ORCID Profile
0000-0002-5854-6909
Current Organisation
Dalian University of Technology
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Publisher: MDPI AG
Date: 19-08-2021
Abstract: Guaiacol is a typical model compound used to investigate and understand the hydrodeoxygenation behaviour of bio-oils, which is critical to their application as an alternative to fossil resources. While extensive research has been carried out on developing catalysts for guaiacol hydrodeoxygenation, the true active sites in these catalysts are often illusive. This study investigated the effect of Au-loading on the catalytic activity of NiTiO3 for the hydrodeoxygenation of guaiacol. It showed that metallic Ni formed by the partial reduction in NiTiO3 was responsible for its catalytic activity. Au-loading in NiTiO3 effectively reduces the temperature required for the NiTiO3 reduction from 400 °C to 300 °C. Consequently, at an Au-loading of 0.86 wt%, the 0.86 Au/NiTiO3-300 °C catalyst was found to deliver a guaiacol conversion of ~32%, more than 6 times higher than that of the pure NiTiO3-300 °C catalyst.
Publisher: American Chemical Society (ACS)
Date: 29-08-2017
DOI: 10.1021/JACS.7B06841
Abstract: Molecular catalysts offer tremendous advantages for stereoselective polymerization because their activity and selectivity can be optimized and understood mechanistically using the familiar tools of organometallic chemistry. Yet, this exquisite control over selectivity comes at an operational price that is generally not justifiable for the large-scale manufacture of polyfolefins. In this report, we identify Co-MFU-4l, prepared by cation exchange in a metal-organic framework, as a solid catalyst for the polymerization of 1,3-butadiene with high stereoselectivity (>99% 1,4-cis). To our knowledge, this is the highest stereoselectivity achieved with a heterogeneous catalyst for this transformation. The polymer's low polydispersity (PDI ≈ 2) and the catalyst's ready recovery and low leaching indicate that our material is a structurally resilient single-site heterogeneous catalyst. Further characterization of Co-MFU-4l by X-ray absorption spectroscopy provided evidence for discrete, tris-pyrazolylborate-like coordination of Co(II). With this information, we identify a soluble cobalt complex that mimics the structure and reactivity of Co-MFU-4l, thus providing a well-defined platform for studying the catalytic mechanism in the solution phase. This work underscores the capacity for small molecule-like tunability and mechanistic tractability available to transition metal catalysis in metal-organic frameworks.
Publisher: Elsevier BV
Date: 12-2018
Publisher: American Chemical Society (ACS)
Date: 25-04-2017
No related grants have been discovered for Guanghui Zhang.