Proton conducting polymers containing 1H‐1,2,3‐triazole moieties

Polyacrylates containing a different number of 1H‐1,2,3‐triazole groups per repeat unit have been synthesized via conventional free radical polymerization. These polymers were characterized by nuclear magnetic resonance spectroscopy (NMR), gel permeation chromatography (GPC), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). Proton conductivity measurements were made using impedance spectroscopy. Introduction of more than one triazole per repeat unit did not result in an increase in conductivity as there was an accompanying increase in glass transition temperature (T_g). A maximum conductivity of 17.5 μS/cm was obtained at 200 °C under anhydrous condition. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 188–196, 2009     

Complexation of Titanium n-butoxide Ti(OBu n )4 and Zirconium n-butoxide Zr(OBu n )4 with Some Oxime Ligands and Structural Analysis of the Complexes

Titanium tetra-n-butoxide, Ti(OBuⁿ)₄, and zirconium tetra-n-butoxide, Zr(OBuⁿ)₄, were reacted with some well-known dioxime and monoxime ligands such as dimethylglyoxime (DMG), salicylaldoxime (SO) and acetone oxime (AO). The structures of the resulting complexes have been determined by elemental analysis, i.r. and ¹H-n.m.r. spectroscopy. The complexation ratio of both Ti(OBuⁿ)₄ and Zr(OBuⁿ)₄ was found to be 1:2 with DMG and SO. On the other hand, both 1:1 and 1:2 complexation ratios of the same metal alkoxides were observed with the ligand AO.     

Spinor Bishop Equations of Curves in Euclidean 3-Space

In this paper, we study spinor Bishop equations of curves in ${\mathbb{E}^3}$ . We research the spinor formulations of curves according to Bishop frames in ${\mathbb{E}^3}$ . Also, the relations between spinor formulations of Bishop frames and Frenet frame are expressed.     

A probe into the chaotic nature of daily streamflow time series by correlation dimension and largest Lyapunov methods

Two chaotic indicators namely the correlation dimension and the Lyapunov exponent methods are investigated for the daily river flow of Kizilirmak River. A delay time of 60 days used for the reconstruction is chosen after examining the first minimum of the average mutual information of the data. The sufficient embedding dimension is estimated using the false nearest neighbor algorithm, which has a value of 11. Based on these embedding parameters the correlation dimension of the resulting attractor is calculated, as well as the average divergence rate of nearby orbits given by the largest Lyapunov exponent. The presence of chaos in the examined river flow time series is evident with the low correlation dimension (2.4) and the positive value of the largest Lyapunov exponent (0.0061).     

Effect of benzyladenine on recovery of cryopreserved shoot tips of grapevine and citrus cultured in vitro

The effect of N6-benzyladenine (BA) on the recovery of cryopreserved shoot tips of the LN33 hybrid (Vitis L.) and Troyer citrange [Poncirus trifoliata (L.) Raf. x Citrus sinensis [L.] Osbeck.] cultured in vitro was examined. For the LN33 hybrid, the presence of BA in the recovery medium was essential for survival of control and cryopreserved shoot tips, although the BA concentration did not influence the survival percentage. BA at 5, 2, and 5 microM or higher induced callus formation in control, and shoot tips cryopreserved by vitrification, and by encapsulation-dehydration, respectively. While a BA concentration of 4 microM was found optimal for recovery of control shoot tips, 1 and 2-4 microM produced the best recovery of shoot tips cryopreserved by vitrification and encapsulation-dehydration, respectively. A similar pattern of effect of BA on recovery was found for 'Troyer' citrange. Low survival of control and cryopreserved shoot tips was observed with a BA-free recovery medium. The addition of BA to the recovery medium significantly increased survival. The BA concentration that induced callus formation in shoot tips cryopreserved by encapsulation-vitrification was higher than that which induced it in those cryopreserved by encapsulation-dehydration. Recovery of control shoot tips was best with an addition of 6-10 microM BA to the medium. Optimal recovery of shoot tips cryopreserved by encapsulation-vitrification and encapsulation-dehydration was achieved with 3-4 and 2 microM BA, respectively. Results from the present study suggest that an optimal BA concentration for recovery of control shoot tips may be different from that for cryopreserved shoot tips; furthermore, the optimal BA concentration for recovery of cryopreserved shoot tips may also differ among different cryogenic procedures.     

Coordination-Induced Band Gap Reduction in a Metal–Organic Framework

Herein, we report on the synthesis of a microporous, three-dimensional phosphonate metal–organic framework (MOF) with the composition Cu₃(H₅-MTPPA)₂ ⋅ 2 NMP (H₈-MTPPA=methane tetra-p-phenylphosphonic acid and NMP=N-methyl-2-pyrrolidone). This MOF, termed TUB1, has a unique one-dimensional inorganic building unit composed of square planar and distorted trigonal bipyramidal copper atoms. It possesses a (calculated) BET surface area of 766.2 m²/g after removal of the solvents from the voids. The Tauc plot for TUB1 yields indirect and direct band gaps of 2.4 eV and 2.7 eV, respectively. DFT calculations reveal the existence of two spin-dependent gaps of 2.60 eV and 0.48 eV for the alpha and beta spins, respectively, with the lowest unoccupied crystal orbital for both gaps predominantly residing on the square planar copper atoms. The projected density of states suggests that the presence of the square planar copper atoms reduces the overall band gap of TUB1, as the beta-gap for the trigonal bipyramidal copper atoms is 3.72 eV.     

