通过 N∩O 螯合肼的钯络合物的位点选择性 CCl 键活化从 3-氯香豆素和芳基硼酸制备 3-芳香豆素支架

IF 3.7 2区 化学 Q2 CHEMISTRY, APPLIED Applied Organometallic Chemistry Pub Date : 2024-08-20 DOI:10.1002/aoc.7709
C. Shalini, M. Akilesh, G. Sathiyaraj, N. S. P. Bhuvanesh, K. S. Neethu, M. V. Kaveri, N. Dharmaraj
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引用次数: 0

摘要

利用钯腙络合物作为 SMC 的均相催化剂,我们合成了 15 种变体 3-芳基香豆素。在此背景下,我们报告了一组通式为[Pd(L)(Cl)(PPh3)]的四配位钯(II)腙配合物 1 和 2,它们是通过前体配合物[PdCl2(PPh3)2]与腙配体 HL1 或 HL2 反应得到的。采用单晶 XRD 和传统光谱技术对这两种配合物进行了表征。从催化应用的角度来看,新的配合物 1 和 2 被测试用作均相催化剂,通过激活具有挑战性的 CCl 官能,将 3-氯香豆素转化为 3-芳基香豆素。络合物 2 的催化剂负载量极低(0.01 摩尔%),就能得到一系列 3-芳基香豆素,收率高达 92%,并可重复使用长达五个周期。本方法简单易行,可在室温下利用绿色溶剂(乙醇)和芳基硼酸谱在开放式烧瓶中进行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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3-Arylcoumarin Scaffolds From 3-Chlorocoumarin and Arylboronic Acids via Site-Selective CCl Bond Activation With Palladium Complexes of N∩O Chelating Hydrazones

Using palladium hydrazone complex as a homogeneous catalyst for SMC, we synthesized a library of 15 variant 3-arylcoumarins. In this context, we report a set of four coordinated palladium(II) hydrazone complexes 1 and 2 having the general formula [Pd(L)(Cl)(PPh3)] by reacting the precursor complex [PdCl2(PPh3)2] with the hydrazone ligands HL1 or HL2. Single crystal XRD and conventional spectroscopic techniques were employed to characterize both complexes. From the catalytic application point of view, the new complexes 1 and 2 were tested as homogeneous catalysts towards the conversion of 3-chlorocoumarins into 3-arylcoumarins by activating the challenging CCl functionality. A minimal catalyst loading of complex 2 (0.01 mol%), afforded a series of 3-arylcoumarins with a maximum of 92% yield and reusability up to five cycles. The present methodology is simple and easy to carry out at room temperature utilizing a green solvent (ethanol) in an open flask with a spectrum of aryl boronic acids.

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来源期刊
Applied Organometallic Chemistry
Applied Organometallic Chemistry 化学-无机化学与核化学
CiteScore
7.80
自引率
10.30%
发文量
408
审稿时长
2.2 months
期刊介绍: All new compounds should be satisfactorily identified and proof of their structure given according to generally accepted standards. Structural reports, such as papers exclusively dealing with synthesis and characterization, analytical techniques, or X-ray diffraction studies of metal-organic or organometallic compounds will not be considered. The editors reserve the right to refuse without peer review any manuscript that does not comply with the aims and scope of the journal. Applied Organometallic Chemistry publishes Full Papers, Reviews, Mini Reviews and Communications of scientific research in all areas of organometallic and metal-organic chemistry involving main group metals, transition metals, lanthanides and actinides. All contributions should contain an explicit application of novel compounds, for instance in materials science, nano science, catalysis, chemical vapour deposition, metal-mediated organic synthesis, polymers, bio-organometallics, metallo-therapy, metallo-diagnostics and medicine. Reviews of books covering aspects of the fields of focus are also published.
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