Abstract
The new dihydroborate [Li(Et2O)][B(C6F5)(2)(H)(2)] (1) has been prepared and characterised by single-crystal X-ray diffraction. In the solid state 1 exhibits a one-dimensional chain structure that is a result of intermolecular Li-F interactions. Reaction between 1 and one equivalent of Cp2TiCl or 0.5 equivalents of Cp2TiCl2 gives the violet compound Cp2Ti{(mu-H)(2)B(C6F5)(2)} (2), which has also been characterised by single-crystal X-ray diffraction. Addition of two equivalents of PM3, to 2 does not result in elimination of a borane:phosphine adduct, but yields the ionic compound [Cp2Ti(PMe3)(2)][H2B(C6F5)(2)] (3). (C) 2000 Elsevier Science Ltd. All rights reserved.
Original language | English |
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Pages (from-to) | 1579-1583 |
Number of pages | 5 |
Journal | POLYHEDRON |
Volume | 19 |
Issue number | 13 |
Publication status | Published - 1 Jul 2000 |
Keywords
- hydroborates
- lithium
- titanium(IV)
- bonding
- crystal structures
- TRANSITION-METAL
- COMPLEXES