Blue light-emitting and hole-transporting amorphous molecular materials based on diarylaminobiphenyl-functionalized bimesitylenes

The diarylaminobiphenyl-functionalized bimesityls and exhibit amorphous nature, high thermal stability and excellent blue emission in the solid state. They serve as both hole-transporting and emissive materials in OLEDs for blue emission with high external quantum efficiencies.     

Light Emitting Materials and Devices of PPV Type Compounds Containing Quinolines

Five derivatives of 1,4‐bis(2′‐quinolinylethenyl)benzene were prepared through Wittig reaction of a diylide of p‐xylene and two molar equivalents of quinolinyl carbaldehyde. Dyes 1a,b and 2a‐c thus obtained exhibit fluorescence in quantum yields of 0.44–0.78. They are fabricated to light‐emitting diodes in the form of ITO/NPB/CBP/TPBI: dye(5% wt)/Mg: Ag. The devices can be turned on at 6 V, and they displayed blue and green light at intensities up to 5000 cd/m² at 15 V. The compounds containing methoxy substituents, i.e. 1b and 2b,c , performed more effectively than those without, i.e. 1a and 2a . The former derivatives also showed a red‐shift in their emission spectra with respect to the latter.     

High‐Performance Organic Materials for Dye‐Sensitized Solar Cells: Triarylene‐Linked Dyads with a 4‐tert‐Butylphenylamine Donor

A series of organic dyes were prepared that displayed remarkable solar‐to‐energy conversion efficiencies in dye‐sensitized solar cells (DSSCs). These dyes are composed of a 4‐tert‐butylphenylamine donor group (D), a cyanoacrylic‐acid acceptor group (A), and a phenylene‐thiophene‐phenylene (PSP) spacer group, forming a D‐π‐A system. A dye containing a bulky tert‐butylphenylene‐substituted carbazole (CB) donor group showed the highest performance, with an overall conversion efficiency of 6.70 %. The performance of the device was correlated to the structural features of the donor groups; that is, the presence of a tert‐butyl group can not only enhance the electron‐donating ability of the donor, but can also suppress intermolecular aggregation. A typical device made with the CB‐PSP dye afforded a maximum photon‐to‐current conversion efficiency (IPCE) of 80 % in the region 400–480 nm, a short‐circuit photocurrent density J_sc=14.63 mA cm^?2, an open‐circuit photovoltage V_oc=0.685 V, and a fill factor FF=0.67. When chenodeoxycholic acid (CDCA) was used as a co‐absorbent, the open‐circuit voltage of CB‐PSP was elevated significantly, yet the overall performance decreased by 16–18 %. This result indicated that the presence of 4‐tert‐butylphenyl substituents can effectively inhibit self‐aggregation, even without CDCA.     

Assessment of Glucose Oxidase Based Enzymatic Fuel Cells Integrated With Newly Developed Chitosan Membranes by Electrochemical Impedance Spectroscopy

Considerably stable enzymatic fuel‐cells (single cell and 5‐cells stack) were prepared by using chitosan based membranes along with glucose oxidase attached bioanode. Continuous operation of fuel‐cells were monitored under short circuit conditions reaching half‐life over a week. Detailed analysis for the effects of pH, temperature, buffer types and concentration on different type of in‐house produced chitosan membranes were performed by electrochemical impedance spectroscopy (EIS). EIS was utilized to observe, total electrolyte resistance, charge transfer properties, mass transfer and double layer effects on integrated fuel cells (single cell and 5‐cells stack). Performance of the fuel cells was also analyzed by the polarization experiments. Current density of the fuel cell increased at higher operation temperatures not only due to better enzyme kinetics, but also due to increase in electrolyte (membrane+buffer solution) conductivity. Buffer concentration in the fuel (glucose) solution was found as an important parameter. Under optimum fuel cell operation conditions (i. e. 30–40 °C, pH 5 0.3 M buffer solution), maximum current densities of 3.0–3.2 mA cm^?2 were reached. Low‐power devices (i. e. a calculator, step motor) were powered with 5‐cell stack producing 3 mW at 1.3 V.     

The Chemistry of Binor-S and its Cyclopropyl Ring Transformations

Selective ring opening of the cyclopropyl moiety of binor-S was accomplished by several methods including acidic hydrolysis, bromination, and bydrobromination. The crystal structure of dibromide adduct 3 was solved by X-ray diffraction analysis. Debrominations of 3 yielded either 1 or 4a , whereas dehydrobromination yielded a 3-substituted monobromide 6a . The mechanism of conversion of 3 to 6a is depicted as involving intermediate 7 ; the existence of 7 is supported by the isolation of olefin 8 . Oxidation of alcohol 4c produced ketone 11a which was either oxidized to lactone 12 or transformed to a methylene derivative 11b . Hydroboration of 11b followed by quenching with hydrogen peroxide produced a hydroxymethyl derivative 14 .     

