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81.
多氯代二苯并呋喃在不同色谱柱上的气相色谱保留行为——定量结构-色谱保留关系(QSRR)的研究 总被引:23,自引:3,他引:23
以一种拟原子的方式处理多氯代二苯并呋喃 (PCDFs)异构体中的苯环 ,将PCDFs异构体中的原子或基团分为 3类 ,即 :氯原子 (Cl) (记为“1”) ,氧原子 (O) (记为“2”)及拟原子 (B) (记为“3”)。在烷烃分子距边矢量的基础上 ,提出一种以基团为基准的分子距离边数矢量 (μ矢量 ) ,借助多元线性回归方法分别建立了多氯代二苯并呋喃在不同色谱柱上的色谱保留指数与表征其结构的 μ矢量间的定量结构 色谱保留关系 (QSRR)相关模型。各样本总体所建模型的相关系数均在 0 98以上。 相似文献
82.
83.
亲核性1,2-重排反应是有机化学的重要反应之一,重排中离去基团的离去和迁移基团的迁移步骤既可以是分步的,也可以是协同的,但是迁移基团的构型始终保持不变。本文用超共轭效应和反应过程中有机立体电子效应解释了此现象,掌握一般规律,希望能够从教学上便于教师讲授和学生学习理解。 相似文献
84.
A. Moutsatsou V. Protonotarios 《中国颗粒学报》2006,4(2):65-69
This paper investigates a treated fly ash to act as a synthetic zeolite to remediate soils polluted with heavy metals and metalloids (As, Pb, Cu, Zn, Fe, Cd and Mn). Four types of such 'zeolites' were synthesized by hydrothermal treatment of a calcareous fly ash derived from Greek lignite-fired power plants: two with excess of sodium hydroxide in a solid/liquid ratio of 50 g·L^-1, and two with excess of fly ash in a solid/liquid ratio of 100g·L^-1. Soil samples were obtained from a former mining site at Lavrion, Greece. Mobilization and transfer of metals to the retention agents was effected by using HCI aq 1M, with satisfactory results with respect to As, Pb, Cu, Mn and Cd. The great variety of metal complexes in soil was found to be of major importance for the effectiveness of the overall process. The final products were solidified either on their own, or by using additives such as lime and cement. 相似文献
85.
建立了高温液相色谱系统,在高温条件下,采用甲醇-水作为流动相,在Polymerx RP-1聚合物(PSDVB)色谱柱上考察了6种酚类样品的色谱行为.实验条件:温度40~160 ℃,流速0.2~5.5 mL/min,流动相中甲醇浓度范围40%~80%.考察了温度、流速和流动相组成对酚类样品的保留、分辨、柱效和系统压力的影响,探讨了酚类样品在聚合物柱上的热力学行为.温度升高2.35℃大约相当于流动相中甲醇浓度增加1%,可以通过改变色谱柱温度调节样品保留和改变选择性.柱温升高,降低了流动相的粘度,允许在高温条件下使用较高的流速实现快速分离.在160℃、V(甲醇):V(水)=40:60,为流动相和3 mL/min流速条件下,可于2.5 min内实现6种酚类的完全分离. 相似文献
86.
Infrared spectroscopic characteristics and gas chromatographic retention indices of tri- and tetramethylcyclohexenyl butenyl ketones were determined at different temperatures of analysis. Thermodynamic characteristics of sorption on the apolar stationary phase were calculated. The sorption characteristics of tri- and tetramethylcyclohexenyl butenyl ketones show that under conditions of capillary gas chromatography these compounds are retained due to the dispersive energy. It was shown by FTIR spectroscopy that the formation of conjugation systems of double bonds is responsible for the higher retention of the -isomers compared with that of the -isomers. The shortening of the distance between the carbonyl and trimethylcyclohexenyl groups was found to be accompanied by a decrease in the retention of the isomeric compounds. 相似文献
87.
88.
The usual concepts of the dynamics of an overloaded solute band fail to explain several phenomena such as the typical “leading-tail” shape and retention deviations exhibited by overloaded peaks, and why these defects are more commonly observed in short columns. These and other related deviations from theory can be rationalized by a non-classical approach to the overloading phenomenon. 相似文献
89.
Beşli S Coles SJ Davies DB Hursthouse MB Ibişoglu H Kiliç A Shaw RA 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(19):4915-4920
X-ray crystallographic evidence shows that nucleophilic substitution reactions of two different types of cyclophosphazene derivatives with relatively rigid nine-membered ansa rings leads to the first demonstration of retention of configuration in these molecular systems. 相似文献
90.
The Kováts retention indices of all 93 acyclic octenes on polydimethylsiloxane and squalane as stationary phases as well as their mass spectra were measured. The means of gas chromatography-mass spectrometry (GC-MS) were used for confirmation of GC identification as well as for mass spectrometric deconvolution of the majority of gas chromatographic unseparated isomeric octene peaks. The distinction between corresponding E and Z acyclic octenes, that is either difficult or even impossible by means of GC-MS, was obtained on the basis of larger temperature coefficients of retention indices for Z isomeric octenes than for corresponding E isomers. The retention data expressed as homomorphy factors were correlated with the degree of branching, position of double bond, and position of alkyl group with respect to the double bond of acyclic octenes, and the structure-retention relationships were formulated. The 81 acyclic octenes were identified in FCC gasoline. 相似文献