Understanding Structure Does Not Always Explain Reactivity:  A Phosphinoamide Anion Reacts as an Iminophosphide Anion

The aminophosphine C6H4(o-CN)NHPPh2, 1, containing an electron-withdrawing nitrile group, was prepared from the lithiation of 2-aminobenzonitrile followed by addition of Ph2PCl. Lithiation of 1 using n BuLi affords the anion [Ph2PN(Li)C6H4(o-CN)(thf)]2, 2. Compound 2 reacts with Ph2PCl or MeI to aff...

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Bibliographic Details
Published in:Inorganic chemistry 2003-03, Vol.42 (6), p.2125-2130
Main Authors: Fei, Zhaofu, Scopelliti, Rosario, Dyson, Paul J
Format: Article
Language:English
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Summary:The aminophosphine C6H4(o-CN)NHPPh2, 1, containing an electron-withdrawing nitrile group, was prepared from the lithiation of 2-aminobenzonitrile followed by addition of Ph2PCl. Lithiation of 1 using n BuLi affords the anion [Ph2PN(Li)C6H4(o-CN)(thf)]2, 2. Compound 2 reacts with Ph2PCl or MeI to afford C6H4(o-CN)NPPh2PPh2, 3, and [C6H4(o-CN)NPPh2(CH3)(LiI)(C2H5O)]2, 4, respectively. In these products new P−P and P−C bonds have been formed rather than N−P and N−C bonds. The structures of 1−4 have been determined by single-crystal X-ray diffraction analysis, and the synthetic results are discussed in terms of the structural data and NMR spectroscopic studies.
ISSN:0020-1669
1520-510X
DOI:10.1021/ic0262841