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Multiferroic Behavior Associated with an Order−Disorder Hydrogen Bonding Transition in Metal−Organic Frameworks (MOFs) with the Perovskite ABX3 Architecture

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TLDR
This research opens up a new class of multiferroics in which the electrical ordering is achieved by means of hydrogen bonding, and the compounds become canted weak ferromagnets below 40 K.
Abstract
Multiferroic behavior in perovskite-related metal−organic frameworks of general formula [(CH3)2NH2]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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Organic–Inorganic Perovskites: Structural Versatility for Functional Materials Design

TL;DR: This review will explore beyond the current focus on three-dimensional (3-D) lead(II) halide perovskites, to highlight the great chemical flexibility and outstanding potential of the broader class of 3-D and lower dimensional organic-based perovSKite family for electronic, optical, and energy-based applications as well as fundamental research.
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Ferroelectric Metal–Organic Frameworks

TL;DR: The ferroelectric properties of some lately reported MOFs will be presented in this talk, covering their triggering mechanism, designing strategies and potential applications as multifunctional materials.
Journal ArticleDOI

Chemically diverse and multifunctional hybrid organic–inorganic perovskites

TL;DR: Hybrid organic-inorganic perovskites (HOIPs) as mentioned in this paper can have a diverse range of compositions including halides, azides, formates, dicyanamides, cyanides, and Dicyanometallates.
Journal ArticleDOI

Metal-organic frameworks as a tunable platform for designing functional molecular materials.

TL;DR: Through the combination of molecular synthesis and crystal engineering, MOFs present an unprecedented opportunity for the rational and precise design of functional materials.
Journal ArticleDOI

Solid-state principles applied to organic–inorganic perovskites: new tricks for an old dog

TL;DR: In this paper, the authors extend the classical concept of ionic tolerance factors to hybrid organic-inorganic materials and predict the existence of several hitherto undiscovered hybrid perovskite phases.
References
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Journal ArticleDOI

Functional porous coordination polymers.

TL;DR: The aim is to present the state of the art chemistry and physics of and in the micropores of porous coordination polymers, and the next generation of porous functions based on dynamic crystal transformations caused by guest molecules or physical stimuli.
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Hybrid porous solids: past, present, future

TL;DR: The state-of-the-art on hybrid porous solids, their advantages, their new routes of synthesis, the structural concepts useful for their 'design', aiming at reaching very large pores are presented.
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Metal-organic frameworks: a new class of porous materials

TL;DR: A review of the synthesis, structure, and properties of metal-organic frameworks (MOFs) is presented in this paper, highlighting the important advances in their research over the past decade.
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Structural diversity and chemical trends in hybrid inorganic–organic framework materials

TL;DR: The diversity of this complex class of materials is examined, a simple but systematic classification is proposed, and the growing evidence that many hybrid frameworks tend to form under thermodynamic rather than kinetic control when the synthesis is carried out under hydrothermal conditions is discussed.
Journal ArticleDOI

Electric-field-induced spin flop in BiFeO3 single crystals at room temperature.

TL;DR: It is argued here that the coupling between the two orders may be stronger in the bulk than in thin films where the cycloid is absent, and that the antiferromagnetic and ferroelectric order parameters are intimately coupled.
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