Endocyclic P-P bond cleavage in carbaborane-substituted 1,2-diphosphetane: a new route to secondary phosphinocarbaboranes |
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Authors: | Anika Kreienbrink Peter Lönnecke Matthias Findeisen Evamarie Hey-Hawkins |
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Institution: | Institut für Anorganische Chemie, Universit?t Leipzig, Johannisallee 29, 04103 Leipzig, Germany. hey@rz.uni-leipzig.de. |
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Abstract: | Carbaborane-substituted 1,2-diphosphetane reacts with elemental lithium and hydrogen chloride to give exclusively secondary mono- and bis(phosphino)carbaboranes. The latter reacts with two equivalents of formaldehyde and one equivalent of aniline to give a carbaborane-substituted 1-aza-3,6-diphosphepane. |
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