Probing Local pH Change during Electrode Oxidation of TEMPO Derivative: Implication of Redox-Induced Acidity Alternation by Imidazolium-Linker Functional Groups.

The chemical degradation of 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-based aqueous energy storage and catalytic systems is pH sensitive. Herein, we voltammetrically monitor the local pH (pHlocal) at a Pt ultramicroelectrode (UME) upon electro-oxidation of imidazolium-linker functionalized TEMPO and show that its decrease is associated with the greater acidity of the cationic (oxidized) rather than radical (reduced) form of TEMPO. The protons that drive the decrease in pH arise from hydrolysis of the conjugated imidazolium-linker functional group of 4-[2-(N-methylimidazolium)acetoxy]-2,2,6,6-tetramethylpiperidine-1-oxyl chloride (MIMAcO-T), which was studied in comparison with 4-hydroxyl-TEMPO (4-OH-T). Voltammetric hysteresis is observed during the electrode oxidation of 4-OH-T and MIMAcO-T at a Pt UME in an unbuffered aqueous solution. The hysteresis arises from the pH-dependent formation and dissolution of Pt oxides, which interact with pHlocal in the vicinity of the UME. We find that electrogenerated MIMAcO-T+ significantly influences pHlocal, whereas 4-OH-T+ does not. Finite element analysis reveals that the thermodynamic and kinetic acid-base properties of MIMAcO-T+ are much more favorable than those of its reduced counterpart. Imidazolium-linker functionalized TEMPO molecules comprising different linking groups were also investigated. Reduced TEMPO molecules with carbonyl linkers behave as weak acids, whereas those with alkyl ether linkers do not. However, oxidized TEMPO+ molecules with alkyl ether linkers exhibit more facile acid-base kinetics than those with carbonyl ones. Density functional theory calculations confirm that OH- adduct formation on the imidazolium-linker functional group of TEMPO is responsible for the difference in the acid-base properties of the reduced and oxidized forms.

Triiodide-in-Iodine Networks Stabilized by Quaternary Ammonium Cations as Accelerants for Electrode Kinetics of Iodide Oxidation in Aqueous Media.

The Zn-polyiodide redox flow battery is considered to be a promising aqueous energy storage system. However, in its charging process, the electrode kinetics of I- oxidation often suffer from an intrinsically generated iodine film (I2-F) on the cathode of the battery. Therefore, it is critical to both understand and enhance the observed slow electrode kinetics of I- oxidation by an electrochemically generated I2-F. In this article, we introduced an electrogenerated N-methyl-N-ethyl pyrrolidinium iodide (MEPI)-iodine (I2) solution, designated as MEPIS, and demonstrated that the electrode kinetics of I- oxidation were dramatically enhanced compared to an I2-F under conventional electrolyte conditions, such as NaI. We showed that this result mainly contributed to the fast electro-oxidation of triiodide (I3-), which exists in the shape of a I3--in-I2 network, [I3-·(I2)n]. Raman spectroscopic and electrochemical analyses showed that the composition of electrogenerated MEPIS changed from I3- to [I3-·(I2)n] via I5- as the anodic overpotential increased. We also confirmed that I- was electrochemically oxidized on a MEPIS-modified Pt electrode with fast electrode kinetics, which is clearly contrary to the nature of an I2-F derived from a NaI solution as a kinetic barrier of I- oxidation. Through stochastic MEPIS-particle impact electrochemistry and electrochemical impedance spectroscopy, we revealed that the enhanced electrode kinetics of I- oxidation in MEPIS can be attributed to the facilitated charge transfer of I3- oxidation in [I3-·(I2)n]. In addition, we found that the degree of freedom of I3- in a quaternary ammonium-based I2-F can also be critical to determine the kinetics of the electro-oxidation of I-, which is that MEPIS showed more enhanced charge-transfer kinetics of I- oxidation compared to tetrabutylammonium I3- due to the higher degree of freedom of I3-.

Mechanistic approaches for chemically modifying the coordination sphere of copper-amyloid-ß complexes.

