共查询到20条相似文献,搜索用时 114 毫秒
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2′-芳基-3-(1,4,5,6-四氢-6-哒嗪酮-3-羰基)氨基硫脲及其环化产物的合成 总被引:4,自引:1,他引:4
以α-酮戊二酸为起始原料,合成了1,4,5,6-四氢-6-哒嗪酮-3-甲酰肼(2),然后将2与异硫氰酸芳基酯反应得到相应的芳基氨基硫脲衍生物3a~3f.用硫酸、醋酸汞或氢氧化钠分别将芳基氨基硫脲环化得到一系列新的1,3,4-噻二唑、1,3,4-噁二唑和1,2,4-三唑的衍生物.化合物的结构经元素分析,IR,1H NMR和MS谱得以证实. 相似文献
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将邻羟苯基引入1,2,3-三唑结构中, 设计合成了10个1-(4-取代苯基)-4-苯基-5-取代-1,2,3-三唑类衍生物. 首先, 以对位取代的芳胺为原料, 经重氮化、叠氮化、闭环和缩合反应制得1-(4-取代苯基)-4-苯基-5-水杨醛亚胺-1,2,3-三唑类衍生物(3a~3e), 再用硼氢化钠还原制得1-(4-取代苯基)-4-苯基-5-(2-羟基苄基)氨基-1,2,3-三唑类衍生物(4a~4e). 目标化合物的结构经核磁、IR及元素分析确认. 抑菌活性测试表明, 当质量浓度为0.1 mg/L时, 除化合物3e和4e外, 所有化合物对白色念球菌的抑菌率均达95%以上, 对大肠杆菌的抑菌率达85%以上, 具有强抑菌活性, 表明该类化合物在抗菌药物开发方面有重要应用价值. 相似文献
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高能量密度材料3,3′-偶氮-1,2,4,5-四嗪衍生物的分子设计 总被引:1,自引:0,他引:1
运用密度泛函理论(DFT)方法,计算系列3,3′-偶氮-1,2,4,5-四嗪衍生物的生成热.结果显示:—N3取代基在增加3,3′-偶氮-1,2,4,5-四嗪衍生物的生成热方面起了非常重要的作用.通过分析标题化合物的最弱键离解能发现:—NH2或—N3取代基非常有利于增加衍生物的热稳定性.计算的爆速(D)和爆压(p)数值表明:—NO2或—NF2取代基有利于提高3,3′-偶氮-1,2,4,5-四嗪衍生物的爆轰性能.综合爆轰性能和热稳定性的计算结果,3种3,3′-偶氮-1,2,4,5-四嗪衍生物可以作为潜在的品优高能量密度材料(HEDM)候选物. 相似文献
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报道了一种全合成3-氧-11,12,13-三羟基桉烷-4-烯(1)的简便方法. 对于该化合物及其衍生物的药理活性研究目前正在进行中. 相似文献
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Zusammenfassung Mo3CoB3, Mo3NiB3, W3CoB3 und W3NiB3 kristallisieren in einem eigenen Typ (W3CoB3-Struktur). Das trigonal prismatische Bauelement [T
6B]* ist zu Ketten vereinigt, wobei B3-Gruppen entstehen. Die Phasen sind vermutlich Bor-reicher als obiger Formel entspricht.
Mit 2 Abbildungen 相似文献
The crystal structure of W3CoB3 and the isotypic phases Mo3CoB3, Mo3NiB3, and W3NiB3
Mo3CoB3, Mo3NiB3, W3CoB3, and W3NiB3 were found to possess a new type of crystal structure (W3CoB3-structure type). Trigonal prismatic groups [T 6B]* are linked together forming chains in such a way that B3-groups occur. These borides do probably exist with a larger amount of boron as to compared with the formula.
