Modular Design of Highly Stable Semiconducting Porous Coordination Polymer for Efficient Electrosynthesis of Ammonia.

Developing highly stable porous coordination polymers (PCPs) with integrated electrical conductivity is crucial for advancing our understanding of electrocatalytic mechanisms and the structure-activity relationship of electrocatalysts. However, achieving this goal remains a formidable challenge because of the electrochemical instability observed in most PCPs. Herein, we develop a "modular design" strategy to construct electrochemically stable semiconducting PCP, namely, Fe-pyNDI, which incorporates a chain-type Fe-pyrazole metal cluster and π-stacking column with effective synergistic effects. The three-dimensional electron diffraction (3D ED) technique resolves the precise structure. Both theoretical and experimental investigation confirms that the π-stacking column in Fe-pyNDI can provide an efficient electron transport path and enhance the structural stability of the material. As a result, Fe-pyNDI can serve as an efficient model electrocatalyst for nitrate reduction reaction (NO3RR) to ammonia with a superior ammonia yield of 339.2 µmol h-1 cm-2 (14677 µg h-1 mgcat. -1) and a faradaic efficiency of 87 % at neutral electrolyte, which is comparable to state-of-the-art electrocatalysts. The in-situ X-ray absorption spectroscopy (XAS) reveals that during the reaction, the structure of Fe-pyNDI can be kept, while part of the Fe3+ in Fe-pyNDI was reduced in situ to Fe2+, which serves as the potential active species for NO3RR.

Molecular elastic crystals exhibiting slow magnetic relaxations.

We report an elastic crystal of a copper(II) porphyrinato complex that exhibits slow magnetic relaxations and is a promising candidate for an external-force-responsive spin qubit.

Width-dependent band gap of arm-chair graphene nanoribbons formed on vicinal SiC substrates by MBE.

Formation and electronic states of graphene nanoribbons with arm-chair edges (AGNR) are studied on the SiC(0001) vicinal surfaces toward the [11-00] direction. The surface step and terrace structures of both 4H and 6H-SiC substrates are used as the growth templates of one-dimensional arrays of AGNRs, which are prepared using the carbon molecular beam epitaxy followed by hydrogen intercalation. A band gap is observed above theπ-band maximum by angle-resolved photoelectron spectroscopy (ARPES) for the both samples. The average widths of the AGNRs are 6 and 10 nm, and the estimated average band gaps are 0.40 and 0.28 eV for the 4H- and 6H- substrates, respectively. A simple and phenomenological inverse relation between the energy gap and AGNR width works in the analyses of the ARPES data.

Photoinduced Catalytic Organic-Hydride Transfer to CO2 Mediated with Ruthenium Complexes as NAD+ /NADH Redox Couple Models.

The catalytic organic-hydride transfer to CO2 was first achieved through the photoinduced two-electron reduction of the [Ru(bpy)2 (pbn)]2+ /[Ru(bpy)2 (pbnHH)]2+ (bpy=2,2'-bipyridine, pbn=2-(pyridin-2-yl)benzo[b]-1,5-naphthyridine, and pbnHH=2-(pyridin-2-yl)-5,10-dihydrobenzo[b]-1,5-naphthyridine) redox couple in the presence of 1,3-dimethyl-2-phenyl-2,3-dihydro-1H-benzo[d]imidazole (BIH). The active species for the catalytic hydride transfer to carbon dioxide giving formate is [Ru(bpy)(bpy⋅- )(pbnHH)]+ formed by one-electron reduction of [Ru(bpy)2 (pbnHH)]2+ with BI⋅.

Fine Pore-Structure Engineering by Ligand Conformational Control of Naphthalene Diimide-Based Semiconducting Porous Coordination Polymers for Efficient Chemiresistive Gas Sensing.

