共查询到20条相似文献,搜索用时 171 毫秒
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对1992-2007年间氢化物发生-原子荧光光谱法在金属材料中痕量元素测定中的应用的新进展作了评述,对氢化物发生-原子荧光光谱法的发展前景作了展望.引述文献39篇. 相似文献
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有机染料共振光散射法测定蛋白质的研究进展 总被引:1,自引:0,他引:1
对用有机染料作试剂的共振光散射光谱法测定蛋白质研究的进展情况(主要包括1990年至2004年间)作了评述。对测定蛋白质的反应体系中有机染料作用的基本原理作了简要论述。文中涉及的有机染料主要有:三苯甲烷类、偶氮类、酞菁类及羟基蒽醌类等(引用文献58篇)。 相似文献
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5-Br-PADAP作为高灵敏显色剂已被广泛研究及应用,但对锆显色反应的研究似未见报导。本文对某些含氧有机溶剂与水的混溶介质中,锆(Ⅳ)与5-Br-PADAP显色反应作了较系统的研究,对该体系中的溶剂化效应作了初步探讨,为络合显色反应中有机溶剂化效应的研究和应用又提供了一例。 相似文献
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Mixed-valence (MV) compounds are excellent model systems for the investigation of basic electron-transfer (ET) or charge-transfer (CT) phenomena. These issues are important in complex biophysical processes such as photosynthesis as well as in artificial electronic devices that are based on organic conjugated materials. Organic MV compounds are effective hole-transporting materials in organic light emitting diodes (OLEDs), solar cells, and photochromic windows. However, the importance of organic mixed-valence chemistry should not be seen in terms of the direct applicability of these species but the wealth of knowledge about ET phenomena that has been gained through their study. The great variety of organic redox centers and spacer moieties that may be combined in MV systems as well as the ongoing refinement of ET theories and methods of investigation prompted enormous interest in organic MV compounds in the last decades and show the huge potential of this class of compounds. The goal of this Review is to give an overview of the last decade in organic mixed valence chemistry and to elucidate its impact on modern functional materials chemistry. 相似文献
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Dr. Milan Pramanik Michael G. Guerzoni Dr. Emma Richards Prof. Dr. Rebecca L. Melen 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2024,136(9):e202316461
The development of new methods for enantioselective reactions that generate stereogenic centres within molecules are a cornerstone of organic synthesis. Typically, metal catalysts bearing chiral ligands as well as chiral organocatalysts have been employed for the enantioselective synthesis of organic compounds. In this review, we highlight the recent advances in main group catalysis for enantioselective reactions using the p-block elements (boron, aluminium, phosphorus, bismuth) as a complementary and sustainable approach to generate chiral molecules. Several of these catalysts benefit in terms of high abundance, low toxicity, high selectivity, and excellent reactivity. This minireview summarises the utilisation of chiral p-block element catalysts for asymmetric reactions to generate value-added compounds. 相似文献
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Covalent Organic Frameworks and Cage Compounds: Design and Applications of Polymeric and Discrete Organic Scaffolds 下载免费PDF全文
Priv.‐Doz. Dr. Florian Beuerle Dr. Bappaditya Gole 《Angewandte Chemie (International ed. in English)》2018,57(18):4850-4878
Porous organic materials are an emerging class of functional nanostructures with unprecedented properties. Dynamic covalent assembly of small organic building blocks under thermodynamic control is utilized for the intriguingly simple formation of complex molecular architectures in one‐pot procedures. In this Review, we aim to analyze the basic design principles that govern the formation of either covalent organic frameworks as crystalline porous polymers or covalent organic cage compounds as shape‐persistent molecular objects. Common synthetic procedures and characterization techniques will be discussed as well as more advanced strategies such as postsynthetic modification or self‐sorting. When appropriate, comparisons are drawn between polymeric frameworks and discrete organic cages in terms of their underlying properties. Furthermore, we highlight the potential of these materials for applications ranging from gas storage to catalysis and organic electronics. 相似文献
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The UV and visible spectra of some arylazo barbituric acids and arylazo pyrimidine in pure and mixed organic solvents of varying polarities have been studied. The different absorption bands displayed in the electronic spectra of these compounds are assigned and the possibility of the existence of these compounds in tautomeric equilibrium as well as in intra‐ and intermolecular H‐bonding were examined. The solute‐solvents molecular complexes liable to exist in polar‐nonpolar mixed solvents are investigated. The structure of the azo compounds were confirmed by 1H NMR and IR spectroscopy. The ionization processes of the compounds were investigated and the possible ionization constants were determined and discussed in terms of molecular structure of the azo compounds. 相似文献
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Methods have been developed for the determination of organic compounds in solid wastes and sludges. The methods involve sequential extraction with acid, base, and organic solvent, as well as dynamic headspace stripping of the volatile components. Methods for assessing the mobility of organic compounds in the environment have been evaluated, including four batch extractions and an upward-flow column extraction. Batch extractions in closed vessels are most effective for the determination of volatile components. The upward-flow column arrangement is shown to be the most aggressive leaching procedure for semi-volatile organic compounds. 相似文献
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This paper deals with the specific identification of several thiazide, potassium-sparing and loop diuretics. The liquid chromatographic behaviour of these compounds is studied. Different organic modifiers (methanol, acetonitrile and tetrahydrofuran) are compared in terms of selectivity for the thiazide diuretics. An acetonitrile-water (40:60) eluent can be used to identify the thiazide diuretics. The loop and potassium-sparing diuretics are well chromatographed at an acidic pH in the presence of propylamine hydrochloride. This study enables us to select the right mobile phase composition for any given selectivity or resolution. The determination of the dead volume in different chromatographic systems is also discussed. A mixture of organic solvent and deuterium oxide in the same volume ratio as the eluent is used as dead volume marker. The signal is monitored with a UV detector at low wavelength. 相似文献
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比较了中国化学会《有机化合物命名原则2017》与1980版命名原则的不同,指出了新版的主要变化之处。通过举例,说明母体氢化物、特性基团的概念、含义及其在命名有机化合物时的重要意义。归纳出命名有机物时确定母体氢化物和主特性基团所依据原则和方法,梳理出命名有机化合物的一般步骤,并通过实例来说明2017版命名原则的实施方法。 相似文献
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纳米金属铁降解有机卤化物的研究进展 总被引:23,自引:0,他引:23
有机卤化物是一种毒性强、难生物降解的环境污染物,传统处理技术存在着降解不完全、效率低等不足。纳米技术的发展给有机卤化物的处理带来了一种新的颇具潜力的方法,即应用纳米金属/双金属颗粒对有机卤化物进行脱卤。目前,以Fe(Ⅱ) 和 Fe(Ⅲ)等常见原料合成纳米铁颗粒的技术已经成熟,纳米颗粒对有机卤化物也显示出高效的降解性能。更重要的是,其可灵活应用于地下水和土壤的原位和异位修复,尤其适用于原位修复。本文综述了纳米铁颗粒降解有机卤化物的研究进展,包括纳米铁颗粒的合成与修饰, 降解效能、降解机理、降解动力学、示范工程等,以及发展前景和今后的研究方向。 相似文献
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Differences in various properties of organic compounds of different classes of the same or similar composition but of different structure, as well as complexes of such compounds and transient complexes in their chemical reactions are associated with different mobility of terminal molecular fragments and can be explained in terms of the “hot termini” effect.__________Translated from Zhurnal Obshchei Khimii, Vol. 75, No. 1, 2005, pp. 82–88.Original Russian Text Copyright © 2005 by Golovanov, Zhenodarova. 相似文献