Effects of galvanic vestibular stimulation on postural righting reactions in hemiplegia.

Patients with post-stroke hemiplegia often exhibit reduced ability to maintain sitting balance, a crucial factor for predicting prognosis. Galvanic vestibular stimulation (GVS) influences postural control by stimulating vestibular organ. Although several studies have focused on GVS in static postures, no studies have demonstrated the influence of GVS on righting reactions. Therefore, we aimed to investigate the effects of GVS on postural righting reactions in seated patients with stroke-induced hemiplegia. Using a vertical board (VB), righting reactions were induced by tilting the VB at 10° after patients sat for 1 min. Patients adjusted their bodies until feeling vertical upon prompt. Twenty-two left hemiplegic patients with cerebrovascular disease participated, divided into two groups undergoing right cathode GVS (RC-GVS) followed by left cathode GVS or vice versa, preceded by sham stimulation. Centre of pressure and the joint angle were measured. During the postural righting reactions towards the paralysed side, RC-GVS enhanced the righting reactions and moved the mean position on the x-axis (COPx) to the right and the mean position on the y-axis (COPy) to the front. During the postural righting reaction towards the right side, RC-GVS induced resistance against the righting reaction, COPx was deflected to the right, COPy was deflected backward, and the angle of the neck tilt increased. The findings revealed that GVS with anodal stimulation on the paralysed side could promote righting reactions in patients with post-stroke hemiplegia. SIGNIFICANCE STATEMENT: The study findings suggest that using the contralesional placement of the anode promotes righting reactions, and galvanic vestibular stimulation can induce joint movements in the neck and trunk by polarising it to act as resistance against righting reactions.

Design of a robust and strong-acid MOF platform for selective ammonium recovery and proton conductivity.

Metal-organic frameworks (MOFs) are potential candidates for the platform of the solid acid; however, no MOF has been reported that has both aqueous ammonium stability and a strong acid site. This manuscript reports a highly stable MOF with a cation exchange site synthesized by the reaction between zirconium and mellitic acid under a high concentration of ammonium cations (NH4+). Single-crystal XRD analysis of the MOF revealed the presence of four free carboxyl groups of the mellitic acid ligand, and the high first association constant (pKa1) of one of the carboxyl groups acts as a monovalent ion-exchanging site. NH4+ in the MOF can be reversibly exchanged with proton (H+), sodium (Na+), and potassium (K+) cations in an aqueous solution. Moreover, the uniform nanospace of the MOF provides the acid site for selective NH4+ recovery from the aqueous mixture of NH4+ and Na+, which could solve the global nitrogen cycle problem. The solid acid nature of the MOF also results in the proton conductivity reaching 1.34 × 10-3 S cm-1 at 55 °C by ion exchange from NH4+ to H+.

Effects of paddy irrigation-drainage system on water quality and productivity of small rivers in the Himi region of Toyama, Central Japan.

The aim of this study was to clarify the impact of differences between historical and recently introduced irrigation and drainage management systems on water quality in the rivers around paddy fields. We investigated the seasonal variation in nutrients concentration and dissolved organic carbon (DOC) components in single- (used for intake only) and dual-purpose (used for both intake and drainage) channels during a 4-year period in the Himi region of Toyama, Central Japan. The system of dual-purpose channel has traditionally been used in the region of this study. A total of 197 three-dimensional excitation-emission matrix (3DEEM) fluorescence spectra of DOM in waters were applied for the parallel factor analysis (PARAFAC) modeling. Based on the 3DEEM and PARAFAC, the abundance of terrestrial humic-like components in the dual-purpose channel was significantly higher than that in the single-purpose channel. The even long-chain n-fatty acids derived associated with rice cropping in sediments of the dual-purpose channels were 22-30-fold higher than that of the single-purpose channel. In addition, the turbidity values of the river waters had significantly positive linear correlations with concentrations of K+, DOC, and humic-like components. These observations indicate that the dissolved nutrient concentrations in the river water were higher in the dual-purpose channel compared to those of the single-purpose channel, which may be supplied by leaching from the inflow of soil particles from the paddy fields. During the mid-irrigation period, the quantity of epiphytic chlorophyll a on artificial substrate tiles in the dual-purpose channel were 3.1-4.1-fold higher than that in the single-purpose channel. This study clear that the input of paddy drainage during the irrigation season significantly changes the DOC components in river waters and irrigation management is strongly linked to the primary production in agricultural channels. Therefore, it is important to consider the impact of the introduction of different irrigation and drainage management systems on water quality and productivity in order to maintain the riverine ecosystems around rice paddies, which are based on historical water use systems.

