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Uncritical application of portable X‐ray fluorescence (PXRF) to non‐destructive analysis of archaeological ceramics has been received with scepticism. In this article, we present a methodological evaluation of the parameters and constraints for PXRF analysis of archaeological ceramics. We use experimental matrices that simulate characteristics of archaeological artefacts to demonstrate the impact of (1) surface morphology, (2) organic surface coatings and (3) grain size and mineralogy on non‐destructive PXRF analysis. We then apply these parameters to PXRF analysis of heterogeneous handmade ceramics from central Turkey. We conclude that with appropriate methodology, non‐destructive PXRF analysis can be demonstrated to provide a high level of accurate and precise geochemical discrimination for archaeological ceramics. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
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Prof. Kun Liu Ariella Lukach Kouta Sugikawa Siyon Chung Dr. Jemma Vickery Dr. Heloise Therien‐Aubin Prof. Bai Yang Prof. Michael Rubinstein Prof. Eugenia Kumacheva 《Angewandte Chemie (International ed. in English)》2014,53(10):2648-2653
The resemblance between colloidal and molecular polymerization reactions is very useful in fundamental studies of polymerization reactions, as well as in the development of new nanoscale systems with desired properties. Future applications of colloidal polymers will require nanoparticle ensembles with a high degree of complexity that can be realized by hetero‐assembly of NPs with different dimensions, shapes, and compositions. A method has been developed to apply strategies from molecular copolymerization to the co‐assembly of gold nanorods with different dimensions into random and block copolymer structures (plasmonic copolymers). The approach was extended to the co‐assembly of random copolymers of gold and palladium nanorods. A kinetic model validated and further expanded the kinetic theories developed for molecular copolymerization reactions. 相似文献
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Covering up to the end of 2011Many pharmaceuticals on the market today belong to a large class of natural products called nonribosomal peptides (NRPs). Originating from bacteria and fungi, these peptide-based natural products consist not only of the 20 canonical l-amino acids, but also non-proteinogenic amino acids, heterocyclic rings, sugars, and fatty acids, generating tremendous chemical diversity. As a result, these secondary metabolites exhibit a broad array of bioactivity, ranging from antimicrobial to anticancer. The biosynthesis of these complex compounds is carried out by large multimodular megaenzymes called nonribosomal peptide synthetases (NRPSs). Each module is responsible for incorporation of a monomeric unit into the natural product peptide and is composed of individual domains that perform different catalytic reactions. Biochemical and bioinformatic investigations of these enzymes have uncovered the key principles of NRP synthesis, expanding the pharmaceutical potential of their enzymatic processes. Progress has been made in the manipulation of this biosynthetic machinery to develop new chemoenzymatic approaches for synthesizing novel pharmaceutical agents with increased potency. This review focuses on the recent discoveries and breakthroughs in the structural elucidation, molecular mechanism, and chemical biology underlying the discrete domains within NRPSs. 相似文献
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以香豆素为基用以识别氟离子的新型比色化学传感器 总被引:2,自引:1,他引:1
以香豆素作为发色团,胺基为氢键供体,以—C=N键桥连设计合成了可裸眼识别氟离子的化学传感器1,吸收光谱结果表明在乙腈中它可以高选择性识别氟离子,光谱红移70 nm,溶液颜色由橙色变为蓝紫色,而其它离子如Cl~-、Br~-、I~-、H_2PO_4~-、NO_3~-、HSO_4~-、AcO~-等均不影响其对氟离子的识别.通过核磁共振氢谱考察其识别机制,表明传感分子通过与F~-间的质子转移反应,使整个体系电子离域,分子内电荷转移更加显著,从而导致吸收光谱大幅红移. 相似文献
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G. W. Pucher H. B. Vickery und A. J. Wakeman 《Fresenius' Journal of Analytical Chemistry》1938,112(5-6):229-233
Ohne Zusammenfassung 相似文献
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G. W. Pucher H. B. Vickery und C. S. Leavenworth 《Fresenius' Journal of Analytical Chemistry》1936,107(3-4):157-159
Ohne Zusammenfassung 相似文献