SiO2/Al2O3=38)为载体,偏钨酸铵为钨源制备了双功能催化剂WC/HZSM-5,考察了其催化正己烷芳构化反应性能,并采用X射线衍射、扫描电子显微镜、X射线能量散射谱和程序升温氨脱附等手段对催化剂进行了表征,探讨了制备方法和WC含量对WC/HZSM-5催化剂性能的影响.结果表明,采用原位还原碳化法制备的WC/HZSM-5(RC)催化剂上正己烷芳构化反应性能优于浸渍法制备的WC/HZSM-5(IP).5%WC/HZSM-5(RC)样品在反应初始阶段芳烃选择性为10.28%,而HZSM-5上的仅为2.56%.WC/HZSM-5(RC)催化剂上反应产物中轻质芳烃(苯、甲苯和二甲苯)含量增加,重质芳烃C9+含量降低,其催化性能优于Pt/HZSM-5催化剂.产物分布的变化可能是由于WC与分子筛间的协同作用所致. 相似文献
120.
首次研究了碳化钨负载S2 O2 -8 ZrO2 (PSZ)固体超强酸催化剂 (WC PSZ)上正戊烷的反应情况及影响催化剂活性的各种因素 ,并用GC MS ,XRD ,BET等手段分析了正戊烷反应产物和催化剂的物理化学性质等 .结果表明 :WC PSZ对正戊烷具有异构化和裂解的双重催化作用 .PSZ在负载适量碳化钨后对正戊烷反应的活性和选择性显著提高 ,显示出优于Pt PSZ催化剂的效果 ,碳化钨的负载量为 2 0 %的效果最佳 .适当的焙烧、活化和反应温度等条件是取得良好反应效果的关键 相似文献