4.7 Article

Diamondoid Phosphines - Selective Phosphorylation of Nanodiamonds

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 352, Issue 4, Pages 609-615

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.200900774

Keywords

diamondoids; nanodiamonds; phosphorylation; Sonogashira-Hagihara reaction; Suzuki-Miyaura reaction

Funding

  1. Deutsche Forschungsgemeinschaft
  2. Fonds der Chemischen Industrie

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The diamondoids (nanodiamonds) diamantane and triamantane were selectively converted into diorganophosphinic acid chlorides by reacting them with phosphorus trichloride under Friedel Crafts-like conditions. The di-diamondoid phosphinic acid chlorides were subsequently reduced with trichlorosilane to give the hitherto unknown corresponding di-diamondoid phosphines. These diamondoid phosphinic acid chlorides and phosphines are of great utility as starting materials in organo-element and coordination chemistry due to their extraordinary rigidity and steric bulk.

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