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Abstract
An oxygen atom is selectively inserted into the P-B bond of a borylphosphine (L1) by reaction with Me3NO to afford the corresponding borylphosphinite (L2). This transformation can also be effected when L1 is coordinated to rhodium. The ν(CO) values for trans-[RhCl(CO)(L)2] reveal very different electronic properties for coordinated L1 and L2 which translate into the strikingly different performances of the complexes [RhCl(L)(cod)] (L=L1 or L2, cod=1,5-cyclooctadiene) in hydrosilylation and hydroboration catalysis.
| Original language | English |
|---|---|
| Pages (from-to) | 5360-5363 |
| Number of pages | 4 |
| Journal | Chemistry - A European Journal |
| Volume | 21 |
| Issue number | 14 |
| Early online date | 20 Feb 2015 |
| DOIs | |
| Publication status | Published - 27 Mar 2015 |
Bibliographical note
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.Research Groups and Themes
- Inorganic & Materials
Keywords
- hydroboration
- hydrosilylation
- oxygen insertion
- phosphane ligands
- phosphinoboranes
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Dive into the research topics of 'Single Oxygen-Atom Insertion into P-B Bonds: On- and Off-Metal Transformation of a Borylphosphine into a Borylphosphinite'. Together they form a unique fingerprint.Projects
- 1 Finished
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3-month Core Capability for Chemistry Research
Crosby, J. (Principal Investigator)
1/01/13 → 1/04/13
Project: Research