| Literature DB >> 34757730 |
Tim Görlich1, Daniel S Frost1, Nico Boback1, Nathan T Coles1, Birger Dittrich2, Peter Müller3, William D Jones4, Christian Müller1.
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.Entities:
Year: 2021 PMID: 34757730 DOI: 10.1021/jacs.1c07370
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419