TY - JOUR
T1 - Brønsted Acid Promoted Reduction of Tertiary Phosphine Oxides
AU - Krachko, Tetiana
AU - Lyaskovskyy, Volodymyr
AU - Lutz, Martin
AU - Lammertsma, Koop
AU - Slootweg, J. Chris
N1 - Publisher Copyright:
© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2017/8/3
Y1 - 2017/8/3
N2 - Recently, Brønsted acids, such as phosphoric acids, carboxylic acids, and triflic acid, were found to catalyze the reduction of phosphine oxides to the corresponding phosphines. In this study, we fully characterize the HCl, HOTf, and Me2SiHOTf adducts of triphenylphosphine oxide and find that the thermally stable adduct Ph3POH+OTf– is efficiently converted into triphenylphosphine at 100 °C in the presence of readily available hydrosiloxanes. Under the same reaction conditions, also Ph3POSiMe2H+OTf– selectively affords triphenylphosphine indicating that silylated phosphine oxides are likely intermediates in this process.
AB - Recently, Brønsted acids, such as phosphoric acids, carboxylic acids, and triflic acid, were found to catalyze the reduction of phosphine oxides to the corresponding phosphines. In this study, we fully characterize the HCl, HOTf, and Me2SiHOTf adducts of triphenylphosphine oxide and find that the thermally stable adduct Ph3POH+OTf– is efficiently converted into triphenylphosphine at 100 °C in the presence of readily available hydrosiloxanes. Under the same reaction conditions, also Ph3POSiMe2H+OTf– selectively affords triphenylphosphine indicating that silylated phosphine oxides are likely intermediates in this process.
KW - 1,1,3,3-Tetramethyldisiloxane
KW - Brønsted acid
KW - Poly(methylhydrosiloxane)
KW - Reduction
KW - Triphenylphosphine oxide
UR - http://www.scopus.com/inward/record.url?scp=85020421283&partnerID=8YFLogxK
U2 - 10.1002/zaac.201700125
DO - 10.1002/zaac.201700125
M3 - Article
AN - SCOPUS:85020421283
SN - 0044-2313
VL - 643
SP - 916
EP - 921
JO - Zeitschrift fur Anorganische und Allgemeine Chemie
JF - Zeitschrift fur Anorganische und Allgemeine Chemie
IS - 14
ER -