Abstract
The organolanthanide complexes Ln{C(SiHMe2)3}3 (Ln = La, 1a; Ce, 1b; Pr, 1c; Nd, 1d) react with 1 or 2 equiv of B(C6F5)3 to yield the well-defined zwitterionic species Ln{C(SiHMe2)3}2HB(C6F5)3 (Ln = La, 2a; Ce, 2b; Pr, 2c; Nd, 2d) or LnC(SiHMe2)3{HB(C6F5)3}2 (Ln = La, 3a; Ce, 3b; Pr, 3c; Nd, 3d), respectively. These complexes are shown to contain labile, bridging Si–H⇀Ln and o-F→Ln interactions based upon the observation of low one-bond silicon–hydrogen coupling constants (1JSiH) in 1H NMR spectra of 2a and 3a, the presence of one set of C6F5 signals in the 19F NMR spectra of 2a and 3a, the detection of only m-F and p-F resonances in the 19F NMR spectra of 2b–d and 3b–d, two νSiH bands in the IR spectra of 2a–d, and X-ray crystallography analyses of 2b and 3d. In addition, a hexahaptotoluene molecule is coordinated to neodymium in 3d. Reactions of 1a and (AlMe3)2 yield labile adducts. With greater than 3 equiv of AlMe3, exchange between free and bound AlMe3 groups was observed in EXSY NMR experiments. Com...
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