Exploring new porous coordination polymers (PCPs) that have tunable structure and conductivity is attractive but remains challenging. Herein, fine pore structure engineering by ligand conformation control of naphthalene diimide (NDI)-based semiconducting PCPs with π stacking-dependent conductivity tunability is achieved. The π stacking distances and ligand conformation in these isoreticular PCPs were modulated by employing metal centers with different coordination geometries. As a result, three conjugated PCPs (Co-pyNDI, Ni-pyNDI, and Zn-pyNDI) with varying pore structure and conductivity were obtained. Their crystal structures were determined by three-dimensional electron diffraction. The through-space charge transfer and tunable pore structure in these PCPs result in modulated selectivity and sensitivity in gas sensing. Zn-pyNDI can serve as a room-temperature operable chemiresistive sensor selective to acetone.

Rotating magnetocaloric effect in highly anisotropic TbIII and DyIII single molecular magnets.

The magnetocaloric effect (MCE) was investigated in highly anisotropic single crystals of two single molecule magnets (SMMs): [LnIII(ZnIIL)2]CF3SO3, where Ln = Tb, Dy and L = tripodal hexadentate Schiff base ligand. The structure of these paramagnetic compounds consists of identically oriented linear trinuclear clusters in a trigonal system with an easy direction c∥Zn-Ln-Zn array and a hard plane ab⊥Zn-Ln-Zn array. The magnitude of MCE measured for c∥H was significantly greater than MCE for ab∥H at a wide temperature range regardless of the studied SMM. Therefore, the rotating magnetocaloric effect (RMCE) was evaluated. The maxima of the magnetic entropy change for RMCE were obtained at 2.0 K and moderate fields: 3.9 J K-1 kg-1 at µ0H = 1.3 T for Ln = Tb and 3.3 J K-1 kg-1 at µ0H = 1.1 T for Ln = Dy. The relative efficiency of RMCE compared to the MCE measured in c∥H was as high as 99% at low magnetic fields.

Ultrasmall Copper Nanoclusters in Zirconium Metal-Organic Frameworks for the Photoreduction of CO2.

Encapsulating ultrasmall Cu nanoparticles inside Zr-MOFs to form core-shell architecture is very challenging but of interest for CO2 reduction. We report for the first time the incorporation of ultrasmall Cu NCs into a series of benchmark Zr-MOFs, without Cu NCs aggregation, via a scalable room temperature fabrication approach. The Cu NCs@MOFs core-shell composites show much enhanced reactivity in comparison to the Cu NCs confined in the pore of MOFs, regardless of their very similar intrinsic properties at the atomic level. Moreover, introducing polar groups on the MOF structure can further improve both the catalytic reactivity and selectivity. Mechanistic investigation reveals that the CuI sites located at the interface between Cu NCs and support serve as the active sites and efficiently catalyze CO2 photoreduction. This synergetic effect may pave the way for the design of low-cost and efficient catalysts for CO2 photoreduction into high-value chemical feedstock.

Effect of Micropores of a Porous Coordination Polymer on the Product Selectivity in RuII Complex-catalyzed CO2 Reduction.

To develop an efficient CO2 reduction catalyst, hybridizing a molecular catalyst and a porous coordination polymer (PCP) is a promising strategy because it can combine both advantages of the precise reactivity control of the former and the CO2 adsorption property of the latter. Although several PCP hybrid catalysts have been reported to date, the CO2 sorption behavior and the CO2 reduction reactivity have been investigated separately, and the CO2 enrichment during the catalysis is still unclear. We report CO2 photoreduction under different temperatures and pressures using a PCP-RuII complex hybrid catalyst. The product selectivity (CO or HCOOH) varied depending on the reaction conditions. The altered selectivity could be interpreted in terms of the CO2 capture in the micropores of a PCP.

Xylene Recognition in Flexible Porous Coordination Polymer by Guest-Dependent Structural Transition.