A Series of D-A-D Structured Disilane-Bridged Triads: Structure and Stimuli-Responsive Luminescence Studies.

A series of σ-π extended octamethyltetrasilanes, which have phenothiazine, 9,9-dimethyl-9,10-dihydroacridine, or phenoxazine (1, 2, and 3) groups as donor moieties and thienopyrazine or benzothiadiazole (a and b) groups as acceptor fragments, has been prepared, and their optical properties have been studied as an extension of our work. All six compounds exhibited fluorescence in the solid state with maximum wavelengths centered in the range of 400 and 650 nm upon excitation by a UV lamp. Compound 2b showed apparent dual emission behavior in solution, which depends on solvent polarity, and a reversible photoluminescent change under mechanical and thermal stimuli in the solid state. Quantum chemical calculations suggest the contribution of a quasi-axial conformer of the 9,9-dimethyl-9,10-dihydroacridine moiety in 2b to the dual emission in solution and the mechanofluoroluminescence in the solid state, similarly to 1a. These studies provide new insight into the preparation of disilane-bridged triads capable of responding to multiple stimuli.

Synthesis, Structure, and Photophysical Properties of Yellow-Green and Blue Photoluminescent Dinuclear and Octanuclear Copper(I) Iodide Complexes with a Disilanylene-Bridged Bispyridine Ligand.

The synthesis, structural, and photophysical investigations of CuI complexes with a disilanylene-bridged bispyridine ligand 1 are herein presented. Dinuclear (2) and ladder-like (3) octanuclear copper(I) complexes were straightforwardly prepared by exactly controlling the ratio of CuI/ligand 1. Single-crystal X-ray analysis confirmed that dinuclear complex 2 had no apparent π…π stacking whereas octanuclear complex 3 had π…π stacking in the crystal packing. In the solid state, the complexes display yellow-green (λem = 519 nm, Φ = 0.60, τ = 11 µs, 2) and blue (λem = 478 nm, Φ = 0.04, τ = 2.6 µs, 3) phosphorescence, respectively. The density functional theory calculations validate the differences in their optical properties. The difference in the luminescence efficiency between 2 and 3 is attributed to the presence of π…π stacking and the different luminescence processes.

Luminescent Behavior Elucidation of a Disilane-Bridged D-A-D Triad Composed of Phenothiazine and Thienopyrazine.

A σ-π extended aryldisilane, comprising a thienopyrazine group as an acceptor fragment and phenothiazine groups as the donor moiety, has been prepared through the introduction of two Si-Si bridges (compound 1). X-ray diffraction analysis determined the crystal structure of 1, and experimental and theoretical approaches investigated its optical properties. Solvatochromic studies revealed the dual emission of 1 in all solvents tested. Compound 1 also exhibited fluorescence in the solid state upon excitation with a hand-held UV lamp, as well as mechanochromic luminescent properties. The packing mode in the crystal structure, variation of phenothiazine conformation, morphological changes between crystalline and amorphous phases are the major factors showing reversible fluorescence under external stimuli. A theoretical conformer study found that 1 exists in distinct conformational groups differing in Gibbs free energy by less than 3 kcal mol-1 . The conformer in the crystalline state of 1 can promote the complete separation of the HOMO and LUMO between the phenothiazine donor and the thienopyrazine acceptor, linked by the disilane linker. HOMO-LUMO energy transition in the crystalline state is forbidden due to the lack of frontier orbital overlap. Crystalline state emission showed LUMO → HOMO-1 transition (locally excited (LE) state). In the amorphous state, the partial presence of quasi-axial conformers allows intramolecular charge-transfer type emission via energy transfer from dominant quasi-equatorial conformers. The strategy proposed in this work provides important guidance for developing stimuli-responsive materials with controlled excited states.

