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可溶性β-二酮亚胺碱土金属配合物的化学(M=Mg、Ca、Sr;X=OH、卤化物、H)。

Chemistry of soluble β-diketiminatoalkaline-earth metal complexes with M-X bonds (M=Mg, Ca, Sr; X=OH, Halides, H).

机构信息

Institut für Anorganische Chemie, Universität Göttingen, Tammannstrasse 4, D-37077 Göttingen, Germany.

出版信息

Acc Chem Res. 2011 Mar 15;44(3):157-70. doi: 10.1021/ar100103h. Epub 2011 Jan 19.

Abstract

Victor Grignard's Nobel Prize-winning preparation of organomagnesium halides (Grignard reagents) marked the formal beginning of organometallic chemistry with alkaline earth metals. Further development of this invaluable synthetic route, RX+Mg→RMgX, with the heavier alkaline earth metals (Ca and Sr) was hampered by limitations in synthetic methodologies. Moreover, the lack of suitable ligands for stabilizing the reactive target molecules, particularly with the more electropositive Ca and Sr, was another obstacle. The absence in the literature, until just recently, of fundamental alkaline earth metal complexes with M-H, M-F, and M-OH (where M is the Group 2 metal Mg, Ca, or Sr) bonds amenable for organometallic reactions is remarkable. The progress in isolating various unstable compounds of p-block elements with β-diketiminate ligands was recently applied to Group 2 chemistry. The monoanionic β-diketiminate ligands are versatile tools for addressing synthetic challenges, as amply demonstrated with alkaline earth complexes: the synthesis and structural characterization of soluble β-diketiminatocalcium hydroxide, β-diketiminatostrontium hydroxide, and β-diketiminatocalcium fluoride are just a few examples of our contribution to this area of research. To advance the chemistry beyond synthesis, we have investigated the reactivity and potential for applications of these species, for example, through the demonstration of dip coating surfaces with CaCO(3) and CaF(2) with solutions of the calcium hydroxide and calcium fluoride complexes, respectively. In this Account, we summarize some recent developments in alkaline earth metal complex chemistry, particularly of Mg, Ca, and Sr, through the utilization of β-diketiminate ligands. We focus on results generated in our laboratory but give due mention to work from other groups as well. We also highlight the closely related chemistry of the Group 12 element Zn, as well as the important chemistry developed by other groups using the complexes we have reported. Although Mg and Ca are more abundant in living organisms, no other metal has as many biological functions as Zn. Thus Zn, the nontoxic alternative to the heavier Group 12 elements Cd and Hg, occupies a unique position ripe for further exploration.

摘要

维克多·格林尼亚(Victor Grignard)因制备有机镁卤化物(格氏试剂)而获得诺贝尔奖,这标志着碱土金属有机金属化学的正式开始。由于合成方法的限制,进一步发展这种非常宝贵的合成路线 RX+Mg→RMgX,用较重的碱土金属(Ca 和 Sr)受到阻碍。此外,缺乏合适的配体来稳定反应性靶分子,特别是对于更具正电性的 Ca 和 Sr,这是另一个障碍。直到最近,文献中才出现具有 M-H、M-F 和 M-OH(其中 M 是第 2 族金属 Mg、Ca 或 Sr)键的基本碱土金属配合物,这些配合物可用于有机金属反应,这是非常值得注意的。最近,将带有β-二酮亚胺配体的 p 区元素各种不稳定化合物分离的进展已应用于第 2 族化学。单价阴离子β-二酮亚胺配体是解决合成挑战的多功能工具,如用碱土金属配合物充分证明:可溶性β-二酮亚胺钙氢氧化物、β-二酮亚胺锶氢氧化物和β-二酮亚胺钙氟化物的合成和结构表征只是我们在该研究领域贡献的几个例子。为了超越合成推进化学,我们已经研究了这些物质的反应性和潜在应用,例如,通过用钙氢氧化物和钙氟化物配合物的溶液分别对 CaCO(3)和 CaF(2)进行浸涂表面来证明。在本报告中,我们总结了通过利用β-二酮亚胺配体的碱土金属配合物化学的一些最新进展,特别是对 Mg、Ca 和 Sr 的研究。我们专注于我们实验室生成的结果,但也适当提到其他小组的工作。我们还突出了与 Group 12 元素 Zn 密切相关的化学,以及其他小组使用我们报告的配合物开发的重要化学。虽然 Mg 和 Ca 在生物体中更为丰富,但没有其他金属具有像 Zn 那样多的生物学功能。因此,作为较重的 Group 12 元素 Cd 和 Hg 的无毒替代品,Zn 占据了一个有待进一步探索的独特位置。

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