Abstract
Reaction of [(dppf)Au2Br2] (3) {dppf = 1,1′-bis(diphenylphosphino)ferrocene} and [(dippf)Au2Br2] (4) {dippf = 1,1′-bis(diisopropylphosphino)ferrocene} with excess bromine yields two new complexes [(C5H4Br3)(PR2)AuBr] (R = Ph, 5; R = i-Pr, 6). Bromination of the free diphosphinoferrocene ligands produces the expected brominated cyclopentenes (C5H4Br3)(PR2) (R = Ph, 7; R = i-Pr, 8) in good yields; however, these compounds could not be complexed to gold due to reduced basicity of 7 and 8. When the bromination is performed under wet aerobic conditions the oxidized pseudo-centrosymmetric product, [doppf][FeBr4] (9) {doppf = 1,1′-bis(oxodiphenylphosphino)ferrocene, is formed as the major product. Solid-state structures of 1, 2, 4, 6, and 9 have been established by means of single-crystal X-ray crystallography.
Original language | English |
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Pages (from-to) | 701-708 |
Number of pages | 8 |
Journal | Journal of Organometallic Chemistry |
Volume | 693 |
Issue number | 4 |
DOIs | |
Publication status | Published - 15 Feb 2008 |
Keywords
- Bromination
- Diisopropylphosphinoferrocene
- Diphenylphosphinoferrocene
- Gold(I) complexes
- Ligands
- Phosphinocyclopentene
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
- Materials Chemistry