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Keishi Yamamoto

Researcher at ETH Zurich

Publications -  9
Citations -  463

Keishi Yamamoto is an academic researcher from ETH Zurich. The author has contributed to research in topics: Chemical shift & Organosilicon. The author has an hindex of 8, co-authored 9 publications receiving 345 citations.

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Bridging the Gap between Industrial and Well-Defined Supported Catalysts

TL;DR: This Review discusses how surface organometallic chemistry (SOMC) engineers surface sites with well-defined structures and provides insight into the nature of the active sites of industrial catalysts; the Review focuses in particular on olefin production and conversion processes.
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Metathesis Activity Encoded in the Metallacyclobutane Carbon-13 NMR Chemical Shift Tensors

TL;DR: In the metathesis active metallacyclobutanes, the α-carbons retain some residual alkylidene character, while their β-carbon is shielded, especially in the direction perpendicular to the ring.
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Orbital Analysis of Carbon-13 Chemical Shift Tensors Reveals Patterns to Distinguish Fischer and Schrock Carbenes.

TL;DR: Orbital analysis of the principal components of the chemical shift tensors determined by solid-state NMR spectroscopy and calculated by a 2-component DFT method shows specific patterns that act as fingerprints for each type of complex.
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Metal alkyls programmed to generate metal alkylidenes by α-H abstraction: prognosis from NMR chemical shift.

TL;DR: In this article, solid-state NMR measurements combined with DFT/ZORA calculations and a chemical shift tensor analysis reveal that this remarkable deshielding originates from an empty metal d-orbital oriented in the M −Cα-Cα′ plane.
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NMR chemical shift analysis decodes olefin oligo- and polymerization activity of d0 group 4 metal complexes.

TL;DR: It is shown by a combined experimental and computational study that the 13C NMR chemical shift tensors of the α-carbon of metal alkyls that undergo olefin insertion signal the presence of partial alkylidene character in the metal–carbon bond, which facilitates this reaction.