Multi-Noncentrosymmetric Polar Order in 2D Hybrid Lead Chloride with Broadband Emission and High-Temperature Second-Harmonic Generation Switching.

Two-dimensional lead halide perovskites represent a fascinating class of hybrid semiconductors for solar cell, light-emitting, nonlinear optical (NLO), and ferroelectric applications. A notable subset within this category is luminescent ferroelectrics, which have garnered considerable attention for their potential in integrated photoelectronic devices. In this study, we employed an organic amine halogenation strategy (also referred to as halogen engineering), which is renowned for its efficacy in inducing polar order through crystal engineering. Consequently, we synthesized a layered Ruddlesden-Popper (RP) lead chloride comprising 3-chloropropylammonium cations (CPA+), with the chemical formula CPA2PbCl4. This compound features as many as four temperature-dependent crystal phases, with phase transitions observed at T1 = 353.1 K (343.9 K), T2 = 211.7 K (208.6 K), and T3 = 182.0 K (178.2 K) in the heating (cooling) cycles. Employing a multitechnique approach─including thermal analysis, X-ray diffraction, dielectric and pyroelectric current measurements, Raman spectroscopy, and second-harmonic generation (SHG) studies─we determined the mechanisms of the structural phase transitions. Our findings demonstrate polar order of phase II (space group Cmc21), phase III (space group Pna21), and phase IV (space group Pca21), while also confirming the centrosymmetric nature of phase I (space group Cmce). X-ray diffraction data revealed that the I to II PT is of a ferroelectric nature, devoid of ferroelastic strain, a conclusion further supported by pyroelectric measurements. CPA2PbCl4 features negative linear thermal expansion and broadband emission, which transitions to white light above 180 K. Remarkably, CPA2PbCl4 also demonstrates high-temperature SHG on-off switching with a high contrast ratio of 300:1 along with good switching stability, as evidenced by SHG cycling studies at heating/cooling rates ranging from 5 to 50 K/min. This SHG study also sets new standards for the field of SHG switching by providing a method to quantify the thermal responsiveness of SHG-switchable materials using the treq (time requirement) parameter. Overall, our findings show that the halogenation strategy has led to the discovery of a rare example of an RP perovskite exhibiting coexistence of white-light emission, SHG on-off thermal bistability, ferroelectricity, and negative linear thermal expansion.

Temperature and volumetric effects on structural and dielectric properties of hybrid perovskites.

Three-dimensional organic-inorganic perovskites are rapidly evolving materials with diverse applications. This study focuses on their two representatives - acetamidinium manganese(II) formate (AceMn) and formamidinium manganese(II) formate (FMDMn) - subjected to varying temperature and pressure. We show that AceMn undergoes atypical pressure-induced structural transformations at room temperature, increasing the symmetry from ambient-pressure P21/n phase II to the high-pressure Pbca phase III. In turn, FMDMn in its C2/c phase II displays temperature- and pressure-induced ordering of cage cations that proceeds without changing the phase symmetry or energy barriers. The FMD+ cations do not order under constant volume across the pressure-temperature plane, despite similar pressure and temperature evolution of the unit-cell parameters. Temperature and pressure affect the cage cations differently, which is particularly pronounced in their relaxation dynamics seen by dielectric spectroscopy. Their motion require a rearrangement of the metal-formate framework, resulting in the energy and volumetric barriers defined by temperature-independent activation energy and activation volume parameters. As this process is phonon-assisted, the relaxation time is strongly temperature-dependent. Consequently, relaxation times do not scale with unit-cell volume nor H-bond lengths in formates, offering the possibility of tuning their electronic properties by external stimuli (like temperature or pressure) even without any structural changes.

Three-State Dielectric Switching within a Narrow Temperature Range in Isopropylammonium Lead Iodide, a One-Dimensional Perovskite with Polar Phase.

