The reaction of [Pt6(CO)6(SnCl2)2(SnCl3)4]4–(1) with CO under atmospheric pressure resulted in the new [Pt6(CO)8(SnCl2)(SnCl3)4]4–(2) cluster by the addition of two CO ligands and the elimination of a stannylene SnCl2group. In turn, 2 reacted with 2 equivalents of PPh3under a CO atmosphere to afford [Pt6(CO)8(SnCl2)(SnCl3)2(PPh3)2]2–(3) by elimination of two stannyl [SnCl3]–ligands. Conversely, the reaction of 2 with 2 equivalents of PPh3under a N2atmosphere resulted in a species tentatively formulated as [Pt6(CO)5(SnCl2)2(SnCl3)2(PPh3)2]2–(4–5CO) on the basis of13C NMR,31P NMR spectroscopy and ESI-MS studies. Compounds 2–4 were spectroscopically characterized by IR spectroscopy and multinuclear (13C and31P) variable-temperature NMR spectroscopy. The crystal structures of 2 and 3 were determined by means of single-crystal X-ray diffraction, and their bonding was computationally investigated by DFT calculations. The possible structure of 4–5CO was predicted by means of DFT methods.

Bortoluzzi, M., Ceriotti, A., Cesari, C., Ciabatti, I., DELLA PERGOLA, R., Femoni, C., et al. (2016). Syntheses of [Pt6(CO)8(SnCl2)(SnCl3)4]4–and [Pt6(CO)8(SnCl2)(SnCl3)2(PPh3)2]2–Platinum–Carbonyl Clusters Decorated by SnIIFragments. EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2016(24), 3939-3949 [10.1002/ejic.201600597].

Syntheses of [Pt6(CO)8(SnCl2)(SnCl3)4]4–and [Pt6(CO)8(SnCl2)(SnCl3)2(PPh3)2]2–Platinum–Carbonyl Clusters Decorated by SnIIFragments

DELLA PERGOLA, ROBERTO;
2016

Abstract

The reaction of [Pt6(CO)6(SnCl2)2(SnCl3)4]4–(1) with CO under atmospheric pressure resulted in the new [Pt6(CO)8(SnCl2)(SnCl3)4]4–(2) cluster by the addition of two CO ligands and the elimination of a stannylene SnCl2group. In turn, 2 reacted with 2 equivalents of PPh3under a CO atmosphere to afford [Pt6(CO)8(SnCl2)(SnCl3)2(PPh3)2]2–(3) by elimination of two stannyl [SnCl3]–ligands. Conversely, the reaction of 2 with 2 equivalents of PPh3under a N2atmosphere resulted in a species tentatively formulated as [Pt6(CO)5(SnCl2)2(SnCl3)2(PPh3)2]2–(4–5CO) on the basis of13C NMR,31P NMR spectroscopy and ESI-MS studies. Compounds 2–4 were spectroscopically characterized by IR spectroscopy and multinuclear (13C and31P) variable-temperature NMR spectroscopy. The crystal structures of 2 and 3 were determined by means of single-crystal X-ray diffraction, and their bonding was computationally investigated by DFT calculations. The possible structure of 4–5CO was predicted by means of DFT methods.
Articolo in rivista - Articolo scientifico
Carbonyl ligands; Cluster compounds; Platinum; Structure elucidation; Tin;
Platinum; Tin; Heterometallic cluster; 13C and 31P-NMR; coordination chemistry
English
2016
2016
24
3939
3949
none
Bortoluzzi, M., Ceriotti, A., Cesari, C., Ciabatti, I., DELLA PERGOLA, R., Femoni, C., et al. (2016). Syntheses of [Pt6(CO)8(SnCl2)(SnCl3)4]4–and [Pt6(CO)8(SnCl2)(SnCl3)2(PPh3)2]2–Platinum–Carbonyl Clusters Decorated by SnIIFragments. EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2016(24), 3939-3949 [10.1002/ejic.201600597].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/129547
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