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 P-31{H-1} NMR spectroscopy.
Original language | English |
---|---|
Pages (from-to) | 5372-5375 |
Number of pages | 4 |
Journal | Dalton Transactions |
Issue number | 46 |
DOIs | |
Publication status | Published - 2007 |