The phenomenon of dielectric switching has garnered considerable attention due to its potential applications in electronic and photonic devices. Typically, hybrid organic-inorganic perovskites, HOIPs, exhibit a binary (low-high) dielectric state transition, which, while useful, represents only the tip of the iceberg in terms of functional relevance. One way to boost the versatility of applications is the discovery of materials capable of nonbinary switching schemes, such as three-state dielectric switching. The ideal candidate for that task would exhibit a trio of attributes: two reversible, first-order phase transitions across three distinct crystal phases, minimal thermal hysteresis, and pronounced, step-like variations in dielectric permittivity, with a substantial change in its real part. Here, we demonstrate a one-dimensional lead halide perovskite with the formula (CH3)2C(H)NH3)PbI3, abbreviated as ISOPrPbI3, that fulfills these criteria and demonstrates three-state dielectric switching within a narrow temperature range of ca. 45 K. Studies on ISOPrPbI3 also revealed the polar nature of the low-temperature phase III below 266 K through pyrocurrent experiments, and the noncentrosymmetric character of the intermediate phase II and low-temperature phase III is confirmed via second harmonic generation measurements. Additionally, luminescence studies of ISOPrPbI3 have demonstrated combined broadband and narrow emission properties. The introduction of ISOPrPbI3 as a three-state dielectric switch not only addresses the limitations posed by the wide thermal gap between dielectric states in previous materials but also opens new avenues for the development of nonbinary dielectric switchable materials.

Revisiting a (001)-oriented layered lead chloride templated by 1,2,4-triazolium: structural phase transitions, lattice dynamics and broadband photoluminescence.

This study revisits a (001)-oriented layered lead chloride templated by 1,2,4-triazolium, Tz2PbCl4, which recently has been an object of intense research but still suffers from gaps in characterization. Indeed, the divergent reports on the crystal structures of Tz2PbCl4 at various temperatures, devoid of independent verification of chiral phases through second harmonic generation (SHG), have led to an unresolved debate regarding the existence of a low-temperature phase transition (PT) and the noncentrosymmetric nature of the low-temperature phase. Now, by combining differential scanning calorimetry, single-crystal X-ray diffraction, dielectric, as well as linear and nonlinear optical spectroscopies on Tz2PbCl4, we reveal a sequence of reversible PTs at T1 = 361 K (phase I-II), T2 = 339 K (phase II-III), and T3 = 280 K (phase III-IV). No SHG activity could be registered for any of the four crystal phases, as checked by wide-temperature range SHG screening, supporting their centrosymmetry. The dipole relaxation processes indicate a decrease in activation energy with increasing temperature, from 0.60, 0.38, to 0.24 eV observed for phase IV (space group P21/c), phase III (Pnma), and phase II (Cmcm), respectively. This change is interpreted as a result of the diminishing strength of H-bonds as the system transforms from phase IV to III and subsequently to II. The weaker H-bonds facilitate the reorientation of Tz+ cations in the presence of an external electric field. The photoluminescence spectra of Tz2PbCl4 reveal an intriguing interplay of narrow and broadband emission, linked respectively to free excitons and excitons trapped on defects. Notably, as the temperature decreases from 300 K to 16 K, both the emission bands exhibit distinctive blue and red shifts, indicative of increased in-plane octahedral distortion. This dynamic behaviour transforms the photoluminescence of Tz2PbCl4 from greenish-blue at 300 K to yellowish-green at 13 K, enriching our understanding of 2D lead halide perovskites and highlighting the optoelectronic potential of Tz2PbCl4.

Mixology of MA1-x EA x PbI3 Hybrid Perovskites: Phase Transitions, Cation Dynamics, and Photoluminescence.

Mixing molecular cations in hybrid lead halide perovskites is a highly effective approach to enhance the stability and performance of optoelectronic devices based on these compounds. In this work, we prepare and study novel mixed 3D methylammonium (MA)-ethylammonium (EA) MA1-x EA x PbI3 (x < 0.4) hybrid perovskites. We use a suite of different techniques to determine the structural phase diagram, cation dynamics, and photoluminescence properties of these compounds. Upon introduction of EA, we observe a gradual lowering of the phase-transition temperatures, indicating stabilization of the cubic phase. For mixing levels higher than 30%, we obtain a complete suppression of the low-temperature phase transition and formation of a new tetragonal phase with a different symmetry. We use broad-band dielectric spectroscopy to study the dielectric response of the mixed compounds in an extensive frequency range, which allows us to distinguish and characterize three distinct dipolar relaxation processes related to the molecular cation dynamics. We observe that mixing increases the rotation barrier of the MA cations and tunes the dielectric permittivity values. For the highest mixing levels, we observe the signatures of the dipolar glass phase formation. Our findings are supported by density functional theory calculations. Our photoluminescence measurements reveal a small change of the band gap upon mixing, indicating the suitability of these compounds for optoelectronic applications.

