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Successive modification of polydentate complexes gives access to planar carbon- and nitrogen-based ligands

机译:多齿复合物的连续修饰使得可以使用基于碳和氮的平面配体

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摘要

Polydentate complexes containing combinations of nitrogen and carbon (N and C) ligating atoms are among the most fundamental and ubiquitous molecules in coordination chemistry, yet the formation of such complexes with planar high-coordinate N/C sites remains challenging. Herein, we demonstrate an efficient route to access related complexes with tetradentate CCCN and pentadentate CCCCN and NCCCN cores by successive modification of the coordinating atoms in complexes with a CCCC core. Combined experimental and computational studies reveal that the rich reactivity of metal-carbon bonds and the inherent aromaticity of the metallacyclic skeletons play key roles in these transformations. This strategy addresses the paucity of synthetic approaches to mixed N/C planar pentadentate chelating species and provides valuable insights into the synthesis of carbon-based high-coordinate complexes. Furthermore, the resulting complexes are the examples of organometallic species with combined photoacoustic, photothermal, and sonodynamic properties, which makes them promising for application in related areas.
机译:含有氮和碳(N和C)连接原子的多齿配合物是配位化学中最基本和最普遍的分子之一,但是这种具有平面高配位N / C位的配合物的形成仍然具有挑战性。在本文中,我们证明了通过连续修饰具有CCCC核的配合物中的配位原子,可以有效地访问四齿CCCN和五齿CCCCN和NCCCN核的相关配合物。组合的实验和计算研究表明,金属-碳键的丰富反应性和金属环骨架的固有芳香性在这些转变中起关键作用。该策略解决了用于混合N / C平面五齿螯合物种的合成方法的不足,并为合成基于碳的高配位络合物提供了宝贵的见识。此外,所得的配合物是具有组合的光声,光热和声动力学性质的有机金属物质的实例,这使得它们有希望在相关领域中应用。

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