Single-molecule Magnet Properties of Silole- and Stannole-ligated Erbium Cyclo-octatetraenyl Sandwich Complexes.

The synthesis, structures and magnetic properties of an η5-silole complex and an η5-stannole complex of erbium are reported. The sandwich complex anions [(η5-CpSi)Er(η8-COT)]- and [(η5-CpSn)Er(η8-COT)]-, where CpSi is [SiC4-2,5-(SiMe3)2-3,4-Ph2]2- (1Si), CpSn is [SnC4-2,5-(SiMe3)2-3,4-Me2]2- (1Sn) and COT = cyclo-octatetraenyl, were obtained as their [K(2.2.

Photochromic Dysprosium Single-Molecule Magnet Featuring Reversible Redox Transformation of Polyoxomolybdate Moiety.

A photochromic dysprosium-based single-molecule magnet [Dy(CyPhPO)(HO)](PMoO) ⋅ 3CyPhPO⋅HO (1-Dy) is synthesized via cocrystal engineering of a polyoxomolybdate (POMo) anion and an Ising-type cation with pseudo pentagonal bipyramidal geometry. Upon ultraviolet irradiation, Mo-to-Mo single-electron photoreduction occurs in the POMo moiety, resulting in significant changes of optical and magnetic properties. The emergence of intervalence charge-transfer transitions in heteropoly blue state 1-Dy* facilitates photothermal conversion in near-infrared region.

Synergetic spin crossover and fluorescence in a mononuclear iron(III) complex.

Two mononuclear iron(III) complexes (XEA)[Fe(azp)]·HO (Hazp = 2,2'-azodiphenol, XEA = 2-fluoroethylammonium and 2-chloroethylammonium) are synthesized, which exhibit the counterion dependence of magnetic and fluorescent properties. The synergetic effect between abrupt spin crossover and fluorescence is observed in an iron(III) complex for the first time.

Integrating Polyoxometalate into Dy(III)-based Single-molecule Magnets with Pentagonal Bipyramidal Symmetry.

Polyoxometalates (POMs) with various coordination fashions are versatile ligands for constructing single-ion magnets (SIMs), but enforcing POM-SIMs with a specific geometry remains a synthetic challenge. Herein, we synthesized a POM-cocrystallized Dy-SIM [Dy(OPPh)(HO)][PWO]·4EtOH () and a POM-ligated Dy-SIM [{Dy(OPPh)(HO)}{PWO}]·PhPO·HO () with pentagonal bipyramidal local coordination geometry. Magnetic measurements indicate that displays field-induced single-molecule magnet (SMM) behavior and the relaxation is dominated by under-barrier processes.

Integrating Molecular Motions in Ternary Cocrystals for NIR-II Photothermal Conversion.

Organic photothermal conversion materials hold immense promise for various applications owing to their structural flexibility. Recent research has focused on enhancing near-infrared (NIR) absorption and mitigating radiative transition processes. In this study, we have developed a viable approach to the design of photothermal conversion materials through the construction of ternary organic cocrystals, by introducing a third component as a molecular blocker and motion unit into a binary donor-acceptor system.

Bidirectional photomagnetism, exciplex fluorescence and dielectric anomalies in a spin crossover Hofmann-type coordination polymer.

Stepped spin crossover (SCO) complexes with three or more spin states have promising applications in high-order data storage, multi-switches and multi-sensors. Further synergy with other functionalities, such as luminescence and dielectric properties, will provide a good chance to develop novel multifunctional SCO materials. Here, a bent pillar ligand and luminescent pyrene guest are integrated into a three-dimensional (3D) Hofmann-type metal-organic framework (MOF) [Fe(dpoda){Au(CN)}]·pyrene (dpoda = 2,5-di-(pyridyl)-1,3,4-oxadiazole).

Phase Transition Control in Molecular Solids via Complementarity of Hydrogen-Bond Strength.

Phase transitions in molecular solids involve synergistic changes in chemical and electronic structures, leading to diversification in physical and chemical properties. Despite the pivotal role of hydrogen bonds (H-bonds) in many phase-transition materials, it is rare and challenging to chemically regulate the dynamics and to elucidate the structure-property relationship. Here, four high-spin Co compounds were isolated and systematically investigated by modifying the ligand terminal groups (X=S, Se) and substituents (Y=Cl, Br).

Spin-State Control in Dysprosium(III) Metallacrown Magnets via Thioacetal Modification.

Integrating controllable spin states into single-molecule magnets (SMMs) enables precise manipulation of magnetic interactions at a molecular level, but remains a synthetic challenge. Herein, we developed a 3d-4f metallacrown (MC) magnet [DyNi(quinha)(sal)(py)](ClO) ⋅ 4HO (Hquinha=quinaldichydroxamic acid, Hsal=5-chlorosalicylaldehyde) wherein a square planar Ni is stabilized by chemical stacking. Thioacetal modification was employed via post-synthetic ligand substitutions and yielded [DyNi(quinha)(saldt)(py)](ClO) ⋅ 3HO (Hsaldt=4-chloro-2-(1,3-dithiolan-2-yl)phenol).