Effect of Dimensionality on Photoluminescence and Dielectric Properties of Imidazolium Lead Bromides.

Hybrid organic-inorganic lead halide perovskites have emerged as promising materials for various applications, including solar cells, light-emitting devices, dielectrics, and optical switches. In this work, we report the synthesis, crystal structures, and linear and nonlinear optical as well as dielectric properties of three imidazolium lead bromides, IMPbBr3, IM2PbBr4, and IM3PbBr5 (IM+ = imidazolium). We show that these compounds exhibit three distinct structure types. IMPbBr3 crystallizes in the 4H-hexagonal perovskite structure with face- and corner-shared PbBr6 octahedra (space group P63/mmc at 295 K), IM2PbBr4 adopts a one-dimensional (1D) double-chain structure with edge-shared octahedra (space group P1̅ at 295 K), while IM3PbBr5 crystallizes in the 1D single-chain structure with corner-shared PbBr6 octahedra (space group P1̅ at 295 K). All compounds exhibit two structural phase transitions, and the lowest temperature phases of IMPbBr3 and IM3PbBr5 are noncentrosymmetric (space groups Pna21 at 190 K and P1 at 100 K, respectively), as confirmed by measurements of second-harmonic generation (SHG) activity. X-ray diffraction and thermal and Raman studies demonstrate that the phase transitions feature an order-disorder mechanism. The only exception is the isostructural P1̅ to P1̅ phase transition at 141 K in IM2PbBr4, which is of a displacive type. Dielectric studies reveal that IMPbBr3 is a switchable dielectric material, whereas IM3PbBr5 is an improper ferroelectric. All compounds exhibit broadband, highly shifted Stokes emissions. Features of these emissions, i.e., band gap and excitonic absorption, are discussed in relation to the different structures of each composition.

[Methylhydrazinium]2PbCl4, a Two-Dimensional Perovskite with Polar and Modulated Phases.

Two-dimensional (2D) lead halide perovskites are a family of materials at the heart of solar cell, light-emitting diode, and photodetector technologies. This perspective leads to a number of synthetic efforts toward materials of this class, including those with prescribed polar architectures. The methylhydrazinium (MHy+) cation was recently presumed to have an unusual capacity to generate non-centrosymmetric perovskite phases, despite its intrinsically nonchiral structure. Here, we witness this effect once again in the case of the Ruddlesden-Popper perovskite phase of formula MHy2PbCl4. MHy2PbCl4 features three temperature-dependent crystal phases, with two first-order phase transitions at T1 = 338.2 K (331.8 K) and T2 = 224.0 K (205.2 K) observed in the heating (cooling) modes, respectively. Observed transitions involve a transformation from high-temperature orthorhombic phase I, with the centrosymmetric space group Pmmn, through the room-temperature modulated phase II, with the average structure being isostructural to I, to the low-temperature monoclinic phase III, with non-centrosymmetric space group P21. The intermediate phase II is a rare example of a modulated structure in 2D perovskites, with Pmmn(00γ)s00 superspace symmetry and modulation vector q ≅ 0.25c*. MHy2PbCl4 beats the previous record of MHy2PbBr4 in terms of the shortest inorganic interlayer distance in 2D perovskites (8.79 Šat 350 K vs 8.66 Šat 295 K, respectively). The characteristics of phase transitions are explored with differential scanning calorimetry, dielectric, and Raman spectroscopies. The non-centrosymmetry of phase III is confirmed with second harmonic generation (SHG) measurements, and polarity is demonstrated by the pyroelectric effect. MHy2PbCl4 also exhibits thermochromism, with the photoluminescence (PL) color changing from purplish-blue at 80 K to bluish-green at 230 K. The demonstration of polar characteristics for one more member of the methylhydrazinium perovskites settles a debate about whether this approach can present value for the crystal engineering of acentric solids similar to that which was recently adopted by a so-called fluorine substitution effect.