Mit 2 Abbildungen 相似文献
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γ-Nitro-γ-butyrolactone By oxidation of 3-(1-nitro-2-oxocyclohexyl)propanal ( 1 ) with KMnO4, besides 3-(1′-nitro-2′-oxocyclohexyl)pripionic acid ( 2 ), the complete hydrolysis product 4-oxononanedioic acid ( 4 ) and the oxidized semi-hydrolysis product 5-(2-nitro-5-oxotetrahydro-2-furyl)pentanoic acid ( 3 ) were formed. The crystalline 3 decomposes at r.t. forming 4 and nitrous gases; its structure was established by X-ray determination. 相似文献
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γγγ-Trifluorocarbonyl compounds are easily obtained in a good yield by introduction of the 1,1,1-trifluoroethyl moiety (CF3-CH2-) on the -methylene group of a ketone. 相似文献
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L. N. Sobenina A. I. Mikhaleva M. P. Sergeeva D. -S. D. Toryashchinova O. B. Kozyreva B. A. Trofimov 《Chemistry of Heterocyclic Compounds》1996,32(1):43-47
Condensation of pyrrole-2-dithiocarboxylates with CH acids containing ester groups, in the KOH-DMSO system, was used to prepare previously unknown 1-alkylthio-3H pyrrolizin-3-ones. The latter, treated with secondary amines, are readily converted to the corresponding 1-amino derivatives. 相似文献
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L. N. Sobenina A. I. Mikhaleva M. P. Sergeeva D. -S. D. Toryashinova O. B. Kozyrea B. A. Trofimov 《Chemistry of Heterocyclic Compounds》1996,32(7):783-788
Previously unknown 1-alkylthio-3H-pyrrolizin-3-ones have been obtained by the condensation of pyrrole-2-dithiocarboxylates with CH acids containing ester groupings in the KOH-DMSO system. On treating the products with secondary amines they are readily converted into the corresponding 1-amino derivatives.Irkutsk Branch of the Russian Academy of Sciences, Irkutsk 664033. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 919–924, July, 1996. Original article submitted May 2, 1996. 相似文献
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K3BiSe3, Rb3BiSe3, and Cs3BiSe3 – Derivatives of the Th3P4 Structure Type The compounds K3BiSe3, Rb3BiSe3, and Cs3BiSe3 were synthesized by heating mixtures of Bi2O3 and the respective alkalicarbonate in a stream of hydrogen saturated by selenium at 850°C. Thin crystals of the compounds appear red in transmitted light. They crystallize isostructural with Na3AsS3, space group P213, lattice constants a = 9.771(5) Å, a = 10.161(3) Å, and a = 10.587(5) Å for K3BiSe3, Rb3BiSe3, and Cs3BiSe3, respectively. The Na3AsS3 structure type is a derivative of the Th3P4 structure type. 相似文献
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Zusammenfassung Es wurden die Enthalpien der Reaktionen von AsCl3, AsBr3, AsJ3, SbCl3, SbBr3 und SbJ3 mit Tributylphosphat, N,N-Dimethylacetamid und Hexamethylphosphorsäuretriamid bestimmt. Das Verhalten der Addukte bei Gegenwart eines Überschusses der Donoren wird beschrieben.
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Acceptor properties of AsCl3, AsBr3, AsI3, SbCl3, SbBr3, and SbI3
The enthalpies of the reactions of AsCl3, AsBr3, AsI3, SbCl3, SbBr3 and SbI3 with tributylphosphate, N,N-dimethylacetamide and hexamethylphosphoric acid triamide were measured. The behavior of the adducts in the presence of excess donor molecules is described.
Mit 5 Abbildungen 相似文献
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Thin films of methylammonium lead halides, CH3NH3PbI3 and CH3NH3PbI3-xClx, were deposited onto symmetrical microstructured electrode arrays of gold or platinum on Si/SiO2 wafers. Polarization studies were carried out on perovskite films under vacuum in the dark. For poling, a constant voltage was applied to the samples while the temperature was cycled between 295 K and 4 K. The measured current densities depending on the temperature showed distinct characteristics relating strongly to the crystal phase and the dielectric properties of the perovskite films. Voltage sweeps were carried out at different scan rates at specific temperature intervals after poling. The polarization of the films due to the migration of iodide vacancies in direction of the blocking perovskite/metal interface was frozen almost up to room temperature. Charge carriers were only able to cross the blocking barrier and contribute to the current where the ions have accumulated during poling. All J-V curves showed hysteresis: inverted and regular hysteresis at room temperature and below, respectively. Inverted hysteresis originates from the slow accumulation of ions at the blocking barrier, while regular hysteresis arises from a distortion in the adjacent crystals which will be discussed. 相似文献