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Synthesis of a series of complexes of the type LLBX2 + BX4 − where X = F− and CI− and LL = 1,10-phenanthroline, 2,2′-bipyridine and 1,8-bis(dimethylamino)naphthalene was achieved by the direct interaction of the ligand and BX3. No reaction was observed for X = CH3. The reactions provide a direct route for the preparation of tetra-coordinate boronium cations. The boron-11 nmr and infrared spectra of these complexes confirm the ionic nature of the compounds. 2,2′-Bipyridine functions as a chelating agent rather than as a bis-monodentate donor. 1,8-Bis(dimethylamino)naphthalene is found to be able to chelate cations much larger than protons. The steric implications of donor-acceptor interactions of boron with rigid and semi-rigid chelating donor molecules are discussed.
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Axtell et al. (1976) studied this question.
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