Near-Infrared Phosphorescent Hybrid Organic-Inorganic Perovskite with High-Contrast Dielectric and Third-Order Nonlinear Optical Switching Functionalities.

Hybrid organic-inorganic perovskites providing integrated functionalities for multimodal switching applications are widely sought-after materials for optoelectronics. Here, we embark on a study of a novel pyrrolidinium-based cyanide perovskite of formula (C4H10N)2KCr(CN)6, which displays thermally driven bimodal switching characteristics associated with an order-disorder phase transition. Dielectric switching combines two features important from an application standpoint: high permittivity contrast (Δε' = 38.5) and very low dielectric losses. Third-order nonlinear optical switching takes advantage of third-harmonic generation (THG) bistability, thus far unprecedented for perovskites and coordination polymers. Structurally, (C4H10N)2KCr(CN)6 stands out as the first example of a three-dimensional stable perovskite among formate-, azide-, and cyanide-based metal-organic frameworks comprising large pyrrolidinium cations. Its stability, reflected also in robust switching characteristics, has been tracked down to the Cr3+ component, the ionic radius of which provides a large enough metal-cyanide cage for the pyrrolidinium cargo. While the presence of polar pyrrolidinium cations leads to excellent switchable dielectric properties, the presence of Cr3+ is also responsible for efficient phosphorescence, which is remarkably shifted to the near-infrared region (770 to 880 nm). The presence of Cr3+ was also found indispensable to the THG switching functionality. It is also found that a closely related cobalt-based analogue doped with Cr3+ ions displays distinct near-infrared phosphorescence as well. Thus, doping with Cr3+ ions is an effective strategy to introduce phosphorescence as an additional functional property into the family of cobalt-cyanide thermally switchable dielectrics.

Multiple rotor modes and how to trigger them: complex cation ordering in the family of relaxing hybrid formates.

A combination of structural, dielectric and calorimetric studies is used to describe a highly atypical behaviour of novel hybrid formate [NH3(CH2)3NH2(CH2)3NH3][Mn(HCOO)3]3, incorporating large triprotonated molecular cations. Two successive phase transitions, switching between fast multiple rotor modes, and the surprising probable coexistence of static and dynamic disorder are discussed for this compound.

Metal-Formate Framework Stiffening and Its Relevance to Phase Transition Mechanism.

In the last decade, one of the most widely examined compounds of motal-organic frameworks was undoubtedly ((CH3)2NH2)(Zn(HCOO)3), but the problem of the importance of framework dynamics in the order-disorder phase change of the mechanism has not been fully clarified. In this study, a combination of temperature-dependent dielectric, calorimetric, IR, and Raman measurements was used to study the impact of ((CH3)2NH2)(Zn(DCOO)3) formate deuteration on the phase transition mechanism in this compound. This deuteration led to the stiffening of the metal-formate framework, which in turn caused an increase in the phase transition temperature by about 5 K. Interestingly, the energetic ordering of DMA+ cations remained unchanged compared to the non-deuterated compound.

Benzyltrimethylammonium cadmium dicyanamide with polar order in multiple phases and prospects for linear and nonlinear optical temperature sensing.

