Abstract
Deprotonation of [Ru(C6Me6)2]2+ generates the new o-xylylene complex Ru(C6Me6)[C6Me4(CH2)2]. The X-ray crystallographic study confirms that the metal is coordinated to the endocyclic diene system. The exocyclic methylenes are nucleophilic and can be reacted with electrophiles in a stepwise manner. This has allowed the isolation of a new exo-(methylene)cyclohexadienyl complex.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1716-1718 |
| Number of pages | 3 |
| Journal | Organometallics |
| Volume | 1 |
| Issue number | 12 |
| DOIs | |
| State | Published - 1982 |
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