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Magnetic properties of closo-carborane-based Co(II) single-ion complexes with O, S, Se, and Te bridging atoms

Ofelia B Oñ; a; Diego R Alcoba; Gustavo E Massaccesi; Alicia Torre; Luis Lain; Juan I Melo; Josep M Oliva Enrich; Juan E Peralta
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摘要

We present a detailed computational analysis of a newly proposed family of Co(II) single-ion complexes with large magnetic anisotropy. Starting from previously proposed structures based on oxy- and thio-bridged 1,2-dicarba-closo-dodecaborane and 1,2-dicarba-closo-hexaborane, we explore the substitution of O and S bridging atoms by Se and Te atoms. Our calculations, based on CASSCF/NEVPT2 methods, show that these substitutions also lead to some large magnetic anisotropy complexes. Particularly, one of the proposed single-ion Se-bridged Co(II) chelated by 1,2-dicarba-closo-dodecaborane has a calculated anisotropy parameter D=-144cm-1, and a single-ion Se-bridged Co(II) chelated by 1,2-dicarba-closo-hexaborane gives a calculated D=-133 cm-1. These large D values can be attributed in part to geometric distortion from Td symmetry at the Co(II) ion caused by the ligand structure, and in part to the electric effect of the Se atoms. Our results suggest that this strategy could be a feasible alternative to increase the magnetic anisotropy of single-ion transition metal complexes. Graphical abstract We present a detailed computational analysis of a newly proposed family of Co(II) single-ion complexes with large magnetic anisotropy. Starting from previously proposed structures based on oxy- and thio-bridged 1,2-dicarba-closo-dodecaborane and 1,2-dicarba-closo-hexaborane, we explore the substitution of O and S bridging atoms by Se and Te atoms. Based on CASSCF/NEVPT2 calculations, we find some of these complexes to have a large magnetic anisotropy D parameter of about 140 cm-1.Download : Download high-res image (173KB)Download : Download full-size image

关键词

CarboranesCo(II) complexesMagnetic anisotropySpin relaxation

出版信息

论文状态
公开发表
期刊名称
Polyhedron
发表日期
2019-12-6
卷
-
期
-
页码
114257
DOI
10.1016/j.poly.2019.114257

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