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Phone: (843) 588-2001
Edgar Allan Poe/Sullivan's Island Library
Closed for renovations
Phone: (843) 883-3914
West Ashley Library
9 a.m. – 7 p.m.
Phone: (843) 766-6635
Wando Mount Pleasant Library
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9 a.m. – 6 p.m.
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A metal–organic framework-supported dinuclear iron catalyst for hydroboration of carbonyl compounds.
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- Author(s): Zhu, Yi-Jie1 (AUTHOR); Wang, Jun-Jie2 (AUTHOR); Li, Jun-Yu3 (AUTHOR); Zhang, Teng4 (AUTHOR)
- Source:
Dalton Transactions: An International Journal of Inorganic Chemistry. 6/14/2023, Vol. 52 Issue 22, p7581-7589. 9p.- Subject Terms:
- Source:
- Additional Information
- Abstract: Preparation of catalytically active dinuclear transition metal complexes with an open coordination sphere is a challenging task because the metal sites tend to be "saturated" with excess donor atoms around during synthesis. By isolating the binding scaffolds with the metal–organic framework (MOF) skeleton and installing metal sites through post-synthetic modification, we succeed in constructing a MOF-supported metal catalyst, namely FICN-7-Fe2, with dinuclear Fe2 sites. FICN-7-Fe2 effectively catalyses the hydroboration of a broad range of ketone, aldehyde, and imine substrates with a low loading of 0.05 mol%. Remarkably, kinetic measurements showed that FICN-7-Fe2 is 15 times more active than its mononuclear counterpart FICN-7-Fe1, indicating that cooperative substrate activation on the two Fe centres significantly enhances the catalysis. [ABSTRACT FROM AUTHOR]
- Abstract: Copyright of Dalton Transactions: An International Journal of Inorganic Chemistry is the property of Royal Society of Chemistry and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Abstract:
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