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Tuning Pd-nanoparticle@MIL-101(Cr) Catalysts for Tandem Reductive Amination.


ABSTRACT: Abstract:The versatility of MOFs as highly porous Lewis acidic supports for precious metal nanoparticles has been exploited for one-pot tandem reductive amination catalysis. MIL-101(Cr) loaded with Pd nanoparticles ca. 3 nm in size at 0.2-1 wt% has been used to catalyse the reaction of 4'-fluoroacetophenone with benzylamine under 10 bar of H2 to give the secondary amine, 4'-fluoro-?-methyl-N-phenylmethylbenzenemethanamine. For the highest Pd loading, major hydrogenolysis of the secondary amine occurs in a second tandem reaction, but by changing the ratio of Pd to Lewis acidic Cr3+ active sites it is possible to tune the catalytic selectivity to the desired 2° amine product. An empirical kinetic analysis was performed to demonstrate this active site complementarity. Graphical Abstract:

SUBMITTER: Anderson AE 

PROVIDER: S-EPMC6566290 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature

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Tuning Pd-nanoparticle@MIL-101(Cr) Catalysts for Tandem Reductive Amination.

Anderson Amanda E AE   Baddeley Christopher J CJ   Wright Paul A PA  

Catalysis letters 20171127 1


<h4>Abstract</h4>The versatility of MOFs as highly porous Lewis acidic supports for precious metal nanoparticles has been exploited for one-pot tandem reductive amination catalysis. MIL-101(Cr) loaded with Pd nanoparticles ca. 3 nm in size at 0.2-1 wt% has been used to catalyse the reaction of 4'-fluoroacetophenone with benzylamine under 10 bar of H<sub>2</sub> to give the secondary amine, 4'-fluoro-α-methyl-<i>N</i>-phenylmethylbenzenemethanamine. For the highest Pd loading, major hydrogenolysi  ...[more]

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