Regioselective B-H/C-H activation and metal-metal bond formation induced by half-sandwich metals complexes at hydroxy-substituted o-carboranes
A binuclear iridium complex, (Cp2*Ir2(CH2O)C2B10H8) (6), with a unique metal-metal bond has been synthesized and fully characterized. Importantly, this complex is constructed via selective C-H and B(3)-H bond activation on the carborane precursor. Additionally, when the proligand (2-pyridine)(o-carb...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2018, Vol.47 (38), p.13641-13646 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A binuclear iridium complex, (Cp2*Ir2(CH2O)C2B10H8) (6), with a unique metal-metal bond has been synthesized and fully characterized. Importantly, this complex is constructed via selective C-H and B(3)-H bond activation on the carborane precursor. Additionally, when the proligand (2-pyridine)(o-carboranyl)methanol ligand was combined with a half-sandwich iridium complex, selective B(6)-H bond activation or metal-carbon bond formation can be induced by the use of different bases. And the rhodium complex constructed from (2-pyridine)(o-carboranyl)methanol ligand containing a metal-carbon bond has been obtained and fully characterized. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c8dt03104e |