Structural and Mechanistic Insights into the Metalation of Fluoroarenes Mediated by a Superbasic Co(II) Bis(amide) Complex.

IF 1.1 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Chimia Pub Date : 2025-04-30 DOI:10.2533/chimia.2025.224
Na Jin, Eva Hevia
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引用次数: 0

Abstract

Over the past decades, s-block metal amides including LiTMP and TMPMgCl.LiCl (TMP = 2,2,6,6-tetramethylpiperidide) have found widespread applications in the deprotonative metalation of aromatic compounds. In contrast, transition metal amides usually exhibit diminished basicity to metalate these substrates. Here we present an overview of the synthesis of a highly reactive TMP-based cobalt(II) bis(amide) complex Co(TMP)2 and its relevance in the direct Co-H exchange processes with fluoroarenes. This deprotonative metalation reactivity can be further extended to cyclopentadiene to generate cobaltocene. Exhibiting an unusual reactivity, Co(TMP)2 has also been found to be highly nucleophilic, as evidenced by the insertion of CO2 molecules into both of its Co-NTMP bonds.

超碱式Co(II)双(酰胺)配合物介导的氟芳烃金属化反应的结构和机理研究。
在过去的几十年里,五嵌段金属酰胺包括LiTMP和TMPMgCl。LiCl (TMP = 2,2,6,6-四甲基哌啶酯)在芳香化合物的脱质子金属化反应中有广泛的应用。相反,过渡金属酰胺通常表现出减弱的碱度来金属化这些底物。在这里,我们概述了高活性TMP基钴(II)双(酰胺)配合物Co(TMP)2的合成及其与氟芳烃直接Co- h交换过程的相关性。这种脱质子金属化反应性可进一步扩展到环戊二烯生成钴二烯。Co(TMP)2表现出一种不同寻常的反应活性,也被发现是高度亲核的,其Co- ntmp键中都插入了CO2分子。
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来源期刊
Chimia
Chimia 化学-化学综合
CiteScore
1.60
自引率
0.00%
发文量
144
审稿时长
2 months
期刊介绍: CHIMIA, a scientific journal for chemistry in the broadest sense covers the interests of a wide and diverse readership. Contributions from all fields of chemistry and related areas are considered for publication in the form of Review Articles and Notes. A characteristic feature of CHIMIA are the thematic issues, each devoted to an area of great current significance.
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