Palladium-catalysed aryl/monofluoroalkylation of allenamides: access to fluoroalkyl indoles and isoquinolones.

A palladium catalysed construction of fluoroalkyl indoles and isoquinolones through aryl/monofluoroalkylation of allenamides has been developed. Monofluoromethyl-substituted heterocycles could be accessed under mild conditions with broad functional group tolerance. In addition, indole-oxindole bisheterocyclic scaffolds bearing a fluorine atom were successfully synthesized with 3-fluoro-oxindole as the nucleophile by applying this method.

Identifying Element-Modulated Reactivity and Stability of the High-Voltage Spinel Cathode Materials via In Situ Time-Resolved X-Ray Diffraction.

Designing and identifying a dopant-involved material is quite significant, especially for battery science. LiNi0.5Mn1.5O4, being one of the most appealing candidates for high-potential lithium-ion batteries, has attracted immense attention and been investigated with Al or F dopants for its undesirable inherent structural challenges. Although the excellent performance of Al- or F-doped LiNi0.5Mn1.5O4 has been reported previously, the relationship between dopants, structural variation, and electrochemistry has not been fully identified. Hence, synchronous time-resolved XRD techniques are applied for identifying a guideline of the phase variations in cathodic (Al3+)- and anodic (F-)-substituted LiNi0.5Mn1.5O4, which revealed a three-phase evolution as a function of structural stability. Also, the Al-substituted materials exhibit excellent reactivity and stability, which can be clearly identified via the stable buffer phase existing in high power density or after long cycling due to the improvement in reaction kinetics of phase transition and the lithium-ion diffusion coefficient, just opposite to F doping. This provides a good guideline for identifying an element-modulated mechanism of reactivity or stability of materials science.

Copper-Catalyzed Cascade 1,4-Addition/Annulation/Hydrolysis of Propargylamines with 2-Hydroxynaphthalene-1,4-diones: Direct Formation of 12-Phenacyl-11H-benzo[b]xanthenes.

A novel and versatile approach to construct 12-phenacyl-11H-benzo[b]xanthene-6,11(12H)-dione derivatives through copper-catalyzed cascade reaction of propargylamines with 2-hydroxynaphthalene-1,4-diones has been developed. The procedure is proposed to go through a sequence of 1,4-conjugate addition, intramolecular nucleophilic addition/dehydration, and hydrolysis of alkyne followed by an enol-ketone tautomerization. The reaction provides a new and highly efficient method for the synthesis of 12-phenacyl-11H-benzo[b]xanthene-6,11(12H)-diones by formation of three new bonds and one heterocycle from readily available starting materials in good to high yields (70-88%) with broad functional group compatibility in a single step.

Synthesis of 4-styrylcoumarins via FeCl3-promoted cascade reactions of propargylamines with ß-keto esters.

A versatile and highly regioselective FeCl3-promoted tandem cyclization reaction of in situ generated alkynyl o-quinone methides (o-AQMs) with ß-keto esters has been developed on the basis of the mode involving an intermolecular 1,4-conjugate addition/alkyne-allene isomerization/intramolecular transesterification/isomerization cascade. Using this method, a variety of diversely substituted 4-styryl-2H-chromen-2-ones were prepared with good efficiency and exclusive site-selectivity.

Octahedral and Porous Spherical Ordered LiNi0.5Mn1.5O4 Spinel: the Role of Morphology on Phase Transition Behavior and Electrode/Electrolyte Interfacial Properties.

LiNi0.5Mn1.5O4 compound as positive electrode of the lithium ion battery with high specific energy or high specific power, has a good application prospect in the field of electric vehicles such as PHEV/EVs. The influence of the morphology of ordered LiNi0.5Mn1.5O4 on phase transition behavior and electrode/electrolyte interfacial properties is investigated, including octahedral and porous spherical morphologies. Three phases named LiNi0.5Mn1.5O4 (Li1), Li0.5Ni0.5Mn1.5O4 (Li0.5) and Ni0.5Mn1.5O4 (Li0) are detected by in situ X-ray diffraction (XRD) measurement with high time resolution in the octahedral and porous spherical ordered LiNi0.5Mn1.5O4 materials during charge and discharge, and the phase transition kinetics of the two samples at high discharge rate and after charge-discharge cycles are elucidated. It is a clear demonstration that the high-rate capability and cycle life of LiNi0.5Mn1.5O4 material are influenced by crystal morphology. The porous spherical LiNi0.5Mn1.5O4 material exhibits better rate performance, associated with the fast reaction kinetic of Li0.5 phase formation. It is noticed that the coexistence of three cubic phases in the initial discharge stage is observed in the cycled octahedral sample, resulting in a higher capacity fading after 200 cycles at room temperature and 1 C. However, the porous spherical sample exhibits a poor cyclic performance at 55 °C and 1 C. This may be attributed to the fact that the porous spherical sample with high specific surface area leads to an accelerated decomposition of the electrolyte at 55 °C, and the thick interfacial film and high content of LiF on the electrode surface are formed.

