Phosphine-ligated palladium sulfonate palladacycles
Described are palladium precatalysts, and methods of making and using them. The palladium precatalysts show improved stability and improved reactivity in comparison to previously-described palladium precatalysts.
1. A precatalyst of formula III:
wherein, independently for each occurrence,
X is a non-coordinating anion;
R 1 is H, alkyl, haloalkyl, hydroxy, alkoxy, aryloxy, aryl, or halo;
L is a trialkylphosphine, triarylphosphine, dialkylarylphosphine, alkyldiarylphosphine, bis(phosphine), phosphoramide, amine, bis(amine), or N-heterocyclic carbene; and
R 2 is alkyl, haloalkyl or aryl.
2. The precatalyst of claim 1 , wherein L is selected from the group consisting of PPh 3 , Ph 2 P—CH 3 , PhP(CH 3 ) 2 , P(o-tol) 3 , PCy 3 , P(tBu) 3 , BINAP, dppb, dppe, dppf, dppp,
R x is alkyl, aralkyl, cycloalkyl, or aryl;
X 1 is CH or N;
R 3 is H or alkyl;
R 4 is H, alkoxy, or alkyl;
R 5 is alkyl or aryl; and
n is 1, 2, 3, or 4.
3. The precatalyst of claim 1 , wherein X is selected from the group consisting of boron tetrafluoride, tetraarylborates, hexafluoroantimonate, phosphorus tetrafluoride, phosphorus hexafluoride, alkylsulfonate, haloalkylsulfonate, arylsulfonate, perchlorate, bis(alkylsulfonyl)amide, bis(fluoroalkylsulfonyl)amide, bis(arylsulfonyl)amide, (fluoroalkylsulfonyl)(fluoroalkylcarbonyl)amide, nitrate, nitrite, sulfate, hydrogensulfate, alkyl sulfate, aryl sulfate, carbonate, bicarbonate, carboxylate, phosphate, hydrogen phosphate, dihydrogen phosphate, phosphinate, and hypochlorite.
4. The precatalyst of claim 1 , wherein R 1 is H or alkyl.
5. The precatalyst of claim 1 , wherein R 2 , where present, is substituted or unsubstituted alkyl.
6. The precatalyst of claim 1 , wherein R 2 , where present, is substituted or unsubstituted aryl.
7. The precatalyst of claim 1 , wherein the precatalyst is selected from the group consisting of:
wherein R is H, alkyl, or aryl; L is selected from the group consisting of PPh 3 , Ph 2 P—CH 3 , PhP(CH 3 ) 2 , P(o-tol) 3 , PCy 3 , P(tBu) 3 , BINAP, dppb, dppe, dppf, dppp,
R x is alkyl, aralkyl, cycloalkyl, or aryl; X 1 is CH or N; R 3 is H or alkyl; R 4 is H, alkoxy, or alkyl; R 5 is alkyl or aryl; and n is 1, 2, 3, or 4.
8. A dimer of:
wherein, independently for each occurrence,
X is a non coordinating anion; and
R 1 is H, alkyl, haloalkyl, hydroxy, alkoxy, aryloxy, aryl, or halo;
R 2 is alkyl, haloalkyl or aryl.
9. The dimer of claim 8 , wherein X is selected from the group consisting of boron tetrafluoride, tetraarylborates, hexafluoroantimonate, phosphorus tetrafluoride, phosphorus hexafluoride, alkylsulfonate, haloalkylsulfonate, arylsulfonate, perchlorate, bis(alkylsulfonyl)amide, bis(fluoroalkylsulfonyl)amide, bis(arylsulfonyl)amide, (fluoroalkylsulfonyl)(fluoroalkylcarbonyl)amide, nitrate, nitrite, sulfate, hydrogensulfate, alkyl sulfate, aryl sulfate, carbonate, bicarbonate, carboxylate, phosphate, hydrogen phosphate, dihydrogen phosphate, phosphinate, and hypochlorite.
10. The dimer of claim 8 , wherein R 1 is H or alkyl.
11. The dimer of claim 8 , wherein R 2 , where present, is substituted or unsubstituted alkyl.
12. The dimer of claim 8 , wherein R 2 , where present, is substituted aryl or unsubstituted aryl.