Xylene isomers are crucial chemical intermediates in great demand worldwide; the almost identical physicochemical properties render their current separation approach energy consuming. In this study, we utilized the soft porous coordination polymer (PCP)'s isomer-specific structural transformation, realizing o-xylene (oX) recognition/separation from the binary and ternary isomer mixtures. This PCP has a flexible structure that contains flexible aromatic pendant groups, which both work as recognition sites and induce structural flexibility of the global framework. The PCP exhibits guest-triggered "breathing"-type structural changes, which are accompanied by the rearrangement of the intraframework π-π interaction. By rebuilding π-π stacking with isomer species, the PCP discriminated oX from the other isomers by its specific guest-loading configuration and separated oX from the isomer mixture via selective adsorption. The xylene-selective property of the PCP is dependent on the solvent; in diluted hexane solution, the PCP favors p-xylene (pX) uptake. The separation results combined with crystallographic analyses revealed the effect of the isomer selectivity of the PCP on xylene isomer separation via structural transition and demonstrated its potential as a versatile selective adsorptive medium for challenging separations.

Coexistence of Two Types of Spin Splitting Originating from Different Symmetries.

The symmetry of a surface or interface plays an important role in determining the spin splitting and texture of a two-dimensional band. Spin-polarized bands of a triangular lattice atomic layer (TLAL) consisting of Sn on a SiC(0001) substrate is investigated by spin- and angle-resolved photoelectron spectroscopy. Surprisingly, both Zeeman- and Rashba-type spin-split bands, without and with spin degeneracy, respectively, coexist at a K point of the Sn TLAL. The K point has a threefold symmetry without inversion symmetry according to the crystal structure including the SiC periodicity, meaning that the Zeeman-type is consistent with the symmetry of the lattice while the Rashba-type is inconsistent. Our density functional calculations reveal that the charge density distribution of the Rashba-type (Zeeman-type) band shows (no) inversion symmetry at the K point. Therefore, the symmetry of the charge density distribution agrees with both types of the spin splitting.

Electrochemical behavior of a Rh(pentamethylcyclopentadienyl) complex bearing an NAD+/NADH-functionalized ligand.

A RhCp* (Cp* = pentamethylcyclopentadienyl) complex bearing an NAD+/NADH-functionalized ligand, [RhCp*(pbn)Cl]Cl ([1]Cl, pbn = (2-(2-pyridyl)benzo[b]-1,5-naphthyridine)), was synthesized. The cyclic voltammogram of [1]Cl in CH3CN shows two reversible redox waves at E1/2 = -0.58 and -1.53 V (vs. the saturated calomel electrode (SCE)), which correspond to the RhIII/RhI and pbn/pbn˙- redox couples, respectively. The addition of acetic acid to the solution afforded the proton-coupled two-electron reduction of [1]Cl at -0.62 V, from which [RhCp*(pbnHH)Cl]+ was selectively generated, probably via a hydride transfer from a RhIII-hydride intermediate to the pbn ligand. Complex [1]Cl is stable under acidic conditions, whereas a methyl proton of the Cp* moiety dissociates under basic conditions. The resulting anionic methylene group attacks the para carbon of the free pyridine of pbn, accompanied by protonation of the nitrogen atom of the ligand. As a result, treatment of [1]Cl with a base produces selectively the cyclic complex [1CH]Cl, which bears a reduced pbn framework (pbnCH). [1CH]Cl forms 1 : 1 adducts with PhCOO-via hydrogen bonding. A similar adduct, formed by a Ru-pbnHH scaffold and RCOO- (R = CH3, C6H5), has been reported to react with CO2 to produce HCOO- under concomitant regeneration of Ru-pbn. The adduct of [1CH]Cl with PhCOO-, however, lacks such hydride-donor ability, due to a steric barrier in the molecular structure of [1CH]Cl, which hampers the hydride transfer.

Catalytic Hydride Transfer to CO2 Using Ru-NAD-Type Complexes under Electrochemical Conditions.

The catalytic performance of Ru-NAD-type complexes [Ru(tpy)(pbn)(CO)]2+ ([1]2+; tpy = 2,2';6',2″-terpyridine; pbn = 2-(pyridin-2-yl)benzo[b][1,5]naphthyridine) and the Ru-CO-bridged metallacycle [2]+ was investigated in the context of the electrochemical reduction of CO2 in H2O/CH3CN at room temperature. A controlled-potential electrolysis of [1]2+ and [2]+ afforded formate (HCOO-) as the main product, under concomitant formation of minor amounts of CO and H2. Metallacycle [2]+ showed a higher selectivity toward the formation of HCOO- than [1]2+ (HCOO-/CO for [1]2+, 2.7; HCOO-/CO for [2]+, 7). The generation of HCOO- via a catalytic hydride transfer from the NADH-type ligands of [1]2+ and [2]+ to CO2 was supported by the experimental results and a comparison with the reduction of CO2 catalyzed by [Ru(tpy)(bpy)(CO)]2+ under similar conditions. A mechanism for the catalytic reduction of CO2 by [1]2+ and [2]+ was proposed based on the experimental evidence. The thus-obtained results may help to expand the field of NADH-assisted reduction reactions.

