Dual Emission with Efficient Phosphorescence Promoted by Intermolecular Halogen Interactions in Luminescent Tetranuclear Zinc(II) Clusters.

The development of Zn-based phosphorescent materials, associated with a ligand-centered (LC) transition, is extremely limited. Herein, we demonstrated dual emissions including fluorescence and phosphorescence in luminescent tetranuclear Zn(II) clusters [ZnL(μ-OMe)X] ( = methyl-5-iode-3-methoxysalicylate; X = I, Br, Cl), incorporating iodine-substituted ligands. Single-crystal X-ray structural analyses and variable-temperature emission spectra studies revealed the presence of iodine substitutions, and intermolecular halogen interactions produced the internal/external heavy-atom effects and yielded strong green phosphorescence with a long emission lifetime (λ = 510-522 nm, Φ = 0.

Covalently Linked 5,6,11,12-Tetraazanaphthacene Dimer and Its Triptycene-Capped Derivatives as Electron Acceptors.

The development of electron transport and n-type materials is still largely dominated by a limited number of organic semiconductors, with fullerenes at the forefront. In contrast, substantial progress has been made in developing hole transport and p-type materials. Therefore, expanding the range of electron acceptors, making them solution-processable, and elucidating their structural arrangement by X-ray crystallography is essential.

Solvent vapour-responsive structural transformations in molecular crystals composed of a luminescent mononuclear aluminium(III) complex.

Investigations into the construction of functional molecular crystals and their external stimuli-induced structural transformations represent compelling research topics, particularly for the advancement of sensors and memory devices. However, reports on the development of molecular crystals constructed from discrete mononuclear complex units and exhibiting structural transformations the adsorption/desorption of guest molecules are scarce. In this study, we synthesised three molecular crystals composed of [Al(sap)(acac)(HO)]·(solvent) (Hsap = 2-salicylideneaminophenol, acac = acetylacetonate, solvent = MeCO (Al·Me2CO), MeCN (Al·MeCN), or DMSO (Al·DMSO)), and demonstrated solvent vapour-responsive reversible crystal-to-crystal structural transformations in Al·Me2CO and Al·MeCN.

Polarity and Dielectric Property Control Triggered by a Coordinated Solvent Molecule Exchange in Luminescent Mononuclear Aluminium(III) Complexes.

The development of molecule-based multifunctional switchable materials that exhibit a switch of polarity and dielectric property are extremely limited. We have demonstrated solvent-vapour-induced reversible molecular rearrangements between nonpolar crystals [Al(sap)(acac)(sol)] (H sap=2-salicylideneaminophenol, acac=acetylacetonate, sol=MeOH (1), EtOH (2)) and polar crystal [Al(sap)(acac)(DMSO)] (3). This crystal-to-crystal structural transformation was accompanied by a switch of second harmonic generation (SHG) and dielectric properties, including the formation of ferroelectric domains, thus reflecting the SHG-active polar Cc space group of 3.

Mechanism of high photoluminescence quantum yield of melem.

To produce high-efficiency organic light-emitting diodes, materials that exhibit thermally activated delayed fluorescence (TADF) are attracting attention as alternatives to phosphorescent materials containing heavy metallic elements. Melem, a small molecule with a heptazine backbone composed only of nitrogen, carbon, and hydrogen, is known to emit light in the near-ultraviolet region and exhibit high photoluminescence (PL) quantum yield and delayed fluorescence. However, the mechanism underlying the high PL quantum yield remains unclear.

Proton Conduction at High Temperature in High-Symmetry Hydrogen-Bonded Molecular Crystals of Ru Complexes with Six Imidazole-Imidazolate Ligands.

Invited for the cover of this issue is mainly the group of Makoto Tadokoro and co-workers at Tokyo University of Science. Other co-workers are Masaki Itoh, Ryota Nishimura, Kensuke Sekiguchi (TUS students), Dr. Norihisa Hoshino (Tohoku Univ.

