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(XantPhos)AgBr as a cheap and readily available catalyst for the bromofluorocyclopropanation of electron-rich alkenes (XantPhos)AgBr 作为富电子烯溴氟环丙烷化反应的廉价易得催化剂
IF 1.8 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-09-01 DOI: 10.1016/j.mencom.2024.09.023
Maxim A. Novikov, Angelina Yu. Bobrova, Anton A. Servetnik, Elena I. Chernoburova, Igor V. Zavarzin, Yury V. Tomilov
A silver phosphine complex (XantPhos)AgBr proved to be a cheap and readily accessible catalyst for bromofluoro- cyclopropanation of electron-rich alkenes with CFBr2CO2Na. Ozonolysis followed by treatment with NaHSO3 was shown to be an effective protocol to purify gem-bromofluoro- cyclopropanes from unreacted alkene precursors.
事实证明,膦银络合物 (XantPhos)AgBr 是一种廉价且易于获得的催化剂,可用于富电子烯与 CFBr2CO2Na 的溴氟环丙烷化反应。研究表明,先用臭氧分解,再用 NaHSO3 处理,是从未反应的烯烃前体中提纯溴氟环丙烷的有效方法。
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引用次数: 0
Anisotropy of elastic properties of disordered cubic titanium monoxide TiOy 无序立方氧化钛 TiOy 弹性特性的各向异性
IF 1.8 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-09-01 DOI: 10.1016/j.mencom.2024.09.007
Aleksandr I. Gusev, Albina A. Valeeva
For the first time, the elastic constants c11, c12, and c44 of disordered cubic titanium monoxide TiOy were determined depending on the oxygen content y in the homogeneity region from TiO0.80 to TiO1.25. It has been established that the values of the elastic moduli depend on the oxygen content y and the crystallographic direction [hkl ]. Large changes in the elastic characteristics of TiOy depending on the [hkl ] direction indicate a strong anisotropy of the elasticity of disordered cubic titanium monoxide.
首次测定了无序立方氧化钛 TiOy 的弹性常数 c11、c12 和 c44,它们取决于从 TiO0.80 到 TiO1.25 的均匀性区域内的氧含量 y。已确定弹性模量值取决于氧含量 y 和晶体学方向 [hkl]。TiOy 的弹性特性随 [hkl ] 方向的巨大变化表明,无序立方氧化钛的弹性具有很强的各向异性。
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引用次数: 0
Kinetics of N2O decomposition over bulk and supported LaCoO3 perovskites 块状和支撑型 LaCoO3 包晶上的 N2O 分解动力学
IF 1.8 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-09-01 DOI: 10.1016/j.mencom.2024.09.009
Petr V. Zemlianskii , Alexander L. Kustov , Gennady I. Kapustin , Nikolay A. Davshan , Konstantin B. Kalmykov , Vladimir V. Chernyshev , Leonid M. Kustov
For the first time, kinetic data on the decomposition of N2O over mixed oxide LaCoO3 with a perovskite structure have been obtained. Bulk LaCoO3 synthesized using microwave activation exhibited an increased intrinsic reaction rate with a 30 kJ mol–1 lower activation energy. Perovskite samples supported on ZrO2-La demonstrated lower intrinsic reaction rates due to the lower content of the LaCoO3 phase, but the activation energies were also lower by 50–80 kJ mol–1.
该研究首次获得了在具有包晶结构的混合氧化物 LaCoO3 上分解 N2O 的动力学数据。使用微波活化法合成的块状 LaCoO3 表现出更高的本征反应速率,活化能降低了 30 kJ mol-1。由于 LaCoO3 相的含量较低,支撑在 ZrO2-La 上的包晶样品的固有反应速率较低,但活化能也降低了 50-80 kJ mol-1。
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引用次数: 0
Formation of active centers of polymer catalysts for radical-coordination polymerization 用于自由基配位聚合的聚合物催化剂活性中心的形成
IF 1.8 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-09-01 DOI: 10.1016/j.mencom.2024.09.031
Olga Yu. Vdovina, Ruslan R. Galimullin, Marat F. Abdullin, Alexander V. Smirnov, Sergey V. Kolesov
Chromatography–mass spectrometry of samples representing the interaction products of ferrocene, radical initiator and monomer taken in the molar ratio of 1:2:10 in toluene solution was used for experimental detection of products indicating the structure and mechanism of formation of metal complex active centers of radical-coordination polymerization. Structures similar to those proposed by the quantum-chemical modeling were demonstrated to be formed with the participation of secondary radicals.