A Holmium(III)-Based Single-Molecule Magnet with Pentagonal-Bipyramidal Geometry.

The right environment: The remarkable properties of a recently reported holmium(III)-based single-ion magnet have been ascribed to the hyperfine interactions with the half-integer nuclear spin in combination with the pentagonal-bipyramidal coordination environment. These results provide insight into the complicated magnetic properties of nanosized magnetic materials.

Modulation of Electron-Phonon Coupling in One-Dimensionally Nanorippled Graphene on a Macrofacet of 6H-SiC.

Local electron-phonon coupling of a one-dimensionally nanorippled graphene is studied on a SiC(0001) vicinal substrate. We have characterized local atomic and electronic structures of a periodically nanorippled graphene (3.4 nm period) prepared on a macrofacet of the 6H-SiC crystal using scanning tunneling microscopy/spectroscopy (STM/STS) and angle-resolved photoelectron spectroscopy (ARPES). The rippled graphene on the macrofacets distributes homogeneously over the 6H-SiC substrate in a millimeter scale, and thus replica bands are detected by the macroscopic ARPES. The STM/STS results indicate the strength of electron-phonon coupling to the out-of-plane phonon at the K̅ points of graphene is periodically modified in accordance with the ripple structure. We propose an interface carbon nanostructure with graphene nanoribbons between the surface rippled graphene and the substrate SiC that periodically modifies the electron-phonon coupling in the surface graphene.

Pancreas volume reduction and metabolic effects in Japanese patients with severe obesity following laparoscopic sleeve gastrectomy.

This study aimed to assess the relationship between the metabolic effect after laparoscopic sleeve gastrectomy (LSG) in morbidly obese Japanese patients, with or without type 2 diabetes mellitus (T2DM), and improved pancreatic steatosis (PS). The study enrolled 27 morbidly obese Japanese patients who were undergoing LSG. Their clinical and metabolic effects were evaluated at baseline and six months after LSG. Pancreas volume (PV), pancreatic attenuation (PA), and splenic attenuation (SA) were measured using a 64-row computed tomography (CT). Changes in PV, PA-SA, and PA/SA were evaluated. The mean body-weight loss, body mass index loss, and percentage of excess weight loss (%EWL) were -34.4 kg (p < 0.001), -11.0 kg/m2 (p < 0.001), and 43.7%, respectively. The mean PV was 96.7 mL at baseline, and it decreased six months after LSG (-16.3mL, p < 0.001). The mean PA significantly increased six months after LSG (9.5 HU, p < 0.001). PA-SA (-23.2 HU vs. -13.3 HU, p = 0.003), and PA/SA (0.54 vs. 0.73, p < 0.001) also significantly increased six months after LSG. In T2DM patients, decreased PV correlated with decreased fasting blood sugar, decreased insulin, and reduced liver volume. In conclusion, PV significantly decreased after LSG in morbidly obese Japanese patients, and that decrease correlated with improvements in PS. In addition, PS plays an important role of development and progression of insulin resistance and T2DM.

Light Lanthanide Complexes with Crown Ether and Its Aza Derivative Which Show Slow Magnetic Relaxation Behaviors.

