Double stimuli-responsive cellulose nanocrystals reinforced electrospun PHBV composites membrane for intelligent drug release.

Double stimuli-responsive functionalized cellulose nanocrystal-poly[2-(dimethylamino)ethyl methacrylate] (CNC-g-PDMAEMA) reinforced poly(3-hydroxybutyrate-co-3-hydroxy valerate) (PHBV) electrospun composite membranes were explored as drug delivery vehicles using tetracycline hydrochloride (TH) as a model drug. It was found that rigid CNC-g-PDMAEMA nanoparticles enhanced thermal, crystallization and hydrophilic properties of PHBV. Moreover, great improvements in fiber diameter uniformity, crystallization ability and maximum decomposition temperature (Tmax) could be achieved at 6 wt% CNC-g-PDMAEMA. Furthermore, by introducing stimuli-responsive CNC-g-PDMAEMA nanofillers, intelligent and long-term sustained release behavior of composite membranes could be achieved. The releasing mechanism of composite membranes based on zero order, first order, Higuchi and Korsmeyere-Peppas mathematical models was clearly demonstrated, giving effective technical guidance for practical drug delivery systems.

Green one-step synthesis of ZnO/cellulose nanocrystal hybrids with modulated morphologies and superfast absorption of cationic dyes.

Zinc oxide/cellulose nanocrystal (ZnO/CNC) hybrids with modulated morphologies were prepared by using bamboo CNC as templates via green one-step technique. The effect of pH values on the morphology, microstructure, thermal stability, antibacterial efficiency and dye absorption kinetics of hybrids were investigated. A possible mechanism for various hybrid morphologies at different pH values was provided. All the samples exhibited high antibacterial ratios of 91.4%-99.8% against both Escherichia coli and Staphylococcus aureus. ZnO/CNC8.5 gave quick removal efficiency with high dye removal ratios in methylene blue (MB, 93.55%) and malachite green (MG, 99.02%), especially >91.47% and 97.85% within 5 min. The absorption capacity could reach up to 46.77 mg/g for MB and 49.51 mg/g for MG. Besides, absorption kinetics showed that the absorption behavior followed the pseudo-second-order kinetic model (R2 > 0.99996). Such ZnO/CNC hybrids show outstanding and low-cost adsorbent for efficient absorption of cationic dyes in wastewater treatment field.

Robust 1D open rack-like architecture in coordination polymers of Anderson POMs [{Na4(H2O)14}{Cu(gly)}2][TeMo6O24] and [{Cu(en)2}3{TeW6O24}]: synthesis, characterization and heterogeneous catalytic epoxidation of olefines.

Two novel organic-inorganic hybrid tungsto- and molybdo-telurates having formula [{Na(4)(H(2)O)(14)}{Cu(gly)}(2)][TeMo(6)O(24)] (1){gly = glycine} and [{Cu(en)(2)}(3){TeW(6)O(24)}]·6H(2)O {en = ethyline-diamine} (2) based on Anderson type heteropolyoxometalates (POMs) have been synthesized and characterized by X-ray crystallography. Common structural feature of both 1 and 2 is the presence of a unique 1D open rack-like architecture, where the disc shaped Anderson POMs act as steps and cationic Cu-organic complexes act as handles of the rack. In 1 the independent structural unit is a 1D coordination polymer with the above mentioned rack type architecture, while in 2, these independent rack-like architectures are further extended to a 2D coordination polymer. Heterogeneous catalysis for the epoxidation of cyclohexene and styrene by complexes 1 and 2 showed very good catalytic efficiency resulting epoxides of ~60% yield, with dialcohol formed by the hydrolysis of epoxides, as the other major product (~28%). Cyclic voltammetric studies of [{Na(4)(H(2)O)(14)}{Cu(gly)}(2)][TeMo(6)O(24)] (1) in aqueous KCl solution indicates that the redox changes occur only on the copper centers and supported by carrying out parallel experiments on the precursors like ([Cu(gly)(2)](2+) and [TeMo(6)O(24)](6-), under the identical experimental conditions. The E(1/2) = 0.662, -0.142 and -0.332 V(vs. SCE) correspond to Cu(III) → Cu(II), Cu(II) → Cu(I) and Cu(I) → Cu(0) reductions, respectively. Thermal analyses reveal identical phase transition reactions with an exothermic peak in the DTA curve at 380 °C for 1 and an endothermic peak appears at comparatively higher temperature (408 °C) for 2 manifesting the higher stability of tungstane based POM over the molybdenum ones. EPR as well as magnetic moment results indicate that both the complexes 1 and 2 are paramagnetic with one unpaired electron per copper(II) ion.

catena-Poly[potassium [copper(II)-mu-isothiocyanato-mu-N-salicylidene-beta-alaninato2-]].

The title polymeric compound, catena-poly[dipotassium [bis[mu-N-salicylidene-beta-alaninato(2-)]-kappa(4)O,N,O':O";kappa(4)O":O,N,O'-dicopper(II)]-di-mu-isothiocyanato-kappa(2)N:S;kappa(2)S:N], [K[Cu(NCS)(C(10)H(9)NO(3))]](n), consists of [isothiocyanato(N-salicylidene-beta-alaninato)copper(II)](-) anions connected through the two three-atom thiocyanate (mu-NCS) and the two anti,anti-mu-carboxylate bridges into infinite one-dimensional polymeric anions, with coulombically interacting K(+) counter-ions with coordination number 7 constrained between the chains. The Cu(II) atoms adopt a distorted tetragonal-bipyramidal coordination, with three donor atoms of the tridentate Schiff base and one N atom of the bridging mu-NCS ligand in the basal plane. The first axial position is occupied by a thiocyanate S atom of a symmetry-related mu-NCS ligand at an apical distance of 2.9770 (8) A, and the second position is occupied by an O atom of a bridging carboxylate group from an adjacent coordination unit at a distance of 2.639 (2) A.