Görlich, Tim, Frost, Daniel S., Boback, Nico, Coles, Nathan T. ![]() |
Official URL: https://doi.org/10.1021/jacs.1c07370
Abstract
The photochemical activation of the C(sp)–C(sp2) bond in Pt(0)-η2-aryl-phosphaalkyne complexes leads selectively to coordination compounds of the type LnPt(aryl)(C≡P). The oxidative addition reaction is a novel, clean, and atom-economic route for the synthesis of reactive terminal Pt(II)-cyaphido complexes, which can undergo [3 + 2] cycloaddition reactions with organic azides, yielding the corresponding Pt(II)-triazaphospholato complexes. The C–C bond cleavage reaction is thermodynamically uphill. Upon heating, the reverse and quantitative reductive elimination toward the Pt(0)-phosphaalkyne-π-complex is observed.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Chemistry |
Publisher: | American Chemical Society |
ISSN: | 0002-7863 |
Last Modified: | 12 Nov 2024 15:30 |
URI: | https://orca.cardiff.ac.uk/id/eprint/173580 |
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