Ylide-functionalised phosphanes for use in metal complexes and homogeneous catalysis

Abstract

The invention relates to ylide-functionalized phosphane ligands, the production of same and use in transition metal compounds, as well as the use of same as catalysts in organic reactions.

1 - 40 . (canceled) 
     
     
         41 . Metal complexes having phosphane ligands of formula (II) 
       
         
           
           
               
               
           
         
         wherein On is a phosphonium group —P(R 3 R 4 R 5 ), in which R 3 , R 4  and R 5  are independently selected from the group consisting of C 1-6  alkyl groups, C 4-10  cycloalkyl groups, C 6-10  aryl groups, X is selected from the group consisting of linear, branched-chain or cyclic C 1-6  alkyl groups, C 6-10  aryl groups, mono- or polyunsaturated linear, branched-chain or cyclic C 2-6  alkenyl groups, a trialkylsilyl (—SiR 3 R 4 R 5 ), arylsulfonyl group, and R 1  and R 2  are C 6-10  aryl groups or C 1-6  alkyl and cycloalkyl groups. 
       
     
     
         42 . The metal complexes according to  claim 41 , wherein R 3 , R 4  and R 5  are independently selected from the group consisting of methyl, ethyl, butyl, cyclohexyl, phenyl, and combinations thereof. 
     
     
         43 . The metal complexes according to  claim 41  wherein R 3 , R 4  and R 5  are the same and are selected from the group consisting of methyl, ethyl, butyl, cyclohexyl, phenyl, and combinations thereof, especially cyclohexyl and phenyl. 
     
     
         44 . The metal complexes according to  claim 41 , wherein X is selected from the group consisting of methyl, ethyl, cyclohexyl, phenyl, p-tolyl, trimethylsilyl, p-tolylsulfonyl, or combinations thereof. 
     
     
         45 . The metal complexes according to  claim 41 , wherein R 1  and R 2  are independently selected from the group consisting of phenyl, cyclohexyl, methyl, tert-butyl and combinations thereof. 
     
     
         46 . The metal complexes according to  claim 41 , wherein said complex is a palladium allyl complex having the following structure (V) or (VI): 
       
         
           
           
               
               
           
         
         wherein X′ is an anion, 
         Y is On-C—X, 
         R 33 , R 34  and R 35  are independently selected from H, alkyl, aryl and heteroaryl groups that may be unsubstituted or substituted with functional groups; or 
         at least two of R 33 , R 34  and R 35  form a carbocyclic ring with 5 to 14 carbon atoms, 
         Ar represents a substituted or unsubstituted aryl group. 
       
     
     
         47 . The metal complexes according to  claim 46 , wherein R 33 , R 34  and R 35  are independently selected from linear, branched-chain or cyclic C 1-10  alkyl groups, the aryl groups are selected from C 6-14  aryl groups, the alkenyl groups are selected from mono- or polyunsaturated linear, branched-chain or cyclic C 2-10  alkenyl groups, and the heteroaryl groups are selected from C 6-14  heteroaryl groups, wherein all of the groups mentioned are optionally substituted with functional groups; or
 at least two of R 33 , R 34  and R 35  form a carbocyclic ring that is a C 4-10  cycloalkyl group, or a C 6-14  aryl group, optionally substituted with one or more functional groups; and   Ar are selected from C 6-14  aryl groups and the heteroaryl groups are selected from C 6-14  heteroaryl groups, wherein all of the groups mentioned are optionally substituted with functional groups; and   the functional groups are selected from alkyl, C 1-6  alkyl groups, C 6-10  aryl, halogen, hydroxy, cyano, alkoxy, amino, or mercapto.   
     
     
         48 . The metal complexes according to  claim 46 , wherein X is selected from the group of halogen, tosylate, nosylate and mesylate. 
     
     
         49 . The metal complexes according to  claim 41 , wherein X is selected from the group of fluorine, chlorine, bromine, iodine, tosylate, nosylate and mesylate, and/or aryl is selected from phenyl, m-tolyl, p-tolyl, o-tolyl, mesityl, 1,3-diisopropylphenyl. 
     
     
         50 . A process for performing a coupling reaction containing the steps of
 providing a reaction mixture containing at least a substrate, coupling partner, and the metal complex according to  claim 41 ; and   reacting said substrate with said coupling partner in the presence of the metal complex or its derivative to form a coupling product.   
     
     
         51 . The process according to  claim 50 , wherein the metal of said metal complex is a precious metal or a transition metal. 
     
     
         52 . The process according to  claim 50 , wherein the metal of said metal complex is a metal of group 10 or 11 of the Periodic Table of the elements. 
     
     
         53 . The process according to  claim 50 , wherein the metal of said metal complex is selected from the group consisting of copper, silver, gold, platinum, palladium, nickel, and combinations thereof. 
     
     
         54 . The metal complexes of  claim 41 , wherein the metal of the metal complex is selected from the group consisting of copper, silver, gold, platinum, palladium, nickel, and combinations thereof.