For the first time, polyketone (poly-3-oxotrimethylene, PK) has been employed as support for Pd nanoparticles. Three different approaches have been adopted: (i) reduction of Pd(OAc)2 in EtOH under microwave irradiation, (ii) hydrothermal reduction of the same precursor in EtOH or n-BuOH employing traditional heating and (iii) vaporization of Pd metal through metal vapour synthesis. These supported systems have been characterized by solid state NMR, TEM, ICP, XPS, BET and tested in the selective hydrogenation of cinnamaldehyde (CAL) to hydrocinnamaldehyde (HCAL) as probe reaction. Their catalytic performances have been compared in relation to their preparation procedure and morphology. It is remarkable that these catalysts do not show significant leaching even after several catalytic recycles, thus indicating their high stability and recyclability, ascribed to a stabilizing capacity of this particular polymeric support. © 2012 Elsevier B.V.
New palladium catalysts on polyketone prepared through different smart methodologies and their use in the hydrogenation of cinnamaldehyde
TONIOLO, Luigi;
2012-01-01
Abstract
For the first time, polyketone (poly-3-oxotrimethylene, PK) has been employed as support for Pd nanoparticles. Three different approaches have been adopted: (i) reduction of Pd(OAc)2 in EtOH under microwave irradiation, (ii) hydrothermal reduction of the same precursor in EtOH or n-BuOH employing traditional heating and (iii) vaporization of Pd metal through metal vapour synthesis. These supported systems have been characterized by solid state NMR, TEM, ICP, XPS, BET and tested in the selective hydrogenation of cinnamaldehyde (CAL) to hydrocinnamaldehyde (HCAL) as probe reaction. Their catalytic performances have been compared in relation to their preparation procedure and morphology. It is remarkable that these catalysts do not show significant leaching even after several catalytic recycles, thus indicating their high stability and recyclability, ascribed to a stabilizing capacity of this particular polymeric support. © 2012 Elsevier B.V.I documenti in ARCA sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.