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991.
Dezhu Wu Qingwang Chen Ginfu Li 《Journal of Radioanalytical and Nuclear Chemistry》2003,258(3):697-698
The synthesis of [1,2-3H2]-polystyrene consisted of a two step reaction. First catalytic tritium gas addition to phenylacetylene was used to prepare [1,2-3H2]-styrene and then it was polymerized to [1,2-3H2]-polystyrene in the present of an initiator. 相似文献
992.
A cytotoxic compound from the leaves of Juglans mandshurica 总被引:1,自引:0,他引:1
From Juglans mandshurica leaves, a new quinone compound was isolated through bioassay-guided fractionation. The structure elucidation of the compound was established based on spectroscopic studies, notably of the 2D NMR spectra. The compound exhibited moderate cytotoxic activities against Hela, MCF-7, BGC823 and 3T3-Llcell lines with IC50 ranges from 7.5 to 26.8 μmol/L. 相似文献
993.
Hyphenation of flow injection/sequential injection with chemical hydride/vapor generation atomic fluorescence spectrometry 总被引:1,自引:0,他引:1
The dominant role played by flow injection/sequential injection (FI/SI, including lab-on-valve, LOV) in automatic on-line sample pretreatments coupling to various detection techniques is amply demonstrated by the large number of publications it has given rise to. Among these, its hyphenation with hydride/vapor generation atomic fluorescence spectrometry (HG/VG-AFS) has become one of the most attractive sub-branches during the last years, attributed not only to the high sensitivity of this technique, but also to the superb separation capability of hydride/vapor forming elements from complex sample matrices. In addition, it also provides potentials for the speciation of the elements of interest.It is worth mentioning that quite a few novel developments of sample pretreatment have emerged recently, which attracted extensive attentions from the related fields of research. The aim of this mini-review is thus to illustrate the state-of-the-art progress of implementing flow injection/sequential injection and miniaturized lab-on-valve systems for on-line hydride/vapor generation separation and preconcentration of vapor forming elements followed with detection by atomic fluorescence spectrometry, within the period from 2004 up to now. Future perspectives in this field are also discussed. 相似文献
994.
制成了光学解偏振法测定高聚物结晶过程的仪器,测试了聚丙烯、尼龙6等几种试样。本方法的优点是:样品用量少,测试温度范围宽,可以测定较快的结晶过程。由于设计了透射光强度自动控制电路,实验结果可靠,重复性好,并能自动记录。 相似文献
995.
996.
Chen Zhixing 《Theoretical chemistry accounts》1983,62(4):293-299
Various semiempirical MO methods for predicting regioselectivity in Diels-Alder reactions are compared in order to examine their reliability. They are the frontier molecular orbital method using CNDO/2, HMO and MNDO molecular orbitals and the HMO approach on pericyclic reactions presented by Tang. 相似文献
997.
Yechen Hu Zhongcheng Wang Liang Liu Jianhua Zhu Dongxue Zhang Mengying Xu Yuanyuan Zhang Feifei Xu Yun Chen 《Chemical science》2021,12(23):7993
Precision medicine has been strongly promoted in recent years. It is used in clinical management for classifying diseases at the molecular level and for selecting the most appropriate drugs or treatments to maximize efficacy and minimize adverse effects. In precision medicine, an in-depth molecular understanding of diseases is of great importance. Therefore, in the last few years, much attention has been given to translating data generated at the molecular level into clinically relevant information. However, current developments in this field lack orderly implementation. For example, high-quality chemical research is not well integrated into clinical practice, especially in the early phase, leading to a lack of understanding in the clinic of the chemistry underlying diseases. In recent years, mass spectrometry (MS) has enabled significant innovations and advances in chemical research. As reported, this technique has shown promise in chemical mapping and profiling for answering “what”, “where”, “how many” and “whose” chemicals underlie the clinical phenotypes, which are assessed by biochemical profiling, MS imaging, molecular targeting and probing, biomarker grading disease classification, etc. These features can potentially enhance the precision of disease diagnosis, monitoring and treatment and thus further transform medicine. For instance, comprehensive MS-based biochemical profiling of ovarian tumors was performed, and the results revealed a number of molecular insights into the pathways and processes that drive ovarian cancer biology and the ways that these pathways are altered in correspondence with clinical phenotypes. Another study demonstrated that quantitative biomarker mapping can be predictive of responses to immunotherapy and of survival in the supposedly homogeneous group of breast cancer patients, allowing for stratification of patients. In this context, our article attempts to provide an overview of MS-based chemical mapping and profiling, and a perspective on their clinical utility to improve the molecular understanding of diseases for advancing precision medicine.An overview of MS-based chemical mapping and profiling, indicating its contributions to the molecular understanding of diseases in precision medicine by answering "what", "where", "how many" and "whose” chemicals underlying clinical phenotypes. 相似文献
998.
