Abstract:The combination of some three-atom bridges with paramagnetic 3d transition metal ions results in the systematic isolation of molecular magnetic materials, ranging from single-molecule and singlechain magnets to layered weak ferromagnets and three-dimensional porous magnets. The design strategy and role of secondary components, such as co-ligands, templates and other mixed short ligands are discussed.
“…One class of compounds for which this methodology is particularly well--suited is the range of transition metal (II) formates, which can form a variety of structures ranging from mesoporous 3D frameworks [2,3] to isolated 1D chains [4]. As these structures are usually composed of M 2+ octahedra linked by various 1--or 3--atom bridging ligands [5], they often exhibit rather exotic magnetic interactions and are of interest as low--dimensional, highly anisotropic magnetic materials [6] and potentially as multiferroics [7]. We Figure 1.…”
An ambient-pressure solution route and an improved solvothermal synthetic method have been developed to produce polycrystalline powders and large single crystals of NH 4 MCl 2 (HCOO) (M = Fe, Co, Ni). The magnetic structure of the 1D linear chain compound NH 4 FeCl 2 (HCOO) has been determined by low-temperature neutron powder diffraction, revealing ferromagnetic intra-chain interactions and antiferromagnetic inter-chain interactions. The newly-reported Co and Ni analogues are isostructural with NH 4 FeCl 2 (HCOO), but there are significant differences in the magnetic properties of each compound; the Ni analogue behaves similarly to the Fe compound but with stronger magnetic coupling, exhibiting antiferromagnetic ordering (T N = 8.5 K) and a broad metamagnetic transition between 2-5 T, while the Co analogue does not order magnetically above 2 K, despite strong antiferromagnetic nearest-neighbor interactions.
“…One class of compounds for which this methodology is particularly well--suited is the range of transition metal (II) formates, which can form a variety of structures ranging from mesoporous 3D frameworks [2,3] to isolated 1D chains [4]. As these structures are usually composed of M 2+ octahedra linked by various 1--or 3--atom bridging ligands [5], they often exhibit rather exotic magnetic interactions and are of interest as low--dimensional, highly anisotropic magnetic materials [6] and potentially as multiferroics [7]. We Figure 1.…”
An ambient-pressure solution route and an improved solvothermal synthetic method have been developed to produce polycrystalline powders and large single crystals of NH 4 MCl 2 (HCOO) (M = Fe, Co, Ni). The magnetic structure of the 1D linear chain compound NH 4 FeCl 2 (HCOO) has been determined by low-temperature neutron powder diffraction, revealing ferromagnetic intra-chain interactions and antiferromagnetic inter-chain interactions. The newly-reported Co and Ni analogues are isostructural with NH 4 FeCl 2 (HCOO), but there are significant differences in the magnetic properties of each compound; the Ni analogue behaves similarly to the Fe compound but with stronger magnetic coupling, exhibiting antiferromagnetic ordering (T N = 8.5 K) and a broad metamagnetic transition between 2-5 T, while the Co analogue does not order magnetically above 2 K, despite strong antiferromagnetic nearest-neighbor interactions.
“…As we known, the azido anion is af avorite bridging ligand for constructing magnetic molecule materials due to its versatile coordination modes and efficient mediating different types of magnetic exchange interactions [1]. In particularly, alarge number of copper-azido compounds with interesting topologies have been well documented thanks to many possible bridging modes of the azido ligand and flexible coordination numbers of the Cu(II) ion [2][3][4][5][6][7].The molecular structure of the title compound consists of centrosymmetric tetranuclear molecule of formula [Cu 4 (mesalen) 2 (m 1,1 -N 3 ) 2 (N 3 ) 2 ](mesalen =(bis(ethane-1,2-diylbis((1-(2-oxidophenyl)ethyl)amido)), whicha re similara sthe previous tetranuclear copper compounds [8].…”
Section: Discussionmentioning
confidence: 99%
“…While, the central copper Cu(2) ions takes on a square pyramid geometry with two phenoxo oxygen atomsfrom one ligand, and three nitrogen atomsfrom one terminal azido and two bridging azido ligands respectively. In the title compound, the bond lengths of Cu-O are in the range of 1 ( …”
“…Magnetic MOFs and molecular magnets reported with their designs, synthetic approaches, structures, and physical properties [25][26][27][28][29][30][31][32][33] are both branches of coordination chemistry where metals are bound in a solid by coordination bonds to organic linkers. There exist several reviews dealing with the different aspects of magnetism [34][35][36][37][38].…”
Section: Magnetic Metal-organic Frameworkmentioning
Metal-organic frameworks (MOFs), also known as hybrid inorganic-organic materials, represent an emerging class of materials that have attracted the imagination of solid-state chemists because MOFs combine unprecedented levels of porosity with a range of other functional properties that occur through the metal moiety and/or the organic ligand. The purpose of this critical review is to give a representative and comprehensive overview of the arising developments in the field of functional metal-organic frameworks, including luminescence, magnetism, and porosity through presenting examples. This review will be of interest to researchers and synthetic chemists attempting to design multifunctional MOFs.
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