Two sets of isostructural Ln(III) mononuclear complexes, [Ln(NO3)3(18-crown-6)] (Ln = Ce (1), Pr (2), and Nd (3)) and [Ln(NO3)3(1,10-diaza-18-crown-6)] (Ln = Ce (4), Pr (5), and Nd (6)), were synthesized, and their slow magnetic relaxation behavior was investigated. Since Ln(III) ions are located in an axially stressed ligand field in both sets of complexes, they can exhibit single-molecule magnet (SMM) behavior owing to the oblate-type electronic distributions of the ground sublevels found in Ce(III), Pr(III), and Nd(III). Field-induced slow magnetic relaxation was observed for Ce(III) and Nd(III) complexes 1, 3, 4, and 6 under an applied bias dc field of 1000 Oe, whereas no slow relaxation was observed for Pr(III) complexes 2 and 5. The slow magnetic relaxation behavior of 1, 3, 4, and 6 was correlated with the even-numbered Jz sublevels of Ce(III) and Nd(III) ions, known as the Kramers system.

One-dimensional Magnus-type platinum double salts.

Interest in platinum-chain complexes arose from their unusual oxidation states and physical properties. Despite their compositional diversity, isolation of crystalline chains has remained challenging. Here we report a simple crystallization technique that yields a series of dimer-based 1D platinum chains. The colour of the Pt(2+) compounds can be switched between yellow, orange and blue. Spontaneous oxidation in air is used to form black Pt(2.33+) needles. The loss of one electron per double salt results in a metallic state, as supported by quantum chemical calculations, and displays conductivity of 11 S cm(-1) at room temperature. This behaviour may open up a new avenue for controllable platinum chemistry.

Association of Advanced Glycation End Products with coronary Artery Calcification in Japanese Subjects with Type 2 Diabetes as Assessed by Skin Autofluorescence.

AIM: Advanced glycation end products (AGE) are considered to be among the critical pathogenic factors involved in the progression of diabetic complications. Skin autofluorescence (AF), a noninvasive measurement of AGE accumulation, has been recognized as a useful and convenient marker for diabetic vascular diseases in Caucasians. This study aimed to evaluate the association of tissue AGE, assessed using skin AF, with coronary artery calcification in Japanese subjects with type 2 diabetes. METHODS: In total, 122 Japanese subjects with type 2 diabetes enrolled in this cross-sectional study underwent multi-slice computed tomography for total coronary artery calcium scores (CACS) estimation and examination with a skin AF reader. RESULTS: Skin AF positively correlated with age, sex, diabetes duration, pulse wave velocity, systolic blood pressure, serum creatinine, and CACS. In addition, skin AF results negatively correlated with BMI, eGFR, and serum C-peptide concentration. According to multivariate analysis, age and systolic blood pressure showed strong positive correlation and eGFR showed negative correlation with skin AF values. Multiple linear regression analyses revealed a significant positive correlation between skin AF values and logCACS, independent of age, sex, diabetes duration, HbA1c, BMI, IMT, and blood pressure. However, skin AF showed no association with serum levels of AGE, such as Nε-(carboxymethyl) lysine and 3-deoxyglucosone. CONCLUSION: Skin AF results positively correlated with CACS in Japanese subjects with type 2 diabetes. This result indicates that AGE plays a role in the pathogenesis of diabetic macrovascular disease. Measurement of skin AF values may be useful for assessing the severity of diabetic complications in Japanese subjects.

Photochemical Reduction of Low Concentrations of CO2 in a Porous Coordination Polymer with a Ruthenium(II)-CO Complex.

Direct use of low pressures of CO2 as a C1 source without concentration from gas mixtures is of great interest from an energy-saving viewpoint. Porous heterogeneous catalysts containing both adsorption and catalytically active sites are promising candidates for such applications. Here, we report a porous coordination polymer (PCP)-based catalyst, PCP-Ru(II) composite, bearing a Ru(II) -CO complex active for CO2 reduction. The PCP-Ru(II) composite showed improved CO2 adsorption behavior at ambient temperature. In the photochemical reduction of CO2 the PCP-Ru(II) composite produced CO, HCOOH, and H2 . Catalytic activity was comparable with the corresponding homogeneous Ru(II) catalyst and ranks among the highest of known PCP-based catalysts. Furthermore, catalytic activity was maintained even under a 5 % CO2 /Ar gas mixture, revealing a synergistic effect between the adsorption and catalytically active sites within the PCP-Ru(II) composite.