Neurotoxic implications of the interactions between Cu(I/II) and amyloid-ß (Aß) indicate a connection between amyloid cascade hypothesis and metal ion hypothesis with respect to the neurodegeneration associated with Alzheimer's disease (AD). Herein, we report a mechanistic strategy for modifying the first coordination sphere of Cu(II) bound to Aß utilizing a rationally designed peptide modifier, L1. Upon reacting with L1, a metal-binding histidine (His) residue, His14, in Cu(II)-Aß was modified through either covalent adduct formation, oxidation, or both. Consequently, the reactivity of L1 with Cu(II)-Aß was able to disrupt binding of Cu(II) to Aß and result in chemically modified Aß with altered aggregation and toxicity profiles. Our molecular-level mechanistic studies revealed that such L1-mediated modifications toward Cu(II)-Aß could stem from the molecule's ability to 1) interact with Cu(II)-Aß and 2) foster copper-O2 chemistry. Collectively, our work demonstrates the development of an effective approach to modify Cu(II)-Aß at a metal-binding amino acid residue and consequently alter Aß's coordination to copper, aggregation, and toxicity, supplemented with an in-depth mechanistic perspective regarding such reactivity.

Time Transient Electrochemical Monitoring of Tetraalkylammonium Polybromide Solid Particle Formation: Observation of Ionic Liquid-to-Solid Transitions.

Energy storage systems (ESSs) using a Br-/Br2 redox reaction such as a Zn/Br redox flow battery (RFB) or a redox-enhanced electrochemical capacitor (Redox-EC) suffer from self-discharge reactions resulting in significant Coulombic loss. To inhibit the self-discharge, quaternary ammonium (Q+) and tetraalkylammonium (T+) bromide are added to form ionic liquid (QBr2 n+1) and solid (TBr3) polybromides during the ESS charging process. The electrochemical formation of liquid QBr2 n+1 and its electrochemical properties have been examined. The detailed mechanisms of ionic solid TBr3 formation, however, have not yet been explored. In this article, we analyzed the ionic liquid-to-solid phase transition of TBr3 particles using a time transient electrochemical method. We suggest the formation of ionic solid TBr3 particles via hydrated TBr3 droplets as an intermediate phase, which are generated by electro-oxidation of Br- in an aqueous TBr solution. We found the phase transition time of TBr3 particles is strongly dependent on the chemical structure of T+ and the concentration of TBr in an aqueous solution.

Probing the speciation of quaternary ammonium polybromides by voltammetric tribromide titration.

The speciation of quaternary ammonium polybromides (QBr2n+1) was quantitatively determined by voltammetric tribromide titration on a Pt ultramicroelectrode (UME). The concentration of Br3- in a QBr2n+1-water mixed solution (QBr2n+1-WMS) was electrochemically estimated by measuring the steady state current associated with the electro-reduction of Br3- in a linear sweep voltammogram (LSV). The pBr3- titration curves of QBr2n+1-WMSs show 2-4 plateaus, each of which relates to the formation of QBr2n+1 from Br3- and Br2. The values of pBr3- at these plateaus can be regarded as corrected equilibrium constants of QBr2n+1, K'eq(n), which is Keq(n)/γ±, where γ± is a mean activity coefficient in QBr2n+1-WMS. Based on the estimated K'eq(n), fractional diagrams of QBr2n+1 were obtained, which gave information on QBr2n+1 speciation.

Tuning Structures and Properties for Developing Novel Chemical Tools toward Distinct Pathogenic Elements in Alzheimer's Disease.

Multiple pathogenic factors [e.g., amyloid-ß (Aß), metal ions, metal-bound Aß (metal-Aß), reactive oxygen species (ROS)] are found in the brain of patients with Alzheimer's disease (AD). In order to elucidate the roles of pathological elements in AD, chemical tools able to regulate their activities would be valuable. Due to the complicated link among multiple pathological factors, however, it has been challenging to invent such chemical tools. Herein, we report novel small molecules as chemical tools toward modulation of single or multiple target(s), designed via a rational structure-property-directed strategy. The chemical properties (e.g., oxidation potentials) of our molecules and their coverage of reactivities toward the pathological targets were successfully differentiated through a minor structural variation [i.e., replacement of one nitrogen (N) or sulfur (S) donor atom in the framework]. Among our compounds (1-3), 1 with the lowest oxidation potential is able to noticeably modify the aggregation of both metal-free Aß and metal-Aß, as well as scavenge free radicals. Compound 2 with the moderate oxidation potential significantly alters the aggregation of Cu(II)-Aß42. The hardly oxidizable compound, 3, relative to 1 and 2, indicates no noticeable interactions with all pathogenic factors, including metal-free Aß, metal-Aß, and free radicals. Overall, our studies demonstrate that the design of small molecules as chemical tools able to control distinct pathological components could be achieved via fine-tuning of structures and properties.

