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Transformation of Nickelalactones to Methyl Acrylate: On the Way to a Catalytic Conversion of Carbon Dioxide
Author(s) -
Lee S. Y. Tina,
Cokoja Mirza,
Drees Markus,
Li Yang,
Mink János,
Herrmann Wolfgang A.,
Kühn Fritz E.
Publication year - 2011
Publication title -
chemsuschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.412
H-Index - 157
eISSN - 1864-564X
pISSN - 1864-5631
DOI - 10.1002/cssc.201000445
Subject(s) - methyl acrylate , methyl iodide , catalysis , carbon dioxide , chemistry , acrylate , transformation (genetics) , nickel , ethylene , combinatorial chemistry , organic chemistry , polymer , copolymer , biochemistry , gene
Mu‐nick: The methyl iodide‐mediated ring opening of nickelalactones, which can be formed by oxidative coupling of carbon dioxide and ethylene at Ni 0 complexes, induces β‐H elimination, producing methyl acrylate in yields of up to 56 %. This reaction is found to be very sensitive to the ligands coordinated to the central nickel atom.

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