Abstract
Coupling of the N,N-dimethylacrylamides 6a-c with cyclopentadienide resulted in the formation of the substituted 3-dimethylamino-1,2- dihydropentalnenes 2a-c. Deprotonation followed by metallation with CpZrCl 3·DME gave the substituted zirconocenes 12a-c. The reaction of 3-dimethylamino-1-methyl-dihydropentalene 2a with ZrCl2(NMe 2)2·2THF resulted in a unique coupling between a pair of the aminodihydropentalene derivatives to yield an unsymmetrically bridged novel ansa-zirconocene framework (9a). Treatment of the 1,1-dimethyl-substituted substrate 2b with this Zr-amido reagent in contrast resulted in a clean deprotonation and formation of the unbridged bis(dimethylaminohydropentalenyl)ZrCl2 complexes 10b. The compounds 2a, 9a, meso-10b, 12a and 12c were characterized by X-ray diffraction.
Original language | English |
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Pages (from-to) | 9973-9981 |
Number of pages | 9 |
Journal | Dalton Transactions |
Volume | 39 |
Issue number | 41 |
DOIs | |
Publication status | Published - 7 Nov 2010 |
Externally published | Yes |