Significant Enhancement in the Efficiency and Selectivity of Iron‐Catalyzed Oxidative Cross‐Coupling of Phenols by Fluoroalcohols

Significant enhancement of both the rate and the chemoselectivity of iron‐catalyzed oxidative coupling of phenols can be achieved in fluorinated solvents, such as 1,1,1,3,3,3‐hexafluoropropan‐2‐ol (HFIP), 2,2,2‐trifluoroethanol (TFE), and 1‐phenyl‐2,2,2‐trifluoroethanol. The generality of this effect was examined for the cross‐coupling of phenols with arenes and polycyclic aromatic hydrocarbons (PAHs) and of phenol with β‐dicarbonyl compounds. The new conditions were utilized in the synthesis of 2′′′‐dehydroxycalodenin B in only four synthetic steps.     

Quinoxaline-imidazolium receptors for unique sensing of pyrophosphate and acetate by charge transfer

[structure: see text] Quinoxaline derivatives (1-4) bearing two imidazolium moieties are found to strongly bind anions and show unique charge-transfer fluorescent responses to pyrophosphate and acetate, whereas they show excimer formation with other anions. Anion-binding studies are investigated with fluorescence and 1H NMR analysis, single-crystal X-ray analysis, and theoretical calculations.     

Green Sources Derived Carbon Dots for Multifaceted Applications

For the past decade, the Carbon dots (CDs) a tiny sized carbon nanomaterial are typically much attentive due to their outstanding properties. Nature is a fortune of exciting starting materials that provides many inexpensive and renewable resources which have received the topmost attention of researchers because of non-hazardous and eco-friendly nature that can be used to prepare green CDs by top-down and bottom-up synthesis including hydrothermal carbonization, microwave synthesis, and pyrolysis due to its simple synthetic process, speedy reactions and clear-cut end steps. Compared to chemically derived CDs, green CDs are varied by their properties such as less toxicity, high water dispersibility, superior biocompatibility, good photostability, bright fluorescence, and ease of modification. These nanomaterials are a promising material for sensor and biological fields, especially in electrochemical sensing of toxic and trace elements in ecosystems, metal sensing, diagnosis of diseases through bio-sensing, and detection of cancerous cells by in-vitro and in-vivo bio-imaging applications. In this review, the various synthetic routes, fluorescent mechanisms, and applications of CDs from discovery to the present are briefly discussed. Herein, the latest developments on the synthesis of CDs derived from green carbon materials and their promising applications in sensing, catalysis and bio-imaging were summarized. Moreover, some challenging problems, as well as upcoming perspectives of this powerful and tremendous material, are also discussed.

     

Controlled Radical Polymerization of Furfuryl Methacrylate

Atom transfer radical polymerization provides a new method of controlled radical polymerization. The most important advantage of ATRP is that it is tolerant to the different functional groups present in the initiator as well as in the monomer. Furfuryl Methacrylate (FMA) is a specialty monomer, which has applications in coatings, adhesives and in biomedicals. Conventional radical polymerization of FMA leads to excessive gel formation, which limits its applications. In this investigation homo and co-polymerization of FMA has been carried out via ATRP. ATRP of FMA was carried out using CuBr as catalyst and 1, 1, 4, 7, 10, 10 hexamethyltriethylenetetramine (HMTETA) as ligand. There was no gel formation during the polymerization. ATRP of FMA was well controlled with a linear increase of molecular weight (Mn) with monomer conversion. The polymers were characterized by using ¹HNMR, FT-IR and GPC analysis. Interestingly, it was observed that the furfuryl ring was not affected during polymerization.     

Sensing of Pyrophosphate Anion by a Fluorescent Zn(II) Complex Bearing Acenaphthene Imidazole Moiety

Journal of Analytical Chemistry - Acenaphthene imidazole ligand (AIMP) reacted with zinc acetate for the synthesis of Zn-AIMP complex which was used to detect pyrophosphate (PPi) ions in the...     

Current-driven magnetization reversal dynamics and breather-like EM soliton propagation in biaxial anisotropic weak ferromagnetic nanowire

Nonlinear Dynamics - We investigate the effect of spin torque on the switching dynamics of magnetic solitons in a weak ferromagnetic nanowire under the influence of an electromagnetic wave (EMW)....     

Stair and Step Soliton Solutions of the Integrable (2+1) and (3+1)-Dimensional Boiti-Leon-Manna-Pempinelli Equations

The multiple exp-function method is a new approach to obtain multiple wave solutions of nonlinear partial differential equations (NLPDEs). By this method one can obtain multi-soliton solutions of NLPDEs. In this paper, using computer algebra systems, we apply the multiple exp-function method to construct the exact multiple wave solutions of a (2+1)-dimensional Boiti-Leon-Manna-Pempinelli equation. Also, we extend the equation to a (3+1)-dimensional case and obtain some exact solutions for the new equation by applying the multiple exp-function method. By these applications, we obtain single-wave, double-wave and multi-wave solutions for these equations.     

Modified extended tanh-function method and nonlinear dynamics of microtubules

We here present a model of nonlinear dynamics of microtubules (MT) in the context of modified extended tanh-function (METHF) method. We rely on the ferroelectric model of MTs published earlier by Satari? et al. [1] where the motion of MT subunits is reduced to a single longitudinal degree of freedom per dimer. It is shown that such nonlinear model can lead to existence of kink solitons moving along the MTs. An analytical solution of the basic equation, describing MT dynamics, was compared with the numerical one and a perfect agreement was demonstrated. It is now clearer how the values of the basic parameters of the model, proportional to viscosity and internal electric field, impact MT dynamics. Finally, we offer a possible scenario of how living cells utilize these kinks as signaling tools for regulation of cellular traffic as well as MT depolymerisation.     

Ultrasound assisted free radical polymerization of glycidyl methacrylate by a new disite phase-transfer catalyst system: A kinetic study

The kinetics of multi-site phase-transfer catalyzed free radical polymerisation of glycidyl methacrylate (GMA) using potassium peroxy disulphate (PDS) as water soluble initiator and newly synthesized 1,4-dihexadecylpyrazine-1,4-diium dibromide as multi-site phase-transfer catalyst (MPTC) has been investigated in ethyl acetate/water two phase system at constant temperature 65±1°C under nitrogen atmosphere and ultrasound irradiation conditions. The rate of polymerization increases with an increase in concentrations of GMA, PDS and MPTC. The order with respect to monomer, initiator and MPTC were found to be 1.0, 0.5 and 1.0, respectively. The comparative study reveals that the Rp of GMA determined in the presence of PTC combined with ultrasound has shown more enhancements in the activity than PTC alone. Based on the observed results a suitable mechanism has been proposed to account for the experimental observations and its significance was discussed.