Coordination polymers with multiple non-centrosymmetric phases have sparked substantial research efforts in the materials community. We report the synthesis and properties of a hitherto unknown cadmium dicyanamide coordination polymer comprising benzyltrimethylammonium cations (BeTriMe+). The room-temperature (RT) crystal structure of [BeTriMe][Cd(N(CN)2)3] (BeTriMeCd) is composed of Cd centers linked together by triple dca-bridges to form one-dimensional chains with BeTriMe+ cations located in void spaces between the chains. The structure is polar, the space group is Cmc21, and the spontaneous polarization in the c-direction is induced by an arrangement of BeTriMe+ dipoles. BeTriMeCd undergoes a second-order phase transition (PT) at T1 = 268 K to a monoclinic polar phase P21. Much more drastic structural changes occur at the first-order PT observed in DSC at T2 = 391 K. Raman data prove that the PT at T2 leads to extensive rearrangement of the Cd-dca coordination sphere and pronounced disorder of both dca and BeTriMe+. On cooling, the HT polymorph transforms at T3 = 266 K to another phase of unknown symmetry. Temperature-resolved second harmonic generation (TR-SHG) studies at 800 nm confirm the structural non-centrosymmetry of all the phases detected. Optical studies indicate that BeTriMeCd exhibits at low temperatures an intense emission under 266 nm excitation. Strong temperature dependence of both one-photon excited luminescence and SHG response allowed for the demonstration of two disparate modes of optical thermometry for a single material. One is the classic ratiometric luminescence thermometry employing linear excitation in the ultraviolet region while the other is single-band SHG thermometry, a thus far unprecedented subtype of nonlinear optical thermometry. Thus, BeTriMeCd is a rare example of a dicyanamide framework exhibiting polar order, SHG activity, photoluminescence properties and linear and nonlinear optical temperature sensing capability.

Cadmium and manganese hypophosphite perovskites templated by formamidinium cations: dielectric, optical and magnetic properties.

The recently discovered hypophosphite perovskites are promising functional materials. This contribution is devoted to the structural, thermal, dielectric, Raman and optical studies of a new hybrid organic-inorganic perovskite, [FA]Cd(H2POO)3 (FA = formamidinium, NH2CHNH2+). We also report the thermal, magnetic, dielectric and optical properties of the known perovskite [FA]Mn(H2POO)3. [FA]Cd(H2POO)3 crystallizes in a monoclinic structure, with the space group C2/c, and transforms at 190 K to another monoclinic structure, with the space group P21/n. For both compounds, the FA+ is disordered through the two-fold axis in the high-temperature (HT) phases. However, lowering of the temperature of [FA]Mn(H2POO)3 results in the complete ordering of FA+, while the organic cations still occupy two positions in [FA]Cd(H2POO)3. Raman data provide strong evidence that both FA+ cations have the same or a very similar structure and that the phase transition is triggered by an ordering of the FA+ cations. The dielectric studies confirm the order-disorder nature of the phase transition and reveal the presence of two dipolar relaxations observed in the 320-220 K range and near the phase transition temperature. The low-temperature (LT) process exhibits the classical Arrhenius-type behaviour, whereas the behaviour of the HT relaxation suggests glass-like behaviour. Magnetic studies show that [FA]Mn(H2POO)3 is an example of a canted antiferromagnet with a low ordering temperature of 2.4 K. Diffuse reflectance studies show that the Mn (Cd) hypophosphite is a wide bandgap material with Eg = 5.20 eV (5.42 eV). Upon ultraviolet excitation (266 nm), [FA]Mn(H2POO)3 exhibits reddish-orange emission at 656 nm associated with the 4T1g(G) →6A1g(S) transition of octahedrally coordinated Mn2+ ions. [FA]Cd(H2POO)3 shows significantly weaker purplish-blue emission at low temperatures composed of two bands at 425 and 443 nm, which are almost completely quenched at 160 K. For both compounds, CIE chromaticity coordinates show negligible change with temperature. Furthermore, the intensity of the observed emissions decreases quickly with increasing temperature, suggesting the possible application of [FA]Mn(H2POO)3 in non-contact optical thermometry.

Suppression of phase transitions and glass phase signatures in mixed cation halide perovskites.

Cation engineering provides a route to control the structure and properties of hybrid halide perovskites, which has resulted in the highest performance solar cells based on mixtures of Cs, methylammonium, and formamidinium. Here, we present a multi-technique experimental and theoretical study of structural phase transitions, structural phases and dipolar dynamics in the mixed methylammonium/dimethylammonium MA1-xDMAxPbBr3 hybrid perovskites (0 ≤ x ≤ 1). Our results demonstrate a significant suppression of the structural phase transitions, enhanced disorder and stabilization of the cubic phase even for a small amount of dimethylammonium cations. As the dimethylammonium concentration approaches the solubility limit in MAPbBr3, we observe the disappearance of the structural phase transitions and indications of a glassy dipolar phase. We also reveal a significant tunability of the dielectric permittivity upon mixing of the molecular cations that arises from frustrated electric dipoles.

