The extraction of Bi(III) in nitrate media has been investigated using aminododecyldimethylenediphosphonic acid, ADDMDPA, which was previously synthesized and characterized. The extraction of the cation was carried ou...The extraction of Bi(III) in nitrate media has been investigated using aminododecyldimethylenediphosphonic acid, ADDMDPA, which was previously synthesized and characterized. The extraction of the cation was carried out in different media with the addition of CH3COONa, KNO3 and HNO3. The maximum extraction yield for Bismuth is 70% after addition of 0.01 M of potassium nitrate at pHi = 2.9, in one step.展开更多
Enantiopure 2-(dicyclohexylphosphino)-1,1'-biphenyl derivatives substituted in the 2'-position by a chiral amino group were prepared.For the compound bearing an acyclic chiral chain,the key step was a Suzuki c...Enantiopure 2-(dicyclohexylphosphino)-1,1'-biphenyl derivatives substituted in the 2'-position by a chiral amino group were prepared.For the compound bearing an acyclic chiral chain,the key step was a Suzuki coupling between bromobenzeneboronic acid and N-Boc-iodoaniline whereas an aromatic nucleophilic substitution allowed the introduction of a chiral pyrrolidine in the 2'-position of the biphenyl backbone.The efficiency of the P,N-biphenyl pyrrolidine derivatives as ligands in Pd-catalyzed arylaminations compares well with that of DavePhos ligand.展开更多
文摘The extraction of Bi(III) in nitrate media has been investigated using aminododecyldimethylenediphosphonic acid, ADDMDPA, which was previously synthesized and characterized. The extraction of the cation was carried out in different media with the addition of CH3COONa, KNO3 and HNO3. The maximum extraction yield for Bismuth is 70% after addition of 0.01 M of potassium nitrate at pHi = 2.9, in one step.
基金the Ministry of Education, the CNRS and the European Union (FEDER funding) for financial supports
文摘Enantiopure 2-(dicyclohexylphosphino)-1,1'-biphenyl derivatives substituted in the 2'-position by a chiral amino group were prepared.For the compound bearing an acyclic chiral chain,the key step was a Suzuki coupling between bromobenzeneboronic acid and N-Boc-iodoaniline whereas an aromatic nucleophilic substitution allowed the introduction of a chiral pyrrolidine in the 2'-position of the biphenyl backbone.The efficiency of the P,N-biphenyl pyrrolidine derivatives as ligands in Pd-catalyzed arylaminations compares well with that of DavePhos ligand.
