A Hexagonal Covalent Porphyrin Framework as an Efficient Support for Gold Nanoparticles toward Catalytic Reduction of 4‐Nitrophenol

A hexagonal porphyrin‐based porous organic polymer, namely, CPF‐1, was constructed by 3+2 ketoenamine condensation of the C₂‐symmetric porphyrin diamine 5,15‐bis(4‐aminophenyl)‐10,20‐diphenylporphyrin and 1,3,5‐triformylphloroglucinol. This material exhibits permanent porosity and excellent thermal and chemical stability. CPF‐1 can be employed as a superior supporting substrate to immobilize Au nanoparticles (NPs) as a result of the strong interactions between Au NPs and the CPF support. An Au@CPF‐1 hybrid was synthesized by an interfacial solution infiltration method with NaBH₄ as reducing agent. Au NPs (5 nm) grew on CPF‐1 and were distributed without aggregation. Moreover, Au@CPF‐1 exhibits superior catalytic activity compared to many other reported Au‐based catalysts for the reduction of 4‐nitrophenol in the presence of NaBH₄. In addition, Au@CPF‐1 has excellent stability and recyclability, and it can be reused for three successive reaction cycles without loss of activity. The dense distribution of phenyl rings on the channel walls of the CPF support can reasonably be regarded as the active sites that adsorb the 4‐nitrophenol molecule through hydrogen‐bonding and C?H ??? π interactions, as was confirmed by the X‐ray structure of model compound DAPP‐Benz.     

Bio-inspired synthesis of ZnO polyhedral single crystals under eggshell membrane direction

A simple and versatile technique was developed to prepare hierarchical ZnO single crystals by introducing eggshell membrane (ESM) to a bio-inspired approach. Based on the control of nucleation and gestation, ZnO nanocrystallites could grow at three dimensions into polyhedral single crystals through a surface sol-gel process followed by a calcination treatment. Different from traditional wet chemical techniques, our synthetic process depends more on the restrictive or directing functions of the ESM biomacromolecules. The hierarchical ZnO nanostructures doped with polyhedral single crystallites could be desirable for catalysts, photoelectrochemical devices, especially solar cells.     

Passively Q-switched mode-locking Erbium-doped fiber laser with net-normal dispersion using nonlinear polarization rotation technique

We experimentally demonstrate a passively Q-switched mode-locking (QML) operation in an Erbium-doped fiber ring laser with net normal dispersion by using nonlinear polarization rotation technique. A 2 m long section of dispersion compensating fiber (DCF) with extra large positive dispersion was inserted into the cavity to ensure the fiber laser working in the region of net positive dispersion. By carefully adjusting the polarization controller, both uniform dissipative mode-locking pulses with fundamental repetition rate and QML pulse trains with tunable repetition rate from 71.58 to 98.83 kHz are achieved. It is found that the QML operation is caused by the interaction between the polarization state of the pulse and the intracavity polarizer.     

Facile and green synthesis of Co3O4 nanoplates/graphene nanosheets composite for supercapacitor

Journal of Solid State Electrochemistry - A series of Co3O4 nanoplates/graphene nanosheets (GNS) composites are fabricated using a facile and green method by hydrothermal treatment and subsequent...     

Synthesis of one-dimensional graphene-encapsulated TiO2 nanofibers with enhanced lithium storage capacity for lithium-ion batteries

Journal of Solid State Electrochemistry - The one-dimensional graphene/TiO2 composite nanofibers with the unique microstructures have been successfully synthesized via an efficient method and...     

A new class of multi-wavelet bases: V-system

The V-system is a complete orthogonal system of functions defined on the interval [0, 1], generated by finite Legendre polynomials and the dilation and translation of a function generator, which consists of a finite number of continuous and discontinuous functions. The V-system has interesting properties, such as orthogonality, symmetry, completeness and short compact support. It is shown in this paper that the V-system is essentially a special multi-wavelet basis. As a result, some basic properties of the V-system are established through the well-developed theory of multi-wavelets. From this point of view, more other V-systems are constructed.     

A “Mitsubishi emblem” tetrauclear aluminum complex containing two unsymmetric N2O2‐ligands and a symmetric NO3‐ligand as initiator for polymerization of rac‐lactide

A novel hydroxy‐, methoxy‐, and phenoxy‐bridge “Mitsubishi emblem” tetranuclear aluminum complex ( 1 ) is synthesized from an unsymmetric amine‐pyridine‐bis(phenol) N₂O₂‐ligand (H₂L¹) and a symmetric amine‐tris(phenol) NO₃‐ligand (H₂L²). Two same configuration chiral nitrogen atoms are formed in the tetranuclear Al complex upon coordination of the unsymmetric tertiary amine ligand to central Al. Complex 1 initiates controlled ring‐opening polymerization (ROP) of rac‐lactide and afford polylactide (PLA) with narrow molecular weight distributions (M_w/M_n = 1.05–1.19). The analysis of ¹H NMR spectra of the oligomer indicates that the methoxy group is the initiating group and the ring‐opening polymerization of lactide follows a coordination‐insertion mechanism. The Homonuclear decoupled ¹H NMR spectroscopy suggests the isotactic‐rich chains is preferentially formed in PLA. The study on kinetics of the ROP of lactide reveals the homopropagation rate is higher than the cross‐propagation rate, which is in agreement with the observed isotactic selectivity in the ROP of rac‐lactide. The stereochemistry of the polymerization was also supported by activation parameters. The introduction of unsymmetric ligand H₂L¹ has an effect on stereoslectivity of polymerization. This result may be of interest for the design of multinuclear metal complex catalysts containing functionalized ligands. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 2084–2091