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Reactions of Indene and Indoles with Platinum Methyl Cations: Indene C-H Activation, Indole ? vs. Nitrogen Lone-Pair Coordination.


ABSTRACT: Reactions of indene and various substituted indoles with [(diimine)PtII(Me)(TFE)]+ cations have been studied (diimine = ArN = C(Me) - C(Me) = NAr; TFE = 2,2,2-trifluoroethanol). Indene displaces the TFE ligand from platinum to form a stable ? coordination complex that, upon heating, undergoes C-H activation with first order kinetics, ?H‡ = 29 kcal/mol, ?S‡ = 10 eu, and a kinetic isotope effect of 1.1 at 60 °C. Indoles also initially form coordination complexes through the C2=C3 olefin, but these undergo rearrangement to the corresponding N-bound complexes. The relative rates of initial coordination and rearrangement are affected by excess acid or methyl substitution on indole.

SUBMITTER: Williams TJ 

PROVIDER: S-EPMC4833004 | biostudies-literature | 2007

REPOSITORIES: biostudies-literature

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Reactions of Indene and Indoles with Platinum Methyl Cations: Indene C-H Activation, Indole π <i>vs.</i> Nitrogen Lone-Pair Coordination.

Williams Travis J TJ   Labinger Jay A JA   Bercaw John E JE  

Organometallics 20070101 2


Reactions of indene and various substituted indoles with [(diimine)Pt<sup>II</sup>(Me)(TFE)]<sup>+</sup> cations have been studied (diimine = ArN = C(Me) - C(Me) = NAr; TFE = 2,2,2-trifluoroethanol). Indene displaces the TFE ligand from platinum to form a stable π coordination complex that, upon heating, undergoes C-H activation with first order kinetics, <i>ΔH</i><sup>‡</sup> = 29 kcal/mol, <i>ΔS</i><sup>‡</sup> = 10 eu, and a kinetic isotope effect of 1.1 at 60 °C. Indoles also initially form  ...[more]

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