Two-dimensional spin-crossover coordination polymers based on the 1,1,2,2-tetra(pyridin-4-yl)ethene ligand.

A series of two-dimensional (2D) spin-crossover coordination polymers (SCO-CPs) [Fe(TPE)(NCX)]·solv (1: X = BH, solv = HO·2CHOH·DMF; 2: X = Se, solv = HO·2CHOH·0.5DMF; 3: X = S, solv = HO·2CHOH·0.5DMF) were synthesized by employing 1,1,2,2-tetra(pyridin-4-yl)ethene (TPE) and pseudohalide (NCX) coligands.

Cyanometallic charge engineering in spin crossover metal-organic frameworks.

In this study, we successfully synthesize cationic/neutral/anionic inverse-Hofmann-type spin crossover (SCO) frameworks with 1,1,2,2-tetrakis(4-(pyridine-4-yl)phenyl)-ethene ligand by means of cyanometallic charge engineering strategy. The cationic and neutral frameworks exhibit single-step thermally induced spin transition behaviors, while the SCO capability of anionic framework can be aroused by partial desolvation. This strategy provides a new idea to construct ionic SCO frameworks and extends the toolkit for SCO materials.

Radical-Induced Photochromic Silver(I) Metal-Organic Frameworks: Alternative Topology, Dynamic Photoluminescence and Efficient Photothermal Conversion Modulated by Anionic Guests.

Photogenerated radicals are an indispensable member of the state-of-the-art photochromic material family, as they can effectively modulate the photoluminescence and photothermal conversion performance of radical-induced photochromic complexes. Herein, two novel radical-induced photochromic metal-organic frameworks (MOFs), [Ag(TEPE)](AC) ⋅ /HO ⋅ /EtOH (1) and [Ag(TEPE)](NC) ⋅ 3HO ⋅ EtOH (2), are reported. Distinctly different topological networks can be obtained by judiciously introducing alternative π-conjugated anionic guests, including a new topological structure (named as sfm) first reported in this work, describing as 4,4,4,4-c net.

NIR-II photothermal conversion and imaging based on a cocrystal containing twisted components.

On account of the scarcity of molecules with a satisfactory second near-infrared (NIR-II) response, the design of high-performance organic NIR photothermal materials has been limited. Herein, we investigate a cocrystal incorporating tetrathiafulvalene (TTF) and tetrachloroperylene dianhydride (TCPDA) components. A stable radical was generated through charge transfer from TTF to TCPDA, which exhibits strong and wide-ranging NIR-II absorption.

Single-Crystal Transformation Engineering the Spin Change of Metal-Organic Frameworks via Cluster Deconstruction.

Spin crossover (SCO) materials with new architectures will expand and enrich the research in the SCO field. Here, we report two metal-organic frameworks (MOFs) containing tetradentate organic ligands and hexatopic linkers [Ag X (CN) ] (X=Br and I), which represents the first SCO MOF with clusters as building blocks. The silver halide cluster can be further removed after reacting with lithium tetracyanoquinodimethan (LiTCNQ).

High-stability spherical lanthanide nanoclusters for magnetic resonance imaging.

High-nuclear lanthanide clusters have shown great potential for the administration of high-dose mononuclear gadolinium chelates in magnetic resonance imaging (MRI). The development of high-nuclear lanthanide clusters with excellent solubility and high stability in water or solution has been challenging and is very important for expanding the performance of MRI. We used -methylbenzimidazole-2-methanol (HL) and LnCl·6HO to synthesize two spherical lanthanide clusters, Ln (Ln = Ho, Ho; and Ln = Gd, Gd), which are highly stable in solution.

Lanthanide-radical single-molecule magnets: current status and future challenges.

In the field of molecular magnetism, the lanthanide-radical (Ln-Rad) method has become one of the most appealing tactics for introducing strong magnetic interactions and has spurred on the booming development of heterospin single-molecule magnets (SMMs). The article is a timely retrospect on the research progress of Ln-Rad heterospin systems and special attention is invested on low dimensional Ln-Rad compounds with SMM behavior, primarily concerning with nitrogen-based radicals, semiquinone and nitroxide radicals. Rational design, molecular structures, magnetic behaviors and magneto-structural correlations are highlighted.

Dynamic Magnetic Properties of Germole-ligated Lanthanide Sandwich Complexes.

