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Imine Nitrogen Bridged Binuclear Nickel Complexes
via N–H Bond Activation: Synthesis, Characterization, Unexpected
C,N-Coupling Reaction, and Their Catalytic Application in Hydrosilylation
of Aldehydes
The
reactions of NiMe<sub>2</sub>(PMe<sub>3</sub>)<sub>3</sub> with
2,6-difluoroarylimines were explored. As a result, a series of binuclear
nickel complexes (<b>5</b>–<b>8</b>,<b> 11</b>) were synthesized. Meanwhile, from the reactions of NiMe<sub>2</sub>(PMe<sub>3</sub>)<sub>3</sub> with [2-CH<sub>3</sub>C<sub>6</sub>H<sub>4</sub>-C(NH)-2,6-F<sub>2</sub>C<sub>6</sub>H<sub>3</sub>] (<b>9</b>) and [2,6-(CH<sub>3</sub>)<sub>2</sub>C<sub>6</sub>H<sub>3</sub>-C(NH)-2,6-F<sub>2</sub>C<sub>6</sub>H<sub>3</sub>] (<b>10</b>), two unexpected C,N-coupling products (<b>12</b> and <b>13</b>) were obtained. It is believed that
these coupling reactions underwent activation of the N–H and
C–F bonds. The binuclear nickel complexes showed excellent
catalytic activity in the hydrosilylation of aldehydes. The mechanism
of the reaction was studied through stoichiometric reactions, and
the double-(η<sup>2</sup>-Si–H)–Ni<sup>II</sup> intermediate was detected by in situ <sup>1</sup>H NMR spectroscopy,
which may be the key point in the catalytic cycle
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