A new method for the synthesis of functionalized maleimides

An effective route to novel maleimides is described, which involves the reaction of an enamine derived from the addition of a secondary amine to a dialkyl acetylenedicarboxylate with an arylsulfonyl isocyanate. These maleimides in solution indicate dynamic NMR because of restricted rotation around the carbon-nitrogen bond, resulting from conjugation of the side-chain nitrogen with the adjacent α,β-unsaturated ester group.     

Molybdenum (VI)‐functionalized UiO‐66 provides an efficient heterogeneous nanocatalyst in oxidation reactions

A novel heterogeneous nanocatalyst was established by supporting molybdenum (VI) on Zr₆ nodes in the structure of the well‐known UiO‐66 metal–organic framework (MOF). The structure of the UiO‐66 before and after Mo (VI) immobilization was confirmed with XRD, DR‐FTIR and UV–vis spectroscopy, and the presence and amount of Mo (VI) was identified by X‐ray photoelectron spectroscopy and inductively coupled plasma atomic emission spectroscopy. TEM imaging confirmed the absence of Mo clusters on the MOF surface, while SEM confirmed that the appearance of the MOF has not changed upon immobilizing the Mo (VI) catalyst. BET adsorption measurements were used to confirm the porosity of the catalyst. The catalytic activity of this heterogeneous catalyst was investigated in oxidation of sulfides with H₂O₂ in acetonitrile and oxidative desulfurization of dibenzothiophene. Easy work up, convenient and steady reuse and high activity and selectivity are prominent properties of this new hybrid material.     

Direct breath figure formation on PMMA and superhydrophobic surface using in situ perfluoro-modified silica nanoparticles

Breath figure formation was carried out directly on the surface of poly(methylmethacrylate) using a mixture of a good solvent, tetrahydrofuran, and a nonsolvent, water. Direct breath figure formation was coined for this method and a mechanism was proposed to describe the figure formation by the method based on hypothesizes available for the normal breath figure formation. The proposed mechanism is such that the sonication effect, immersion time, and water content on characteristics of the obtained figures can be explained. The figured surface was then made superhydrophobic with a water contact angle of 175° using in situ growing of perfluoro modified silica nanoparticles inside the figure cell by one-pot method. The spherical modified silica nanoparticles were detected being trapped by figure features providing a mechanical entrapment of the low-surface energy nanoparticles. © 2013 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2013     

The Effect of Calcium Perovskite and Newly Developed Magnetic CaFe2O4/CaTiO3 Perovskite Nanocomposite on Degradation of Toxic Dyes Under UV–Visible Radiation

Journal of Cluster Science - In this research, we used a fast and simple method for synthesis of calcium titanate (CaTiO3) and calcium ferrite (CaFe2O4) nanostructures: microwave assisted...     

Structure Characterization and Lead Detoxification Effect of Carboxymethylated Melanin Derived from <Emphasis Type="Italic">Lachnum</Emphasis> Sp.

In the present study, an intracellular melanin, named LIM205, was separated from Lachnum YM205 mycelia and was purified on a Sephadex G-15 column. The molecular weight of LIM205 was determined as 522 Da, and its molecular formula was speculated as C₂₈H₁₄N₂O₇S. The possible chemical structure of LIM205 was determined according to the results of Fourier transform infrared (FT-IR), ¹H NMR, ¹³C NMR, and pyrolysis/GC-MS analysis. With the aim to increase its water solubility, its carboxymethylated derivative, named CLIM205, was formed by the substitution of hydrogen atoms in LIM205 with one, two, and three carboxymethylate groups. FT-IR, UV, and ESI-MS analysis demonstrated that the carboxymethylate groups were conjugated onto LIM205. The lead detoxification activities of LIM205 and CLIM205 had also been investigated. In vivo test showed that both LIM205 and CLIM205 reduced the tissue lead concentration, enhanced lead excretion, and reversed lead-induced alterations in superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and malondialdehyde (MDA) concentrations in mice, with CLIM205 showed better efficacy. The study indicates that LIM205 and CLIM205 have significant lead detoxification effect which will contribute to solve related problems.     

TiO2 as a Reusable Catalyst for the One‐Pot Synthesis of 3,4‐Dihydropyrimidin‐2(1H)‐ones under Solvent‐Free Conditions

An efficient solvent‐free method for the synthesis of various 3,4‐dihydropyrimidin‐2(1H)‐ones using TiO₂ as a recyclable heterogeneous catalyst is described. Compared to known methods, satisfactory results are obtained with excellent yields, short reaction times, and simplicity in the experimental procedure.     

Acid-catalyzed reactions of (3-(naphthalen-2-yl)-2,2-bis(trimethylsilyl)oxiran. A new synthesis of functional-group-substituted vinylsilanes

The magnesium bromide-diethyl etherate-catalyzed ring-opening of (3-(naphthalen-2-yl)-2,2-bis(trimethylsilyl)oxiran 2 with thiophenols affords (1-trimethylsilylvinyl)sulfides 3 and the (1-bromovinyl)silane 4. Nucleophilic attack occurs regioselectively at the position α- to silicon. The compound 2 has been converted into the (1-trimethylsilylvinyl)amide 5 with an excess of acetonitrile and into the (1-trimethylsilylvinyl)acetate 6 with acetic acid/acetic anhydride. These reactions proceed with catalytic amounts of boron trifluoride-diethylether. Treatment of 2 with acetic acid alone gives naphthaldehyde. The epoxide 2 reacts also with MgBr₂·OEt₂, MeLi/CuI, HX (XBr or Cl) and LiAlH₄ with nucleophilic attack at the bis(trimethylsilyl)-substituted carbon.     

Effects of electron‐withdrawing group on the photoisomerization of tetraaryl‐4H‐thiopyran‐1,1‐dioxides

Syntheses and photoisomerization of the new sulfone derivatives, 4,4‐di (p‐trifluoromethylphenyl)‐2,6‐diphenyl‐4H‐thiopyran‐1, 1‐dioxide and 4‐(p‐trifluoromethylphenyl)‐2,4,6‐triphenyl‐4H‐thiopyran‐1,1‐dioxide, have been investigated. The relative molar ratios of the photoproducts are compared with those of 2,4,4,6‐tetraphenyl‐4H‐thiopyran‐1,1‐dioxide as well as electron‐donating substituted 4‐methyl‐2,4,6‐triaryl‐4H‐thiopyran‐1,1‐dioxides as model compounds under identical experimental conditions using ¹H NMR spectroscopy. The results observed are discussed on the basis of a triplet excited state di‐π‐methane rearrangement. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:557–561, 2008; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/hc.20455