The first germole-ligated single-molecule magnets are reported, with contrasting properties found for the near-linear sandwich complexes [(η -COT)Ln(η -Cp ] , where Ln=Dy (1 ) or Er (1 ), COT is cyclo-octatetraenyl and Cp is [GeC -2,5-(SiMe ) -3,4-Me ] . Whereas 1 has an energy barrier of 120(1) cm in zero applied field and open hysteresis loops up to 10 K, the relaxation in 1 is characterized by quantum tunneling within the ground state.

Magnetic and Luminescent Dual Responses of Photochromic Hexaazamacrocyclic Lanthanide Complexes.

Herein, hexaazamacrocyclic ligand L was employed to construct a series of photochromic rare-earth complexes, [Ln(L)(NO)](BPh) [, Ln = Dy, Tb, Eu, Gd, Y; L = (3,5,10,12)-3,6,10,13-tetraaza-1,8(2,6)-dipyridinacyclotetradecaphane-3,5,10,12-tetraene]. The behavior of photogenerated radicals of hexaazamacrocyclic ligands was revealed for the first time. Upon 365 nm light irradiation, complexes exhibit photochromic behavior induced by photogenerated radicals according to EPR and UV-vis analyses.

Single-molecule magnets beyond a single lanthanide ion: the art of coupling.

The promising future of storing and processing quantized information at the molecular level has been attracting the study of Single-Molecule Magnets (SMMs) for almost three decades. Although some recent breakthroughs are mainly about the SMMs containing only one lanthanide ion, we believe SMMs can tell a much deeper story than the single-ion anisotropy. Here in this , we will try to draw a unified picture of SMMs as a delicately coupled spin system between multiple spin centres.

Redox-Programmable Spin-Crossover Behaviors in a Cationic Framework.

Metal-organic frameworks (MOFs) provide versatile platforms to construct multi-responsive materials. Herein, by introducing the neutral tetradentate ligand and the linear dicyanoaurate(I) anion, we reported a rare cationic MOF [Fe(TPB){Au(CN)}]I·4HO·4DMF (TPB = 1,2,4,5-tetra(pyridin-4-yl)benzene) with hysteretic spin-crossover (SCO) behavior near room temperature. This hybrid framework with an open metal site (Au) exhibits redox-programmable capability toward dihalogen molecules.

Single-Crystal to Single-Crystal Transformation of a Spin-Crossover Hybrid Perovskite via Thermal-Induced Cyanide Linkage Isomerization.

Linkage isomers involving changes in the bonding mode of ambidentate ligands have potential applications in data storage, molecular machines, and motors. However, the observation of the cyanide-linkage-isomerism-induced spin change (CLIISC) effect characterized by single-crystal X-ray diffraction remains a considerable challenge. Meanwhile, the high-spin and low-spin states can be reversibly switched in spin-crossover (SCO) compounds, which provide the potential for applications to data storage, switches, and sensors.

Reversible Switchability of Magnetic Anisotropy and Magnetodielectric Effect Induced by Intermolecular Motion.

Introducing magnetic switchability into artificial molecular machines is fascinating for precise control of magnetism via external stimuli. Herein, a field-induced Co single-molecule magnet was found to exhibit the reversible switch of Jahn-Teller distortion near room temperature, along with thermal conformational motion of the 18-crown-6 rotor, which pulls the coordinated H O to rotate through intermolecular hydrogen bonds and triggers a single-crystal-to-single-crystal phase transition with T =282 K and T =276 K. Interestingly, the molecular magnetic anisotropy probed by single-crystal angular-resolved magnetometry revealed the reorientation of easy axis by 14.

Discovery of a Dysprosium Metallocene Single-Molecule Magnet with Two High-Temperature Orbach Processes.

Magnetic bistability in single-molecule magnets (SMMs) is a potential basis for new types of nanoscale information storage material. The standard model for thermally activated relaxation of the magnetization in SMMs is based on the occurrence of a single Orbach process. Here, we show that incorporating a phosphorus atom into the framework of the dysprosium metallocene [(Cp)Dy(Cp)][B(CF)] (Cp is penta-isopropylcyclopentadienyl, Cp is tetraethylphospholyl) leads to the occurrence of two distinct high-temperature Orbach processes, with energy barriers of 1410(10) and 747(7) cm, respectively.

Synergistic Experimental and Theoretical Studies of Luminescent-Magnetic LnZn Clusters.

The present work is part of our ongoing quest for developing functional inorganic complexes using unorthodox pyridyl-pyrazolyl-based ligands. Accordingly, we report herein the synthesis, characterization, and luminescence and magnetic properties of four 3d-4f mixed-metal complexes with a general core of LnZn (Ln = Dy, Gd, Tb, and Eu). In stark contrast to the popular wisdom of using a compartmental ligand with separate islands of and coordinating sites for selective coordination, we have vindicated our approach of using a ligand with overcrowded N-coordinating sites that show equal efficiency with both 4f and 3d metals toward multinuclear cage-cluster formation.