Abstract
The reaction of the new platinaboratrane salt [PtH(PTol3){B(mt)3}]Cl(Pt-->B)8 (mt = methimazolyl, Tol = C6H4Me-4) with 2 equivalents of PR3 (R = Me, Et) affords, via hydride migration to boron and ligand substitution, the salts [Pt(PR3)2{kappa 2-S,S'-HB(mt)3}]Cl, which slowly undergo B-H reactivation, to afford, ultimately, the platinaboratrane salts [PtH(PR3){B(mt)3}]Cl(Pt-->B)8.
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