Proton Conduction at High Temperature in High-Symmetry Hydrogen-Bonded Molecular Crystals of Ru Complexes with Six Imidazole-Imidazolate Ligands.

A new H-bonded crystal [Ru (Him) (Im) ] with three imidazole (Him) and three imidazolate (Im ) groups was prepared to obtain a higher-temperature proton conductor than a Nafion membrane with water driving. The crystal is constructed by complementary N-H⋅⋅⋅N H-bonds between the Ru complexes and has a rare Icy-c* cubic network topology with a twofold interpenetration without crystal anisotropy. The crystals show a proton conductivity of 3.

Preparation of a magnetic metal-organic square and metal-organic cubes using 4,5-bis(2-imidazolinyl)imidazolate: slow magnetization relaxation behavior in mixed-valent octamanganese(ii/iii) clusters.

Functional metal-organic squares (MOSs) and metal-organic cubes (MOCs) are important building units for zeolite-like metal-organic frameworks (ZMOFs), which are required to exhibit solid-state properties, such as dielectric, conductive, and magnetic properties. This work describes the preparation and magnetism of a tetracopper(ii) macrocyclic complex [Cu(im-Hbizn)(DMSO)(THF)](ClO)·8DMSO (1) (Him-Hbizn = 4,5-bis(4,5-dihydro-1H-imidazol-2-yl)imidazole) as a MOS and octametallic clusters [Ni(im-Hbizn)](ClO)·10MeOH·3HO (2) and [MnMn(im-Hbizn)](ClO)·14MeOH (3) as MOCs. The Cu ion in 1 possesses a five-coordinated square pyramidal geometry, resulting in the formation of an ML-type square, which gives an estimated intramolecular antiferromagnetic interaction with an exchange coupling constant of J = -95 K.

Interface Structures and Electronic States of Epitaxial Tetraazanaphthacene on Single-Crystal Pentacene.

The structural and electronic properties of interfaces composed of donor and acceptor molecules play important roles in the development of organic opto-electronic devices. Epitaxial growth of organic semiconductor molecules offers a possibility to control the interfacial structures and to explore precise properties at the intermolecular contacts. 5,6,11,12-tetraazanaphthacene (TANC) is an acceptor molecule with a molecular structure similar to that of pentacene, a representative donor material, and thus, good compatibility with pentacene is expected.

Gas sorption of nano-porous supramolecules formed by multi-hydrogen bonded coordination capsules.

[{Re(CO)(Hbim)}(tpta)] (1, Hbim = 2,2'-biimidazolate monoanion, tpta = 2,4,6-tripyridyl-1,3,5-triazine) was prepared as a nano-space supramolecule by using a new group of H-bonded coordination capsules. The hamburger bun-shaped half unit [{Re(CO)(Hbim)}(tpta)] contains six intermolecular H-bonds of Hbim ligands with complementary dual NHN types, and three [Re(CO)(Hbim)] are coordinated by bridging tridentate tpta. Interestingly, mechanical grinding easily would convert single crystals of 1 to an amorphous state with minor crystallinity while maintaining the nano-space pores.

A Novel Thermocell System Using Proton Solvation Entropy.

The entropy change associated with proton-coupled electron transfer (PCET) reactions significantly enhance the Seebeck coefficient (S ) of thermocells. A redox pair of [Ru(H im) ] (Him=imidazole, x=0≈1) releases three protons in their one-electron redox reactions in thermocells, which gave a remarkably high S of -3.7 mV K as confirmed by temperature-dependent square wave voltammetry.

Synthesis of Double-Bridged Cofacial Nickel Porphyrin Dimers with 2,2'-Bipyridyl Pillars and Their Restricted Coordination Space.

