[HDBU][HSO4]-catalyzed facile synthesis of new 1,2,3-triazole-tethered 2,3-dihydroquinazolin-4[1H]-one derivatives and their DPPH radical scavenging activity

Research on Chemical Intermediates - A simple and efficient protocol has been developed for the synthesis of new1,2,3-triazole-2,3-dihydroquinazolin-4[1H]-one (DHQ) conjugates(6a?j) via...     

Silica-supported sodium carbonate: an efficient heterogeneous catalyst for the synthesis of new thiazolopyrimidine derivatives

Research on Chemical Intermediates - Herein we describe a new convenient strategy for the synthesis of substituted thiazolopyrimidines. The present approach delivers the use of silica-supported...     

Synthesis and Characterization of Four-Arm Star Poly(ϵ-caprolactone)-Block-Poly(cyclic-carbonate methacrylate) Copolymers by Combining Ring-Opening Polymerization With Atom Transfer Radical Polymerization

Well-defined four-arm star poly(?-caprolactone)-block-poly(cyclic carbonate methacrylate) (PCL-b-PCCMA) copolymers were synthesized by combining ring-opening polymerization (ROP) with atom transfer radical polymerization (ATRP). First, a four-arm poly(?-caprolactone) (PCL) macroinitiator [(PCL-Br)₄] was prepared by the ROP of ?-CL catalyzed by stannous octoate at 110°C in the presence of pentaerythritol as the tetrafunctional initiator followed by esterification with 2-bromoisobutyryl bromide. The sequential ATRP of CCMA monomer was carried out by using the (PCL-Br)₄ tetrafunctional macroinitiator (MI) and in the presence of CuBr/2, 2′-bipyridyl system in DMF at 80°C with [(MI)]:[CuBr]:[bipyridyl] = 1:1:3 to yield block polymers with controlled molecular weights (M_n (NMR) = 10700 to 27300 g/mol) by varying block lengths and with moderately narrow polydispersities (M_w/M_n = 1.2–1.4). Block copolymers with different PCL: PCCMA copolymer composition such as 50:50, 70:30 and 74:26 were prepared with good yields (48-74%). All these block copolymers were well characterized by NMR, FTIR and GPC and tested their thermal properties by DSC and TGA.     

Polyethylene glycol-promoted synthesis of pyrimido[1,2-a]benzimidazole and pyrano[2,3-c]pyrazole derivatives in water

Synthesis of pyrimido[1,2-a]benzimidazole and pyrano[2,3-c]pyrazole derivatives were achieved using polyethylene glycol (PEG-400) as promoting reaction medium in water under catalyst-free conditions at reflux and room temperature, respectively. The structure of pyrimido[1,2-a]benzimidazole was confirmed using ¹H NMR, ¹³C NMR, DEPT, and HMBC experiments. The promising points for the present methodology are efficiency, generality, high yield, short reaction time, cleaner reaction profile, ease of product isolation, simplicity, potential of recycling reaction medium, and finally agreement with green chemistry protocols.     

A Positive Solution of Mixed Non-Linear Fractional Delay Differential Equations with Integral Boundary Conditions

In this paper, we study mixed non-linear fractional delay differential equations with integral boundary conditions. We obtain an equivalence result between the proposed problem and non-linear Fredholm integral equation of the second kind. Further, we establish existence and uniqueness of positive solutions for the problem using Guo-Krasnoseleskii''s fixed point theorem and Banach contraction principle.     

Structural study and electrical properties of Zr-doped Nd<Subscript>2</Subscript>Sn<Subscript>2</Subscript>O<Subscript>7</Subscript> pyrochlore compounds

Nd₂Sn₂O₇ pyrochlores with the substitution of Zr⁴⁺ were prepared by conventional ceramic double sintering technique. The single-phase formation was confirmed by X-ray diffraction and neutron diffraction techniques. Relative intensity calculations for X-ray diffraction analysis were performed for oxygen positional parametersx = 0.331 and 0.375, while Rietveld refinements were employed for neutron diffraction data. The neutron diffraction study revealed that there are only two anion sites with 48f and 8b positions. This indicates that the 8a site, i.e. O(3) sublattice, is completely vacant and the structure is a perfect cubic pyrochlore with space group Fd3m (O _h ⁷ ). From the conductivity measurements, it is observed that the electronic conductivity dominates from room temperature up to about 525 K and forT > 525 K, the oxygen ion conduction dominates the charge transport in these compositions. Complex impedance spectroscopy indicates the existence of grain and grain boundary as two separate elements.     

Novel porous anatase TiO2 nanorods and their high lithium electroactivity

We demonstrated a simple approach for the synthesis of a kind of novel porous anatase TiO₂ nanorods. The method is based on a reaction in composite-hydroxide eutectic system and normal atmosphere without using an organic dispersant or capping agent. The synthesis technique is cost effective, easy to control and is adaptable to mass production. This is the first time TiO₂ nanorods with a porous structure are fabricated by using this method. The as-prepared material was characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM), nitrogen adsorption and desorption experiments and electrochemical measurements. The results showed that the anatase TiO₂ nanorods obtained in our experiment have a large specific surface area with a porous structure which makes it have a potential application in catalysts and battery materials, especially in lithium ion batteries. In this study, we mainly tested their electrochemical performance as negative materials for lithium ion batteries. Further research to optimize synthesis conditions, particularly to develop their application in the field of catalysis is currently in progress.     

Ni<Superscript>2+</Superscript>-substituted Mg–Cu–Zn ferrites: a colloidal approach of tuning structural and electromagnetic properties

A robust synthesis approach to Ni²⁺-substituted Mg_0.25-xNi _x Cu_0.25Zn_0.5Fe₂O₄ (0?≤?x?≤?0.25?mol.) ferrimagnetic oxides using citrate assisted sol–gel process is reported. The route utilizes simple metal nitrate precursors in aqueous solution, thus eliminating the need for organometallic precursors. Citric acid acts as a fuel for the combustion reaction and forms stable complexes with metal ions preventing the precipitation of hydroxilated compounds to yield the composite ferrite structure by auto-combustion process. The XRD signatures, especially (3 1 1) plane, confirmed the formation of spinel structure. The linear growth of lattice constant from 8.385 to 8.409?Å was observed by Ni²⁺ substitution from 0 to 0.25. The dense microstructure is observed with the average grain size of 0.42–2.18?µm. The transport properties revealed the semiconducting behavior of as-prepared ferrite material, with an increase in the DC-electrical resistivity by the incorporation of nickel. The magnetic properties viz. initial permeability (µ_i) and magnetic moment (n_B) are explained, based on the deviation in saturation magnetization (M_s), anisotropy constant (K₁)_, density values, and exchange interactions. Furthermore, the effect of adding Ni²⁺ on the Curie temperature, frequency-dependent dielectric properties of the ferrite material are also discussed.

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