Project description:The one-pot synthesis of a target molecule in the same reaction vessel is widely considered to be an efficient approach in synthetic organic chemistry. In this review, the characteristics and limitations of various one-pot syntheses of biologically active molecules are explained, primarily involving organocatalytic methods as key tactics. Besides catalysis, the pot-economy concepts presented herein are also applicable to organometallic and organic reaction methods in general.
Project description:Polyphosphazene microspheres were fabricated by ultrasonic-assisted precipitation polymerization using 4,4'-(hexafluoroisopropylidene)diphenol, 4,4'-sulfonyldiphenol, 4,4-(9-fluorenylidene)diphenol, and phenolphthalein to obtain poly[4,4'-(hexafluoroisopropylidene)diphenol]phosphazene (PZAF), poly(4,4'- sulfonyldiphenol)phosphazene (PZS), poly[4,4'-(9-fluorenylidene)diphenol]phosphazene, and poly(phenolphthalein)phosphazene (PZPT) and were incorporated into polybenzoxazines (PBa) to obtain corresponding PZAF/PBa, PZS/PBa, fluorenyl polyphosphazene (PZFP)/PBa, and PZPT/PBa composites. Addition of 5 wt % of PZAF, PZS, PZFP, and PZPT microspheres improved the thermal stability and fire retardancy of PBa resin significantly. Notably, addition of PBa with 5% PZAF led to a 62.5% decrease in the peak heat release rate and 49.3% reduction in total heat release. The role of microspheres in the gas-phase flame-retardancy mechanism in the PBa matrix was studied. Dynamic mechanical analysis results demonstrated that the T g of PBa flame-retardant composites was still around 210 °C compared to 221 °C of pure PBa. Hence, the synthesized PBa composites had potential applications as high flame-retardancy materials.
Project description:Impurity element doping is extensively taken as one of the most efficient strategies to regulate the electronic structure as well as the rate of photogenerated charge separation of photocatalysts. Herein, a one-pot hydrothermal synthesis process was exploited to obtain La-doped ZnIn2S4 microspheres, aiming at gaining insight into the role that doping ions played in the improvement of pollutant photodegradation. Systematical characterization means, comprising of X-ray photoelectron spectroscopy (XPS), ultraviolet-visible (UV-vis) diffuse reflection spectroscopy and Raman spectra, combination with high-resolution transmission electron microscopy (HRTEM), were employed to in depth reveal the concomitancy of La ions and ZnIn2S4 crystal lattice. The results showed that the La-doped ZnIn2S4 samples exhibited a slightly wider and stronger spectral absorption than pristine ZnIn2S4; and the specific surface area of doped ZnIn2S4 samples was a bit larger. The La-doped ZnIn2S4 electrodes showed improved photocurrent response, and the photocurrent density reached a maximum value at La content of 1.5 wt%. As expected, La-doped ZnIn2S4 samples exhibited a remarkable enhancement of photocatalytic behaviour toward the photodegradation of tetracycline hydrochloride (TCH) and methyl orange (MO). The prominently enhanced photoactivity of doped ZnIn2S4 samples was due to the synergistic effect of the elevated visible-light absorption ability and effective photogenerated charge carriers' separation.
Project description:The fabrication of manganese oxide-carbon composite microspheres with open nanochannels and their electrochemical performance as anode materials for lithium ion batteries are investigated. Amorphous-like Mn3O4 nanoparticles embedded in a carbon matrix with three-dimensional channels are fabricated by one-pot spray pyrolysis. The electrochemical properties of the Mn3O4 nanopowders are also compared with those of the Mn3O4-C composite microspheres possessing macropores resembling ant-cave networks. The discharge capacity of the Mn3O4-C composite microspheres at a current density of 500 mA g(-1) is 622 mA h g(-1) after 700 cycles. However, the discharge capacity of the Mn3O4 nanopowders is as low as 219 mA h g(-1) after 100 cycles. The Mn3O4-C composite microspheres with structural advantages and high electrical conductivity have higher initial discharge and charge capacities and better cycling and rate performances compared to those of the Mn3O4 nanopowders.
