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Advances in the chemistry of heterocyclic azides 杂环叠氮化物的化学研究进展
IF 7.7 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.1070/rcr5042
V. Bakulev, Yu. M. Shafran, Nikolai A. Beliaev, T. Beryozkina, N. Volkova, M. N. Joy, Zhijin Fan
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引用次数: 2
Modeling biologically important NH⋯π interactions 模拟生物学上重要的NH⋯π相互作用
IF 7.7 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.1070/rcr5047
A. Pozharskii, O. V. Dyablo, V. Ozeryanskii, Olga G Pogosova
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引用次数: 0
Porous porphyrin-based metal-organic frameworks: synthesis, structure, sorption properties and application prospects 多孔卟啉基金属有机骨架:合成、结构、吸附性能及应用前景
IF 7.7 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.1070/RCR5038
Yulia G. Gorbunova, Y. Y. Enakieva, M. Volostnykh, A. Sinelshchikova, I. A. Abdulaeva, K. P. Birin, A. Tsivadze
The unique properties of porous metal-organic frameworks are responsible for the increasing research interest in the design and synthesis of this type of materials. A general strategy towards targeted design of metal-organic frameworks possessing desired properties is a choice of optimal linkers, which are usually represented by polytopic organic ligands. Porphyrins are promising building blocks for such frameworks due to their tunable physicochemical properties and wide possibilities of macrocycle modification. The achievements of the last decade in the development of synthetic approaches to porphyrin functionalization have promoted fast progress of tetrapyrrole chemistry as the basis of metal-organic frameworks. This review gives analysis of the current literature devoted to the synthesis of porphyrin-based metal-organic frameworks and the prospects for their application in modern materials science. The bibliography includes 262 references.
多孔金属-有机框架的独特性能使得人们对这类材料的设计和合成越来越感兴趣。有针对性地设计具有理想性能的金属有机框架的一般策略是选择最佳连接体,通常以多面体有机配体为代表。卟啉由于其可调的物理化学性质和广泛的大环修饰可能性而成为这种框架的有希望的构建块。近十年来卟啉功能化合成方法的发展,促进了作为金属有机骨架基础的四吡咯化学的快速发展。本文对卟啉类金属有机骨架的合成及其在现代材料科学中的应用前景进行了综述。参考书目包括262篇参考文献。
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引用次数: 9
Acetylene derivatives of quinones and their transformation products: synthesis, reactivity and applied aspects 醌类乙炔衍生物及其转化产物:合成、反应性及应用
IF 7.7 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.1070/RCR5020
S. Vasilevsky, A. A. Stepanov
The review summarizes the data on the methods of synthesis, reactivity and practical applications of acetylene derivatives of quinones and their transformation products published for the last 15 years. The specificity of alkynylquinones associated with the activation of the triple bond by the quinoid moiety is addressed. The triple bond activation is responsible for high reactivity of these compounds, which makes it possible to design and perform complex cascade transformations, providing a rational route to multipurpose products. The general patterns and specific features of the reactivity of this class of compounds are systematically reviewed. Particular attention is given to fundamentally important redox processes and new heterocyclization reactions. The mechanisms of these transformations are considered. The prospects of the practical application of alkynylquinones and their transformation products in optics, electronics, medicinal chemistry and other areas of human activity are discussed. The bibliography includes 141 references.
综述了近15年来醌类乙炔衍生物及其转化产物的合成方法、反应性和实际应用等方面的研究进展。炔基醌的特异性与激活的三键的奎尼类部分的讨论。三键活化是这些化合物具有高反应活性的原因,这使得设计和执行复杂的级联转化成为可能,为多用途产品提供了合理的途径。本文系统地评述了这类化合物反应性的一般规律和特殊特征。特别注意基本重要的氧化还原过程和新的杂环化反应。考虑了这些转换的机制。讨论了炔基醌及其转化产物在光学、电子、药物化学等人类活动领域的实际应用前景。参考书目包括141篇参考文献。
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引用次数: 0
Transition metal-free cross-coupling reactions to form carbon–heteroatom bonds 过渡无金属交叉偶联反应形成碳杂原子键
IF 7.7 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.1070/RCR5022
Dmitry I. Bugaenko, A. Karchava, M. Yurovskaya
The formation of carbon–heteroatm bond is the key step of synthesis of numerous organic compounds, including socially important products such as pharmaceuticals, crop protection agents and organic functional materials. These reactions proceed most efficiently when catalyzed by compounds of transition metals, first of all palladium. However, this approach has considerable drawbacks, in particular, high cost and toxicity of transition metal compounds and harsh reaction conditions required in some cases, resulting in limited functional group tolerance. This review describes the recent advances in the development of methodology of transition metal-free carbon–heteroatom bond-forming cross-coupling. It is shown that single-electron transfer and homolytic bond cleavage result in the generation of highly reactive radical and/or radical ion intermediates, enable the formation of new carbon–heteroatom bonds. These intermediates are generated using either visible light or electricity as energy sources or simple organic compounds acting as electron donors. Methods for carbon–heteroatom bond formation based on radical reactions proceeding under mild conditions and in the presence of labile functional groups are considered. The key mechanistic aspects of the reactions are highlighted. The review mainly covers the original publications of the current decade. The bibliography includes 302 references.