Evidence and evolution of magnetic polaron in HgCr2Se4 investigated by electron spin resonance.

The evidence and evolution of magnetic polarons (MPs) in HgCr2Se4 have been studied by electron spin resonance (ESR), magnetism and conductivity measurements in a temperature range of 5-300 K. A single paramagnetic resonance line is observed in the high-temperature range while multiple resonance lines appear in the low-temperature range. As temperature decreases, the peak-to-peak linewidth ΔH pp shows a minimum at T min ≈ 210 K, with the activation energy fitted by small polaron hopping model consistent with the bottleneck mechanism, providing an evidence for existence of small MPs above T min. The analysis of the temperature dependence of ΔH pp, double integrated intensity I, and g factor of ESR signals, combined with the temperature dependence of magnetization and conductivity, reveals an evolution process from small MPs at zone I (T > T min) to correlated MPs at zone II (T c < T * ⩽ T ⩽ T min) in the paramagnetic regime. Three critical temperatures, T min (≈210 K), T th (≈175 K), and T * (≈121 K), which determine the evolution characteristics of MPs, are distinguished. The magnetic correlation length ξ of Cr3+-Se2--Cr3+ should account for the evolution of MPs.

Giant magnetoelectric effects achieved by tuning spin cone symmetry in Y-type hexaferrites.

Multiferroics materials, which exhibit coupled magnetic and ferroelectric properties, have attracted tremendous research interest because of their potential in constructing next-generation multifunctional devices. The application of single-phase multiferroics is currently limited by their usually small magnetoelectric effects. Here, we report the realization of giant magnetoelectric effects in a Y-type hexaferrite Ba0.4Sr1.6Mg2Fe12O22 single crystal, which exhibits record-breaking direct and converse magnetoelectric coefficients and a large electric-field-reversed magnetization. We have uncovered the origin of the giant magnetoelectric effects by a systematic study in the Ba2-x Sr x Mg2Fe12O22 family with magnetization, ferroelectricity and neutron diffraction measurements. With the transverse spin cone symmetry restricted to be two-fold, the one-step sharp magnetization reversal is realized and giant magnetoelectric coefficients are achieved. Our study reveals that tuning magnetic symmetry is an effective route to enhance the magnetoelectric effects also in multiferroic hexaferrites.Control of the electrical properties of materials by means of magnetic fields or vice versa may facilitate next-generation spintronic devices, but is still limited by their intrinsically weak magnetoelectric effect. Here, the authors report the existence of an enhanced magnetoelectric effect in a Y-type hexaferrite, and reveal its underlining mechanism.

Enhanced Rate Capability and Low-Temperature Performance of Li4Ti5O12 Anode Material by Facile Surface Fluorination.

A commercial Li4Ti5O12 material was modified by NH4F using a facile and dry method at a low temperature in air. X-ray diffraction reveals that the fluorination did not change the bulk structure of Li4Ti5O12. X-ray photoelectron spectroscopy demonstrates that LiF was formed at the surface and Ti4+ was partially changed into Ti3+. Microscopic images show that some nanoislands were formed on the surface, which enlarged the surface area. Consequently, the NH4F-modified Li4Ti5O12 material exhibited significantly enhanced capacities and rate capabilities, even at low temperatures. The discharge capacity was increased from 149 to 167 mA h g-1 at 1 C, and the capacity retention was increased from 17.8 to 52.0% at 15 C. The capacity retention of NH4F-modified Li4Ti5O12 was greater than that of Li4Ti5O12 at each low-temperature point. Additionally, the introduction of F can protect the Li4Ti5O12 material from side reactions with the electrolyte and the atmosphere, enhancing the surface stability and reducing the release of gaseous products. It is believed that the NH4F-modified Li4Ti5O12 with enhanced electrochemical performance is a promising anode material for lithium ion batteries. Furthermore, this facile surface fluorination strategy is amenable to large-scale production.

Electrochemical-reaction-induced synaptic plasticity in MoOx-based solid state electrochemical cells.

