期刊
ACS CATALYSIS
卷 5, 期 12, 页码 7399-7414出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.5b01671
关键词
single-site catalysts; carbonyl hydroboration; zirconium hydride; interfacial catalysis; mesoporous silica; solid-state NMR
资金
- U.S. Department of Energy, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences [DE-AC02-07CH11358]
The hydroboration of aldehydes and ketones using a silica-supported zirconium catalyst is reported. Reaction of Zr(NMe2)(4) and mesoporous silica nanoparticles (MSN) provides the catalytic material Zr(NMe2)(5)@MSN. Exhaustive characterization of Zr(NMe2)(5)@MSN with solidstate (SS)NMR and infrared spectroscopy, as well as through reactivity studies, suggests its surface structure is primarily an SiOZr(NMe2)(3). The presence of these nitrogen-containing zirconium sites is supported by I5N NMR spectroscopy, including natural abundance '5N NMR measurements using dynamic nuclear polarization (DNP) SSNMR. The Zr(NMe2)(5)@MSN material reacts with pinacolborane (HBpin) to provide Me(2)NBpin and the material ZrH/Bpin@MSN that is composed of interacting surface-bonded zirconium hydride and surface-bonded borane =-SiOBpin moieties in an approximately 1:1 ratio, as well as zirconium sites coordinated by dimethylamine. The ZrH/Bpin@MSN is characterized by 'H/H-2 and HB SSNMR and infrared spectroscopy and through its reactivity with D-2. The zirconium hydride material or the zirconium amide precursor Zr(NMe2)(5)@MSN catalyzes the selective hydroboration of aldehydes and ketones with HBpin in the presence of functional groups that are often reduced under hydroboration conditions or are sensitive to metal hydrides, including olefins, alkynes, nitro groups, halides, and ethers. Remarkably, this catalytic material may be recycled without loss of activity at least eight times, and air-exposed materials are catalytically active. Thus, these supported zirconium centers are robust catalytic sites for carbonyl reduction and that surface-supported, catalytically reactive zirconium hydride may be generated from zirconium-amide or zirconium alkoxide sites.
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