Facile Synthesis and Versatilities of Polyanthraquinoylamine Nanofibril Bundles with Self Stability and High Carbon Yield

A facile synthesis for nanosized conducting polymers with inherent self-stability and multi-functionalities is a main challenge. Here we simply synthesize intrinsically self-stabilized nanofibril bundles of poly(1-anthraquinoylamine) (PAQ) by a template-free method. The critical polymerization parameters were studied to significantly optimize the synthesis, size, properties, and functionalities of the resulted fine nanofibrils with a diameter of ca. 30 nm and length of ~6 μm. The PAQ obtained with ammonium persulfate possesses higher polymerization yield, purer composition, higher conductivity, better melting behaviour, higher thermostability, lower burning enthalpy, and slower degradation than that with other oxidants. Furthermore, the polymer nanofibrils exhibit high self-stability, powerful redispersibility, high purity, and clean surface because of a complete avoidance of the contamination from external stabilizer. The PAQ exhibits widely controllable conductivity moving across ten orders of magnitudes from 10^-9^ to 50 S/cm, photoluminescence, lead-ion adsorbability, very high thermostability in air and extremely high char yield in nitrogen at 1000˚C. These materials would be useful as advanced materials including photoluminescent materials, highly cost-effective carbon precursors, sorbents of toxic metal ions, and cost-efficient conductive nanocomposite with low percolation threshold

Interfacial chemical oxidative synthesis of multifunctional polyfluoranthene.

A novel polyfluoranthene (PFA) exhibiting strong visual fluorescence emission, a highly amplified quenching effect, and widely controllable electrical conductivity is synthesized by the direct cationic oxidative polymerization of fluoranthene in a dynamic interface between n-hexane and nitromethane containing fluoranthene and FeCl3, respectively. A full characterization of the molecular structure signifies that the PFAs have a degree of polymerization from 22-50 depending on the polymerization conditions. A polymerization mechanism at the interface of the hexane/nitromethane biphasic system is proposed. The conductivity of the PFA is tunable from 6.4 × 10-6 to 0.074 S cm-1 by doping with HCl or iodine. The conductivity can be significantly enhanced to 150 S cm-1 by heat treatment at 1100 °C in argon. A PFA-based chemosensor shows a highly selective sensitivity for Fe3+ detection which is unaffected by other common metal ions. The detection of Fe3+ likely involves the synergistic effect of well-distributed π-conjugated electrons throughout the PFA helical chains that function as both the fluorophore and the receptor units

Effect of Astragalus membranaceus (Fisch) Bunge extract on streptozocin-induced diabetic in rats

Purpose: To investigate the effect of Astragalus membranaceus (Fisch.) Bunge. extract (AMBE) on streptozotocin-induced diabetic rats.Methods: The aqueous extract of AMB was obtained by steeping the dried  Astragalus membranaceus (Fisch.) Bunge. in water at 60 oC three times, each for 1 h, before first drying in an oven at 100 oC and then freeze-drying the last extract thus obtained. Diabete model rats was induced by a single intraperitoneal injection of a freshly prepared solution of streptozotocin (50 mg/kg). The rats were randomly divided into 6 groups of ten rats each: negative control group, normal control group, reference group (glibenclamide1 mg/kgbody weight) as well as AMB extract groups, namely, 40, 80 and 160 mg/kg body weight. Antihyperglycemic effect was measured by blood glucose and plasma insulin levels. Oxidative stress was evaluated in liver and kidney by antioxidant markers, viz, lipidperoxidation (LPO), superoxide  dismutase (SOD), reduced glutathione (GSH), glutathione peroxidase (GPx) and catalase (CAT), while blood serum levels of creatinine and urea were also determined in both diabetic control and treated rats.Results: Compared with diabetic rats, oral administration of AMBE at a  concentration of 160 mg/kg daily for 30 days showed a significant decrease in fasting blood glucose (109.438 ± 3.52, p < 0.05) and increased insulin level (13.96 ± 0.74, p < 0.05). Furthermore, it significantly reduced biochemical parameters (serum creatinine, 0.86 ± 0.29, p < 0.05) and serum urea (45.14 ± 1.79, p < 0.05). The treatment also resulted in significant increase in GSH (49.21 ± 2.59, p < 0.05), GPx (11.96 ± 1.16, p < 0.05), SOD (14.13 ± 0.49, p < 0.05), CAT (83.25 ± 3.14, p < 0.05) level in the liver and kidney of diabetic rats.Conclusion: The results suggest that AMBE may effectively normalize impaired  antioxidant status in streptozotocin-induced diabetes in a dose-dependent manner. AMBE has a protective effect against lipid peroxidation by scavenging free radicals and is thus capable of reducing the risk of diabetic complications.Keywords: Astragalus membranaceus, Diabetic, Antihyperglycemic, Antioxidant Oxidative stress, Fasting blood glucos

Mid-frequency prediction of transmission loss using a novel hybrid deterministic and statistical method

