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Single-Crystal to Single-Crystal Addition of H2 to [Ir(iPr-PONOP)(propene)][BArF 4] and Comparison Between Solid-State and Solution Reactivity.


ABSTRACT: The reactivity of the Ir(I) PONOP pincer complex [Ir(iPr-PONOP)(η2-propene)][BArF 4], 6, [iPr-PONOP = 2,6-(iPr2PO)2C6H3N, ArF = 3,5-(CF3)2C6H3] was studied in solution and the solid state, both experimentally, using molecular density functional theory (DFT) and periodic-DFT computational methods, as well as in situ single-crystal to single-crystal (SC-SC) techniques. Complex 6 is synthesized in solution from sequential addition of H2 and propene, and then the application of vacuum, to [Ir(iPr-PONOP)(η2-COD)][BArF 4], 1, a reaction manifold that proceeds via the Ir(III) dihydrogen/dihydride complex [Ir(iPr-PONOP)(H2)H2][BArF 4], 2, and the Ir(III) dihydride propene complex [Ir(iPr-PONOP)(η2-propene)H2][BArF 4], 7, respectively. In solution (CD2Cl2) 6 undergoes rapid reaction with H2 to form dihydride 7 and then a slow (3 d) onward reaction to give dihydrogen/dihydride 2 and propane. DFT calculations on the molecular cation in solution support this slow, but productive, reaction, with a calculated barrier to rate-limiting propene migratory insertion of 24.8 kcal/mol. In the solid state single-crystals of 6 also form complex 7 on addition of H2 in an SC-SC reaction, but unlike in solution the onward reaction (i.e., insertion) does not occur, as confirmed by labeling studies using D2. The solid-state structure of 7 reveals that, on addition of H2 to 6, the PONOP ligand moves by 90° within a cavity of [BArF 4]- anions rather than the alkene moving. Periodic DFT calculations support the higher barrier to insertion in the solid state (ΔG = 26.0 kcal/mol), demonstrating that the single-crystal environment gates onward reactivity compared to solution. H2 addition to 6 to form 7 is reversible in both solution and the solid state, but in the latter crystallinity is lost. A rare example of a sigma amine-borane pincer complex, [Ir(iPr-PONOP)H21-H3B·NMe3)][BArF 4], 5, is also reported as part of these studies.

SUBMITTER: Royle CG 

PROVIDER: S-EPMC9709992 | biostudies-literature | 2022 Nov

REPOSITORIES: biostudies-literature

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Single-Crystal to Single-Crystal Addition of H<sub>2</sub> to [Ir(<sup>i</sup>Pr-PONOP)(propene)][BAr<sup>F</sup> <sub>4</sub>] and Comparison Between Solid-State and Solution Reactivity.

Royle Cameron G CG   Sotorrios Lia L   Gyton Matthew R MR   Brodie Claire N CN   Burnage Arron L AL   Furfari Samantha K SK   Marini Anna A   Warren Mark R MR   Macgregor Stuart A SA   Weller Andrew S AS  

Organometallics 20220726 22


The reactivity of the Ir(I) PONOP pincer complex [Ir(<sup>i</sup>Pr-PONOP)(η<sup>2</sup>-propene)][BAr<sup>F</sup> <sub>4</sub>], <b>6</b>, [<sup>i</sup>Pr-PONOP = 2,6-(<sup>i</sup>Pr<sub>2</sub>PO)<sub>2</sub>C<sub>6</sub>H<sub>3</sub>N, Ar<sup>F</sup> = 3,5-(CF<sub>3</sub>)<sub>2</sub>C<sub>6</sub>H<sub>3</sub>] was studied in solution and the solid state, both experimentally, using molecular density functional theory (DFT) and periodic-DFT computational methods, as well as in situ single-crys  ...[more]

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