Pyrrolidinium-Based Cyanides: Unusual Architecture and Dielectric Switchability Triggered by Order-Disorder Process.

Two three-dimensional metal-organic compounds of the formula Pyr2KM(CN)6, where M = Co, Fe and Pyr = pyrrolidinium ((CH2)4NH2+), have been found to crystallize at room temperature in a monoclinic structure, space group P21/c. They are cyano-bridged compounds with an unprecedented type of architecture containing pyrrolidinium cations in the voids. The materials have been investigated by X-ray diffraction, dielectric, and spectroscopic methods as a function of temperature in order to determine their properties and the mechanism of the reversible phase transitions occurring at ca. 345-370 K. The phase transitions in both crystals are first order and are associated with a symmetry increase to a rhombohedral structure (space group R3̅m) as well as a significant disorder of organic cations above Tc. On the basis of Raman scattering and IR spectroscopy it has been assumed that the phase transition in both crystals is triggered by thermally induced pseudorotation of the organic cation and large out-of-plane motions of its atoms followed by a "click-in" of the cyanide bridges. The materials have been proposed as possible switchable dielectrics due to their respective high differences in dielectric permittivities across the phase transition.

Crystal growth, IR specular reflectance and polarized Raman studies of LiNa5Mo9O30 polar single crystal.

A non-centrosymmetric, polar LiNa5Mo9O30 single crystal was grown using Kyropoulos technique and characterized by polarized Raman scattering and polarized infrared specular reflection spectroscopy at room temperature. The comparison to the polycrystalline spectra has been made and assignment of all observed modes to the respective vibrations and their symmetry has been proposed. Based on the four parameter model the infrared reflection spectra were analyzed and the LO-TO splitting has been determined for the observed modes. Stronger anharmonicity of bands assigned to stretching vibrations of the Mo-O⋯Mo bridges has been evidenced. Our results show that this crystal is attractive and promising SRS-active nonlinear optical material for up- and down-Raman laser-frequency converters with the most intense lasing lines at 947 and 884 cm-1. Dielectric permittivity studies in the frequency domain exhibit two anomalies that are assigned to thermally activated relaxation and conductivity processes. The observed increase in electrical conductivity above 400 K is dominated by ionic contribution and change of the conductivity mechanism.

Phase transition in the extreme: a cubic-to-triclinic symmetry change in dielectrically switchable cyanide perovskites.

Two novel three-dimensional metal-organic compounds of formula FA2KM(CN)6, where M = Co, Fe and FA = formamidinium (CH(NH2)2+), have been found to crystallize in a perovskite-like architecture. They have been investigated by X-ray diffraction, dielectric and spectroscopic methods as a function of temperature in order to determine the interactions in the crystals and the mechanism of phase transitions occurring at ca. 321 K upon heating. The phase transitions in both crystals are of first order and originate from the ordering of the formamidinium cations below TC. Symmetry reduction (cubic-to-triclinic) seems to be the strongest upon temperature decrease among known metal-organic frameworks. These materials have been proposed as possible switchable dielectrics with a convenient near-room-temperature transition temperature.

Structural, phonon, magnetic and optical properties of novel perovskite-like frameworks of TriBuMe[M(dca)3] (TriBuMe = tributylmethylammonium; dca = dicyanamide; M = Mn2+, Fe2+, Co2+, Ni2+).

We report the synthesis, crystal structures, thermal, optical and phonon properties of four new metal dicyanamide frameworks templated using tributylmethylammonium cations (TriBuMe+). Our results show that these compounds crystallize in a three-dimensional perovskite-like monoclinic structure, space group P21/n, with two inequivalent TriBuMe+, one well-ordered and the second one showing distinct disorder. DSC and X-ray diffraction show that TriBuMeMn undergoes an order-disorder structural phase transition near 380 K associated with an increase in the symmetry to the orthorhombic Pnma. Phase transitions are also observed for Ni and Fe analogues. The associated change in the phase transition entropy is very large (up to 66.7 J kg-1 K-1 for TriBuMeNi), suggesting that these compounds might be promising barocaloric materials. Raman and IR data confirm the same monoclinic structures for all compounds and show that all changes on heating to 430-450 K are reversible after cooling the samples to room temperature. Magnetic studies indicate that all studied compounds are paramagnets at least down to 2 K. Optical studies indicate that TriBuMeMn has an energy band gap of 4.95 eV and exhibits orange emission under 420 nm excitation with the activation energy for thermal quenching of 0.0673 eV.