二茂铁、自由基引发剂和单体在甲苯溶液中以 1:2:10 的摩尔比相互作用的产物样品的色谱-质谱法,用于实验检测表明自由基配位聚合的金属络合物活性中心的结构和形成机制的产物。结果表明,在次级自由基的参与下,形成了与量子化学模型所提出的结构相似的结构。
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引用次数: 0
Star-shaped thermosensitive poly-N-acyl-1,3-propylenimines with trianglamine core 以三聚氰胺为核心的星形热敏性聚 N-酰基-1,3-丙烯亚胺
IF 1.8 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-09-01 DOI: 10.1016/j.mencom.2024.09.038
Mikhail P. Kurlykin, Nina D. Kozina, Tatyana Yu. Kirila, Alexander P. Filippov, Andrey V. Tenkovtsev
Thermosensitivestar-shapedpoly-N-acyl-1,3-propylenimines with a macrocyclic trianglamine core were synthesized using a ‘grafting-on’ approach involving polymerization of 2-alkyl-5,6-dihydro-4H-oxazines at free trianglamine. The resulting polymers form complexes with europium ions and curcumin and can be used in the creation of delivery systems for drugs as well as contrast agents for NMR tomography.
本研究采用 "接枝 "方法合成了具有大环三角胺核心的热敏性星形聚 N-酰基-1,3-丙烯亚胺,该方法涉及在游离三角胺上聚合 2-烷基-5,6-二氢-4H-噁嗪。由此产生的聚合物与铕离子和姜黄素形成复合物,可用于制造药物输送系统以及核磁共振断层扫描的造影剂。
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引用次数: 0
New 4-azatetracyclo[5.3.2.02,6.08,10]dodec-11-ene-3,5-diones via the cycloaddition of N-phenylmaleimide and cyclohepta-1,3,5-trienes 通过 N-苯基马来酰亚胺和环庚烷-1,3,5-三烯的环化反应制备新的 4-氮杂四环[5.3.2.02,6.08,10]十二-11-烯-3,5-二酮
IF 1.8 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-09-01 DOI: 10.1016/j.mencom.2024.09.024
Gulnara N. Kadikova, Ekaterina S. Meshcheryakova, Leonard M. Khalilov
The cycloaddition reactions of N-phenylmaleimide with 7-substituted cyclohepta-1,3,5-trienes afforded new 4-aza- tetracyclo[5.3.2.02,6.08,10]dodec-11-ene-3,5-diones in high yields (87–97%). The true substrates which underwent the [4 + 2] cycloaddition were the 7-R-bicyclo[4.1.0]hepta-2,4-diene tautomers. The structures of the synthesized compounds were proved by NMR spectroscopy and X-ray diffraction analysis.
通过 N-苯基马来酰亚胺与 7-取代的环庚烷-1,3,5-三烯的环加成反应,可以得到新的 4-氮杂四环[5.3.2.02,6.08,10]十二-11-烯-3,5-二酮,收率高达 87-97%。发生[4 + 2]环加成反应的真正底物是 7-R-双环[4.1.0]庚-2,4-二烯同系物。核磁共振光谱和 X 射线衍射分析证明了合成化合物的结构。
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引用次数: 0
An alternative synthesis of 7-amino-6-nitro-substituted azolo[1,5-a]pyrimidines 7-氨基-6-硝基取代偶氮并[1,5-a]嘧啶的另一种合成方法
IF 1.8 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-09-01 DOI: 10.1016/j.mencom.2024.09.026
Ilya I. Butorin , Olga A. Konovalova , Pavel A. Slepukhin , Svetlana K. Kotovskaya , Vladimir L. Rusinov
New 7-amino-6-nitro-substituted [1,2,4]triazolo- and pyrazolo[1,5-a]pyrimidines were synthesized by an alternative strategy based on amino azoles and 2-nitro-3-(p-tolylamino)acrylonitrile. Unexpectedly, 3,5-dinitro-N-(p-tolyl)pyridine-2,6-diamine was formed when the starting 5-amino-1,2,4-triazoles contained NO2 or CF3 substituents.
