INQUIMAE   12526
INSTITUTO DE QUIMICA, FISICA DE LOS MATERIALES, MEDIOAMBIENTE Y ENERGIA
Unidad Ejecutora - UE
artículos
Título:
NO+, NO·, NO? ! Nitrosyl Siblings from [IrCl5NO] ?
Autor/es:
NATALIA ESCOLA; DAMIAN E. BIKIEL; RICARDO BAGGIO; FLORENCIA DI SALVO; FABIO DOCTOROVICH
Revista:
INORGANICA CHIMICA ACTA
Editorial:
ELSEVIER SCIENCE SA
Referencias:
Año: 2011 vol. 374 p. 528 - 528
ISSN:
0020-1693
Resumen:
Pentachloronitrosyliridate(III) ([IrCl5NO]?), the most nucleophilic NO+ known to date, can bereduced chemically and/or electrochemically by one or two electrons to produce the NO● andHNO/NO? forms. The nitroxyl complex can be formed either by hydride attack to the NO+ in organicsolvent, or by decomposition of iridium-coordinated nitrosothiols in aqueous solutions, while NO● isproduced electrochemically or by reduction of [IrCl5(NO)]? with H2O2. Both NO● and HNO/NO?complexes are stable under certain conditions but tend to labilize the trans chloride and even thecis ones after long periods of time. As expected, the NO+ is practically linear, although the IrNOmoiety is affected by the counterions due to dramatic changes in the solid state arrangement. Theother two nitrosyl redox states comprise bent structures.