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Homogeneous CO Hydrogenation: Ligand Effects on the Lewis Acid ...

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Figure S119. 31 P{ 1 H} NMR.<br />

Reacti<strong>on</strong> of [1-P 2][BF 4] with 2 equiv [HPt][PF 6].<br />

19.3 mg (0.017 mmol) [1-P 2][BF 4], 22.9 mg (0.0357 mmol, 2 equiv) [HPt] + , 4.5 mg (0.017<br />

mmol) 18-crown-6, and 2.9 mg (0.017 mg) NaPF 6 were added to a small vial, and dissolved in<br />

C 6D 5Cl. The mixture was transferred to a J-Young NMR tube, and <strong>the</strong> reacti<strong>on</strong> was m<strong>on</strong>itored by<br />

1 H and 31 P NMR. After initial formati<strong>on</strong> of carbene 2-P2, no fur<strong>the</strong>r reducti<strong>on</strong> was observed over<br />

3 days. The crown e<strong>the</strong>r and NaPF 6 were added in an attempt to favor formati<strong>on</strong> of soluble<br />

coupled products. In a separate experiment, <strong>on</strong>ly cati<strong>on</strong> [1-P 2][BF 4] and 2 equiv [HPt] + were<br />

mixed, and <strong>the</strong> same results were observed.<br />

S105

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