Nanoinhibitory Impacts of Salicylic Acid,Glycyrrhizic Acid Ammonium Salt,and Boric Acid Nanoparticles against Phytoplasma Associated with Faba Bean

Phytoplasmas are economically important plant pathogenic bacterial diseases, causing severe yield losses worldwide. In this study, we tested nanoformulations such as glycyrrhizic acid ammonium salt (GAS), salicylic acid (SA), and boric acid (BA) as novel antimicrobial agents inducing the resistance against the phytoplasma disease in faba bean. The nanoparticles (NP) were foliar-applied to naturally phytoplasma-infected faba bean with three concentrations from each of SA, GAS, and BA, under field conditions. Nested PCR (using universal primer pairs P1/P7 and R16F2n/R16R2) were reacted positively with all symptomatic samples and gave a product size of approximately 1200 bp, while the healthy plant gave no results. Transmission electron microscopy examinations of phytoplasma-infected faba bean plants treated with different nanoparticles revealed that severe damage occurred in phytoplasma particle’s structure, degradation, malformation, lysis in the cell membrane, and the cytoplasmic leakage followed by complete lysis of phytoplasma cells. Exogenous application of GAS-NP (1.68 µM), SA-NP (0.28 µM), and BA-NP (0.124 µM) suppressed the infection percentage of phytoplasma by 75%, 50%, and 20%, and the disease severity by 84%, 64%, and 54%, respectively. Foliar application of nanoparticles improved Fv/Fm (maximum quantum efficiency of PSII Photochemistry), PI (the performance index), SPAD chlorophyll (the relative chlorophyll content), shoots height, and leaves number, thus inducing recovery of the plant biomass and green pods yield. The most effective treatment was GAS-NP at 1.68 µM that mediated substantial increases in the shoots’ fresh weight, shoots’ dry weight, number of pods per plant, and green pods yield by 230%, 244%, 202% and 178%, respectively, compared to those of infected plants not sprayed with nanoparticles. This study demonstrated the utility of using nanoparticles, particularly GAS-NP at 1.68 µM to suppress the phytoplasma infection.     

Effect of ultrasound treatment on steady and dynamic shear properties of glucomannan based salep dispersions: optimization of amplitude level, sonication time and temperature using response surface methodology

The present study investigated effect of different amplitude levels (40, 70 and 100%), sonication temperatures (40, 50 and 60 °C) and exposure times (3, 7 and 11 min) on steady shear properties; apparent viscosity (η), shear stress (σ), consistency coefficient (K), flow behavior index (n) and dynamic shear properties; storage modulus (G′), loss modulus (G″), complex viscosity (η^∗), complex modulus (G^∗) and loss tangent (tan δ) values of glucomannan based salep solution (SS) and salep drink (SD) samples. In addition, the steady and dynamic shear properties were optimized using ridge analysis in terms of amplitude level, sonication temperature and exposure times levels. Increasing amplitude level and sonication time decreased considerably the η, σ, K, G′, G″ and η^∗ values of salep dispersions (SS and SD samples). However, sonication temperature did not have a remarkable effect on these properties.     

A new tetracyclic triterpenoid from the leaves of Azadirachta indica

A new tetracyclic triterpenoid zeeshanol [25,26,27-trinor-apotirucalla-(apoeupha)-6alpha-, 21-dihydroxy, 7alpha-acetoxy, 1,14,22-tri-en-3, 16-dione] (1) along with a known constituent desfurano-6alpha-hydroxyazadiradione (2) have been isolated from the methanolic extract of the leaves of Azadirachta indica. The structure and the relative configurations of 1 were determined by the spectroscopic method (1H- and 13C-NMR, IR, and MS) and 2D-NMR experiments.     

On minimizing the jump number for interval orders

The purpose of this paper is to give an effective characterization of all interval orders which are greedy with respect to the jump number problem.This research (Math/1406/30) was supported by the Research Center, College of Science, King Saud University, Riyadh, Saudi Arabia.     

Novel Barium Beryllates Ba[Be2N2] and Ba3[Be5O8]: Syntheses,Crystal Structures and Bonding Properties

Ba[Be₂N₂] was prepared as a yellow‐green microcrystalline powder by reaction of Ba₂N with Be₃N₂ under nitrogen atmosphere. The crystal structure Rietfeld refinements (space group I4/mcm, a = 566.46(5) pm, c = 839.42(9) pm, R_int = 4.73 %, R_prof = 9.16 %) reveal the compound to crystallize as an isotype of the nitridoberyllates A[Be₂N₂] (A = Ca, Sr) consisting of planar 4.8² nets of mutually trigonal planar coordinated Be and N species. Averaged magnetic susceptibility values for the anion [(Be₂N₂)^2?] determined from measurements on A[Be₂N₂] with A = Mg, Ca, Ba allow to derive a diamagnetic increment for N^3? χ_dia = (?13±1stat.) · 10^?6emu mol^?1. Colorless Ba₃[Be₅O₈] was first obtained as an oxidation product of Ba[Be₂N₂] in air. The crystal structure was solved and refined from single crystal X‐ray diffaction data (space group Pnma, a = 942.9(1) pm, b = 1163.47(7) pm, c = 742.1(1) pm, R1 = 2.99 %, wR2 = 7.15 %) and contains infinite rods of Be in trigonal planar, tetrahedral and 3 + 1 coordination by O. The crystal structure is discussed in context with other known oxoberyllates. Electronic structure calculations and electron localization function diagrams for both compounds support the classification as nitrido‐ and oxoberyllate, respectively.