A facile and controllable one-pot synthesis approach to amino-functionalized hollow silica nanoparticles with accessible ordered mesoporous shells

The development of a practical synthetic method to functionalize hollow mesoporous silica with organic groups is of current intere st for selective adsorption and ene rgy storage applications.Herein,a facile and controllable one-pot approach for the synthesis of monodisperse amino-functionalized hollow mesoporous silica nanoparticles is presented.A novel solid-to-hollow structural transformation procedure of the silica nanoparticles is presented.The structural transformation is easily designed,as obse rved through transmission electro n microscopy,by tailo ring the HCl and N-lauroylsarcosine sodium molar ratio and the water content in the sol-gel.Ordered and radially oriented in situ aminofunctionalized mesochannels were successfully introduced into the shells of the hollow silica nanoparticles.A formation mechanism for the hollow mesoporous silica materials is discussed.     

A new controllable approach to synthesize hyperbranched poly(siloxysilanes)

A new controllable approach to synthesize hyperbranched poly(siloxysilanes) via hydrosilylation of A₂‐ and B′B_x‐type monomers was developed in this work. A₂ monomers (dimethylbis(dimethylsiloxy)siloxane and tetramethyldisiloxane), B′B_x monomers (methylvinyldiallylsilane and vinyltriallylsilane), and the resultant hyperbranched poly(siloxysilanes) were well characterized using FTIR, ¹H NMR, ¹³C NMR, ²⁹Si NMR, and SEC/MALLS. The In situ FTIR results indicate that the controllable polymerization can be carried out quickly and the reaction process was obviously performed in two stages. At the first stage, silicon hydride selectively reacts with vinyl silane groups, which produces intermediate structures with one Si? H and two (or three) allyl groups. Consequently, at the second stage, these intermediates act as new AB₂ (or AB₃) type monomers and continue to be self‐polymerized to generate hyperbranched polymers. By this novel controllable approach, molecular weights and their polydispersity of the resulted hyperbranched poly(siloxysilanes) can be conveniently regulated via adjusting the process parameters, such as feeding ratio of two monomers. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 2708–2720, 2008     

A facile one-step route to synthesize titania hollow microspheres with incontinuous multicavities

The titania hollow microspheres with incontinuous multicavities were successfully fabricated via an oil/ water(O/W) emulsion process accompanied by sol–gel reaction in the presence of polyvinylpyrrolidone(PVP). In the one-step route, the addition of PVP to the tetrabutyl titanate(TBT) 1-octanol solution as the oil phase of the O/W emulsion clearly expands the size of the cavities inside the microspheres. The and atoleine alters the polarity of the oil phase to affect the interior structure significantly. The Span 80 is used as a stabilizer to preserve spherical shape. A preliminary mechanism based on phaseseparation for the structural evolution of titania hollow microspheres with multicavities is suggested. Zirconia and alumina hollow microspheres with incontinuous multicavities can also be prepared by this one-step route successfully.     

A facile route to synthesize silver nanoparticles in polyelectrolyte capsules

We are reporting a novel green approach to incorporate silver nanoparticles (NPs) selectively in the polyelectrolyte capsule shell for remote opening of polyelectrolyte capsules. This approach involves in situ reduction of silver nitrate to silver NPs using PEG as a reducing agent (polyol reduction method). These nanostructured capsules were prepared via layer by layer (LbL) assembly of poly(allylamine hydrochloride) (PAH) and dextran sulfate (DS) on silica template followed by the synthesis of silver NPs and subsequently the dissolution of the silica core. The size of silver nanoparticles synthesized was 60±20 nm which increased to 100±20 nm when the concentration of AgNO(3) increased from 25 mM to 50 mM. The incorporated silver NPs induced rupture and deformation of the capsules under laser irradiation. This method has advantages over other conventional methods involving chemical agents that are associated with cytotoxicity in biological applications such as drug delivery and catalysis.     

A facile approach to synthesize CoO-Co3O4/TiO2 NAs for reinforced photoelectrocatalytic water oxidation

Journal of Solid State Electrochemistry - Photoelectrocatalytic (PEC) water splitting technology is used to convert solar energy into hydrogen energy, and has the potential to alleviate energy...     

一种合成柔红霉素糖基类似物的新方法

与很多蒽环类抗生素一样,柔红霉素分子中含有3-氨基2,3,6-三脱氧己糖单元,糖基部分对药物分子的活性起着至关重要的作用.本文介绍了一种合成柔红霉素糖基类似物的新方法.     

A facile approach to phosphonic acid diesters

The symmetric H‐phosphonates of carbohydrate and other compounds were conveniently prepared by direct transesterification of the corresponding monohydroxylic compounds with diphenyl phosphite. The approach has the merits of mild reaction conditions and high yields. © 2003 Wiley Periodicals, Inc. Heteroatom Chem 14:208–210, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.10130     

A facile approach to synthesize poly(4-vinylpyridine)/multi-walled carbon nanotubes nanocomposites: highly water-dispersible carbon nanotubes decorated with gold nanoparticles

A facile approach to attach high-density and uniform gold nanoparticles on individual multi-walled carbon nanotubes (MWNTs) is achieved. By simple grinding, water-soluble linear polymers poly(4-vinylpyridine) (PVP)-wrapped around nanotubes and thus rendered them reversibly soluble in water, ethanol, and DMF. Individual tubes are clearly observed after PVP-wrapped nanotubes were spin-coated onto a silicon wafer. Subsequently, Au nanoparticles were densely decorated on the individual MWNTs by in situ reduction of HAuCl₄ in the homogeneous aqueous solution of MWNTs–PVP to form stable water-dispersible Au/PVP/MWNTs hybrid. Morphology of Au nanoparticles was determined by scanning electron microscope and atomic force microscope. The diameter of the Au nanoparticles is controlled in the range of 3.5 to 13.5 nm. The presence of gold nanoparticles with decreased particle size was also detected by UV–Vis spectroscopy.     