通过基于氨基唑和 2-硝基-3-(对甲苯氨基)丙烯腈的替代策略,合成了新的 7-氨基-6-硝基取代的 [1,2,4]唑并吡唑并[1,5-a]嘧啶。当起始的 5-氨基-1,2,4-三唑含有 NO2 或 CF3 取代基时,会意外地生成 3,5-二硝基-N-(对甲苯基)吡啶-2,6-二胺。
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引用次数: 0
Octafluorobiphenyl-4,4’-diyl 9-oxothioxanthene-1,4-diyl polyether – a promising material for organic film based memristors: synthesis, memristive effect and charge transport mechanism 八氟联苯-4,4'-二基 9-氧代硫杂蒽-1,4-二基聚醚--一种用于基于有机薄膜的忆阻器的有前途的材料:合成、忆阻效应和电荷传输机制
IF 1.8 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-09-01 DOI: 10.1016/j.mencom.2024.09.013
Inna K. Shundrina , Irina A. Os’kina , Danila S. Odintsov , Andrei A. Gismatulin , Ivan A. Azarov , Leonid A. Shundrin , Vladimir A. Gritsenko
Polycondensation of perfluorobiphenyl with 1,4-dihydroxy- thioxanthen-9-one resulted in the title highly thermally stable polyether containing the thioxanthenone-type electron acceptor in-chain blocks in its structure. Model resistive memory devices based on it as the active medium exhibited a bipolar switching memristive effect with a 4-order difference in resistance between the low and high resistance states. The charge transport in this polyether is quantitatively described by the Nasyrov–Gritsenko model of phonon-assisted electron tunneling between traps.
全氟联苯与 1,4-二羟基-硫杂蒽-9-酮的缩聚反应产生了标题所示的高热稳定性聚醚,其结构中含有硫杂蒽酮型电子受体链块。以这种聚醚为活性介质的模型电阻式存储器件显示出一种双极切换的忆阻效应,在低电阻状态和高电阻状态之间存在 4 阶电阻差。Nasyrov-Gritsenko 声子辅助电子阱间隧道模型定量描述了这种聚醚中的电荷传输。
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引用次数: 0
Visible light-driven decarboxylative alkylation of azomethine imines with carboxylic acids 可见光驱动的偶氮亚胺与羧酸的脱羧烷基化反应
IF 1.8 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-09-01 DOI: 10.1016/j.mencom.2024.09.015
Zakhar M. Rubanov, Mikhail D. Kosobokov, Vitalij V. Levin, Alexander D. Dilman
The alkylation of cyclic five-membered azomethine imines with carboxylic acids proceeds under irradiation with 400 nm light using a dual catalytic system consisting of 9-arylacridine and tetrabutylammonium decatungstate. Azomethine imines containing aromatic, heterocyclic and aliphatic groups are suitable for the process providing pyrazolidin-3-ones in 42–98% yields.
使用由 9-芳基吖啶和四丁基仲钨酸铵组成的双重催化体系,在 400 纳米光照射下,环状五元氮甲基亚胺与羧酸发生烷基化反应。含有芳香族、杂环族和脂肪族基团的偶氮亚胺适用于该工艺,可提供 42-98% 产率的吡唑烷-3-酮。
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引用次数: 0
Lead sulfide quantum dots in an organic solar cell active layer 有机太阳能电池活性层中的硫化铅量子点
IF 1.8 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2024-09-01 DOI: 10.1016/j.mencom.2024.09.012
Jorge Cruz-Gómez , Francisco Javier de Moure-Flores , Sandra Andrea Mayén-Hernández , José Guadalupe Quiñones-Galván , Aruna Devi Rasu Chettiar , Claudia Elena Pérez-García , José Santos-Cruz
Organic solar cells have been fabricated using various concentrations of lead sulfide quantum dots. Data from Mott–Schottky analysis revealed intriguing changes in the bulk heterojunction layer of the solar cells that were directly related to the addition of the quantum dots. Notably, the highest power conversion efficiency of 5.15% was achieved with the addition of 0.4 wt% lead sulfide quantum dots.
利用不同浓度的硫化铅量子点制造了有机太阳能电池。莫特-肖特基分析数据显示,太阳能电池的块状异质结层发生了有趣的变化,这些变化与量子点的添加直接相关。值得注意的是,添加 0.4 wt%硫化铅量子点时,功率转换效率最高,达到 5.15%。
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引用次数: 0
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Mendeleev Communications
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