Abstract
The reaction of the half-sandwich compound Cp *VOCl 2 (Cp * = η 5-pentamethylcyclopentadienyl) with THF solutions of potassium polysulfide, K 2S x ( x > 6), inTHF leads to the pentasulfido-vanadium complex Cp*VO(S 5) ( 1), one which is also found among the soluble side-products of the reaction of Cp *V(CO) 4 with excess sulfur, S 8. Complex 1 contains a six-membered metallacycle in chair conformation, similar to that observed in Cp 2Ti(S 5) and Cp 2V(S 5), although the VS bond distances (average 228.4(2) pm) are shorter and the SVS angles (106.8(1) and 106.1(1)° in the two crystallographically different molecules of 1) are larger than the corresponding parameters in the metallocene derivatives. The vanadium-oxygen bond lengths (159.0(3) and 158.5(4) pm, respectively) are typical of a VO double bond.
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