Mixed-Valence Iron Complexes Containing End-On Bridging Cyaphide Ions

Iron cyanide compounds are among the oldest known synthetic coordination compounds, dating back to the early 18<sup>th</sup> century. By contrast, iron complexes of the cyaphide ion (C≡P<sup>-</sup>)─a heavy valence isoelectronic analog of the cyanide ion─are unknown. Herein we report the synthesis of highly stable mono- and bis-cyaphide complexes of iron(II), namely Fe(depe)<sub>2</sub>(Cl)(CP) and Fe(depe)<sub>2</sub>(CP)<sub>2</sub> (depe = 1,2-bis(diethylphosphino)ethane). These iron(II) cyaphide complexes are capable of further coordination to iron(I) in a hitherto unknown linear coordination geometry, affording the conjugated multimetallic mixed-valence complexes [{Fe(depe)<sub>2</sub>}<sub>2</sub>(μ-CP)(N<sub>2</sub>)][BAr<sup>F</sup><sub>4</sub>]<sub>2</sub> and [{Fe(depe)<sub>2</sub>}<sub>3</sub>(μ-CP)<sub>2</sub>][OTf]<sub>2</sub>.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-10-08
DOI
https://doi.org/10.1021/jacs.4c11741
Citations
8
Primary Topic
Magnetism in coordination complexes
Type
article
Field-Weighted Citation Impact
0.94

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article

Mixed-Valence Iron Complexes Containing End-On Bridging Cyaphide Ions

Christine M. Thomas, José M. Goicoechea, Álvaro García‐Romero, Chenyang Hu et al.
8 citations
Journal of the American Chemical Society
Magnetism in coordination complexes
0.94
article

Mixed-Valence Iron Complexes Containing End-On Bridging Cyaphide Ions

Christine M. Thomas, José M. Goicoechea, Álvaro García‐Romero, Chenyang Hu, Eric S. Yang, Jess Fletcher
article en
8 citations

Abstract

Iron cyanide compounds are among the oldest known synthetic coordination compounds, dating back to the early 18<sup>th</sup> century. By contrast, iron complexes of the cyaphide ion (C≡P<sup>-</sup>)─a heavy valence isoelectronic analog of the cyanide ion─are unknown. Herein we report the synthesis of highly stable mono- and bis-cyaphide complexes of iron(II), namely Fe(depe)<sub>2</sub>(Cl)(CP) and Fe(depe)<sub>2</sub>(CP)<sub>2</sub> (depe = 1,2-bis(diethylphosphino)ethane). These iron(II) cyaphide complexes are capable of further coordination to iron(I) in a hitherto unknown linear coordination geometry, affording the conjugated multimetallic mixed-valence complexes [{Fe(depe)<sub>2</sub>}<sub>2</sub>(μ-CP)(N<sub>2</sub>)][BAr<sup>F</sup><sub>4</sub>]<sub>2</sub> and [{Fe(depe)<sub>2</sub>}<sub>3</sub>(μ-CP)<sub>2</sub>][OTf]<sub>2</sub>.

Journal of the American Chemical SocietyVol. 146(42)
Mansfield University (US), Oxford Research Group (GB), University of Oxford (GB), Indiana University Bloomington (US), The Ohio State University (US)
National Science Foundation, Ohio State University, Engineering and Physical Sciences Research Council
Openalex Percentile: Top 28%
Magnetism in coordination complexes
0.94
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