4.8 Article

Stable, Yet Highly Reactive Nonclassical Iron(II) Polyhydride Pincer Complexes: Z-Selective Dimerization and Hydroboration of Terminal Alkynes

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 139, Issue 24, Pages 8130-8133

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b05051

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Funding

  1. Austrian Science Fund (FWF) [P28866-N34]
  2. FCT, Portugal [UID/QUI/00100/2013, SFRH/BPD/86815/2012]
  3. Austrian Science Fund (FWF) [P28866] Funding Source: Austrian Science Fund (FWF)

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The synthesis, characterization, and catalytic activity of nonclassical iron(II) polyhydride complexes containing tridentate PNP pincer-type ligands is described. These compounds of the general formula [Fe(PNP)(H)(2)(eta(2)-H-2)] exhibit remarkable reactivity toward terminal alkynes. They efficiently promote the catalytic dimerization of aryl acetylenes giving the corresponding conjugated 1,3-enynes in excellent yields with low catalyst loadings. When the reaction is carried out in the presence of pinacolborane, vinyl boronates are obtained. Both reactions take place under mild conditions and are highly chemo-, regio-, and stereoselective with up to 99% Z-selectivity.

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