Magneto-Electric Directional Anisotropy in Polar Soft Ferromagnets of Two-Dimensional Organic-Inorganic Hybrid Perovskites.

Two-dimensional organic-inorganic hybrid perovskites (2D-OIHPs) are attracting interest due to their structural tunability and rich functional characteristics, such as ferroelectricity and ferromagnetism. Here, we report the chiral-polar ferromagnetic 2D-OIHP copper chlorides with discernable electric polarization in the inorganic layers. In these systems, the magneto-electric (ME) correlation has been clearly observed by measuring a magneto-electric directional anisotropy (MEA), in which an optical absorption coefficient changes with reversal of the light propagating direction. We have found that the MEA can be induced by a low magnetic field of about 50 mT, reflecting soft magnetic nature. The present results suggest a new paradigm for designing functional ME multiferroics, which effectively couples magnetic and electric properties.

Ionicity Diagrams for Electron-Donor and -Acceptor Metal-Organic Frameworks: DA Chains and D2A Layers Obtained from Paddlewheel-Type Diruthenium(II,II) Complexes and Polycyano-Organic Acceptors.

Recent developments in research concerning metal-organic frameworks and coordination polymers have provided the successful design of charge-variable molecular frameworks. However, few comprehensive studies exist that investigate the control of charge states in series of molecular frameworks such as these. Herein, we discuss the ionicity diagrams of two series containing electron-donor (D) and -acceptor (A) units: one-dimensional DA chains and two-dimensional D2A layers. The series were obtained by reacting paddlewheel-type diruthenium(II,II) complexes ([Ru2II,II]), which served as D units, with the polycyano-organic acceptors N,N'-dicyanoquinodiimine (DCNQI) and 7,7,8,8-tetracyano-p-quinodimethane (TCNQ), which served as A units. Fifteen novel members of neutral charged DA chains were fabricated in this study to characterize the ionicity diagrams for DA and D2A systems.

Thermosalience in Macrocycle-Based Soft Crystals via Anisotropic Deformation of Disilanyl Architecture.

We describe here the preparation of soft crystals using disilanyl macrocycle C4 possessing four p-phenylenes circularly connected by four flexible disilane bonds. Single crystals of C4 exhibited a reversible thermal single-crystal-to-single-crystal (SCSC) phase transition behavior between two crystal phases accompanied by remarkable mechanical motion (thermosalient effect), as revealed by thermal analyses and X-ray diffraction measurements. Detailed structural analyses implied that flexibility of the parallelogram disilanyl architecture and molecular packing mode via weak intermolecular interactions facilitated a concerted structural transformation (parallel crank motion) of macrocycles in the crystal, thus resulting in the SCSC phase transition accompanied by anisotropic shrinking/elongation of the cells to induce the thermosalient effect. This work explores a new area of organosilicon chemistry and presents the potential utility of disilanyl macrocycles as soft crystals.

Magnetic Sponge with Neutral-Ionic Phase Transitions.

Phase transitions caused by the charge instability between the neutral and ionic phases of compounds, i.e., N-I phase transitions, provide avenues for switching the intrinsic properties of compounds related to electron/spin correlation and dipole generation as well as charge distribution. However, it is extremely difficult to control the transition temperature (Tc) for the N-I phase transition, and only chemical modification based on the original material have been investigated. Here, a design overview of the tuning of N-I phase transition by interstitial guest molecules is presented. This study reports a new chain coordination-polymer [Ru2(3,4-Cl2PhCO2)4TCNQ(EtO)2]∙DCE (1-DCE; 3,4-Cl2PhCO2- = 3,4-dichlorobenzoate; TCNQ(EtO)2 2,5-diethoxy-7,7,8,8-tetracyanoquinodimethane; and DCE = 1,2-dichloroethane) that exhibits a one-step N-I transition at 230 K (= Tc) with the N- and I-states possessing a simple paramagnetic state and a ferrimagnetically correlated state for the high- and low-temperature phases, respectively. The Tc continuously decreases depending on the content of DCE, which eventually disappears with the complete evacuation of DCE, affording solvent-free compound 1 with the N-state in the entire temperature range (this behavior is reversible). This is an example of tuning the in situ Tc for the N-I phase transition via the control of the interstitial guest molecules.

