Size-dependent visible photoluminescence from ZnO nanoparticles prepared via SiO2 network

This study reports a simple method for the synthesis of different size of wurtzite ZnO nanoparticles in assistance of tetraethyl orthosilicate (TEOS). With the increase of the amount of TEOS added, the average size of ZnO nanoparticles was found decreased from ∼14.6 to ∼1.9 nm by characterization of X-ray diffraction (XRD) and high-resolution electron microscopy (HRTEM). The growth of ZnO nanoparticles is proposed to be controlled by the density of the SiO₂ chain mesh which is determined by TEOS amount in precursor. Ultraviolet–visible (UV–VIS) absorption and photoluminescence (PL) spectra show both shift to higher energy in cut-off edge and in visible emission bands respectively. The electron transition process in the mechanism of the visible emission shift was described and related to quantum size effect in ZnO nanoparticles.     

Ferrite nanoparticles supported on natural wool in one‐pot tandem oxidative reactions: strategy to synthesize benzimidazole,quinazolinone and quinoxaline derivatives

Two tandem oxidative two‐component reactions (O‐2CRs) and Ugi‐type three‐component reactions (OU‐3CRs) of aromatic hydrocarbons of petroleum naphtha have been investigated for the synthesis of 2‐phenyl‐1H ‐benzo [d ]imidazole, 2‐aryl‐4‐quinazolinone and 3,4‐dihydroquinoxalin‐2‐amine derivatives using six new biopolymer‐supported ferrite nanocatalysts: CoFe₂O₄@wool‐SO₃H, MnFe₂O₄@wool‐SO₃H, ZnFe₂O₄@wool‐SO₃H, MnCoFe₂O₄@wool‐SO₃H, ZnCoFe₂O₄@wool‐SO₃H and CrCoFeO₄@wool‐SO₃H. The best results are obtained with the CrCoFeO₄@wool‐SO₃H catalyst. All of the catalysts were characterized using flame atomic absorption spectrometry, X‐ray diffraction, thermogravimetric analysis, scanning electron microscopy and energy‐dispersive spectroscopy. To the best of our knowledge, this approach can be considered as the first example of O‐2CRs and OU‐3CRs of aromatic hydrocarbons of petroleum naphtha with ferrite nanocatalysts, which would be very useful from a practical point of view. Copyright © 2016 John Wiley & Sons, Ltd.     

Copper(I) oxide nanoparticles supported on magnetic casein as a bio‐supported and magnetically recoverable catalyst for aqueous click chemistry synthesis of 1,4‐disubstituted 1,2,3‐triazoles

Copper(I) oxide nanoparticles supported on magnetic casein (Cu₂O/Casein@Fe₃O₄NPs) has been synthesized as a bio‐supported catalyst and was characterized using powder X‐ray diffraction, transmission electron microscopy, energy dispersive X‐ray and Fourier transform infrared spectroscopies, thermogravimetric analysis and inductively coupled plasma optical emission spectrometry. The catalytic activity of the synthesized catalyst was investigated in one‐pot three‐component reactions of alkyl halides, sodium azide and alkynes to prepare 1,4‐disubstituted 1,2,3‐triazoles with high yields in water. The reaction work‐up is simple and the catalyst can be magnetically separated from the reaction medium and reused in subsequent reactions.     

Camptothecin@HMSNs/thermosensitive hydrogel composite for applications in preventing local breast cancer recurrence

The CPT was loaded into the HMSNs with the high loading capacity. Then the CPT@HMSNs were loaded into the PLEL thermosensitive hydrogels for local therapy to prevent the recurrence of breast cancer after the tumor was resected.     

A Gold Nanoparticles–Enhanced Carbon Nanotubes Electrochemical Chiral Sensor

The field of enantioselective recognition directly using inherently chiral single‐walled carbon nanotubes (cSWCNTs) still remains unexplored. Herein, the insertion of size‐controlled gold nanoparticles (GNPs) to cSWCNTs brings about superior conductivity, high stability, and excellent electrocatalytic ability, thus an enhanced sensitivity for chiral sensing. The practicability of the GNPs/cSWCNTs based electrochemical sensor was validated by chirally recognizing 3,4‐dihydroxyphenylalanine and tyrosine as model molecules.     

