Abstract
Phosphinines (phosphabenzenes, phosphorins), the higher
homologues of pyridines are low-coordinated phosphorus
compounds that possess significantly different steric and
electronic properties compared to common ligands based on
trivalent phosphorus.[1, 2]
We have recently started to investigate the preparation of
functionalized phosphinines via the pyrylium salt route, originally
described by M#rkl for the synthesis of 2,4,6-triphenylphosphinine.[
1a] It turned out that this procedure allowed
us to introduce substituents into specific positions of the heterocyclic
framework; a feature which is essential for ligand
design and their potential application in homogeneous catalytic
reactions. In this way a variety of donor-functionalized
and axially chiral monophosphinines, as well as a trans-coordinating
diphosphinine have been designed and prepared by
us lately.[3, 4]
Original language | Undefined/Unknown |
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Pages (from-to) | 8803-8807 |
Number of pages | 5 |
Journal | Chemistry-A European Journal |
Volume | 14 |
Publication status | Published - 2008 |