Seasonal variations in bacterioplankton community structures in two small rivers in the Himi region of central Japan and their relationships with environmental factors.

The aim of this study was to improve our understanding of seasonal variations and the effects of physicochemical conditions on the bacterioplankton communities in two small rivers, the Moo and Nakayachi Rivers in the Himi region of central Japan. These rivers are inhabited by unionid freshwater mussels, which are used for oviposition by the endangered Itasenpara bitterling (Acheilognathus longipinnis). Water samples were collected every month between March 2011 and February 2012. Changes in bacterioplankton community structures were analysed using an approach that did not require cultivating the bacteria and involved PCR and denaturing gradient gel electrophoresis. The bacterioplankton community structures in the two rivers were similar in all seasons except winter. The bacterial sequences identified were dominated by typical freshwater Actinobacteria, Bacteroidetes, Cyanobacteria, α-Proteobacteria, and ß-Proteobacteria bacterioplankton. Many ß-Proteobacteria species were detected in all seasons, but Bacteroidetes species were dominant in the winter. The bacterioplankton community structures were affected by biochemical oxygen demand, chemical oxygen demand, chlorophyll-a concentration, water depth, and water temperature. These results provide a foundation for a more detailed understanding of the conditions that provide a suitable unionid habitat.

Tuning of Stepwise Neutral-Ionic Transitions by Acceptor Site Doping in Alternating Donor/Acceptor Chains.

The stepwise neutral-ionic (N-I) phase transition found in the alternating donor/acceptor (DA) chain [Ru2(2,3,5,6-F4PhCO2)4(DMDCNQI)]·2(p-xylene) (0; 2,3,5,6-F4PhCO2(-) = 2,3,5,6-tetrafluorobenzoate; DMDCNQI = 2,5-dimethyl-N,N'-dicyanoquinonediimine) was tuned by partly substituting the acceptor DMDCNQI with 2,5-dimethoxy-N,N'-dicyanoquinonediimine (DMeODCNQI), which displays a poorer electron affinity in an isostructural series. The site-doped series comprised [Ru2(2,3,5,6-F4PhCO2)4(DMDCNQI)1-x(DMeODCNQI)x]·2(p-xylene) for doping rates (x) = 0.05 (0.05-MeO), 0.10 (0.10-MeO), 0.15 (0.15-MeO), and 0.20 (0.20-MeO). The neutral chain [Ru2(2,3,5,6-F4PhCO2)4(DMeODCNQI)]·4(p-xylene) (1), which only contained DMeODCNQI, was also characterized. All site-doped compounds were isostructural to 0 except 1 despite their identical DA chain motif. Except at an x value of 0.20, they displayed a two-step N-I transition involving an intermediate phase. This transition occurred at high temperatures in 0 but shifted to lower temperatures in a parallel manner with increasing doping rate. Simultaneously, each transition broadened with increasing doping rate, leading to a convergence of two transitions at an x value approximating 0.2. Donor/acceptor-site-doping techniques present somewhat different impacts in terms of interchain Coulomb effects.

Magnetic sponge phenomena associated with interchain dipole-dipole interactions in a series of ferrimagnetic chain compounds doped with minor diamagnetic species.