Synthesis and characterization of biodegradable amphiphilic ABC Y‐shaped miktoarm terpolymer by click chemistry for drug delivery

Biodegradable amphiphilic ABC Y‐shaped triblock copolymer (MPBC) containing PEG, PBLA, and PCL segments was synthesized via the combination of enzymatic ring‐opening polymerization (ROP) of epsilon‐caprolactone, ROP of BLA‐N‐carboxyanhydride and click chemistry, where PEG, PBLA, and PCL are poly(ethylene glycol), poly(benzyl‐l ‐aspartate), and polycaprolactone, respectively. Propynylamine was employed as ROP initiator for the preparation of alkynyl‐terminated PBLA and methyloxy‐PEG with hydroxyl and azide groups at the chain‐end was used as enzymatic ROP initiator for synthesis of monoazido‐midfunctionalized block copolymer mPEG‐b‐PCL. The subsequent click reaction led to the formation of Y‐shaped asymmetric heteroarm terpolymer MPBC. The polymer structures were characterized by different analyses. The MPBC terpolymer self‐assembled into micelles and physically encapsulated drug doxorubicin (DOX) to form DOX‐loaded micelles, which showed good stability and slow drug release. In vitro cytotoxicity study indicated that the MPBC micelles were nontoxic and the DOX‐loaded micelles displayed obvious anticancer activity similar to free DOX against HeLa cells. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 3346–3355     

Humic-based bionanocomposites containing stable paramagnetic gold nanoparticles for prospective use in pharmaceuticals

Structural peculiarities and supramolecular organization of medicinally promising nanocomposites, synthesized from humic substances, which essentially differ depending on decomposition degree, have been studied using electron spin resonance, transmission electron, and confocal laser scanning microscopy techniques and some other modern physical–chemical methods. It is shown that stable zero-valent gold nanoparticle of about 10–17?nm in size are formed in a natural macromolecular matrix. The nanocomposites obtained turn out to be stable in aggregative state for a long time and preserve their properties that are extremely important for prospective medicinal substances.     

Removal of permethrin pesticide from water by chitosan–zinc oxide nanoparticles composite as an adsorbent

Synthesis of chitosan–ZnO nanoparticles (CS–ZnONPs) composite beads was performed by a polymer-based method. The resulting bionanocomposite was characterized by scanning electron microscopy (SEM), X-ray powder diffraction (XRD) spectroscopy and infrared spectroscopy (FT-IR). Adsorption applications for removal of pesticide pollutants were conducted. The optimum conditions, including adsorbent dose, agitating time, initial concentration of pesticide and pH on the adsorption of pesticide by chitosan loaded with zinc oxide nanoparticles beads were investigated. Results showed that 0.5 g of the bionanocomposite, in room temperature and pH 7, could remove 99% of the pesticide from permethrin solution (25 ml, 0.1 mg L⁻¹), using UV spectrophotometer at 272 nm. Then, the application of the adsorbent for pesticide removal was studied in the on-line column. The column was regenerated with NaOH solution (0.1 M) completely, and then reused for adsorption application. The CS–ZnONPs composite beads appear to be the new promising material in water treatment application with 56% regeneration after 3 cycles.     

Efficient one‐pot synthesis of water‐compatible and photoresponsive molecularly imprinted polymer nanoparticles by facile RAFT precipitation polymerization

A facile, general, and highly efficient one‐pot approach to obtain azobenzene (azo)‐containing molecularly imprinted polymer (MIP) nanoparticles with photoresponsive template binding and release properties in aqueous media is described, which involves the combined use of hydrophilic macromolecular chain transfer agent‐mediated reversible addition‐fragmentation chain transfer precipitation polymerization and easily available water‐insoluble azo functional monomers. The resulting azo‐containing MIPs were characterized with dynamic laser scattering (DLS), SEM, FTIR, static contact angle and water dispersion studies, and equilibrium binding experiments. They have proven to be nanoparticles (their diameters being around 104–397 nm, as determined by DLS in methanol) with surface‐grafted hydrophilic polymer brushes and exhibit excellent pure water‐compatible template binding properties. Moreover, obvious photoregulated template binding behaviors were observed for such azo‐containing MIP nanoparticles, which led to their largely accelerated template release in the aqueous media under the UV light irradiation. Furthermore, the general applicability of the strategy was also demonstrated. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 1941–1952