Project description:Phenolphthalein type polyphosphazene (PZPT) microspheres were synthesized by an ultrasound assisted precipitation polymerization method, and their structures were confirmed by scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectroscopy. Benzoxazine/PZPT (Ba/PZPT) hybrid materials were fabricated and cured to prepare polybenzoxazine/PZPT (PBa/PZPT) composites. The effects of PZPT microspheres on the curing kinetics and behaviors of Ba were systematically analyzed and supported by differential scanning calorimetry (DSC) and in situ FTIR. The thermogravimetric (TGA) results demonstrated good thermal stability of the PBa composites incorporating PZPT. The peak of heat release rate and total heat release values of PBa/PZPT-5% composites obviously deceased by 57.8% and 17.3% compared to those of the pristine PBa. Moreover, the smoke released from the PZPT/PBa system significantly reduced with the loading of microspheres. Finally, the dynamical mechanical analysis results demonstrated that the T g of PBa flame retardant composites was approximately 210 °C, not affecting further applications of PBa composites.
Project description:(-)-Ambrox is recognised as the prototype of all ambergris odorants. Widely used in perfumery, (-)-Ambrox is an important ingredient due to its unique scent and excellent fixative function. An environmentally friendly and practical preparation of (-)-Ambrox is still unavailable at present although a lot of attention has been paid to this hot research topic for many years. A one-pot synthesis of (-)-Ambrox was studied starting from (-)-sclareol through oxidation with hydrogen peroxide in the presence of a quaternary ammonium phosphomolybdate catalyst {[C5H5NC16H33] [H2PMo12O40]}, which gave the product a 20% overall yield.
Project description:An efficient one-pot synthesis for Janus-type fullerenol derivatives and how to characterize them is reported. This synthesis provides access to asymmetrically substituted fullerenol with five substituents on one pole of the fullerene and polyhydroxylation moieties, mostly ether and hydroxy groups, on the rest of the fullerene core. As substituents a broad variety of primary amines can be used to obtain Janus-type amphiphilic fullerenols in good to excellent yield. These fullerenol amphiphiles can serve as suitable precursors for further reactions resulting in new applications for fullerenols.
Project description:Polypropionates-motifs with alternating methyl and hydroxy groups-are important segments of many natural products possessing high bioactivity and therapeutic value. Synthetic access to these structures remains an area of intensive interest, focusing on the establishment of the contiguous stereocentres and a desire for operational simplicity. Here we report an efficient strategy for the stereoselective assembly of polypropionates with three or four stereocentres through a three-step relay process that include Diels-Alder reaction, silylenol ether hydrolysis and Baeyer-Villiger oxidation. The stereochemistry and functionality of the resulting polypropionates depend on the substitution pattern of the diene and dienophile substrates of the Diels-Alder cycloaddition. More importantly, the relay sequence is effectively performed in one pot, and the product could potentially undergo the same sequence for further elaboration. Finally, the C1-C9 segment of the macrolide etnangien is constructed with four of the six stereogenic centres established using the relay sequence.Polypropionates are present in many natural products possessing high bioactivity and therapeutic value. Here the authors show a strategy for the stereoselective assembly of polypropionates with three or four stereocentres through a process that includes a Diels-Alder reaction, silylenol ether hydrolysis and Baeyer-Villiger oxidation.
Project description:A new method for oligosaccharide assembly that combines the advantages of one-pot synthesis and fluorous separation is described. After one-pot glycosylations are completed, a fluorous tag is introduced into the reaction mixture to selectively "catch" the desired oligosaccharide, which is rapidly separated from non-fluorous impurities by fluorous solid-phase extraction (F-SPE). Subsequent "release" of the fluo rous tag and F-SPE achieved the purification of the desired oligosaccharide without the use of time- and solvent-consuming silica gel chromatography. Linear and branched oligosaccharides have been synthesized with this approach in just a few hours (for the overall oligosaccharide assembly and purification process).
Project description:A promising method for the high-throughput synthesis of linear C-hydroxyalkylamido peptidomimetics and beta-turn cyclic peptidomimetics via "volatilizable" aminoalkyl functionalized silica gels is presented. Boc amino acids and carboxylic acids were coupled on functionalized aminoalkyl silica gels using a standard DIC/HOBt coupling protocol. After peptide synthesis, the resin bound peptide was cleaved using a two-step process to obtain the linear C-hydroxyalkylamido peptidomimetics. Beta-turn cyclic peptidomimetics were generated by intramolecular S(N)Ar cyclization in an aqueous solution. Both the linear and the cyclic peptidomimetics were obtained with good to excellent yields and purities through a "one-pot" reaction.