Double-bridged cofacial Ni porphyrin dimers with 2,2'-bipyridyl pillars were effectively prepared by a one-step reductive homocoupling reaction of bis(chloropyridyl)-substituted Ni porphyrin derivatives followed by a specific separation of a cyanopropyl-modified silica gel column using pyridine eluent systems. The structural analyses of and its Pd complex were carried out in their solid and solution states by means of X-ray single crystal analysis and NMR, respectively. The complexation of η-allylpalladium chloride () with on the spatially restricted 2,2-bipyridine moieties on gave a 2:1 (:) complex, in which the 2,2'-bipyridine ligands only provided one of the N atoms on a 2,2'-bipyridine ligand to a .

Synthesis, X-ray structure, photophysical properties, and theoretical studies of six-membered cyclometalated iridium(iii) complexes: revisiting Ir(pnbi)(acac).

We have determined the X-ray structure of Ir(pnbi)2(acac) (pnbi = 2-phenanthren-9-yl-1-phenyl-1H-benzimidazole; acac = acetylacetonate), which exhibits a six-membered metallocycle around the Ir center. This result stands in sharp contrast to previously postulated structures of Ir(pnbi)2(acac), which assumed a five-membered metallocycle. In this paper, we focus on the relative stability of five- and six-membered Ir(C^N) ring structures.

Synthesis and electrochromic behavior of a multi-electron redox-active N-heteroheptacenequinone.

We report a novel N-heteroheptacenequinone derivative (C6OAHCQ) as a large π-conjugated framework. C6OAHCQ shows good electron-accepting behaviour owing to eight electron-deficient imino-N atoms and two carbonyl moieties and excellent solubility in common organic solvents. When a potential between 0 and -2.

Photo-Modification of Melanin by a Mid-infrared Free-electron Laser.

Melanin is rigidly constructed by several nitrogen-containing aromatic rings, and its excess accumulation in skin tissue is closely associated with melanosis. Although visible lasers (wavelength: 600-1000 nm) are conventionally used for the photo-thermolysis of melanocyte, several pigmented nevi are difficult to be treated. Here, we propose an alternate method for targeting the molecular structure of melanin using an infrared free-electron laser (FEL) tuned to 5.

Evidence of proton-coupled mixed-valency by electrochemical behavior on transition metal complex dimers bridged by two Ag ions.

H-Bonded metal complex dimers with reversible redox behaviour, which are connected by a low-barrier hydrogen bond (LBHB) with a very low energy barrier for proton transfer, can provide a unique mixed-valency state stabilized by the proton-coupled electron transfer (PCET) phenomenon. Using cyclic voltammetry measurements, newly prepared [ReIIICl2(PnPr3)2(Hbim)]2 (2) and [OsIIICl2(PnPr3)2(Hbim)]2 (3) existing as H-bonded dimers in a CH2Cl2 solution showed a four-step and four-electron transfer containing two mixed-valency states of ReIIReIII and ReIIIReIV, and OsIIOsIII and OsIIIOsVI, respectively. Furthermore, [ReIIICl2(PnPr3)2(Agbim)]2 (4) and [OsIIICl2(PnPr3)2(Agbim)]2 (5), bridged by two Ag+ ions instead of two H-bonding protons, were prepared, and their electrochemical behaviours changed to a two-step and four-electron transfer.

Possible Tomonaga-Luttinger spin liquid state in the spin-1/2 inequilateral diamond-chain compound KCuAlO(SO).

KCuAlO(SO) is a highly one-dimensional spin-1/2 inequilateral diamond-chain antiferromagnet. Spinon continuum and spin-singlet dimer excitations are observed in the inelastic neutron scattering spectra, which is in excellent agreement with a theoretical prediction: a dimer-monomer composite structure, where the dimer is caused by strong antiferromagnetic (AFM) coupling and the monomer forms an almost isolated quantum AFM chain controlling low-energy excitations. Moreover, muon spin rotation/relaxation spectroscopy shows no long-range ordering down to 90 mK, which is roughly three orders of magnitude lower than the exchange interaction of the quantum AFM chain.

