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大型十六金属{锰(III)-镧系(III)}轮:合成、结构、磁性及理论表征

Large Hexadecametallic {Mn(III) -Ln(III) } Wheels: Synthesis, Structural, Magnetic, and Theoretical Characterization.

作者信息

Vignesh Kuduva R, Langley Stuart K, Moubaraki Boujemaa, Murray Keith S, Rajaraman Gopalan

机构信息

IITB-Monash Research Academy, IIT Bombay, Mumbai, 400076 (India).

School of Chemistry, Monash University, Victoria, 3800 (Australia).

出版信息

Chemistry. 2015 Nov 9;21(46):16364-9. doi: 10.1002/chem.201503424. Epub 2015 Sep 25.

Abstract

The synthesis, gas sorption studies, magnetic properties, and theoretical studies of new molecular wheels of core type {Mn(III) 8 Ln(III) 8 } (Ln=Dy, Ho, Er, Y and Yb), using the ligand mdeaH2 , in the presence of ortho-toluic or benzoic acid are reported. From the seven wheels studied the {Mn8 Dy8 } and {Mn8 Y8 } analogues exhibit SMM behavior as determined from ac susceptibility experiments in a zero static magnetic field. From DFT calculations a S=16 ground state was determined for the {Mn8 Y8 } complex due to weak ferromagnetic Mn(III) -Mn(III) interactions. Ab initio CASSCF+RASSI-SO calculations on the {Mn8 Dy8 } wheel estimated the Mn(III) -Dy(III) exchange interaction as -0.1 cm(-1) . This weak exchange along with unfavorable single-ion anisotropy of Dy(III) /Mn(III) ions, however, led to the observation of SMM behavior with fast magnetic relaxation. The orientation of the g-anisotropy of the Dy(III) ions is found to be perpendicular to the plane of the wheel and this suggests the possibility of toroidal magnetic moments in the cluster. The {Mn8 Ln8 } clusters reported here are the largest heterometallic Mn(III) Ln(III) wheels and the largest {3d-4f} wheels to exhibit SMM behavior reported to date.

摘要

报道了在邻甲苯酸或苯甲酸存在下,使用配体mdeaH2合成核心类型为{Mn(III)8Ln(III)8}(Ln = Dy、Ho、Er、Y和Yb)的新型分子轮,并对其进行气体吸附研究、磁性研究和理论研究。在所研究的七个分子轮中,{Mn8Dy8}和{Mn8Y8}类似物在零静态磁场下的交流磁化率实验中表现出单分子磁体行为。通过密度泛函理论计算,由于弱铁磁Mn(III)-Mn(III)相互作用,确定{Mn8Y8}配合物的基态为S = 16。对{Mn8Dy8}分子轮进行的从头算CASSCF+RASSI-SO计算估计Mn(III)-Dy(III)交换相互作用为-0.1 cm(-1)。然而,这种弱交换以及Dy(III)/Mn(III)离子不利的单离子各向异性导致观察到具有快速磁弛豫的单分子磁体行为。发现Dy(III)离子的g-各向异性方向垂直于分子轮平面,这表明簇中可能存在环形磁矩。本文报道的{Mn8Ln8}簇是最大的异金属Mn(III)Ln(III)分子轮,也是迄今为止报道的表现出单分子磁体行为的最大的{3d-4f}分子轮。

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