Abstract
The first atropisomeric phosphinine was designed and prepared by introducing substituents into specific positions of the heterocyclic framework; the presence of axial chirality was predicted by means of DFT calculations and experimentally verified by chiral HPLC analysis, derivatization experiments as well as temperature dependent 31P{1H} NMR spectroscopy.
Original language | Undefined/Unknown |
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Pages (from-to) | 5372-5375 |
Number of pages | 4 |
Journal | Dalton Transactions |
Volume | 2007 |
Issue number | 46 |
Publication status | Published - 2007 |