Dialing in single-site reactivity of a supported calixarene-protected tetrairidium cluster catalyst
Author:
Affiliation:
1. Department of Chemical Engineering
2. University of California at Davis
3. Davis
4. USA
5. Department of Chemical and Biomolecular Engineering
6. University of California at Berkeley
7. Berkeley
Abstract
A closed Ir4 carbonyl cluster, 1, comprising a tetrahedral metal frame and three tert-butyl-calix[4]arene(OPr)3(OCH2PPh2) (Ph = phenyl; Pr = propyl) ligands at the basal plane, was silica supported and consists of “*” and “S” sites, which could be dialed in selectively for controlling ethylene hydrogenation catalysis.
Funder
Basic Energy Sciences
Chevron
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/SC/C7SC00686A
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1. Remotely Bonded Bridging Dioxygen Ligands Enhance Hydrogen Transfer in a Silica-Supported Tetrairidium Cluster Catalyst;Journal of the American Chemical Society;2024-02-01
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