We have synthesized three Pd(0) complexes stabilized by the olefin dimethyl fumarate and bidentate ligands based on the quinoline frame with thioetheric or diphenylphosphine function. We have reacted all the synthesized complexes with allyl or propargyl halides and isolated the products of the resulting oxidative addition. The solid state structures in the case of a Pd(0) derivative 1C and of the allenyl complexes 2Af and 2Ag have been resolved and we performed some computational calculations in order to establish whether the formation of allenyl or propargyl derivative as reaction products could be influenced by their reciprocal thermodynamic stability or by kinetic reasons. In this respect we have also carried out some kinetic investigations and hypothesized a plausible mechanism of the oxidative addition.
Oxidative addition of allyl and propargyl halides on palladium(0) complexes bearing bidentate ligands with quinolinic structure
CANOVESE, Luciano;VISENTIN, Fabiano;SANTO, Claudio;
2015-01-01
Abstract
We have synthesized three Pd(0) complexes stabilized by the olefin dimethyl fumarate and bidentate ligands based on the quinoline frame with thioetheric or diphenylphosphine function. We have reacted all the synthesized complexes with allyl or propargyl halides and isolated the products of the resulting oxidative addition. The solid state structures in the case of a Pd(0) derivative 1C and of the allenyl complexes 2Af and 2Ag have been resolved and we performed some computational calculations in order to establish whether the formation of allenyl or propargyl derivative as reaction products could be influenced by their reciprocal thermodynamic stability or by kinetic reasons. In this respect we have also carried out some kinetic investigations and hypothesized a plausible mechanism of the oxidative addition.File | Dimensione | Formato | |
---|---|---|---|
JOM2015(I).pdf
non disponibili
Tipologia:
Documento in Post-print
Licenza:
Licenza non definita
Dimensione
1.11 MB
Formato
Adobe PDF
|
1.11 MB | Adobe PDF | Visualizza/Apri |
I documenti in ARCA sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.