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

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作者
Xiaoxi Zhou
Xin Pang
Liming Nie
Congqing Zhu
Kaiyue Zhuo
Qingde Zhuo
Zhixin Chen
Gang Liu
Hong Zhang
Zhenyang Lin
Haiping Xia
机构
[1] Xiamen University,State Key Laboratory of Physical Chemistry of Solid Surfaces and Collaborative Innovation Centre of Chemistry for Energy Materials (iChEM), College of Chemistry and Chemical Engineering
[2] Xiamen University,State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, Centre for Molecular Imaging and Translational Medicine, School of Public Health
[3] The Hong Kong University of Science and Technology,Department of Chemistry
[4] Nanjing University,State Key Laboratory of Coordination Chemistry, Jiangsu Key Laboratory of Advanced Organic Materials, School of Chemistry and Chemical Engineering
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Nature Communications | / 10卷
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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.
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