Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 55, Issue 46, Pages 14448-14452Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201605838
Keywords
boron; density functional theory; iron; pincer ligands; reduction
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Funding
- DFG [LA 2830/3-1]
- NSFC [21450110063]
- Studienstiftung des deutschen Volkes
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Stabilized borylenes (L2BHD) with weakly pi-accepting substituents L, such as phosphines, were previously believed to be unstable. In the current manuscript, we describe a series of complexes formally containing a phosphine-stabilized borylene or boryl anion. In contrast to common trivalent boron compounds, the boron-based ligands in this study act as electron-donating ligands. The reported iron hydride complexes exhibit a unique reactivity pattern, undergoing a reversible B-H reductive elimination concomitant with oxidation of the boron(I) center.
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