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12.
通过对操作系统启动过程的深入研究,在WINDOWS98 DOS状态下,对当前大容量硬盘主引导扇区的引导过程进行了全面的剖析,导出扩展INT 13H读取大容量硬盘逻辑扇区的方法,这将对大容量硬盘的管理与维护十分有利。 相似文献
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14.
一种新型联萘基旋光共轭聚合物的圆二色谱和圆偏振荧光光谱 总被引:1,自引:0,他引:1
众所周知 ,聚合物的光电性质依赖于聚合物链的构象和 (或 )组成 ,通过在聚合物上引入手性单元 ,采用圆二色谱 ( CD)和圆偏振荧光光谱 ( CPL)等方法可表征聚合物结构 [1] .近年来 ,由于圆偏振光可用作光数据存储和液晶显示器背景光 [2 ] ,人们开始注重共轭聚合物圆偏振光材料的研究 .共轭聚合物的光致和电致圆偏振光的现象由一种带手性侧链的聚噻吩[3 ] 和一种带手性侧链的聚 (对苯撑乙烯 ) [4 ]产生 ,但它们的圆偏振荧光度 (用不对称因子 glum=2 ( IL-IR) / ( IL+IR)表示 ,IL 和 IR 分别指左圆偏振光强度和右圆偏振光强度 )相对较低 … 相似文献
15.
Liquid crystalline ionomers containing sulfonate groups on the terminal unit of the chain were synthesized by an interfacial condensation reaction of 4,4′-dihydroxy-α,α′-dimethyl benzalazine, the monofunctional dye fast yellow (FY), and a 50/50 mixture of sebacoyl and dodecanedioyl dichlorides. The weight-average molecular weights were estimated from inherent viscosity measurements to be between 6000–11,000 and the sodium sulfonate concentrations ranged from 0–18.4 meq/100 g polymer. Elemental analyses, however, indicated much higher molecular weights, which suggested that there was a distribution of chains with one, two, or no FY endgroups. The polymers were semicrystalline and melted at ca. 140°C to form nematic mesophases that were stable over a temperature range of ca. 80°C. They were thermally stable to about 350°C. The ionomeric nature of the polymers was confirmed by the presence of intermolecular associations in nonpolar solvents, as demonstrated by dilute solution viscosity measurements. 相似文献
16.
Roesky HW Murugavel R Walawalkar MG 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(2):324-331
Metal hydroxides represent a very interesting and highly useful class of compounds that have been known to chemists for a very long time. While alkali and alkaline earth metal hydroxides (s‐block) are commonplace chemicals in terms of their abundance and their use in a chemical laboratory as bases, the interest in Brønsted acidic molecular terminal hydroxides of p‐block elements, such as aluminum and silicon, has been of recent origin, with respect to the variety of applications these compounds can offer both in materials science and catalysis. Moreover, these systems are environmentally friendly, relative to the metal halides, owing to their ‐OH functionality (resembling that of water). Design and conceptualization of the corresponding terminal thiols, selenols, and tellurols (M? SH, M? SeH, and M? TeH) offer even more challenging problems to synthetic inorganic chemists. This concept summarizes some of the recent strategies developed to stabilize these otherwise very unstable species. The successful preparation of a number of silicon trihydroxides a few years back resulted in the generation of several model compounds for metal–silicates. The recent synthesis of unusual aluminum compounds such as RAl(OH)2, RAl(SH)2, and RAl(SeH)2 with terminal EH (E=O, Se, or Se) groups is likely to change the ways in which some of the well‐known catalytic conversions are being carried out. The need for very flexible and innovative synthetic strategies to achieve these unusual compounds is emphasized in this concept. 相似文献
17.
本文对汽机房屋盖结构的两种受力体系进行了技术经济比较,阐述了空间网架在我国的应用情况,介绍了平板型网架应用在火力发电厂汽机房屋盖中的可行性及经济性。根据工业厂房建筑中的传力路线,分析了用于汽机房屋盖结构的平板型网架考虑吊车水平刹车力作用时的内力分布特点及其应用,提出了汽机房屋盖结构使用平板型网架的观点 相似文献
18.
将整体双向钢筋混凝土无柱帽式无梁楼盖视为支承于等矩柱网上的正交各向异性板,依据kirchhoff薄板理论,利用变形的对称性,并借助Fourier求解方法,给出了均布荷载作用下楼盖板弯曲挠度的解析解。本文解析解收敛很快,使用较为方便,对该类问题的工程设计有一定的参考价值。 相似文献
19.
王福庆 《辽宁工程技术大学学报(自然科学版)》1998,17(3):325-328
对不同材料的屋盖承重结构在起拱的受力和方式方面进行了分析笔探讨并提出了建设性的意见。 相似文献
20.
The last two decades have seen a dramatic development in the study of metal-metal multiple bonds, particular successes being recorded in the field of organometallic chemistry. Syntheses designed to produce novel transition metal complexes with single, double, triple and quadruple metal-metal bonds occupy a most important place in such research, as also do reactivity studies. A striving to establish general principles has provided much of the motivation for such work, but one less obvious goal—the commercial application of the catalytic properties of metal-metal multiple bonding systems, in the medium and long term—should not be overlooked. All aspects of the investigations of metal-metal multiple bonds also apply to a particular class of compound that has, however, enjoyed little lime-light and thus deserves the present review: complexes with multiple bonds between transition metals and substituent-free (“bare”) main group elements. Although based mostly on accidental discoveries, the few noteworthy examples are now beginning to unfold general concepts of synthesis that are capable of being extended and thus are deserving of exploitation in preparative chemistry. The availability of further structural patterns exhibiting multiple bonds between transition metals and ligand-free main group elements might enable preparative organometallic chemistry to expand in a completely new direction (for instance by the stabilizing or activation of small molecules at the metal complex). This essay discusses the chemistry of complexes of bare carbon, nitrogen, and oxygen ligands (carbido-, nitrido-, and oxo-complexes) and their relationships to higher homologues from both a synthetic and a structural point of view. 相似文献