A geminal antimony(<sc>iii</sc>)/phosphorus(<sc>iii</sc>) frustrated Lewis pair

被引:6
|
作者
Krieft, Jonas [1 ]
Trapp, Pia C. [1 ]
Vishnevskiy, Yury V. [1 ]
Neumann, Beate [1 ]
Stammler, Hans-Georg [1 ]
Lamm, Jan-Hendrik [1 ]
Mitzel, Norbert W. [1 ]
机构
[1] Bielefeld Univ, Fac Chem, Chair Inorgan & Struct Chem, Ctr Mol Mat CM2, Univ Str 25, D-33615 Bielefeld, Germany
关键词
HYDROGEN-EXCHANGE; SUPER ACIDS; C-H; COMPLEXATION; DERIVATIVES; CHEMISTRY; POLYCONDENSATION; INTERMEDIACY; PROTONATION; ACTIVATION;
D O I
10.1039/d4sc02785j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The geminal Lewis pair (F5C2)(2)SbCH2P(tBu)(2) (1) was prepared by reacting (F5C2)(2)SbCl with LiCH2P(tBu)(2). Despite its extremely electronegative pentafluoroethyl substituents, the neutral 1 exhibits a relatively soft acidic antimony function according to the HSAB concept (hard-soft acid-base). These properties lead to a reversibility in the binding of CS2 to 1, as observed by VT-NMR spectroscopy, while no reaction with CO2 is observed. The reaction behaviour towards heterocumulenes and the specific interaction situation in the CS2 adduct were analysed by quantum chemical calculations. The FLP-type reactivity of 1 has also been demonstrated by reaction with a variety of small molecules (SO2, PhNCO, PhNCS, (MePh2P)AuCl). The reactions of 1 with PhNCO and PhNCS led to different types of cyclic addition products: PhNCO adds with its N-C bond and PhNCS adds preferentially with its CS bond. The reaction of 1 with (MePh2P)AuCl gave an adduct {[(F5C2)(2)SbCH2(tBu)(2)P](2)Au}(+) with a clamp-like structure binding a chloride anion by its two antimony atoms in chelate mode. Compound 1 and its adducts have been characterised by X-ray diffraction experiments, multinuclear NMR spectroscopy, elemental analyses and computational calculations (DFT, QTAIM, IQA).
引用
收藏
页码:12118 / 12125
页数:8
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