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Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of Phosphorus(I)
Published on: November 22, 2016
The formation of dimeric phosph(III)azane macrocycles [[P(mu-NtBu)]2.LL]2 [LL = organic spacer]
Felipe García1, Richard A Kowenicki, Istemi Kuzu
1Chemistry Department, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.
Abstract:
The dimeric macrocycles [[P(mu-NtBu)]2.LL]2 [LL = OCH2C(Me)2CH2O (1), 2,6-(NH)2C5H3N (2), 1,2-(NH)2C6H4(3)] have been obtained by the reactions of the appropriate diols and diamines (LLH2) with the dimeric phosph(III)azane [ClP(mu-NtBu)]2. Under different conditions the reaction of 1,2-(NH2)2C6H4 with [ClP(mu-NtBu)]2 gives the monomer [[P(mu-NtBu)]2.[1,2-(NH)2C6H4]] (4) (instead of the dimer 3). Contrary to the literature, the results illustrate that the formation of dimeric macrocycles is common in these reactions and dependent among other factors on the steric demands and length of the organic spacer (LL) as well as the reaction conditions.
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