A facile strategy to synthesize Pd/TiO2 nanotube arrays with high visible light photocatalytic performance

Research on Chemical Intermediates - Novel Pd/TiO2 nanotube arrays (Pd/TNTAs) were fabricated by introducing Pd nanoparticles onto TNTAs via a facile deposition–reduction method. Pd...     

A novel approach to synthesize dichlorobenzonitriles by selective ammoxidation

Research on Chemical Intermediates - Dichlorobenzonitriles are important organic intermediates for the production of many fine chemicals and are produced most economically and environment-friendly...     

A facile approach to hexagonal ZnO nanorod assembly

Nanocrystalline ZnO nanorods were successfully grown by ultrasonication using an acidic ethanolic zinc acetate precursor solution followed by a flow coating process and annealing at 600 °C. The ZnO nanorods obtained were hexagonal in shape and showed a high degree of uniformity in size and distribution. These samples were characterized by X-ray diffraction (XRD), energy dispersive X-ray (EDX) spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and Raman spectrophotometry and the results are discussed. This approach appears to be the easiest way to fabricate bulk ZnO nanorods.     

A facile method to fabricate tough hydrogel with ultra-wide adjustable stiffness,stress, and fast recoverability

In this article, we report a synergistic strategy to develop dual physically cross-linked tough hydrogels via one-pot bulk copolymerization of N-vinyl-2-pyrrolidone, acrylic acid, and stearyl methylacrylate (SMA) without any adscititious surfactant. Due to synergic effects of hydrogen bonding and hydrophobic association, the resulted dual physically cross-linked hydrogels (DP Gel) with ultra-wide range adjustable Young's modulus (0.08–45.6 MPa), tensile stress (0.7–6.9 MPa), and toughness (3.3–23.1 MJ m⁻³). Stretching to 300%, DP Gel exhibited fast recoverability that remained ~95% of initial dissipated energy after resting in 60 °C for 3 min. Finally, scanning electron microscopy revealed that the microstructure of hydrogel changed from phase separation structure to micro phase separation as SMA added, which accounted for excellent performance of DP Gel. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018 , 56, 1469–1474     

A facile and highly atom-economic approach to biaryl-containing medium-ring bislactones

Starting from readily available phenanthrenequinone and alkenes, biaryl containing medium-ring bislactones could be easily prepared through sequential photocycloaddition-photooxidation reactions with good yields and diastereoselectivity.     

A facile two synthon approach to the camptothecin skeleton

A synthesis of deethyldesoxycamptothecin via the reaction of two readily accessible synthons is described. One of the synthons constitutes the ABC ring system of camptothecin, while the second provides all the C atoms of the rings D and E. The synthetic approach is suited for the total synthesis of camptothecin analogues.     

A facile two-step high yield approach to 2-oxasteroids

The base catalyzed autoxidation of 3-oxo-Δ⁴ steroids in aprotic media at circa -25°C occurs nearly exclusively at C₂ of the A-ring, generating rapidly (< 4 hrs) and in high yield the corresponding enol (2-hydroxy-3-oxo-Δ^1,4 analog) When the reaction is then allowed to continue at room temperature for several days, the enol is further autoxidized to the related lactol (1-hydroxy-2-oxa-3-oxo-Δ⁴ analog) in overall yields generally in the range of 85–95%. Sodium borohydride reduction of the lactol yields the pharmacologically important 2-oxasteroids.     

A facile aqueous route to synthesize highly ordered mesoporous polymers and carbon frameworks with Ia3d bicontinuous cubic structure

By employing an organic-organic self-assembly in a dilute aqueous solution, novel ordered bicontinuous cubic mesoporous polymers and carbons with Iad symmetry are directly synthesized.     

A general approach to synthesize asymmetric hybrid nanoparticles by interfacial reactions

Asymmetric multicomponent nanoparticles (AMNPs) offer new opportunities for new-generation materials with improved or new synergetic properties not found in their individual components. There is, however, an urgent need for a synthetic strategy capable of preparing hybrid AMNPs with fine-tuned structural and compositional complexities. Herein, we report a new paradigm for the controllable synthesis of polymer/metal AMNPs with well-controlled size, shape, composition, and morphology by utilizing interfacial polymerization. The hybrid AMNPs display a new level of structural-architectural sophistication, such as controlled domain size and the number of each component of AMNPs. The approach is simple, versatile, cost-effective, and scalable for synthesizing large quantities of AMNPs. Our method may pave a new route to the design and synthesis of advanced breeds of building blocks for functional materials and devices.