Treadmill exercise is associated with reduction of reactive microgliosis and pro-inflammatory cytokine levels in the hippocampus of type 2 diabetic rats.

OBJECTIVES: In the present study, we investigated the effects of treadmill exercise on microglial activation and the subsequent release of tumour necrosis factor-alpha (TNF-alpha), interleukin (IL)-6 and IL-1-beta in the hippocampus in a rat model of type 2 diabetes. METHODS: At 30 weeks of age, diabetic (Zucker diabetic fatty, ZDF) rats and their littermate control (Zucker lean control, ZLC) rats were either placed on a stationary treadmill or made to run for 1 hour/day at 12-16 m/minute on five consecutive days, for 10 weeks. Once the rats reached 40 weeks, they were perfused and their hippocampus collected for immunohistochemistry or hippocampus collected fresh for the Western blotting or enzyme-linked immunosorbent assay (ELISA). RESULTS: The whole blood glucose levels in exercised ZDF rats were significantly higher than in the sedentary or exercised ZLC rats, but were significantly lower than in the sedentary ZDF rats. In the sedentary ZLC and exercised ZLC rats, ionised calcium-binding adapter molecule 1 (Iba-1) immunoreactive microglia showed normal morphology which had small cytoplasm with ramified processes. In the sedentary ZDF rats, some Iba-1 immunoreactive microglia showed abnormal morphology which had hypertrophied cytoplasm with retracted processes. However, exercised ZDF rats had small cytoplasm with highly ramified processes. Levels of TNF-alpha, IL-6 and IL-1beta in the hippocampal homogenates were significantly increased in sedentary ZDF rats compared to sedentary ZLC rats, respectively. However, TNF-alpha, IL-6 and IL-1beta levels in the exercised ZDF rats were significantly decreased compared with those of sedentary ZDF rats, respectively. DISCUSSION: These results suggest that exercise in type 2 diabetic rats reduces microglial activation and the subsequent increase of pro-inflammatory cytokine levels in the hippocampus.

Treadmill exercise prevents diabetes-induced increases in lipid peroxidation and decreases in Cu,Zn-superoxide dismutase levels in the hippocampus of Zucker diabetic fatty rats.

In the present study, we investigated the effects of treadmill exercise on lipid peroxidation and Cu,Zn-superoxide dismutase (SOD1) levels in the hippocampus of Zucker diabetic fatty (ZDF) rats and lean control rats (ZLC) during the onset of diabetes. At 7 weeks of age, ZLC and ZDF rats were either placed on a stationary treadmill or made to run for 1 h/day for 5 consecutive days at 16~22 m/min for 5 weeks. At 12 weeks of age, the ZDF rats had significantly higher blood glucose levels and body weight than the ZLC rats. In addition, malondialdehyde (MDA) levels in the hippocampus of the ZDF rats were significantly higher than those of the ZLC rats whereas SOD1 levels in the hippocampus of the ZDF rats were moderately decreased. Notably, treadmill exercise prevented the increase of blood glucose levels in ZDF rats. In addition, treadmill exercise significantly ameliorated changes in MDA and SOD1 levels in the hippocampus although SOD activity was not altered. These findings suggest that diabetes increases lipid peroxidation and decreases SOD1 levels, and treadmill exercise can mitigate diabetes-induced oxidative damage in the hippocampus.

Copper(II)-catalyzed C-O coupling of aryl bromides with aliphatic diols: synthesis of ethers, phenols, and benzo-fused cyclic ethers.

A highly efficient copper-catalyzed C-O cross-coupling reaction between aryl bromides and aliphatic diols has been developed employing a cheaper, more efficient, and easily removable copper(II) catalyst. A broad range of aryl bromides were coupled with aliphatic diols of different lengths using 5 mol% CuCl2 and 3 equivalents of K2CO3 in the absence of any other ligands or solvents to afford the corresponding hydroxyalkyl aryl ethers in good to excellent yields. In this newly developed protocol, aliphatic diols have multilateral functions as coupling reactants, ligands, and solvents. The resulting hydroxyalkyl aryl ethers were further readily converted into the corresponding phenols, presenting a valuable alternative way to phenols from aryl bromides. Furthermore, it was demonstrated that they are useful intermediates for more advanced molecules such as benzofurans and benzo-fused cyclic ethers.

Copper(II)-catalyzed hydroxylation of aryl halides using glycolic acid as a ligand.