A novel hybrid deterministic-statistical approach named ES-FE-SEA method specially used to predict the sound Transmission loss of panels in mid-frequency is proposed in this paper. The proposed hybrid methods takes the best advantages of edged-based smoothing FEM (ES-FEM) and statistical energy analysis (SEA) to further improve the accuracy of mid-frequency transmission loss predictions. The application of ES-FEM will “soften” the well-known “overly-stiff” behavior in the standard FEM solution and reduce the inherent numerical dispersion error. While the SEA approach will deal with the physical uncertainty in the relatively higher frequency range. Two different types of subsystems will be coupled based on “reciprocity relationship” theorem. The proposed was firstly applied to a standard simple numerical example, and excellent agreement with reference results was achieved. Thus the method is then applied to a more complicated model-a 2D dash panel in a car. The proposed ES-FE-SEA is verified by various numerical examples

3-(4-Chloro­phen­yl)-2-(diisopropyl­amino)-1-benzofuro[3,2-d]pyrimidin-4(3H)-one

In the mol­ecule of the title compound, C22H22ClN3O2, the three fused rings of the benzofuro[3,2-d]pyrimidine system are almost coplanar. This ring system is oriented with respect to the substituted benzene ring at a dihedral angle of 79.05 (3)°. Intra­molecular C—H⋯N hydrogen bonding results in the formation of a six-membered ring. In the crystal structure, π–π stacking inter­actions involving the furan, pyrimidinone and benzene rings are present [centroid-to-centroid distances in the range 3.258 (1)–3.870 (1) Å]

Possible origin of Triticum petropavlovskyi based on cytological analyses of crosses between T. petropavlovskyi and tetraploid, hexaploid, and synthetic hexaploid (SHW-DPW) wheat accessions

Intraspecific hybridization between Triticum petropavlovskyi Udacz. et Migusch., synthetic hexaploid wheat (SHW-DPW), and tetraploid and hexaploid wheat, was performed to collect data on seed set, fertility of F1 hybrid, and meiotic pairing configuration, aiming to evaluate the possible origin of T. petropavlovskyi. Our data showed that (1) seed set of crosses T. petropavlovskyi × T. polonicum and T. petropavlovskyi × T. aestivum cv. Chinese Spring was significantly high; (2) fertility of hybrids T. petropavlovskyi × T. polonicum and T. petropavlovskyi × T. aestivum ssp. yunnanense was higher than that of the other hybrids; (3) fertility of F1 hybrids SHW-DPW × T. dicoccoides and SHW-DPW×T. aestivum ssp. tibetanum was significantly high; and (4) c-value of T. petropavlovskyi × T. polonicum and T. petropavlovskyi × T. aestivum cv. Changning white wheat was also significantly high. The results indicate that the probable origin of T. petropavlovskyi is divergence from a natural cross between T. aestivum and T. polonicum, via either spontaneous introgression or breeding effort

Structure and high-resolution thermogravimetry of liquid-crystalline copoly(p-oxybenzoate- ethylene terephthalate-p-benzamide)

Abstract: Thermotropic liquid-crystalline copoly(ester-amide)s consisting of three units of poxybenzoate (B), ethylene terephthalate (E) and p-benzamide (A) were studied by proton nuclear magnetic resonance at 200 and 400 MHz, wide-angle X-ray diffraction, and high-resolution thermogravimetry to ascertain their molecular and supermolecular structures, thermostability and kinetics parameters of thermal decomposition in both nitrogen and air. The assignments of all resonance peaks of [ 1 H]NMR spectra for the copoly(ester-amide)s are given and the characteristics of X-ray equatorial and meridional scans are discussed. Overall activation energy data of the ®rst major decomposition have been evaluated through three calculating techniques. The thermal degradation occurs in three steps in nitrogen and air. The degradation temperatures are higher than 447°C in nitrogen and 440°C in air and increase with increasing B-unit content at a ®xed A-unit content of 5 mol%. The temperatures at the ®rst maximum weight-loss rate are higher than 455°C in nitrogen and 445°C in air and also increase with an increase in B-unit content. The ®rst maximum weight-loss rates range between 11.1 and 14.5%min À1 in nitrogen and between 11.9 and 13.5%min À1 in air. The char yields at 500°C in both nitrogen and air range from 45.8 to 54.3 wt% and increase with increasing B-unit content. But the char yields at 800°C in nitrogen and air are quite irregular with the variation of copolymer composition and testing atmosphere. The activation energy and Ln (pre-exponential factor) for the ®rst major decomposition are usually higher in nitrogen than in air and increase slightly with an increase in B-unit content at a given A-unit content of 5 mol%. The activation energy, decomposition order, and Ln (pre-exponential factor) of the thermal degradation for the copoly(esteramide)s in two testing atmospheres, are situated in the ranges of 210±292 kJmol À1 , 2.0±2.8, 33±46 min À1 , respectively. The three kinetic parameters of the thermal degradation for the aromatic copoly(esteramide)s obtained by high-resolution thermogravimetry at a variable heating rate are almost the same as those by traditional thermogravimetry at constant heating rate, suggesting good applicability of kinetic methods developed for constant heating rate to the variable heating-rate method. These results indicate that the copoly(ester-amide)s exhibit high thermostability. The isothermal decomposition kinetics of the copoly(ester-amide)s at 450 and 420°C are also discussed and compared with the results obtained based on non-isothermal high-resolution thermogravimetry