Functionalization of P4 using a lewis acid stabilized bicyclo-[1.1.0]tetraphosphabutane anion

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Access status: Embargo until 2050-01-01 , 12836_ftp.pdf (436.64 KB)

Publication date

2014-01-01

Authors

Borger, Jaap E.
Ehlers, Andreas W.
Lutz, M.ORCID 0000-0003-1524-9629ISNI 0000000352600916
Slootweg, Jack C.ISNI 0000000389137347
Lammertsma, Koop

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Abstract

Reacting white phosphorus (P4) with sterically encumbered aryl lithium reagents (aryl=2,6-dimesitylphenyl or 2,4,6-tBu3C6H2) and B(C6F5)3 gives the unique, isolable Lewis acid stabilized bicyclo[1.1.0]tetraphosphabutane anion. Subsequent alkylation of the nucleophilic site of the RP4 anion gives access to non-symmetrical disubstituted bicyclic tetraphosphorus compounds. This novel method enables PC bond formation in a controlled fashion using white phosphorus as starting material.

Keywords

Alkali metals, Anions, Nucleophilic addition, Phosphorus, White phosphorus, General Chemistry, Catalysis

Citation

Borger, J E, Ehlers, A W, Lutz, M, Slootweg, J & Lammertsma, K 2014, 'Functionalization of P4 using a lewis acid stabilized bicyclo-[1.1.0]tetraphosphabutane anion', Angewandte Chemie - International Edition, vol. 53, no. 47, pp. 12836-12839. https://doi.org/10.1002/anie.201405879, https://doi.org/10.1002/ange.201405879