Copper (II) azido complex [CuL(μ-1,3-N3)]n (1) of a NNO donor tridentate Schiff base (HL = 2-[1-(Methylamino-ethylimino)-methyl]-phenol containing single end-to-end μ-1,3-azido bridged 1D infinite chain has been synthesized and characterized by elemental analysis, FT-IR spectroscopy. X-ray single crystal structure analysis reveals that in 1, the central copper (II) ion displays a distorted square pyramidal coordination geometry and are linked by single EE azide bridges forming chains running parallel to the crystallographic b axis. The magnetic interaction revealed that 1 is antiferromagnetic in nature (J = -19.5 (±0.2) cm-1). The catalytic activity of the complex is investigated in a series of solvents for the oxidation of olefins using tert-butyl-hydroperoxide as oxidant. The results showed highest selectivity for 1 in acetonitrile medium.
Single end to end azido bridged adduct of a tridentate schiff base copper(II) complex: synthesis, structure, magnetism and catalytic studies / S., Banerjee; C., Adhikary; Rizzoli, Corrado; R., Pal. - In: INORGANICA CHIMICA ACTA. - ISSN 0020-1693. - 409:(2014), pp. 202-207. [10.1016/j.ica.2013.09.032]
Single end to end azido bridged adduct of a tridentate schiff base copper(II) complex: synthesis, structure, magnetism and catalytic studies
RIZZOLI, Corrado;
2014-01-01
Abstract
Copper (II) azido complex [CuL(μ-1,3-N3)]n (1) of a NNO donor tridentate Schiff base (HL = 2-[1-(Methylamino-ethylimino)-methyl]-phenol containing single end-to-end μ-1,3-azido bridged 1D infinite chain has been synthesized and characterized by elemental analysis, FT-IR spectroscopy. X-ray single crystal structure analysis reveals that in 1, the central copper (II) ion displays a distorted square pyramidal coordination geometry and are linked by single EE azide bridges forming chains running parallel to the crystallographic b axis. The magnetic interaction revealed that 1 is antiferromagnetic in nature (J = -19.5 (±0.2) cm-1). The catalytic activity of the complex is investigated in a series of solvents for the oxidation of olefins using tert-butyl-hydroperoxide as oxidant. The results showed highest selectivity for 1 in acetonitrile medium.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
