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Quo vadis niobium? Divergent coordination behavior of early-transition metals towards MOF-5.


ABSTRACT: Treatment of MOF-5 with NbCl4(THF)2 in acetonitrile leads to incorporation of Nb(iv) centers in a fashion that diverges from the established cation metathesis reactivity of this iconic material. A combination of X-ray absorption spectroscopy analysis and reactivity studies altogether supported by density functional theory computational studies document an unprecedented binding mode for the Zn4O(O2C-)6 secondary building units (SBUs), which in Nb(iv)-MOF-5 function as ? 2-chelating ligands for NbCl4 moieties, with no exchange of Zn2+ observed. This unusual reactivity expands the portfolio of post-synthetic modification techniques available for MOFs, exemplified here by MOF-5, and underscores the diverse coordination environments offered by this and potentially other MOFs towards heterometal species.

SUBMITTER: Korzynski MD 

PROVIDER: S-EPMC6566296 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

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<i>Quo vadis niobium</i>? Divergent coordination behavior of early-transition metals towards MOF-5.

Korzyński Maciej D MD   Braglia Luca L   Borfecchia Elisa E   Lomachenko Kirill A KA   Baldansuren Amgalanbaatar A   Hendon Christopher H CH   Lamberti Carlo C   Dincă Mircea M  

Chemical science 20190509 23


Treatment of MOF-5 with NbCl<sub>4</sub>(THF)<sub>2</sub> in acetonitrile leads to incorporation of Nb(iv) centers in a fashion that diverges from the established cation metathesis reactivity of this iconic material. A combination of X-ray absorption spectroscopy analysis and reactivity studies altogether supported by density functional theory computational studies document an unprecedented binding mode for the Zn<sub>4</sub>O(O<sub>2</sub>C-)<sub>6</sub> secondary building units (SBUs), which i  ...[more]

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