[1-H2N-CB11F11]- -: Synthesis and reactions of a functionalized fluorinated carbadodecaborate anion

被引:27
|
作者
Finze, Maik
Reiss, Guido J.
Zahres, Manfred
机构
[1] Univ Dusseldorf, Inst Anorgan Chem & Strukturchem 2, D-40225 Dusseldorf, Germany
[2] Univ Duisburg Essen, Inst Phys Chem, D-45141 Essen, Germany
关键词
D O I
10.1021/ic701398u
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In anhydrous hydrogen fluoride, K[1-H2N-CB11H11] is fluorinated with elemental fluorine to produce K[(1)-H2N-CB11H11]. Under strong alkaline conditions, two fluorine atoms of the [1-H2N-CB11F11](-) anion are regioselectively exchanged, yielding the [1-H2N-4,6-(HO)(2)-CB11F9](-) anion via [1-H2N-6-HO-CB11F10](-) as an intermediate. Both hydroxycarborate anions were isolated as [Ph4P](+) salts. All of the species were characterized by IR, Raman, and multi-NMR spectroscopy, thermal analysis (DSC) as well as by mass spectrometry (MALDI). The assignment of the NMR signals was supported by DFT calculations. Solid-state structures of K[1-H2N-CB11F11], [BzPh(3)P][1-H2N-CB11F11], [Ph4P][1-H2N-4,6-(HO)(2)-CB11F9], [Ph4P][1-H2N-6-HO-CB11F10], and [BzPh(3)P][1-H2N-CB11H11] were determined by single-crystal X-ray diffraction.
引用
收藏
页码:9873 / 9883
页数:11
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