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Density functional theory calculations modelling selective exo-H/D exchange observed in the Rh σ-alkane complex [(Cy2PCH2CH2PCy2)Rh(η2:η2-endo-NBA)][BArF4], [1-NBA][BArF4], are reported, where ArF=3,5-C6H3(CF3)2 and NBA=norbornane, C7H12. Two models were considered 1) an isolated molecular cation, [1-NBA]+ and 2) a full model in which [1-NBA][BArF4] is treated in the solid state through periodic DFT. After an initial endo-exo rearrangement, both models predict H/D exchange to proceed through D2 addition and oxidative cleavage followed by a rate-limiting C−H activation of the norbornane through a σ-CAM step to form a [1-Rh(D)(η2-HD)(norbornyl)]+ intermediate. HD rotation followed by a σ-CAM C−D bond formation, HD reductive coupling and HD loss then complete the H/D exchange process. exo-H/D exchange is facilitated by a supporting agostic interaction and is consistently more accessible kinetically than the potentially competing endo-H/D exchange (isolated cation: ΔG≠exo=+15.9 kcal/mol, ΔG≠endo=+18.4 kcal/mol; solid state: ΔG≠exo=+22.1 kcal/mol, ΔG≠endo=+25.1 kcal/mol). The solid-state environment has a significant impact on the computed energetics, with barriers increasing by ca. 7 kcal/mol, while only the solid-state model correctly predicts the endo-bound NBA complex to be the resting state of the system. These outcomes reflect solid-state confinement effects within the pocket occupied by the [1-NBA]+ cation and defined by the pseudo-octahedral array of neighbouring [BArF4]− anions. The asymmetry of the solid-state environment also requires a second H/D exchange pathway to be defined to account for reaction at all four exo-C−H bonds. These entail slightly higher barriers (ΔG≠exo=. +24.8 kcal/mol, ΔG≠endo=+27.5 kcal/mol) but retain a distinct preference for exo- over endo-H/D exchange.
|Number of pages||13|
|Journal||HELVETICA CHIMICA ACTA|
|Early online date||31 Jan 2023|
|Publication status||Published - 1 Feb 2023|
Bibliographical noteFunding Information:
The EPSRC for funding through awards EP/K035908/1, EP/K035681/1 and EP/M024210/1.
© 2022 The Authors. Helvetica Chimica Acta published by Wiley-VHCA AG, Zurich, Switzerland.
- C−H activation
- density functional theory calculations
- H/D exchange
- σ-alkane complexes
- 1 Finished
Putting Low Coordination into Practice by the Exploration of Metal-sigma-Interactions: Fundamentals, New Catalysts and Catalysis for New Materials
1/01/20 → 31/03/22
Project: Research project (funded) › Research