Heterogeneous heck coupling in multivariate metal-organic frameworks for 
enhanced selectivity.

Brown, J. W.; Jarenwattananon, N. N.; Otto, T.; Wang, J. L.; Glöggler, S.; .Bouchard, L. S.

doi:10.1016/j.catcom.2015.03.005

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Heterogeneous heck coupling in multivariate metal-organic frameworks for enhanced selectivity.

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Glöggler, S.
Research Group of NMR Signal Enhancement, MPI for Biophysical Chemistry, Max Planck Society;

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Citation

Brown, J. W., Jarenwattananon, N. N., Otto, T., Wang, J. L., Glöggler, S., &.Bouchard, L. S. (2015). Heterogeneous heck coupling in multivariate metal-organic frameworks for enhanced selectivity. Catalysis Communications, 65, 105-107. doi:10.1016/j.catcom.2015.03.005.

Cite as: https://hdl.handle.net/21.11116/0000-0000-2B25-7

Abstract

Highly selective heterogeneous Heck coupling has been demonstrated inside a series of metal–organic frameworks (MOFs). These MOFs, Zn4O(BDC-NH2)n(BDC)(3 − n) (n = 3, 2.4, 1.8, 1.2, 0.9, 0.75, 0.6, 0.3, and 0.15), have been synthesized with different amounts of 1,4-benzenedicarboxylate (BDC) and 2-amino-1,4-benzenedicarboxylate (BDC-NH2) incorporated into their structure. The BDC-NH2 is functionalized by covalent postmodification with salicylic aldehyde for binding catalytically active Pd(II) ions. The catalytic activity of the embedded Pd(II) ions was tested via heterogeneous Heck coupling to produce resveratrol trimethyl ether, a pharmaceutically relevant precursor. It is also found during catalytic testing that a trade-off exists between amount of metalation and pore blocking.