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A significant activation of the C≡N group in organonitriles upon their coordination to a platinum(IV) center has been found in the reaction of [PtCl4(RCN)2] (R = Me, Et, CH2Ph) with the nitrile oxides 2,4,6-R′3C6H2CNO (R′ = Me, OMe) to give the (1,2,4-oxadiazole)platinum(IV) complexes [PtCl4{N=C(R)ON=CC6H2R′3}] (R = Me, R′ = Me (1); R = Et, R′ = Me (2); R = Et, R′ = OMe (3); R = CH2Ph, R′ = Me (4)); the [2 + 3] cycloaddition was performed under mild conditions (unless poor solubility of [PtCl4(RCN)2] precludes the reaction) starting even from complexed acetonitrile and propionitrile, which exhibit low reactivity in the free state. The reaction between complexes 2-4 and 1 equiv of Ph3P=CHCO2Me in CH2Cl2 leads to the appropriate platinum(II) complexes [PtCl2{N=C(R)-ON=CC6H2R′3}] (5-7); the reduction failed only in the case of 1 insofar as this complex is insoluble in the most common organic solvents. All the platinum compounds were characterized by elemental analyses, FAB mass spectrometry, and IR and 1H, 13C{1H}, and 195Pt NMR spectroscopies, and three of them also by X-ray crystallography. The oxadiazoles formed in the course of the metal-mediated reaction were liberated almost quantitatively from their Pt(IV) complexes by reaction of the latter (complexes 2-4) with an excess of pyridine in chloroform, giving free 1,2,4-oxadiazoles and trans-[PtCl4(pyridine)2]; the sequence of the Pt(IV)-mediated [2 + 3] cycloaddition and the liberation opens up an alternative route for the preparation of this important class of heterocycles.
Original language | English |
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Pages (from-to) | 896-903 |
Number of pages | 8 |
Journal | Inorganic Chemistry |
Volume | 42 |
Issue number | 3 |
DOIs | |
State | Published - 10 Feb 2003 |
ID: 97804279