Abstract

AbstractThe reaction between the heteroleptic metal carbonyl complex [W(CO)4(tmeda)] ((tmeda)=N,N,N′,N′‐Tetramethylethane‐1,2‐diamine) with [Si9]4− silicon Zintl clusters in presence of [2.2.2]crypt ([2.2.2]crypt=4,7,13,16,21,24‐Hexaoxa‐1,10‐diazabicyclo[8.8.8]‐hexacosane) in liquid ammonia yielded the compound [(K,Rb)@([2.2.2]crypt)]2(K,Rb)4[Si9W(CO)4] ⋅ 13.4 NH3. The compound was analyzed by single crystal X‐ray diffraction and crystallizes in the space group (a=11.48390(10) Å, b=19.7383(2) Å, c=19.8983(2) Å, α=112.5760(10)°, β=97.4210(10)°, γ=95.3760(10)°, V=4079.01(7) Å3). The compound represents the first group 6 carbonylate‐functionalized silicon Zintl cluster. The central moiety is composed of a tricapped trigonal prismatic nine‐atom silicon species which coordinates with the lone pair of one capping atom to the tungsten tetracarbonylate, forming a pseudo trigonal bipyramidal carbonylate cluster anion [Si9W(CO)4]6−. The chemical bonding in the new cluster entity is analyzed using theoretical calculations and subsequent analysis using QTAIM and NBO.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call