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Synthesis and characterization of a bis(imino)-N-heterocyclic carbene analogue to bis(imino)pyridine iron complexes

机译:双(亚氨基)-N-杂环卡宾类似物的合成和表征双(亚氨基)吡啶铁配合物

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摘要

New bis(imino)-N-heterocyclic carbene ligands have been synthesized, and the corresponding iron complexes have been isolated and characterized. Whereas imidazole-derived complexes exhibited exclusively bidentate binding modes, 4,5,6-trihydropyrimidylidene-based ligands adopted a tridentate pincer conformation analogous to complexes of 2,6-bis(imino)pyridines. Bonding in the five-coordinate bis(imino)-N-heterocyclic carbene complex displayed considerably contracted iron-ligand bond distances in comparison to those in the analogous bis(imino)pyridine iron complex. Of particular note was an extraordinarily short iron-carbene carbon bond distance (1.812(2) ?). In addition to demonstrating differences in bonding, the isoelectronic structures have different electrochemical properties that reflect the ability of the carbene to stabilize both oxidized and reduced forms of the parent organometallic species.
机译:合成了新的双(亚氨基)-N-杂环卡宾配体,并分离和表征了相应的铁配合物。咪唑衍生的复合物仅表现出二齿结合模式,而4,5,6-三氢嘧啶基配体则采用类似于2,6-双(亚氨基)吡啶的三齿钳形构象。与类似的双(亚氨基)吡啶铁络合物相比,五配位双(亚氨基)-N-杂环卡宾配合物中的键合显示出显着收缩的铁-配体键合距离。特别值得注意的是铁碳卡宾碳键的距离非常短(1.812(2)?)。除了证明键合方面的差异外,等电子结构还具有不同的电化学性质,反映了卡宾能够稳定母体有机金属物种的氧化形式和还原形式的能力。

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