Metal alkyls programmed to generate metal alkylidenes by α-H abstraction: prognosis from NMR chemical shift. Issue 7 (19th January 2018)

• Record Type: Journal Article
• Authors: Gordon, Christopher P.; Yamamoto, Keishi; Searles, Keith; Shirase, Satoru; Andersen, Richard A.; Eisenstein, Odile; Copéret, Christophe
• Is Part Of: Chemical science. Volume 9:Issue 7(2018)
• Page Start: 1912
• Page End: 1918
• Publication Date: 2018-01-19
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c7sc05039a
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : Chemical shift analysis predicts the ease of alkylidene formation from bis-alkyl d 0 complexes via α-H abstraction. Abstract : Metal alkylidenes, which are key organometallic intermediates in reactions such as olefination or alkene and alkane metathesis, are typically generated from metal dialkyl compounds [M](CH2 R)2 that show distinctively deshielded chemical shifts for their α-carbons. Experimental 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, interacting with the Cα p-orbital lying in the same plane. This π-type interaction inscribes some alkylidene character into Cα that favors alkylidene generation via α-H abstraction. The extent of the deshielding and the anisotropy of the alkyl chemical shift tensors distinguishes [M](CH2 R)2 compounds that form alkylidenes from those that do not, relating the reactivity to molecular orbitals of the respective molecules. The α-carbon chemical shifts and tensor orientations thus predict the reactivity of metal alkyl compounds towards alkylidene generation.