Caesium carbonate supported on hydroxyapatite‐encapsulated Ni0.5Zn0.5Fe2O4 nanocrystallites as a novel magnetically basic catalyst for the one‐pot synthesis of pyrazolo[1,2‐b]phthalazine‐5,10‐diones

A novel nanomagnetic basic catalyst of caesium carbonate supported on hydroxyapatite‐coated Ni_0.5Zn_0.5Fe₂O₄ magnetic nanoparticles (Ni_0.5Zn_0.5Fe₂O₄@HAP‐Cs₂CO₃) was prepared. This new catalyst was fully characterized using Fourier transform infrared spectroscopy, transmission and scanning electron microscopy, X‐ray diffraction and vibrating sample magnetometry techniques, and then the catalytic activity of this catalyst was investigated in the synthesis of 1H‐pyrazolo[1,2‐b]phthalazine‐5,10‐dione derivatives. Also, Ni_0.5Zn_0.5Fe₂O₄@HAP‐Cs₂CO₃ could be reused at least five times without significant loss of activity and could be recovered easily by applying an external magnet. Thus, the developed nanomagnetic catalyst is potentially useful for the green and economic production of organic compounds. Copyright © 2015 John Wiley & Sons, Ltd.     

Production of benzazepine derivatives via four-component reaction of isatins: study of antioxidant activity

Molecular Diversity - In current research, benzazepine derivative is synthesized via a new process of four-component reaction of isatin or its derivatives, α-haloketones, activated acetylenic...     

N,N′,N,N′-TETRABROMO-BENZENE-1,3-DISULFONYLAMIDE AS A NOVEL REAGENT FOR OXIDATIVE AROMATIZATION OF 1,3,5-TRISUBSTITUTED PYRAZOLINES UNDER HETEROGENEOUS AND SOLVENT-FREE CONDITIONS

1,3,5-Trisubstituted pyrazolines were converted to the corresponding pyrazoles in good yields under heterogeneous and solvent-free conditions by N,N′,N,N′-tetrabromo-benzene-1,3-disulfonylamide [TBBDA] at ambient temperature.     

Magnetic properties in three electrons under Rashba spin-orbit interaction and magnetic field

In this work, we study three-electron magnetic susceptibility in quantum dots under Rashba spin-orbit interaction (SOI) and magnetic field by an analytical methodology. The Hamiltonian of the system is separated to center of mass and relative terms using the Jacobi transformations and the hyperspherical coordinates. By solving Schrodinger equation, energy levels and thereby the susceptibility are calculated using canonical ensemble. At zero temperature, the magnetization reduces with increasing magnetic field with and without Rashba SOI in three-electron-quantum dot without electron-electron (e-e) interaction. Also, SOI slightly changes the magnetization for three-electron-quantum dot without e-e interaction. At nonzero temperature, the magnetization shows a paramagnetic peak when the magnetic field increases. This peak position changes under the SOI. In the presence of e-e interaction, the susceptibility enhances with raising magnetic field and it shows a maximum. The susceptibility at low magnetic field is negative and then it becomes positive. The susceptibility with e-e interaction and without SOI is always diamagnetic and its magnitude reduces with enhancing magnetic field. The susceptibility shows a transition between diamagnetic and paramagnetic with e-e interaction and SOI.     

A novel method for non-destructive Compton scatter imaging based on the genetic algorithm

Compton scattering tomography is widely used in numerous applications such as biomedical imaging, nondestructive industrial testing and environmental survey, etc. This paper proposes the use of the genetic algorithm (GA), which utilizes bio-inspired mathematical models, to construct an image of the insides of a test object via the scattered photons, from a voxel within the object. A NaI(Tl) scintillation detector and a 185 MBq ¹³⁷Cs gamma ray source were used in the experimental measurements. The obtained results show that the proposed GA based method performs well in constructing images of objects.     

Synthesis of new enantiomerically pure spirooxindolopyrrolizidines via a three-component asymmetric 1,3-dipolar cycloaddition reaction of azomethine ylides derived from isatin

An efficient, one-pot, three-component procedure for the synthesis of a small library of new chiral spirooxindolopyrrolizidines with high regio-, diastereo-, and enantioselectivity, from the 1,3-dipolar cycloaddition of azomethine ylides and optically active cinnamoyl oxazolidinone is described. The process occurs at room temperature in aqueous ethanol as a green solvent and in the absence of any Lewis acids. The oxazolidinone chiral auxiliary is removed in a non-destructive manner. The reaction mechanism is discussed on the basis of the assignment of the absolute configuration of the cycloadducts, and on theoretical calculations.     

Exo/endo stereocontrolled synthesis of spiroindoloindolizidines by using classical and microwave conditions via the 1,3-dipolar cycloaddition reaction

Using both classical reflux and microwave-mediated conditions, a series of new spiroindoloindolizidines was synthesized by multicomponent 1,3-dipolar cycloaddition of azomethine ylides in unprecedented exo/endo stereocontrolled. Both conditions easily afforded two identical and separable exo/endo diastereomeric ratios of cycloadducts. However, the ratio of two diastereomeric products obtained from conventional conditions was reversed in all examined cases when the reactions were explored under microwave-mediated conditions. As expected, utilizing the microwave-assisted conditions produced higher yields and reaction rates compared to classical conditions. The structure and exact stereochemistry of synthesized cycloadducts were determined by applying various 2D-NMR spectroscopic techniques and single-crystal X-ray diffraction. Finally, the mechanism of the reaction has been briefly investigated by using density functional theory (DFT) calculations.