Hydride Migration from a Triangular Face to a Tetrahedral Cavity in Tetranuclear Iron Carbonyl Clusters upon Coordination of [AuPPh3]+ Fragments1. (21st May 2014)

• Record Type: Journal Article
• Authors: Bortoluzzi, Marco; Ciabatti, Iacopo; Femoni, Cristina; Hayatifar, Mohammad; Iapalucci, Maria Carmela; Longoni, Giuliano; Zacchini, Stefano
• Is Part Of: Angewandte Chemie. Volume 126:Number 28(2014)
• Page Start: 7361
• Page End: 7365
• Publication Date: 2014-05-21
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201403538
• Languages: English
• ISSNs: 0044-8249

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Metal hydrides are of fundamental importance in chemistry, both as solid‐state materials and molecular compounds. The first low‐valent molecular metal cluster containing an interstitial four‐coordinate hydride in a tetrahedral site is decribed, which undergoes hydride migration from the surface to the tetrahedral cavity of the cluster upon coordination of a [AuPPh₃]⁺ fragment. The [HFe₄(CO)₁₂(AuPPh₃)₂]⁻ mono‐anion, which contains a surface μ₃‐H, was obtained from the reaction of [HFe₄(CO)₁₂]³⁻ with two equivalents of [Au(PPh₃)Cl]. This is, in turn, transformed into the neutral [HFe₄(CO)₁₂(AuPPh₃)₃] upon addition of a third [AuPPh₃]⁺ fragment, with concomitant migration of the unique hydride from the surface of the cluster to its tetrahedral cavity. All of these species have been fully characterized in solution by means of IR and multinuclear NMR spectroscopy, and in the solid state by single‐crystal X‐ray diffractometry.</p> </abstract>