6533b86cfe1ef96bd12c890c
RESEARCH PRODUCT
Sustainable carbon–carbon bond formation catalyzed by new oxamate-containing palladium(II) complexes in ionic liquids
Giovanni De MunnoSalah-eddine StiribaFrancisco R. Fortea-pérezMiguel JulveIsabel SchlegelDonatella Armentanosubject
chemistry.chemical_classificationArylOrganic ChemistryIodidechemistry.chemical_elementBiochemistryMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundchemistrySuzuki reactionCarbon–carbon bondBromideIonic liquidMaterials ChemistryPhysical and Theoretical ChemistryPalladiumdescription
Abstract New and versatile bis(oxamato)palladate(II) complexes of formula ( n -Bu 4 N) 2 [Pd(2-Mepma) 2 ]·4H 2 O ( 1a ) and ( n -Bu 4 N) 2 [Pd(4-Mepma) 2 ]·2H 2 O·MeCN ( 1b ) ( n -Bu 4 N + = tetra- n -buthylammonium, 2-Mepma = N -2-methylphenyloxamate and 4-Mepma = N -4-methylphenyloxamate) have been synthesized and characterized by spectroscopic methods and single crystal X-ray diffraction. Each palladium(II) ion in 1a and 1b is four-coordinate with two oxygen and two nitrogen atoms from two fully deprotonated oxamate ligands building a centrosymmetric square planar surrounding. Their catalytic role has been investigated for both Heck and Suzuki coupling reactions using a series of aryl iodide/bromide derivatives in tetra- n -butylammonium bromide ( n -Bu 4 NBr) as ionic liquid, i.e. molten salt. These precatalysts appear as highly efficient, easily recovered and reused at least eight times without any drastic loss of their exceptional reactivity or leaching from the ionic liquid medium.
year | journal | country | edition | language |
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2013-10-01 | Journal of Organometallic Chemistry |