Martin’s phosphino-triol revisited: unexpected P-C bond cleavage reactions and their suppression via complexation of Al3+ and Sc3+
A revised synthesis of Martin’s phosphino-triols (two derivatives) is reported. Once isolated, these thermally sensitive triols were shown to disassemble selectively via an unexpected P-C bond cleavage reaction. This degradation pathway was effectively suppressed via complexation of Al3+ and Sc3+. I...
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| Main Authors: | , , , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
November 30, 2021
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| In: |
Inorganic chemistry
Year: 2021, Volume: 60, Issue: 24, Pages: 19414-19420 |
| ISSN: | 1520-510X |
| DOI: | 10.1021/acs.inorgchem.1c03232 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/acs.inorgchem.1c03232 |
| Author Notes: | Jean-Marc Mörsdorf, Tim Bruckhoff, Regina Matveeva, Benjamin Rudin, Hubert Wadepohl, and Joachim Ballmann |
MARC
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| 520 | |a A revised synthesis of Martin’s phosphino-triols (two derivatives) is reported. Once isolated, these thermally sensitive triols were shown to disassemble selectively via an unexpected P-C bond cleavage reaction. This degradation pathway was effectively suppressed via complexation of Al3+ and Sc3+. In the resulting half-cage complexes, the ligand scaffold is bound to each metal (Al3+ and Sc3+, respectively) via all four donor atoms. So far, this κ4-P,O,O′,O″-coordination mode has not been observed for any other phosphino-triol. | ||
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