The donor/acceptor ionic chain (i.e., the D(+)A(-) chain) [Ru2(2-MeO-4-ClPhCO2)4(BTDA-TCNQ)]·2.5(benzene) (1; 2-MeO-4-ClPhCO2(-) = 2-methoxy-4-chlorobenzoate; BTDA-TCNQ = bis(1,2,5-thiadiazolo)tetracyanoquinodimethane) is a ferrimagnetic chain with S = 3/2 from [Ru2(II,III)](+) (i.e., D(+)) and S = 1/2 from BTDA-TCNQ(•-) (i.e., A(-)), with J ≈ -100 K, in which long-range antiferromagnetic ordering at TN = 11 K occurs because interchain antiferromagnetic interactions are critical. Compound 1 undergoes a reversible crystal-to-crystal structural transformation with the elimination/absorption of the crystallization solvent to form the dried compound [Ru2(2-MeO-4-ClPhCO2)4(BTDA-TCNQ)] (1'), which has a higher TN (14 K). This change is clearly caused by the shortening of the interchain distances because the exchange coupling parameter for the chain is the same in both 1 and 1'. The chain compounds in 1 can be doped with minor diamagnetic [Rh2(II,II)] species, [{(Ru2)(1-x)(Rh2)(x)(2-MeO-4-ClPhCO2)4}(BTDA-TCNQ)]·2.5(benzene) (x = 0.03 for Rh-3%; x = 0.05 for Rh-5%; x = 0.16 for Rh-16%), which shifts the TN to lower temperatures, the magnitude of the shift being dependent on the doping ratio x (TN = 5.9 K for Rh-3%, TN = 3.7 K for Rh-5%, and TN was not observed above 1.8 K for Rh-16%). Drying a doped compound increased its TN, as was found for 1': TN = 9.9 K for Rh-3%', TN = 9.2 K for Rh-5%', and TN was not observed above 1.8 K for Rh-16%'. TN had a linear relationship with the doping ratio x of the [Rh2] species in both the fresh and dried compounds. The TN linear relationship is associated with the magnitude of the effective magnetic dipole (i.e., the average correlation length) in the chains caused by the [Rh2] defects as well as naturally generated defects in the synthetic process and with the interchain distances affected by the crystal-to-crystal transformations. These results demonstrate that slightly modifying the short-range correlation lengths, which changes the magnetic dipole magnitudes, strongly affects the bulk antiferromagnetic transition, with key dipole-dipole interactions, in low-dimensional anisotropic systems.

Carrier concentration dependent conduction in insulator-doped donor/acceptor chain compounds.

On the basis of the concept that the design of a mixed valence system is a key route to create electronic conducting frameworks, we propose a unique idea to rationally produce mixed valency in an ionic donor/acceptor chain (i.e., D(+)A(-) chain). The doping of a redox-inert (insulator) dopant (P) into a D(+)A(-) chain in place of neutral D enables the creation of mixed valency A(0)/A(-) domains between P units: P-(D(+)A(-))nA(0)-P, where n is directly dependent on the dopant ratio, and charge transfer through the P units leads to electron transport along the framework. This hypothesis was experimentally demonstrated in an ionic DA chain synthesized from a redox-active paddlewheel [Ru2(II,II)] complex and TCNQ derivative by doping with a redox-inert [Rh2(II,II)] complex.

Modification of charge transfer in a two-dimensional donor/acceptor framework by the insertion of another donor-type molecule into electronegative interlayer pockets.

Pyrene-intercalated layered compounds, [{Ru2(O2CCF3)4}2(TCNQR(x))]·2(pyrene) (TCNQR(x) = 7,7,8,8-tetracyano-p-quinodimethane derivatives; R(x) = H4 and F4), were synthesized. Pyrene prohibits intralayer electron transfer of [Ru2(II,II)] → TCNQR(x), even in the compound with R(x) = F4, from occurring.

An ionicity diagram for the family of [{Ru2(CF3CO2)4}2(TCNQR(x))] (TCNQR(x) = R-substituted 7,7,8,8-tetracyano-p-quinodimethane).

A diagram of energies between the HOMO of donor (D) and LUMO of acceptor (A) vs.ΔE(1/2)(DA) (= E(1/2)(D) - E(1/2)(A): E(1/2) = first-redox potential) clearly demonstrates the ionicity in the series of D/A assemblies, [{Ru(2)(CF(3)CO(2))(4)}(2)(TCNQR(x))]·n(solv) (TCNQR(x) = 2,5- or 2,3,5,6-R-substituted 7,7,8,8-tetracyano-p-quinodimethane; R(x) = H(4), F(2), Cl(2), Br(2), F(4), Me(2), (OMe)(2)).

Lanthanide complexes of macrocyclic polyoxovanadates by VO4 units: synthesis, characterization, and structure elucidation by X-ray crystallography and EXAFS spectroscopy.

