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      Synthesis and characterization of novel niccolites [(CH3)2NH2][FeIIIMII(HCOO)6] (MII = Zn, Ni, Cu)

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          Abstract

          We report the synthesis, structural, magnetic, Raman and IR studies of novel niccolite-type heterometallic [(CH 3) 2NH 2][Fe IIIM II(HCOO) 6] compounds (M II = Ni, Zn and Cu). The Ni and Cu compounds order ferromagnetically at 42 and 28.5 K, respectively. The monoclinic Cu member exhibits different structural changes on cooling than the trigonal Zn and Ni compounds.

          Abstract

          We report the synthesis, X-ray diffraction, thermal, magnetic, Raman and IR studies of three heterometallic MOFs, [(CH 3) 2NH 2][Fe IIIM II(HCOO) 6] with M = Zn (DMFeZn), Ni (DMFeNi) and Cu (DMFeCu), crystallizing in the niccolite type structure. DMFeZn and DMFeNi crystallize in the trigonal structure (space group P3̄1 c) while DMFeCu crystallizes in the monoclinic structure (space group C2/ c). Magnetic investigation shows that DMFeZn remains paramagnetic down to the lowest temperature obtained in our experiment while DMFeNi and DMFeCu exhibit ferromagnetic order below 42 and 28.5 K, respectively. IR and Raman data confirm the structural model of the monoclinic DMFeCu and show evidence for stronger hydrogen bonds when compared to trigonal DMFeZn and DMFeNi. A different hydrogen bond network in the monoclinic DMFeCu when compared to trigonal DMFeZn and DMFeNi is responsible for the different behavior of these compounds upon cooling, that is, DMFeCu exhibits a sign of short range ordering of dimethylammonium cations at low temperatures while the trigonal analogues show evolution of dynamic disorder into static disorder.

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          Multiferroic behavior associated with an order-disorder hydrogen bonding transition in metal-organic frameworks (MOFs) with the perovskite ABX3 architecture.

          Multiferroic behavior in perovskite-related metal-organic frameworks of general formula [(CH(3))(2)NH(2)]M(HCOO)(3), where M = Mn, Fe, Co, and Ni, is reported. All four compounds exhibit paraelectric-antiferroelectric phase transition behavior in the temperature range 160-185 K (Mn: 185 K, Fe: 160 K; Co: 165 K; Ni: 180 K); this is associated with an order-disorder transition involving the hydrogen bonded dimethylammonium cations. On further cooling, the compounds become canted weak ferromagnets below 40 K. This research opens up a new class of multiferroics in which the electrical ordering is achieved by means of hydrogen bonding.
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            Coexistence of magnetic and electric orderings in the metal-formate frameworks of [NH4][M(HCOO)3].

            A family of three-dimensional chiral metal-formate frameworks of [NH(4)][M(HCOO)(3)] (M = Mn, Fe, Co, Ni, and Zn) displays paraelectric to ferroelectric phase transitions between 191 and 254 K, triggered by disorder-order transitions of NH(4)(+) cations and their displacement within the framework channels, combined with spin-canted antiferromagnetic ordering within 8-30 K for the magnetic members, providing a new class of metal-organic frameworks showing the coexistence of magnetic and electric orderings.
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              Order-disorder antiferroelectric phase transition in a hybrid inorganic-organic framework with the perovskite architecture.

              [(CH3)2NH2]Zn(HCOO)3, 1, adopts a structure that is analogous to that of a traditional perovskite, ABX3, with A = [(CH3)2NH2], B = Zn, and X = HCOO. The hydrogen atoms of the dimethyl ammonium cation, which hydrogen bond to oxygen atoms of the formate framework, are disordered at room temperature. X-ray powder diffraction, dielectric constant, and specific heat data show that 1 undergoes an order-disorder phase transition on cooling below 156 K. We present evidence that this is a classical paraelectric to antiferroelectric phase transition that is driven by ordering of the hydrogen atoms. This sort of electrical ordering associated with order-disorder phase transition is unprecedented in hybrid frameworks and opens up an exciting new direction in rational synthetic strategies to create extended hybrid networks for applications in ferroic-related fields.
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                Author and article information

                Journal
                ICHBD9
                Dalton Transactions
                Dalton Trans.
                Royal Society of Chemistry (RSC)
                1477-9226
                1477-9234
                2015
                2015
                : 44
                : 29
                : 13234-13241
                Affiliations
                [1 ]Institute of Low Temperature and Structure Research
                [2 ]Polish Academy of Sciences
                [3 ]50-950 Wrocław 2
                [4 ]Poland
                Article
                10.1039/C5DT01608H
                3565fbd0-c43d-4255-a9f2-9849e261997f
                © 2015
                History

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