Magnetic properties of V-substitution effect in an iron mixed valence complex. (4th November 2017)

• Record Type: Journal Article
• Authors: Shida, Norihiro; Suzawa, Yoshiki; Inaba, Michikazu; Okazawa, Atsushi; Kojima, Norimichi; Enomoto, Masaya
• Is Part Of: Polyhedron. Volume 136(2017)
• Page Start: 143
• Page End: 148
• Publication Date: 2017-11-04
• Subjects: Iron mixed valence complex -- Dilution effect on 3d metal ion -- Magnetic property -- Charge transfer phase transition -- Linkage isomerization; Chemistry, Inorganic -- Periodicals; Chimie inorganique -- Périodiques; Organometaalverbindingen; Anorganische chemie; 546.05
• DOI: 10.1016/j.poly.2017.04.006
• Languages: English
• ISSNs: 0277-5387

Abstract

Graphical abstract: A series of magnetically diluted complexes, ( n- C3 H7 )4 N[Fe II Fe III 1− x V III x (dto)3 ] ( x = 0–1), were prepared. In the case of x = 0, novel charge transfer phase transition between Fe II and Fe III was observed. This phenomenon remains whole of substitutional rate x unlike other 3d metal substituted cases. Abstract: The iron mixed-valence complex ( n- C3 H7 )4 N[Fe II Fe III (dto)3 ] (dto = C2 O2 S2 ) exhibits a novel type of phase transition according electron transfer between Fe II and Fe III called charge transfer phase transition (CTPT). The existence of the CTPT highly depends on the 3d metal substitution with Zn, Mn, Cr, or Co for corresponding Fe site in ( n- C3 H7 )4 N[Fe II Fe III (dto)3 ]. Here, we prepared a series of magnetically diluted complexes ( n- C3 H7 )4 N[Fe II Fe III 1− x V III x (dto)3 ] ( x = 0–1), and carried out investigation of magnetic properties. Judging from the magnetic susceptibility measurement, there is no suppression of the CTPT unlike other 3d metal substituted cases. Moreover, 57 Fe Mössbauer spectroscopy revealed that about 60% of Fe II sites changed their spin states from high spin to low spin in case of substitution rate for x = 1.00. Since the difference of hardness and softness between metallic ions (Fe II, Fe III and V III ) and coordination sites of ligand (O or S in dto), this behavior is explained by the linkage isomerization of bridging ligand in formation process of the complex.