碳-杂碳键的形成是许多有机化合物合成的关键步骤,包括药物、作物保护剂和有机功能材料等社会重要产品。在过渡金属化合物(首先是钯)的催化下,这些反应进行得最有效。然而,这种方法有相当大的缺点,特别是过渡金属化合物的高成本和毒性,以及在某些情况下需要苛刻的反应条件,导致官能团耐受性有限。本文综述了过渡金属碳杂原子成键交叉偶联方法的最新进展。结果表明,单电子转移和均裂键导致高活性自由基和/或自由基离子中间体的生成,从而形成新的碳杂原子键。这些中间体是用可见光或电作为能源或简单的有机化合物作为电子供体产生的。考虑了在温和条件和不稳定官能团存在下,基于自由基反应的碳杂原子键形成方法。重点介绍了反应的关键机理。该审查主要包括本十年的原始出版物。参考书目包括302篇参考文献。
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引用次数: 0
High-entropy alloys: properties and prospects of application as protective coatings 高熵合金:作为防护涂层的性能及应用前景
IF 7.7 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.1070/RCR5023
B. Gelchinski, I. A. Balyakin, A. A. Yuryev, A. Rempel
Alloys with high configurational entropy fundamentally differ from traditional alloys as they contain not one, but five or more basic elements with concentrations of 5 to 35 at.% each. Owing to the unique elemental composition, high-entropy alloys can have unusual functional properties such as high strength and wear resistance, exceptional heat resistance, good structural stability and good resistance to corrosion and oxidation. The review considers methods of synthesis of high-entropy alloys, methods and results of computer simulation of the high-entropy alloy structures and applications of such alloys as corrosion-, heat- and radiation-resistant materials and biomedical materials. Particular attention is paid to the prospects for the use of such alloys as protective coatings. The bibliography includes 352 references.
具有高构形熵的合金与传统合金有着根本的区别,因为它们含有的不是一种,而是五种或更多的基本元素,浓度在5到35 at之间。%。由于独特的元素组成,高熵合金可以具有不同寻常的功能性能,如高强度和耐磨性,优异的耐热性,良好的结构稳定性和良好的抗腐蚀和抗氧化性。综述了高熵合金的合成方法、高熵合金结构的计算机模拟方法和结果,以及高熵合金在耐腐蚀、耐热、耐辐射材料和生物医用材料等方面的应用。特别注意了这类合金作为防护涂层的应用前景。参考书目包括352篇参考文献。
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引用次数: 6
Small synthetic molecules with antiglycation activity. Structure–activity relationship 具有抗糖化活性的小合成分子。结构与活性关系
IF 7.7 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.1070/RCR5041
K. Savateev, A. Spasov, V. Rusinov
The accumulation of advanced glycation end products (AGEs) is currently considered as one of the key factors in aging processes, the pathogenesis of late complications of diabetes mellitus, cancer and neurodegenerative diseases. This review is devoted to small synthetic molecules with antiglycation activity, i.e., compounds with the ability to inhibit AGE formation. Molecules with antiglycation activity in the low micromolar range (<10 μM), primarily fused heterocyclic systems containing oxygen or nitrogen as heteroatoms and (thio)ureas, have been discovered to date. The known scaffolds with antiglycation activity are analyzed, structural modifications to enhance antiglycation abilities are highlighted and the structure–activity relationships are discussed. The bibliography includes 125 references.
晚期糖基化终产物(AGEs)的积累目前被认为是衰老过程的关键因素之一,也是糖尿病、癌症和神经退行性疾病晚期并发症的发病机制之一。本综述致力于具有抗糖化活性的小合成分子,即具有抑制AGE形成能力的化合物。在低微摩尔范围(<10 μM)具有抗糖基化活性的分子,主要是含有氧或氮作为杂原子和(硫)脲的融合杂环体系,迄今已被发现。对已知的具有抗糖化活性的支架进行了分析,重点介绍了增强抗糖化能力的结构修饰,并讨论了结构-活性关系。参考书目包括125篇参考文献。
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引用次数: 2
Osmium-catalyzed reductive processes: hydrogen transfer, hydrogen borrowing, hydrogenation, hydroformylation, reductive amination and water gas shift reaction 锇催化的还原过程:氢转移、借氢、加氢、氢甲酰化、还原胺化和水煤气转移反应
IF 7.7 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.1070/rcr5045
Klim O. Biriukov, O. Afanasyev, M. Godovikova, D. Loginov, D. Chusov
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引用次数: 0
SUPERCAPACITORS: PROBLEMS AND DEVELOPMENT PROSPECTS 超级电容器:问题与发展前景
IF 7.7 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.1070/rcr5044
Y. Volfkovich
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引用次数: 2
Avermectin chemistry: recent advances 阿维菌素化学:最新进展
IF 7.7 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2022-01-01 DOI: 10.1070/rcr5051
L. Menchikov, M. Dzhafarov, I. Zavarzin
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引用次数: 0
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