Synthesis, structure, and reactivity of (h5:h1-C5Me4(CH2)2NMe2) Re(CO)2. Electron transfer behavior of a nitrosyl derivative.

FERNANDO GODOY; ALEJANDRA GÓMEZ; RODRIGO SEGURA; FABIO DOCTOROVICH; JUAN PELLEGRINO; CARINA GAVIGLIO; PAULINA GUERRERO; A. HUGO KLAHN; MAURICIO FUENTEALBA; MARÍA TERESA GARLAND

JOURNAL OF ORGANOMETALLIC CHEMISTRY

ELSEVIER SCIENCE SA

Lugar: Amsterdam; Año: 2014 p. 8 - 16

0022-328X

The UV irradiation of an hexane solution of the complex (n5-C5Me4(CH2)2NMe2)Re(CO)3 (1) afforded the chelated species (n5:n1-C5Me4(CH2)2NMe2)Re(CO)2 (2). The molecular structure of 2 has been determined by X-ray crystallography. The reaction of 2 with two-electron donor ligands yields (n5-C5Me4(CH2)2NMe2)Re(CO)2(L) (1, L = CO; 3, L = PMe3). The chelated species 2 also reacts with MeOTf, HBF4, and I2 to form the cationic compounds trans-[(n5-C5Me4(CH2)2NMe2)Re(CO)2X]+ ([4]+, X = Me; [5]+, X = H; [6]+, X = I). The trans stereochemistry of 4-6 have been assigned on the basis of CO IR frequency intensities and 13C-NMR spectroscopy. Also, complex 2 reacts with nitrosyl tetrafluoroborate to yield [(n5-C5Me4(CH2)2NMe2NO)Re(CO)2(NO)]BF4 ([7]2+). The redox behavior of the {ReNO}6 complex [7]2+ was studied and the products obtained after two-electron reduction were characterized by IR. DFT calculations were done to optimize the structure of [7]2+ and to study the effect of the sidearm coordination on the electronic structure of a cyclopentadienyl {ReNO}8 complex.