Temperature-dependent studies of a new two-dimensional cadmium dicyanamide framework exhibiting an unusual temperature-induced irreversible phase transition into a three-dimensional perovskite-like framework.

We report the synthesis, crystal structure, and thermal, dielectric, optical and phonon properties of a new two-dimensional (2D) cadmium(ii) complex [(C3H7)4N][Cd(N(CN)2)3]. Our results show that this compound crystallizes in a two-dimensional monoclinic structure, with the space group P2/n, with ordered tetrapropylammonium cations and disorder of some dicyanamide linkers. It undergoes a structural phase transition at 245 K into another low-temperature (LT) monoclinic structure, with the space group P21/n. X-ray diffraction, dielectric, IR and Raman studies show that freezing of the dca motions stands at the origin of the phase transition. Optical studies indicate that this material has an energy band gap of 4.83 eV and exhibits intense bluish-white emission under 266 nm excitation. Upon heating, this compound undergoes an irreversible phase transition near 390 K associated with significant bond rearrangement. The high-temperature (HT) phase has a three-dimensinal (3D) perovskite-like structure. [(C3H7)4N][Cd(N(CN)2)3] is, therefore, the first example of a hybrid organic-inorganic dicyanamide exhibiting a temperature-induced reconstructive transition from a 2D (layered) structure to a 3D (perovskite-like) structure.

Synthesis and temperature-dependent studies of a perovskite-like manganese formate framework templated with protonated acetamidine.

We report the synthesis, crystal structure, thermal, dielectric, phonon and magnetic properties of the [CH3C(NH2)2][Mn(HCOO)3] (AceMn) compound. Our results show that this compound crystallizes in the perovskite-like orthorhombic structure, space group Imma. It undergoes a structural phase transition at 304 K into a monoclinic structure, space group P21/n. X-ray diffraction, dielectric, IR and Raman studies show that the ordering of the acetamidinium cations triggers the phase transition. Low-temperature magnetic studies show that this compound exhibits weak ferromagnetic properties below 9.0 K.

The effect of K+ cations on the phase transitions, and structural, dielectric and luminescence properties of [cat][K0.5Cr0.5(HCOO)3], where cat is protonated dimethylamine or ethylamine.

We report the synthesis, crystal structure, and dielectric, vibrational and emission spectra of two novel heterometallic perovskite-type metal-organic frameworks (MOFs) of the following formula: [(CH3)2NH2][K0.5Cr0.5(HCOO)3] (DMAKCr) and [C2H5NH3][K0.5Cr0.5(HCOO)3] (EtAKCr). DMAKCr crystallizes in a trigonal structure (R3[combining macron] space group) and undergoes an order-disorder phase transition to the monoclinic system (P1[combining macron] space group) at about 190 K. The dielectric studies confirm the presence of first-order relaxor-like structural transformation. In the high-temperature phase, the dimethylammonium cations are dynamically disordered over three equal positions and upon cooling the dynamical disorder evolves into a two-fold one. This partial ordering is accompanied by a small distortion of the metal-formate framework. EtAKCr crystallizes in a monoclinic structure (P21/n space group) with ordered EtA+ cations and does not experience any phase transition. The differences in the thermal behavior caused by the substitution of Na+ ions by larger K+ ions in the [cat]MIMIII (cat = DMA+, EtA+, MI = Na+, K+ and MIII = Cr3+ and Fe3+) heterometallic MOF family are discussed taking into account the impact of the hydrogen bond (HB) pattern and other factors affecting the stability of metal-formate frameworks. The optical studies show that DMANaCr and EtAKCr exhibit Cr3+-based emission characteristics for intermediate ligand field strength.