Tandem Deacetalization-Knoevenagel Condensation Reactions for the Synthesis of Benzylidene Malononitrile Using Ruthenium(II) Cymene Complexes.

IF 4.7 2区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Pub Date : 2024-12-16 Epub Date: 2024-11-28 DOI:10.1021/acs.inorgchem.4c03109
Noemi Pagliaricci, Riccardo Pettinari, Fabio Marchetti, Alessia Tombesi, Farzaneh Fadaei-Tirani, Paul J Dyson, Anirban Karmakar, Maxim L Kuznetsov, M Fátima C Guedes da Silva, Armando J L Pombeiro
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Abstract

In this study, we report the synthesis and full characterization of five novel ruthenium(II) cymene complexes with the general formula [Ru(cym)(L')Cl], featuring N,O- and N,N-coordinating pyrazolone-based hydrazone ligands. We have characterized these complexes using single X-ray crystallography, Fourier-transform infrared spectroscopy (FT-IR), Nuclear magnetic resonance (NMR), elemental analysis, and Electrospray Ionization Mass Spectroscopy (ESI-MS). Crystallographic analysis confirmed that all of the complexes have a similar type of half-sandwich, pseudo-octahedral "three-legged piano-stool" geometry where the cymene moiety displays the typical η6-coordination mode and the hydrazone ligands coordinate to the Ru(II) center in a bidentate fashion. These complexes, with multiple catalytic sites, demonstrated high efficiency in catalyzing one-pot cascade deacetalization-Knoevenagel condensation reactions under mild conditions, achieving up to 92% of final product yield at 75 °C after 4 h of reaction time under solvent-free condition. Additionally, DFT calculations provided insight into the catalytic mechanism, suggesting a pathway driven by metal-ligand cooperation, assisted by the basic oxygen site of the pyrazolone ring and by the weakly acidic character of the NNH proton of the hydrazone group.

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利用钌(II)亚甲基络合物串联脱乙醛化-Knoevenagel 缩合反应合成亚苄基丙二腈。
在本研究中,我们报告了通式为 [Ru(cym)(L')Cl] 的五种新型钌(II)亚甲基配合物的合成和全面表征,这些配合物具有 N,O- 和 N,N- 配位的吡唑酮基腙配体。我们利用单 X 射线晶体学、傅立叶变换红外光谱(FT-IR)、核磁共振(NMR)、元素分析和电喷雾离子化质谱(ESI-MS)对这些复合物进行了表征。晶体学分析证实,所有这些配合物都具有类似的半夹心假八面体 "三脚琴凳 "几何形状,其中亚甲基呈典型的 η6 配位模式,而腙配体与 Ru(II) 中心的配位方式为双齿配。这些具有多个催化位点的配合物在温和条件下高效地催化了一锅级联脱乙醛-Knoevenagel 缩合反应,在无溶剂条件下于 75 ℃ 反应 4 小时后,最终产物收率高达 92%。此外,DFT 计算深入揭示了催化机理,认为这是一条由金属-配体合作驱动的途径,吡唑酮环的碱性氧位点和腙基团 NNH 质子的弱酸性起了辅助作用。
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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来源期刊
Inorganic Chemistry
Inorganic Chemistry 化学-无机化学与核化学
CiteScore
7.60
自引率
13.00%
发文量
1960
审稿时长
1.9 months
期刊介绍: Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.
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