Utilization of smart hydrogel-metal composites as catalysis media

Various metal nanoparticles such as, Cu, Co, Ni, and Fe were prepared inside poly(1-vinyl imidazole) p(VI) hydrogel by the absorption of the corresponding metal ions from aqueous solutions and the reduction with suitable reducing agents such as NaBH(4) and/or NaOH. TGA and ICP-AES were used to determine the metal particle content of p(VI)-M (M: Cu, Co, and Ni) composites. The prepared hydrogel-metal nanoparticle composites were proven to be resourceful as reaction container for the catalysis of various organic reactions. It was illustrated that p(VI)-M hydrogel-metal composites can be successfully used in the hydrolysis of NaBH(4) for the generation hydrogen form NaBH(4) and NH(3)BH(3). Additionally, p(VI)-M composites were also illustrated in the catalysis of different organic reactions; e.g., these hydrogel-M are very effective in the reduction nitro aromatic compounds such 2-nitrophenol (2-NP) and 4-nitrophenol (4-NP) to their corresponding amine forms in the presence of aqueous NaBH(4). Various parameters in the catalysis of hydrogen production and 4-NP reduction were determined.     

Material binding peptides for nanotechnology

Remarkable progress has been made to date in the discovery of material binding peptides and their utilization in nanotechnology, which has brought new challenges and opportunities. Nowadays phage display is a versatile tool, important for the selection of ligands for proteins and peptides. This combinatorial approach has also been adapted over the past decade to select material-specific peptides. Screening and selection of such phage displayed material binding peptides has attracted great interest, in particular because of their use in nanotechnology. Phage display selected peptides are either synthesized independently or expressed on phage coat protein. Selected phage particles are subsequently utilized in the synthesis of nanoparticles, in the assembly of nanostructures on inorganic surfaces, and oriented protein immobilization as fusion partners of proteins. In this paper, we present an overview on the research conducted on this area. In this review we not only focus on the selection process, but also on molecular binding characterization and utilization of peptides as molecular linkers, molecular assemblers and material synthesizers.     

Fully Developed Forced Convection in a Parallel Plate Channel with a Centered Porous Layer

In this study, fully developed heat and fluid flow in a parallel plate channel partially filled with porous layer is analyzed both analytically and numerically. The porous layer is located at the center of the channel and uniform heat flux is applied at the walls. The heat and fluid flow equations for clear fluid and porous regions are separately solved. Continues shear stress and heat flux conditions at the interface are used to determine the interface velocity and temperature. The velocity and temperature profiles in the channel for different values of Darcy number, thermal conductivity ratio, and porous layer thickness are plotted and discussed. The values of Nusselt number and friction factor of a fully clear fluid channel (Nu _cl = 4.12 and fRe _cl = 24) are used to define heat transfer increment ratio (e_th = Nu_p/Nu_cl)({\varepsilon _{\rm th} =Nu_{\rm p}/Nu_{\rm cl})} and pressure drop increment ratio (e_p = fRe_p/fRe_cl )({\varepsilon_{\rm p} =fRe_{\rm p}/fRe_{\rm cl} )} and observe the effects of an inserted porous layer on the increase of heat transfer and pressure drop. The heat transfer and pressure drop increment ratios are used to define an overall performance (e = e_th/e_p)({\varepsilon = \varepsilon_{\rm th}/\varepsilon_{\rm p})} to evaluate overall benefits of an inserted porous layer in a parallel plate channel. The obtained results showed that for a partially porous filled channel, the value of e{\varepsilon} is highly influenced from Darcy number, but it is not affected from thermal conductivity ratio (k _r) when k _r > 2. For a fully porous material filled channel, the value of e{\varepsilon} is considerably affected from thermal conductivity ratio as the porous medium is in contact with the channel walls.     

Assembly kinetics of nanocrystals via peptide hybridization

The assembly kinetics of colloidal semiconductor quantum dots (QDs) on solid inorganic surfaces is of fundamental importance for implementation of their solid-state devices. Herein an inorganic binding peptide, silica binding QBP1, was utilized for the self-assembly of nanocrystal quantum dots on silica surface as a smart molecular linker. The QD binding kinetics was studied comparatively in three different cases: first, QD adsorption with no functionalization of substrate or QD surface; second, QD adsorption on QBP1-modified surface; and, finally, adsorption of QBP1-functionalized QD on silica surface. The surface modification of QDs with QBP1 enabled 79.3-fold enhancement in QD binding affinity, while modification of a silica surface with QBP1 led to only 3.3-fold enhancement. The fluorescence microscopy images also supported a coherent assembly with correspondingly increased binding affinity. Decoration of QDs with inorganic peptides was shown to increase the amount of surface-bound QDs dramatically compared to the conventional methods. These results offer new opportunities for the assembly of QDs on solid surfaces for future device applications.