Cross-dehydrocoupling: a novel synthetic route to P-B-P-B chains
Souvik Pandey1, Peter Lönnecke, Evamarie Hey-Hawkins
1Institut für Anorganische Chemie, Fakultät für Chemie und Mineralogie, Universität Leipzig , Johannisallee 29, 04103 Leipzig, Germany.
Abstract:
Transition-metal-catalyzed dehydrocoupling of tert-butylferrocenylphosphine-borane (2) with [{Rh(μ-Cl)(1,5-cod)}2] (cod = cyclooctadiene) as the catalyst gave the homocoupled product [Fc(tBu)(H)P(BH2)P(Fc)(tBu)(BH2X)] [3; Fc = Fe(C5H5)(C5H4), X = H/Cl], while cross-dehydrocoupling with the tertiary phosphine-boranes P(tBu)(nBu)2(BH3) (2a) and PPh(nBu)2(BH3) (2b) using [Rh(1,5-cod)2]OTf (OTf = trifluoromethanesulfonate) gave the first cross-dehydrocoupled products reported to date, [Fc(tBu)(BH3)P(BH2)P(tBu)(nBu)2] (4) and [Fc(tBu)(BH3)P(BH2)PPh(nBu)2] (5), in moderate yields. Compounds 2-5 were characterized by NMR spectroscopy ((1)H, (13)C, (31)P, and (11)B), IR spectroscopy, mass spectrometry, and single-crystal X-ray structure determination.
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