Copper(II)-catalyzed hydroxylation of aryl halides has been developed to afford functionalized phenols. The protocol utilizes the reagent combination of Cu(OH)2, glycolic acid, and NaOH in aqueous DMSO, all of which are cheap, readily available, and easily removable after the reaction. A broad range of aryl iodides and activated aryl bromides were transformed into the corresponding phenols in excellent yields. Moreover, it has been shown that C-O(alkyl)-coupled product, instead of phenol, can be predominantly formed under similar reaction conditions.

G-quadruplex binding ligands: from naturally occurring to rationally designed molecules.

Guanine-rich nucleic acid sequences are known to form G-quadruplex - four-stranded DNA or RNA structures stabilized by an array of Hoogsteen hydrogen bonds. G-quadruplex structures are involved in the modulation of gene expression at the transcription and translation levels. Accordingly, G-quadruplexes are considered as novel therapeutic targets for anticancer drug development. In this review, the authors provide a brief, up-to-date summary of G-quadruplex binding ligands, including naturally occurring molecules, synthetic compounds, and molecules identified by computational database screening. The key structural motifs of G-quadruplex binding ligands, that is, an aromatic core and basic side chains, are addressed in the context of how these molecules interact with G-quadruplex. A better understanding of these interactions would facilitate the rational design of ligands selective for DNA or RNA G-quadruplex.

Synthesis and characterization of IMPY derivatives that regulate metal-induced amyloid-ß aggregation.

Metal ions associated with amyloid-ß (Aß) species have been suggested to be involved in neurodegeneration leading to the progression of Alzheimer's disease (AD). The role of metal-involved Aß species in AD neuropathogenesis, however, is not fully elucidated. In order to advance this understanding and contribute to the therapeutic development for AD, the rational structure-based design of small molecules that specifically target metal ions surrounded by Aß species has recently received increased attention. To date, only a few compounds have been fashioned for this purpose. Herein, we report the design strategy, synthesis, characterization, and reactivity of new bifunctional IMPY derivatives K1 and K2. Using UV-vis and high-resolution two-dimensional (2D) NMR spectroscopy, the bifunctionality of K1 and K2 (metal chelation and Aß interaction) was confirmed. These bifunctional IMPY derivatives showed preferential reactivity toward metal-induced Aß aggregation over metal-free conditions in both in vitro inhibition and disaggregation experiments. Taken together, this study provides another example of a bifunctional small molecule framework that can target metal ions associated with Aß species.

Practical demethylation of aryl methyl ethers using an odorless thiol reagent.

A highly practical method for demethylation of aryl methyl ethers employing a long-chain thiol has been developed. Under the conditions described herein, clean and fast conversions to the desired phenolic compounds have been achieved with a broad range of substrates. Unlike other thiolate-mediated methods, this newly developed protocol features in-situ generation of sodium alkylthiolate using NaOH, and is almost free from foul smells and potentially harmful gases. It therefore provides an attractive option for the demethylation of aryl methyl ethers.

One-pot sequential Cu-catalyzed reduction and Pd-catalyzed arylation of silyl enol ethers.

[reaction: see text] Enantiomerically enriched beta-substituted diphenylsilyl enol ethers, which can be prepared from Cu-catalyzed asymmetric conjugate reduction, are utilized in the Pd-catalyzed arylation of various aryl bromides. This new method provides a simple route to alpha-arylated cycloalkanones with excellent levels of enantiomeric and diastereomeric purity. The isolation of the intermediate, diphenylsilyl enol ethers is not necessary; the procedure can be carried out in one-pot.

Syntheses and anti-MRSA activities of the C3 analogs of mansonone F, a potent anti-bacterial sesquiterpenoid: insights into its structural requirements for anti-MRSA activity.

Syntheses and excellent anti-MRSA activities of the mansonone F analogs are reported. In addition, the minimal structural requirements for its anti-MRSA activities as well as its structure-activity relationship including the C3 substituents effects on anti-MRSA activity are also described. In particular, this study revealed that both ortho-quinone and tricyclic systems of mansonone F are essential for anti-MRSA activities.

Palladium-catalyzed regioselective hydrodebromination of dibromoindoles: application to the enantioselective synthesis of indolodioxane U86192A.

A novel approach to the selective preparation of 4-bromoindoles was developed via Pd(OAc)(2)/rac-BINAP catalytic reactions. A variety of 4,6-dibromoindoles were transformed to 4-bromoindoles with high regioselectivity. This methodology, along with C-N and C-O bond-forming reactions developed in our laboratory, was applied to the enantioselective synthesis of indolodioxane U86192A, an antihypertensive agent.