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N-Heterocycle-coordinated λ5-iodanes as IBX alternatives for alcohol oxidations
Chemical Communications ( IF 4.3 ) Pub Date : 2024-12-09 , DOI: 10.1039/d4cc05058d
Nikita S. Antonkin, Yulia A. Vlasenko, Pim Puylaert, Boris J. Nachtsheim, Pavel S. Postnikov

We report the synthesis of novel N-coordinated λ5-iodanes as a unique class of hypervalent iodine compounds. X-ray diffraction analysis revealed their intriguing (pseudo)cyclic structure, showcasing distinctive N⋯I-secondary bonding interactions. We demonstrate the in situ generation of reactive diacetoxy derivatives, which exhibits remarkable efficacy in alcohol oxidation reactions. Thermal stability assessments using TGA/DSC analysis provide crucial insights into the handling and potential applications of these compounds. This work expands the frontier of hypervalent iodine chemistry, offering new tools for selective oxidation reactions.

中文翻译:


N-杂环配位的 λ5-碘作为醇氧化的 IBX 替代品



我们报道了新型 N 配位 λ5-碘的合成,作为一类独特的高价碘化合物。X 射线衍射分析揭示了它们有趣的(伪)循环结构,展示了独特的 N⋯I 次级键相互作用。我们展示了反应性二乙酰氧基衍生物的原位生成,它在醇氧化反应中表现出显着的功效。使用 TGA/DSC 分析进行热稳定性评估,为了解这些化合物的处理和潜在应用提供了重要见解。这项工作扩展了高价碘化学的前沿,为选择性氧化反应提供了新的工具。
更新日期:2024-12-13
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