Transition metals boratabenzenes with

Reaction of the same neutral borabenzene-ligand adduct, C5H5B-PMe3, with a transition, rather than an alkali, metal alkyl or amide can furnish r 6-boratabenzene complexes in a single step (Scheme 8).17 This efficient transformation presumably proceeds through initial ir-coordination of CsHsB-PMes to the transition metal, followedby an intramolecular substitution reaction. In contrast to other approaches to the synthesis of T 6-boratabenzene complexes, this synthetic route does not have a parallel in if-cyclopentadienyl chemistry. 

The X-ray structure of lithium l-(dimethylamido)boratabenzene, reported in 1993, provided the first crystallographic characterization of a transition metal-free boratabenzene (Scheme 13).18a The observed bond lengths are consistent with a delocalized anion and with significant B—N double-bond character. In a separate study, the B—N rotational barrier of [C5H5B—NMeBnjLi has been determined to be 10.1 kcal/mol, and it has been shown that TT-complexation to a transition metal can increase this barrier (e.g., 17.5 kcal/mol for (C5H5B-N(i-Pr)2)Mn(CO)3).24... 

An interesting example of t 3 coordination of a boratabenzene to a transition metal has been observed for a Zr(IV)-boratanaphthalene complex (Scheme 20).35 Thus, treatment of the illustrated 1-boratanaphthalene with Cp+ZrCl3 furnishes an adduct in which the metal-carbon distance for the 3, 4, and 5 positions of the heterocycle (2.53-2.56 A) is significantly shorter than for the 2 and 6 positions (2.77-2.81 A). It is suggested that this distorted bonding mode is the consequence of the high electron demand of Zr(IV), which prefers coordination to the most electron-rich carbon atoms. ... 

Simple transition metal halides react cleanly with alkali metal boratabenzenes. In this way sandwich-type complexes 32 of V (27), Cr (64), Fe (58), Ru (61), and Os (61) have been made. The corresponding nickel complexes seem to be nonexistent, quite in contrast to NiCp2 in attempted preparations, mixtures of diamagnetic C—C linked dimers were obtained (29). In the manganese case, high sensitivity to air and water has precluded preparative success until now. Some organometallic halides have added further variations to the main theme. The complexes 33 of Rh and 34 of Pt were obtained from [(COD)RhCl]2 and [Me3PtI]4, respectively (61). 

Metal complexes of pinene-fused boratabenzene ligands, analogous to chiral metallocenes that have found application in catalysis and enantioselective synthesis, have been prepared.122-124 With late transition metals such as Mn and Fe, the complexes are obtained as mixtures of diastereomers (e.g., 97) with the sterically less congested exo form predominating, but the bis(ligand) Zr complex 98 was obtained as the pure exo,exo product.124 A lithium... 

A large number of boratabenzene transition-metal complexes have been described. For instance, the multinuclear complex (141) has been obtained through the original Herberich route from cobaltocene with FcBBr2 (equation 37). Notably, a rhodium complex has recently been reported to be useful in C-H activation catalysis. ... 

The use of the boratabenzene heterocycle as a ligand for transition metal complexes dates back to 1970 with the synthesis of (C H5B-Ph)CpCo+ (1) (Cp = cyclopentadienyl).1 Since boratabenzene and Cp are 6 it electron donors, 1 can be considered isoelectronic to cobaltocenium. Many other transition metal compounds have been prepared that take advantage of the relationship between Cp and boratabenzene.2 In 1996, the synthesis of bis(diisopropylaminoboratabenzene)zirconium dichloride (CsHsB-NPr ZrCh (2) was reported Of particular interest is that 2 can be activated with methylaluminoxane (MAO) to produce ethylene polymerization catalysts with activities similar to those characteristic of group 4 metallocenes.4 Subsequent efforts showed that, under similar reaction conditions, (CsHjB-Ph ZrCh/MAO (3/MAO) gave predominantly 2-alkyl-1-alkenes5 while (CsHsB-OEt ZrCh/MAO (4/MAO) produced exclusively 1-alkenes.6 Therefore, as shown in Scheme 1, it is possible to modulate the specificity of the catalytic species by choice of the exocyclic group on boron. 

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