Journal
ADVANCED SYNTHESIS & CATALYSIS
Volume 352, Issue 4, Pages 609-615Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.200900774
Keywords
diamondoids; nanodiamonds; phosphorylation; Sonogashira-Hagihara reaction; Suzuki-Miyaura reaction
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Funding
- Deutsche Forschungsgemeinschaft
- 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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