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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.
Pubmed ID: 30940808
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Academic software toolkit for pre-processing of diffusion MRI data, estimation of DTI indices and spatially normalisation of DTI index maps, which fully integrates into the batch system of SPM8. These tools are made for users familiar with the underlying statistical, mathematical and image processing concepts. The ACID toolbox provides the option to write the estimated diffusion tensor in the format of the DTI and Fibertools Software Package.
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