双胍酸镁和钙:不饱和分子氢硼化合的催化活性

IF 4.4 2区 化学 Q2 CHEMISTRY, APPLIED Advanced Synthesis & Catalysis Pub Date : 2025-01-07 DOI:10.1002/adsc.202400843
Carlos Ginés , Blanca Parra‐Cadenas , Rafael Fernández‐Galán , Daniel García‐Vivó , David Elorriaga , Alberto Ramos , Fernando Carrillo‐Hermosilla
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引用次数: 0

摘要

配体在催化活性金属配合物中的作用至关重要。在此,我们对碱土双胍类配合物的合成和催化行为进行了研究。我们探讨了三取代胍类化合物,特别是 (iPrHN)2CNR (R= Ph、2-Ph2PC6H4、2-MeSC6H4)与镁和钙烷基或酰胺的反应性。发现所有化合物在苯乙酮与频哪醇硼烷的硼氢化反应中都非常活跃。值得注意的是,一种钙基复合物在羰基化合物的硼氢化反应中特别有效,对其他活性官能团具有显著的化学选择性。这种复合物在腈的双硼氢化反应中也特别有效,在吡啶的硼氢化脱芳烃反应中也有一定的活性。通过实验和 DFT 研究,我们提出了一种机制,其中胍基配体和金属的参与是不饱和物种和硼烷活化的关键。
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Magnesium and Calcium Bisguanidinates: Catalytic Activity in the Hydroboration of Unsaturated Molecules
The role of ligands in catalytically active metal complexes can be crucial. Herein, we present a study on the synthesis and catalytic behavior of alkaline earth bisguanidinato complexes. The reactivity of trisubstituted guanidines, specifically (iPrHN)2CNR (R=Ph, 2‐Ph2PC6H4, 2‐MeSC6H4), towards magnesium and calcium alkyls or amides was explored. All the compounds were found to be very active in the hydroboration of acetophenone with pinacolborane. Notably, a calcium‐based complex was especially effective in the hydroboration of carbonyl compounds, demonstrating significant chemoselectivity against other reactive functional groups. This complex was also particularly effective in the double hydroboration of nitriles and moderately active in the hydroborative dearomatization of pyridine. Our experimental and DFT studies allow us to propose a mechanism in which the participation of the guanidinato ligands, along with the metal, is key to the activation of both the unsaturated species and borane.
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来源期刊
Advanced Synthesis & Catalysis
Advanced Synthesis & Catalysis 化学-应用化学
CiteScore
9.40
自引率
7.40%
发文量
447
审稿时长
1.8 months
期刊介绍: Advanced Synthesis & Catalysis (ASC) is the leading primary journal in organic, organometallic, and applied chemistry. The high impact of ASC can be attributed to the unique focus of the journal, which publishes exciting new results from academic and industrial labs on efficient, practical, and environmentally friendly organic synthesis. While homogeneous, heterogeneous, organic, and enzyme catalysis are key technologies to achieve green synthesis, significant contributions to the same goal by synthesis design, reaction techniques, flow chemistry, and continuous processing, multiphase catalysis, green solvents, catalyst immobilization, and recycling, separation science, and process development are also featured in ASC. The Aims and Scope can be found in the Notice to Authors or on the first page of the table of contents in every issue.
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