4.7 Article

Uniform distribution of post-synthetic linker exchange in metal-organic frameworks revealed by Rutherford backscattering spectrometry

Journal

CHEMICAL COMMUNICATIONS
Volume 53, Issue 48, Pages 6516-6519

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7cc02631e

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Funding

  1. Swiss National Science Foundation
  2. Swedish Research Council
  3. Swedish Energy Agency
  4. European Research Council [ERC-CoG2015-681895_MOFcat]
  5. Swedish Foundation for Strategic Research (SSF) [RIF-140053]

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Rutherford backscattering spectrometry (RBS) has been used for the first time to study post-synthetic linker exchange (PSE) in metal-organic frameworks. RBS is a non-invasive method to quantify the amount of introduced linker, as well as providing a means for depth profiling in order to identify the preferred localization of the introduced linker. The exchange of benzenedicarboxylate (bdc) by similarly sized 2-iodobenzenedicarboxylate (I-bdc) proceeds considerably slower than migration of I-dbc through the UiO-66 crystal. Consequently, the I-bdc is found evenly distributed throughout the UiO-66 samples, even at very short PSE exposure times.

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