Abstract
The yields for the preparation of a series of di-μ-bromo-bis-(trihapto- cycloalkenyl)palladium(II) compounds increase in the sequence C9 < C8 < C6 < C7. In competitive reactions the reactivity of a series of 3-bromoalkenes with solutions containing palladium(II) increases in the order C8 < C6 < C7. These results parallel the relative ease of hydrogenation of cyclic olefins. The unusual n.m.r. spectrum of di-μ-halogenobis-[(trihapto- cycloheptenyl)palladium(II)] is discussed.
Original language | English |
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Pages (from-to) | 180-181 |
Number of pages | 2 |
Journal | Journal of the Chemical Society - Dalton Transactions |
Issue number | 2 |
DOIs | |
Publication status | Published - 1 Dec 1972 |
Externally published | Yes |