Abstract

The reaction of cationic complex [( 5-C 5Me 5)Re(CO) 3I] + with aliphatic and aromatic primary amines unexpectedly produced the chelated carbamoyl species trans-( 5: 1-C 5Me 4CH 2NRC( O))Re(CO) 2(I) ( 1, R = Me; 2, R = Pr; 3, R = Ph; 4, R = p-tolyl). The 1-coordination of carbamoyl moiety linkages to a methylene group of tetramethylcyclopentadienyl ligand was confirmed by X-ray crystallography of complex 3. All the complexes were isolated as pure samples and fully characterized by IR, 1H and 13C NMR spectroscopies, mass spectrometry and elemental analysis.

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