4.7 Article

Family of Lanthanide-Manganese Heterometallic Metallacrowns: Syntheses, Structures, Magnetic Exchange, and Magnetocaloric Effects

Journal

CRYSTAL GROWTH & DESIGN
Volume 23, Issue 1, Pages 424-433

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.cgd.2c01093

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In this study, a series of Mn-based clusters with different metal arrangements were prepared using salicylhydroxamic acid as organic ligands. It was found that the arrangement of metal ions displaying [M-N-O-M] is more likely to produce weak ferromagnetic coupling, which is crucial for exploring magneto-structure relationship.
The intermetallic magnetic interaction is a key role for exploring magneto-structure relationship. Herein, a series of Mn-based clusters featuring metallacrowns with the formulas [(MnMn4III)-Mn-II(L-1)(4)(HL2)(2)(DMF)(6)]center dot 4MeOH center dot 3H(2)O (1), [GdMn4III(L-1)(4)(OAc)(4)]center dot H(4)TEA center dot 2MeOH center dot H2O (2), [Gd4Mn4III(L-1)(4)(HL2)(2)(H2L1)(4)(OAc)(4)(mu(3)-OH)(2)(DMF)(2)(H2O)(2)]center dot 4DMF center dot H2O center dot 16MeOH center dot H(3)TEA (3), and [(Gd6Mn4Mn2IV)-Mn-III(L-1)(10)(HL1)(2)(H2L1)(4)(DMF)(4)(H2O)(4)(MeOH)(4)]center dot 4DMF center dot 2MeOHmiddot6H(2)O (4) (H3L1 = salicylhydroxamic acid, H2L2 = salicylic acid, MeOH = methanol, DMF = N,N-dimethylformamide, and H(3)TEA = triethylamine) were prepared using salicylhydroxamic acid as organic ligands. The structures of compounds 1-2, 3, and 4 featured 12-metallacrown-4, 16-metallacrown-6, and 28-metallacrown-10, respectively. Magnetic calculations showed that the obvious antiferromagnetic couplings of compounds 1-2 were mainly derived from Mn-III center dot center dot center dot Mn-III. For compound 3, the weak ferromagnetic couplings of Gd-II center dot center dot center dot Mn-III and Mn-III center dot center dot center dot Mn-III bridged through [M-O-N-M] manner were smaller than the antiferromagnetic couplings of Gd-III center dot center dot center dot Gd-III and Gd-III center dot center dot center dot Mn-III bridged by O atoms, resulting in the overall antiferromagnetic behavior. In compound 4, the weak ferromagnetic couplings of Gd-III center dot center dot center dot Mn-III/Mn-III center dot center dot center dot Mn-III/Gd-III center dot center dot center dot Mn-IV/Mn(III)middotmiddotmiddotMn(IV) bridged by the way of [M-O-N-M] were dominant. The abovementioned results revealed that the arrangement of metal ions displaying [M-N-O-M] is more likely to produce weak ferromagnetic coupling between metal ions, which is beneficial to the magnetocaloric effect (MCE). Meanwhile, compounds 3-4 showed considerable MCEs with a magnetic entropy change (-Delta S-m) of 13.86 J kg(-1) K-1 at 3.5 K, 7 T and 16.05 J kg(-1) K-1 at 3 K, 7 T, respectively.

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