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71.
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Managing environmental contamination with Benz[a]anthracene (B[a]A) is essential due to its carcinogenic, teratogenic and mutagenic effects on humans and the environment. At present, the mainly B[a]A degradation methods used are photodegradation, bioremediation and traditional advanced oxidation, although they all have disadvantages. In this study, B[a]A was degraded by hydrodynamic cavitation (HC), chlorine dioxide (ClO2), or an innovative combination of the two methods. According to high performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC–MS) analysed the degradation products and degradation pathway of B[a]A, with the kinetics of different degradation methods discussed. Under optimal conditions, HC combined with ClO2 oxidation can further degrade products to achieve ring cleavage. Compared with the two separate degradation process methods, the combined method exerts a synergistic effect on the degradation of B[a]A, with an enhancement factor of 1.48. Experimental results showed that the combination method can realize enhanced complete degradation of B[a]A, reduce ClO2 requirements, improve efficiency, reduce energy consumption and produce less harmful products with ring cleavage achieved. 相似文献
73.
R.A. Willoughby 《Linear algebra and its applications》1977,18(1):75-94
One aspect of the inverse M-matrix problem can be posed as follows. Given a positive n × n matrix A=(aij) which has been scaled to have unit diagonal elements and off-diagonal elements which satisfy 0 < y ? aij ? x < 1, what additional element conditions will guarantee that the inverse of A exists and is an M-matrix? That is, if A?1=B=(bij), then bii> 0 and bij ? 0 for i≠j. If n=2 or x=y no further conditions are needed, but if n ? 3 and y < x, then the following is a tight sufficient condition. Define an interpolation parameter s via x2=sy+(1?s)y2; then B is an M-matrix if s?1 ? n?2. Moreover, if all off-diagonal elements of A have the value y except for aij=ajj=x when i=n?1, n and 1 ? j ? n?2, then the condition on both necessary and sufficient for B to be an M-matrix. 相似文献
74.
加入1920ppm镧盐,即可在0.6mol/LH_2SO_4与H_3PO_4混合液中同时共存30ppm铜与铁及15ppm钴时,测定30ppm镍,相对误差<5%。 相似文献
75.
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77.
A novel procedure allows the synthesis of spiro[4.5]decane-1,6-dione 1, a key intermediate in the total synthesis of erythrodiene and spirojatamol. The key step is a combination of Claisen rearrangement of allyl vinyl ethers followed by an intramolecular hydroacylation catalysed by RhCl(cod)(dppe). 相似文献
78.
国外聚烯烃树脂工艺进展及新产品开发 总被引:2,自引:0,他引:2
从生产技术和新品种开发方面介绍了国外烯烃树脂最新进展情况,指出茂金属催化剂技术,Catalloy技术,Spherilene技术是人们开发研究的重点,特别是茂金属催化剂技术能按照用户的要求“定制”不同结构的聚合物,茂金属催化剂技术为开发更多的高性能聚烯树脂提供了可能。 相似文献
79.
Jiaxiang Wang Jiahui Gao Tianyun Guo Prof. Dr. Xing Huo Prof. Dr. Wenhua Zhang Prof. Dr. Jian Liu Prof. Dr. Xiaolei Wang 《Angewandte Chemie (International ed. in English)》2023,62(3):e202213810
Herein, bioinspired total syntheses of A201A, A201D, and A201E based on a previously reported biosynthetic pathway are presented. The challenging 1,2-cis-furanoside, a core structure of the A201 family, was obtained by remote 2-quinolinecarbonyl-assisted glycosylation. We accomplished the total synthesis of A201A and A201E based on the critical 1,2-cis-furanoside moiety through late-stage glycosylation without any interference from basic dimethyl adenosine. We also confirmed the absolute configuration of A201E by total synthesis. This modular synthesis strategy enables efficient preparation of A201 family antibiotics, allowing the study of their structure–activity relationships and mode of action. This study satisfies the increasing demand for developing novel antibiotics inspired by the A201 family. 相似文献
80.
Dr. Hannah A. Minas Romain M. M. François Dr. Franziska Hemmerling Dr. Amy E. Fraley Cora L. Dieterich Dr. Simon H. Rüdisser Dr. Roy A. Meoded Sabrina Collin Prof. Dr. Kira J. Weissman Dr. Arnaud Gruez Prof. Dr. Jörn Piel 《Angewandte Chemie (International ed. in English)》2023,62(34):e202304481
Modular trans-acyltransferase polyketide synthases (trans-AT PKSs) are enzymatic assembly lines that biosynthesize complex polyketide natural products. Relative to their better studied cis-AT counterparts, the trans-AT PKSs introduce remarkable chemical diversity into their polyketide products. A notable example is the lobatamide A PKS, which incorporates a methylated oxime. Here we demonstrate biochemically that this functionality is installed on-line by an unusual oxygenase-containing bimodule. Furthermore, analysis of the oxygenase crystal structure coupled with site-directed mutagenesis allows us to propose a model for catalysis, as well as identifying key protein-protein interactions that support this chemistry. Overall, our work adds oxime-forming machinery to the biomolecular toolbox available for trans-AT PKS engineering, opening the way to introducing such masked aldehyde functionalities into diverse polyketides. 相似文献