Solid state electrochemical cells with synaptic functions have important applications in building smart-terminal networks. Here, the essential synaptic functions including potentiation and depression of synaptic weight, transition from short- to long-term plasticity, spike-rate-dependent plasticity, and spike-timing-dependent plasticity behavior were successfully realized in an Ag/MoOx/fluorine-doped tin oxide (FTO) cell with continual resistance switching. The synaptic plasticity underlying these functions was controlled by tuning the excitatory post-synaptic current (EPSC) decay, which is determined by the applied voltage pulse number, width, frequency, and intervals between the pre- and post-spikes. The physical mechanism of the artificial synapse operation is attributed to the interfacial electrochemical reaction processes of the MoOx films with the adsorbed water, where protons generated by water decomposition under an electric field diffused into the MoOx films and intercalated into the lattice, leading to the short- and long-term retention of cell resistance, respectively. These results indicate the possibility of achieving advanced artificial synapses with solid state electrochemical cells and will contribute to the development of smart-terminal networking systems.

Moisture effects on the electrochemical reaction and resistance switching at Ag/molybdenum oxide interfaces.

An important potential application of solid state electrochemical reactions is in redox-based resistive switching memory devices. Based on the fundamental switching mechanisms, the memory has been classified into two modes, electrochemical metallization memory (ECM) and valence change memory (VCM). In this work, we have investigated a solid state electrochemical cell with a simple Ag/MoO3-x/fluorine-doped tin oxide (FTO) sandwich structure, which shows a normal ECM switching mode after an electroforming process. While in the lower voltage sweep range, the switching behavior changes to VCM-like mode with the opposite switching polarity to the ECM mode. By current-voltage measurements under different ambient atmospheres and X-ray photoemission spectroscopy analysis, electrochemical anodic passivation of the Ag electrode and valence change of molybdenum ions during resistance switching have been demonstrated. The crucial role of moisture adsorption in the switching mode transition has been clarified based on the Pourbaix diagram for the Ag-H2O system for the first time. These results provide a fundamental insight into the resistance switching mechanism model in solid state electrochemical cells.

Observation of Resonant Quantum Magnetoelectric Effect in a Multiferroic Metal-Organic Framework.

A resonant quantum magnetoelectric coupling effect has been demonstrated in the multiferroic metal-organic framework of [(CH3)2NH2]Fe(HCOO)3. This material shows a coexistence of a spin-canted antiferromagnetic order and ferroelectricity as well as clear magnetoelectric coupling below TN ≈ 19 K. In addition, a component of single-ion quantum magnets develops below ∼ 8 K because of an intrinsic magnetic phase separation. The stair-shaped magnetic hysteresis loop at 2 K signals resonant quantum tunneling of magnetization. Meanwhile, the magnetic field dependence of dielectric permittivity exhibits sharp peaks just at the critical tunneling fields, evidencing the occurrence of resonant quantum magnetoelectric coupling effect. This resonant effect enables a simple electrical detection of quantum tunneling of magnetization.

Pyrrole-phenylboronic acid: a novel monomer for dopamine recognition and detection based on imprinted electrochemical sensor.

A molecular imprinting polymer (MIP) based electrochemical sensor was successfully prepared for dopamine (DA) recognition and detection using pyrrole-phenylboronic acid (py-PBA) as a novel electropolymerized monomer. py-PBA could form cyclic boronic ester bond with DA, thus endowing a double recognition capacity of the sensor to DA in the combination of the imprinted effect of MIP. Compared with the sensor prepared using pyrrole or phenylboronic acid as electropolymerized monomer, the present sensor exhibited a remarkable high imprinted factor to DA. The influence factors including pH value, the mole ratio between monomer and template molecule, electropolymerization scan rate, and scan cycles of electropolymerization process were investigated and optimized. Under the optimal conditions, the sensor could recognize DA from its analogs and monosaccharides. A linear ranging from 5.0 × 10(-8) to 1.0 × 10(-5) mol/L for the detection of DA was obtained with a detection limit of 3.3 × 10(-8) mol/L (S/N = 3). The sensor has been applied to analyze DA in injection samples with satisfactory results.

Cross coupling between electric and magnetic orders in a multiferroic metal-organic framework.

