TY - JOUR
T1 - Homo- and heterodehydrocoupling of phosphines mediated by alkali metal catalysts
AU - Wu, Lipeng
AU - Annibale, Vincent T.
AU - Jiao, Haijun
AU - Brookfield, Adam
AU - Collison, David
AU - Manners, Ian
PY - 2019/6/26
Y1 - 2019/6/26
N2 - Catalytic chemistry that involves the activation and transformation of main group substrates is relatively undeveloped and current examples are generally mediated by expensive transition metal species. Herein, we describe the use of inexpensive and readily available tBuOK as a catalyst for P-P and P-E (E = O, S, or N) bond formation. Catalytic quantities of tBuOK in the presence of imine, azobenzene hydrogen acceptors, or a stoichiometric amount of tBuOK with hydrazobenzene, allow efficient homodehydrocoupling of phosphines under mild conditions (e.g. 25 °C and < 5 min). Further studies demonstrate that the hydrogen acceptors play an intimate mechanistic role. We also show that our tBuOK catalysed methodology is general for the heterodehydrocoupling of phosphines with alcohols, thiols and amines to generate a range of potentially useful products containing P-O, P-S, or P-N bonds.
AB - Catalytic chemistry that involves the activation and transformation of main group substrates is relatively undeveloped and current examples are generally mediated by expensive transition metal species. Herein, we describe the use of inexpensive and readily available tBuOK as a catalyst for P-P and P-E (E = O, S, or N) bond formation. Catalytic quantities of tBuOK in the presence of imine, azobenzene hydrogen acceptors, or a stoichiometric amount of tBuOK with hydrazobenzene, allow efficient homodehydrocoupling of phosphines under mild conditions (e.g. 25 °C and < 5 min). Further studies demonstrate that the hydrogen acceptors play an intimate mechanistic role. We also show that our tBuOK catalysed methodology is general for the heterodehydrocoupling of phosphines with alcohols, thiols and amines to generate a range of potentially useful products containing P-O, P-S, or P-N bonds.
UR - http://www.scopus.com/inward/record.url?scp=85068033470&partnerID=8YFLogxK
U2 - 10.1038/s41467-019-09832-4
DO - 10.1038/s41467-019-09832-4
M3 - Article (Academic Journal)
C2 - 31243267
AN - SCOPUS:85068033470
SN - 2041-1723
VL - 10
JO - Nature Communications
JF - Nature Communications
M1 - 2786 (2019)
ER -