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Updated: Sep 3, 2025

Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex
Published on: July 27, 2022
Rare-earth-metal half-sandwich complexes incorporating methyl, methylidene, and hydrido ligands
Dennis A Buschmann1, Lion Schumacher1, Reiner Anwander1
1Institut für Anorganische Chemie, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 18, 72076, Tübingen, Germany. reiner.anwander@uni-tuebingen.de.
Abstract:
Complexes Cp*3Ln3(μ2-CH3)3(μ3-CH2)(μ3-H)(thf)3 (Ln = Y, Dy; Cp* = C5Me5) are formed via elimination of CH4 and C2H4 from the respective trinuclear polymethyl complexes [Cp*Ln(μ2-CH3)2]3, involving the methyl/methylidene complex Cp*3Ln3(μ2-CH3)3(μ3-CH2)(μ3-CH3)(thf)2 as an intermediate. Compound Cp*3Y3(μ2-CH3)3(μ3-CH2)(μ3-H)(thf)3 displays "Schrock-type" nucleophilic carbene reactivity, converting ketones into the corresponding terminal alkenes. Treatment of Cp*3Y3(μ2-CH3)3(μ3-CH2)(μ3-H)(thf)3 with [D4]methanol proved accessibility of all small-group functionalities as indicated by the simultaneous formation of deuterated HD and deuterated methanes CH3D and CH2D2.
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