10h -吡嗪[2,3-b][1,4]苯并特拉嗪一种新型含碲杂环体系

IF 1.1 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Diamond S. Smith, D. Alexis, F. Fronczek, T. Junk
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引用次数: 0

摘要

2,3-二氯吡嗪与2-氨基苯碲醇和2-氨基-5-甲基苯碲醇的缩合反应,通过还原相应的二碲化物原位生成,形成了新的10H-吡嗪并[2,3-b][1,4]苯并碲嗪及其7-甲基衍生物。产物通过其结晶良好的5,5-二溴衍生物进行纯化。标题化合物的X射线晶体学分析表明,它具有明显的V形并形成氢键二聚体。含Te,N的杂环具有提供进入超分子组装体的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
10H-Pyrazino[2,3-b][1,4]benzotellurazine, a Novel Tellurium-Containing Heterocyclic System
Condensation of 2,3-dichloropyrazine with 2-aminobenzenetellurole and 2-amino-5-methylbenzenetellurole, generated in situ by reduction of the corresponding ditellurides, resulted in the formation of novel 10H-pyrazino[2,3-b][1,4]benzotellurazine and its 7-methyl derivative. The products were purified via their well-crystallized 5,5-dibromo derivatives. X-ray crystallographic analysis of the title compound indicates that it has a pronounced V-shape and forms hydrogen-bonded dimers. Te, N-containing heterocycles have the potential of offering access to supramolecular assemblies.
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来源期刊
Heteroatom Chemistry
Heteroatom Chemistry 化学-化学综合
CiteScore
1.20
自引率
0.00%
发文量
5
审稿时长
6 months
期刊介绍: Heteroatom Chemistry brings together a broad, interdisciplinary group of chemists who work with compounds containing main-group elements of groups 13 through 17 of the Periodic Table, and certain other related elements. The fundamental reactivity under investigation should, in all cases, be concentrated about the heteroatoms. It does not matter whether the compounds being studied are acyclic or cyclic; saturated or unsaturated; monomeric, polymeric or solid state in nature; inorganic, organic, or naturally occurring, so long as the heteroatom is playing an essential role. Computational, experimental, and combined studies are equally welcome. Subject areas include (but are by no means limited to): -Reactivity about heteroatoms for accessing new products or synthetic pathways -Unusual valency main-group element compounds and their properties -Highly strained (e.g. bridged) main-group element compounds and their properties -Photochemical or thermal cleavage of heteroatom bonds and the resulting reactivity -Uncommon and structurally interesting heteroatom-containing species (including those containing multiple bonds and catenation) -Stereochemistry of compounds due to the presence of heteroatoms -Neighboring group effects of heteroatoms on the properties of compounds -Main-group element compounds as analogues of transition metal compounds -Variations and new results from established and named reactions (including Wittig, Kabachnik–Fields, Pudovik, Arbuzov, Hirao, and Mitsunobu) -Catalysis and green syntheses enabled by heteroatoms and their chemistry -Applications of compounds where the heteroatom plays a critical role. In addition to original research articles on heteroatom chemistry, the journal welcomes focused review articles that examine the state of the art, identify emerging trends, and suggest future directions for developing fields.
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