The coexistence of both electric and magnetic orders in some metal-organic frameworks (MOFs) has yielded a new class of multiferroics beyond inorganic materials. However, the coupling between two orders in multiferroic MOFs has not been convincingly verified yet. Here we present clear experimental evidences of cross coupling between electric and magnetic orders in a multiferroic MOF [(CH3)2NH2]Fe(HCOO)3 with a perovskite structure. The dielelectric constant exhibit a hump just at the magnetic ordering temperature TN. Moreover, both the direct (magnetic field control of dielectric properties) and converse (electric field control of magnetization) magnetoelectric effects have been observed in the multiferroic state. This work opens up new insights on the origin of ferroelectricity in MOFs and highlights their promise as magnetoelectric multiferroics.

Synthesis and characterization of bisoxazolines- and pybox-copper(II) complexes and their application in the coupling of α-carbonyls with functionalized amines.

Binuclear complexes [{(DMOX)CuCl}2(µ-Cl)2] (1), mononuclear complexes [(DMOX)CuBr2] (2) (DMOX = 4,5-dihydro-2-(4,5-dihydro-4,4-dimethyloxazol-2-yl)-4,4-dimethyloxazole) and the pybox Cu(II) complex [(Dm-Pybox)CuBr2] (3) (Dm-Pybox = 2,6-bis[4',4'-dimethyloxazolin-2'-yl]pyridine) were obtained by reactions of CuX2 (X = Cl, Br) with DMOX and Dm-Pybox ligands, respectively. The molecular structures of 1, 2 and 3 have been determined by single-crystal X-ray diffraction analyses. The complexes 2 and 3 are efficient in catalyzing α-amination of ketones and esters through α-bromo carbonyl intermediate. The procedures are environmentally benign methods using molecular oxygen as an oxidant with water as the only byproduct.

Quantum tunneling of magnetization in a metal-organic framework.

Resonant quantum tunneling of magnetization has been observed in a hybrid metal-organic framework where an intrinsic magnetic phase separation leads to the coexistence of long-range canted antiferromagnetic order and isolated single-ion quantum magnets. This unusual magnetic phenomenon is well interpreted based on a selective long-distance superexchange model in which the exchange interaction between transition metal ions through an organic linker depends on the position of hydrogen bonds. Our work not only extends the resonant quantum tunneling of magnetization to a new class of materials but also evokes the important role of hydrogen bonding in organic magnetism.

Field- and temperature-induced evolution of the magnetocaloric effect in Ba0.3Sr1.7Co2Fe12O22 single crystals with heliconical magnetism.

The magnetocaloric effect (MCE) associated with the spin transitions of alternating longitudinal conical (ALC)-mixed conical (MC) and MC-ferrimagnetic (FIM) states in a Ba0.3Sr1.7Co2Fe12O22 single crystal has been investigated. For magnetic field directions applied along either the [120] or [001] directions, the crystal is found to exhibit the conventional and inverse MCE near the ALC-MC (T(N1) = 235 K) and MC-FIM (T(N2) = 348 K) states, respectively. The dependence of the magnetic entropy on the magnetic field also exhibits such sign change behaviors in the MCE, which is attributed to the magnetic field induced gradual collapse of heliconical magnetic order.

Observation of the Josephson effect in Pb/Ba1-xKxFe2As2 single crystal junctions.

We have fabricated c-axis Josephson junctions on single crystals of Ba1-xKxFe2As2 by using Pb as the counterelectrode in two geometries, planar and point contact. Junctions in both geometries show resistively shunted junction I-V curves below the T{C} of the counterelectrode. Microwave induced steps were observed in the I-V curves, and the critical currents are suppressed with an in-plane magnetic field with well-defined modulation periods indicating that the Josephson current is flowing in a manner consistent with the small to intermediate sized junction limit. I{C}R{N} products of up to 0.3 mV have been observed in these junctions at 4.2 K. The observation of Josephson coupling along the c axis between Ba1-xKxFe2As2 and a conventional superconductor suggests the existence of an s-wave symmetry in this class of iron pnictide superconductors.

Evidence for coexistence of superconductivity and magnetism in single crystals of Co-doped SrFe(2)As(2).

In order to investigate whether magnetism and superconductivity coexist in Co-doped SrFe(2)As(2), we have prepared single crystals of SrFe(2-x)Co(x)As(2), x = 0 and 0.4, and characterized them via x-ray diffraction, electrical resistivity in zero and applied field up to 9 T as well as at ambient and applied pressure up to 1.6 GPa, and magnetic susceptibility. At x = 0.4, there is both magnetic and resistive evidence for a spin density wave transition at 120 K, while T(c) = 19.5 K-indicating coexistent magnetism and superconductivity. A discussion of how these results compare with reported results, both in SrFe(2-x)Co(x)As(2) and in other doped 122 compounds, is given.