Reactions of a tetravanadate anion, [V(4)O(12)](4-), with a series of lanthanide(III) salts yield three types of lanthanide complexes of macrocyclic polyoxovanadates: (Et(4)N)(6)[Ln(III)V(9)O(27)] [Ln = Nd (1), Sm (2), Eu (3), Gd (4), Tb (5), Dy (6)], (Et(4)N)(5)[(H(2)O)Ho(III)(V(4)O(12))(2)] (7), and (Et(4)N)(7)[Ln(III)V(10)O(30)] [Ln = Er (8), Tm (9), Yb (10), Lu (11)]. Lanthanide complexes 1-11 are isolated and characterized by IR, elemental analysis, single-crystal X-ray diffraction, and extended X-ray absorption fine structure spectroscopy (EXAFS). Lanthanide complexes 1-6 are composed of a square-antiprism eight-coordinated Ln(III) center with a macrocyclic polyoxovanadate that is constructed from nine VO(4) tetrahedra through vertex sharing. The structure of 7 is composed of a seven-coordinated Ho(III) center, which exhibits a capped trigonal-prism coordination environment by the sandwiching of two cyclic tetravanadates with a capping H(2)O ligand. Lanthanide complexes 8-11 have a six-coordinated Ln(III) center with a 10-membered vanadate ligand. The structural trend to adopt a larger coordination number for a larger lanthanide ion among the three types of structures is accompanied by a change in the vanadate ring sizes. These lanthanide complexes are examined by EXAFS spectroscopies on lanthanide L(III) absorption edges, and the EXAFS oscillations of each of the samples in the solid state and in acetonitrile are identical. The Ln-O and Ln···V bond lengths obtained from fits of the EXAFS data are consistent with the data from the single-crystal X-ray studies, reflecting retention of the structures in acetonitrile.

Vocal acoustic characteristics of patients with Parkinson's disease.

Speech samples obtained from 39 idiopathic Parkinson's disease (PD) patients with vocal pathologies were compared with those from 62 age-matched vocally normal non-PD controls. Voice samples collected from sustained vowel phonation and passage reading were acoustically analyzed using Computer Speech Lab and Multi-Dimensional Voice Program software. Noise-to-harmonic ratio, voice turbulence index (VTI) and soft phonation index (SPI) were incorporated as noise-related measurements, fundamental frequency-tremor intensity index (FTRI), amplitude tremor intensity, fundamental frequency-tremor frequency (Fftr), and amplitude-tremor frequency as tremor-related measurements. Compared with controls, the following results were noted: (1) male and female PD patients exhibited significant differences in acoustic parameters of all frequency and amplitude perturbation measurements and noise-related measurements (except VTI in males); (2) speaking fundamental frequency was significantly higher only in male PD patients; (3) FTRI and Fftr in male (only FTRI in female) PD patients were significantly higher, and (4) disease severity and MDVP analysis showed significant correlations between SPI and the Unified Parkinson's Disease Rating Scale Part I (mentation, behavior, mood) and Part II (activities of daily living) in male PD patients; however, this was not the case in female PD patients.

Organocatalytic alpha-hydroxymethylation of cyclopentanone with aqueous formaldehyde: easy access to chiral delta-lactones.

Optically active lactones are important synthons in perfume and aroma manufacturing. Therefore, developments of efficient asymmetric syntheses are desired. Organocatalytic asymmetric alpha-hydroxymethylations of cyclopentanone with aqueous formaldehyde have been developed, to furnish the corresponding alpha-(hydroxymethyl)cyclopentanone with high enantioselectivity. Further chemical transformation of alpha-(hydroxymethyl)cyclopentanone gave the key intermediate for jasmine lactone, which is widely found in fruits and flowers.

Changes in speaking fundamental frequency characteristics with aging.

Changes in speaking fundamental frequency (SFF) associated with aging were studied in a total of 374 healthy normal speakers (187 males and 187 females) from adolescent to older age groups. Participants were asked to read a sample passage aloud, and acoustic analysis was performed. The main results were as follows: (1) Males exhibited no significant trend for SFF changes in aging. However, a slight increase was observed in participants aged 70 years or older. (2) Females in their 30s and 40s showed obviously lower frequencies than those in their 20s. Across all age groups, including the 80s, SFF tended to decrease markedly in association with aging. (3) The degree of SFF change in association with aging was much larger in females than in males. In addition, reference intervals (mean +/- 1.96 SD) obtained for males and females in each age group are considered useful for clinical detection of abnormalities of SFF, as well as for detection of laryngeal diseases causing SFF abnormality.