TY - JOUR
T1 - Phenanthroline decorated by a crown ether as a module for metallorganic polyoxometalate hybrid catalysts
T2 - The wacker type oxidation of alkenes with nitrous oxide as terminat oxidant
AU - Ettedgui, Jessica
AU - Neumann, Ronny
PY - 2009/1/14
Y1 - 2009/1/14
N2 - A 1,10-phenanthroline ligand decorated at the 5,6-position by a 15-crown-5 ether moiety was prepared. Ligation of PdII at the nitrogen atom positions followed by complexation at the crown ether group of a redox active H5PV2Mo10O40 polyoxometalate yielded a hybrid metallorganic-polyoxometalate complex, PdII(15-crown-5- phen)Cl2-H5PV2Mo10O40. This complex was characterized by IR, UV-vis, ESI-MS, and NMR spectroscopy and elemental analysis that all confirmed the hybrid nature of the complex. Pd II(15-crown-5-phen) Cl2-H5PV2Mo 10O40 was used as a catalyst for the Wacker type oxidation of 1-alkenes to yield the corresponding methylketones in essentially quantitative yields using nitrous oxide as the terminal oxidant.
AB - A 1,10-phenanthroline ligand decorated at the 5,6-position by a 15-crown-5 ether moiety was prepared. Ligation of PdII at the nitrogen atom positions followed by complexation at the crown ether group of a redox active H5PV2Mo10O40 polyoxometalate yielded a hybrid metallorganic-polyoxometalate complex, PdII(15-crown-5- phen)Cl2-H5PV2Mo10O40. This complex was characterized by IR, UV-vis, ESI-MS, and NMR spectroscopy and elemental analysis that all confirmed the hybrid nature of the complex. Pd II(15-crown-5-phen) Cl2-H5PV2Mo 10O40 was used as a catalyst for the Wacker type oxidation of 1-alkenes to yield the corresponding methylketones in essentially quantitative yields using nitrous oxide as the terminal oxidant.
UR - http://www.scopus.com/inward/record.url?scp=67749137432&partnerID=8YFLogxK
U2 - 10.1021/ja808523n
DO - 10.1021/ja808523n
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AN - SCOPUS:67749137432
SN - 0002-7863
VL - 131
SP - 4
EP - 5
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 1
ER -