Hongyang Su Lanlan Chen Yizhen Chen Prof. Rui Si Yuting Wu Xiaonan Wu Dr. Zhigang Geng Prof. Wenhua Zhang Prof. Jie Zeng 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(46):20591-20596
Efforts have been devoted to achieving a highly efficient artificial synthesis of ammonia (NH3). Reported herein is a novel Fe-MoS2 catalyst with Fe atomically dispersed onto MoS2 nanosheets, imitating natural nitrogenase, to boost N2 electroreduction into NH3 at room temperature. The Fe-MoS2 nanosheets exhibited a faradic efficiency of 18.8 % with a yield rate of 8.63 μg mgcat.−1 h−1 for NH3 at −0.3 V versus the reversible hydrogen electrode. The mechanism study revealed that the electroreduction of N2 was promoted and the competing hydrogen evolution reaction was suppressed by decorating the edge sites of S in MoS2 with the atomically dispersed Fe, resulting in high catalytic performance for the electroreduction of N2 into NH3. This work provides new ideas for the design of catalysts for N2 electroreduction and strengthens the understanding about N2 activation over Mo-based catalysts. 相似文献
999.
The pretreatment technique of microwave-assisted extraction on-line headspace solid-phase microextraction (MAE-HS-SPME) was designed and studied for one-step in-situ sample preparation prior to the chromatographic analysis of a pesticide on vegetables. The pesticide on chopped vegetables was extracted into an aqueous solution with the aid of microwave irradiation and then directly onto the SPME fiber in headspace. After being collected on to the SPME fiber and desorbed in the GC injection port, the pesticide (dichlorvos) was analyzed with a GC-electron-capture detection system. The optimum conditions for obtaining extraction efficiency, such as the pH, the polarity modifier, and the salt added in sample solution, the microwave irradiation, as well as the desorption parameters were investigated. Experimental results indicated that the proposed MAE-HS-SPME technique attained the best extraction efficiency of 106% recovery under the optimized conditions, i.e. irradiation of extraction solution (10% aqueous ethylene glycol) at pH 5.0 with medium microwave power for 10 min. Desorption at 220 degrees C for 3 min offered the best detection result. The detection was linear at 5-75 microg/l with correlation coefficient of 0.9985. Detection limit was obtained at approximately 1.0 microg/l level based on S/N=3. The proposed method provided a very simple, fast, and solvent-less procedure to collect pesticides directly from vegetables for GC determination. Its application was illustrated by the analysis of trace dichlorvos in vegetables. 相似文献
1000.
Sh. Yu X. Li A. Ren D. Shao Ch. Chen X. Wang 《Journal of Radioanalytical and Nuclear Chemistry》2006,268(2):387-392
Summary The
removal of heavy metal ion Co(II) from aqueous solution was studied usingg-Al2O3
by batch technique. The experiments were performed at T=20±2 °C, in 0.01M
NaNO3 solutions and under aerobic conditions. The effect of pH,
ionic strength, fulvic acid (FA) and alumina amount on the sorption of Co(II)
on alumina were also investigated. The pH affected the sorption of Co(II)
significantly as compared with the effect of FA and ionic strength. The results
indicated that strong chemical bonds are formed between Co(II) and functional
groups of the bare or FA coated alumina, and a precipitation of Co(II) takes
place on the alumina surface, induced by a transition from the adsorption to
surface. The addition sequences of Co/FA on Co(II) sorption were also studied:
the sorption of Co(II) in the ternary system was found independent of addition
sequences.</p>
</p> 相似文献