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Structures of cationic di-iridium complexes derived from (η<sup>5</sup>-C<sub>5</sub>Me<sub>5</sub>)Ir(CO)<sub>2</sub>, including the dication [(η<sup>5</sup>-C<sub>5</sub>Me<sub>5</sub>)(CO)<sub>2</sub>Ir–Ir(CO)<sub>2</sub>(η<sup>5</sup>-C<sub>5</sub>Me<sub>5</sub>)]<sup>2+</sup>and the bridging methylenetetramethylcyclopentadienyl (tetramethylfulvene) complex [(η<sup>5</sup>-C<sub>5</sub>Me<sub>5</sub>)(CO)Ir–Ir;(CO)<sub>2</sub>(η<sup>5</sup>-CH<sub>2</sub>C<sub>5</sub>Me<sub>4</sub>)]<sup>+</sup>
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1989
Year
(η5-C5Me5)Ir(CO)2(1) reacts with Ph3C+ to give the dinuclear dication [(η5-C5Me5)(CO)2Ir–Ir(CO)2(η5-C5Me5)]2+(4) and with (η5-C5Me5)Ir(CO)Cl2 in presence of one equivalent of Ag+ to give [(η5- C5Me5)(CO)(Cl)Ir–Ir(CO)2(η5-C5Me5)]+(2); both (2) and (4) may be converted to the complex [(η5-C5Me5)(CO)[graphic omitted]H2C5Me4)]+(3) containing a rare bridging methylenetetramethylcyclopentadienyl (tetramethylfulvene) ligand.