Analyses of sizable ZFS and magnetic tensors of high spin metallocomplexes.

The fictitious spin-1/2 Hamiltonian approach is the putative method to analyze the fine-structure/hyperfine ESR spectra of high spin metallocomplexes having sizable zerofield splitting (ZFS), thus giving salient principal g-values far from around g = 2 without explicitly providing their ZFS parameters in most cases. Indeed, the significant departure of the g-values from g = 2 is indicative of the occurrence of their high spin states, but naturally they never agree with true g-values acquired by quantum chemical calculations such as sophisticated DFT or ab initio MO calculations. In this work, we propose facile approaches to determine the magnetic tensors of high spin metallocomplexes having sizable ZFS, instead of performing advanced high-field/high-frequency ESR spectroscopy.

Energy-Storage Applications for a pH Gradient between Two Benzimidazole-Ligated Ruthenium Complexes That Engage in Proton-Coupled Electron-Transfer Reactions in Solution.

The judicious selection of pairs of benzimidazole-ligated ruthenium complexes allowed the construction of a rechargeable proton-coupled electron-transfer (PCET)-type redox battery. A series of ruthenium(II) and -(III) complexes were synthesized that contain substituted benzimidazoles that engage in PCET reactions. The formation of intramolecular Ru-C cyclometalation bonds stabilized the resulting ruthenium(III) complexes, in which pK values of the imino N-H protons on the benzimidazoles are usually lower than those for the corresponding ruthenium(II) complexes.

D3h -Symmetric Porphyrin-Based Rigid Macrocyclic Ligands for Multicofacial Multinuclear Complexes in a One-Nanometer-Sized Cavity.

The one-step synthesis of D3h -symmetric cyclic porphyrin trimers 1 composed of three 2,2'-[4,4'-bis(methoxycarbonyl)]bipyridyl moieties and three porphyrinatozinc moieties was achieved from a nickel-mediated reductive coupling of meso-5,15-bis(6-chloro-4-methoxycarbonylpyrid-2-yl)porphyrinatozinc. Although cyclic trimers 1 were obtained as a mixture that included other cyclic and acyclic porphyrin oligomers, an extremely specific separation was observed only for cyclic trimers 1 when using columns of silica gel modified with pyrenylethyl, cyanopropyl, and other groups. Structural analysis of cyclic trimers 1 was carried out by means of NMR spectroscopy and X-ray crystallography.

Anomalous enhancement of proton conductivity for water molecular clusters stabilized in interstitial spaces of porous molecular crystals.

In an investigation into the proton conductivity of crystallized water clusters confined within low-dimensional nanoporous materials, we have found that water-stable nanoporous crystals are formed by complementary hydrogen bonding between [Co(III) (H2 bim)3 ](3+) (H2 bim: 2,2'-biimidazole) and TATC(3-) (1,3,5- tricarboxyl-2,4,6-triazinate); the O atoms in the -COO(-) groups of TATC(3-) in the porous outer wall are strongly hydrogen bonded with H2 O, forming two types of WMCs (water molecular clusters): a spirocyclic tetramer chain (SCTC) that forms infinite open 1D channels, and an isolated cyclic tetramer (ICT) present in the void space. The ICT is constructed from four H2 O molecules as a novel C2 -type WMC, which are hydrogen bonded with four-, three-, and two-coordination spheres, respectively. The largest structural fluctuation is observed at elevated temperatures from the two-coordinated H2 O molecules, which begin to rapidly and isotropically fluctuate on heating.

Electron transport of photoconductive n-type liquid crystals based on a redox-active tetraazanaphthacene framework.

The preparation of two liquid crystals composed of a redox-active tetraazanaphthacene (TANC) framework is reported. The materials form smectic A (SmA) thin-film liquid-crystalline (LC) phases over a wide temperature range. Cyclic voltammetry analysis revealed that LC TANCs behave as organic electron acceptors.