C–C and C–H coupling reactions by Fe3O4/KCC-1/APTPOSS supported palladium-salen-bridged ionic networks as a reusable catalyst

This study investigates the potential application of an efficient, easily recoverable and reusable magnetically separable Fe₃O₄/KCC-1/APTPOSS nanoparticle-supported salen/Pd(ii) catalyst for C–C and C–H cross-couplings. The Fe₃O₄/KCC-1/APTPOSS/salen/Pd(ii) MNPs were thoroughly characterized by using TEM, FE-SEM, TGA, XRD, VSM, FT-IR, ICP-MS, and BET. This observation was exploited in the direct and selective chemical reaction of 2-acetyl-benzaldehyde with cyclopentadiene for the synthesis of pentafulvene. The recycled catalyst has been analyzed by ICP-MS showing only minor changes in the morphology after the reaction, thus confirming the robustness of the catalyst.

This study investigates the potential application of an efficient, easily recoverable and reusable magnetically separable Fe₃O₄/KCC-1/APTPOSS nanoparticle-supported salen/Pd(ii) catalyst for C–C and C–H cross-couplings.     

99mTc‐(EDDA/tricine)‐HYNIC‐GnRH analogue as a potential imaging probe for diagnosis of prostate cancer

Prostate cancer is a serious threat to men's health, so it is necessary to develop the techniques for early detection of this malignancy. Radiolabeled peptides are the useful tools for diagnosis of prostate cancer. In this research, we designed a new HYNIC‐conjugated GnRH analogue and labeled it by ^99mTc with tricine/EDDA as coligands. We used aminohexanoic acid (Ahx) as a hydrocarbon linker to generate ^99mTc‐(tricine/EDDA)‐HYNIC‐Ahx‐[DLys⁶]GnRH. The radiopeptide exhibited high radiochemical purity and stability in solution and serum. Two human prostate cancer cell lines LN‐CaP and DU‐145 were used for cellular experiments. The binding specificity and affinity of radiopeptide for LN‐CaP were superior to DU‐145 cells. The K_d values for LN‐CaP and DU‐145 cells were 41.91 ± 7.03 nM and 55.96 ± 10.56 nM, respectively. High kidney uptake proved that the main excretion route of radiopeptide was through the urinary system. The tumor/muscle ratio of ^99mTc‐HYNIC‐Ahx‐[DLys⁶]GnRH was 4.14 at 1 hr p.i. that decreased to 2.41 at 4 hr p.i. in LN‐CaP tumor‐xenografted nude mice. The blocking experiment revealed that the tumor uptake was receptor‐mediated. The lesion was visualized clearly using ^99mTc‐[DLys⁶]GnRH at 1 hr p.i. Accordingly, this research highlights the capability of ^99mTc‐(tricine/EDDA)‐HYNIC‐Ahx‐[DLys⁶]GnRH peptide as a promising agent for GnRHR‐expressing tumor imaging.     

Fixed‐structure controller design for polytopic systems via LMIs

In this paper, a new approach for fixed‐structure H₂ controller design in terms of solutions to a set of linear matrix inequalities are given. Both discrete‐time and continuous‐time SISO time‐invariant systems are considered. Then the results are extended to systems with polytopic uncertainty. The presented methods are based on an inner convex approximation of the non‐convex set of fixed‐structure H₂ controllers. The designed procedures are initialized either with a stable polynomial or with a stabilizing controller. An iterative procedure for robust controller design is given that converges to a suboptimal solution. The monotonic decreasing of the upper bound on the H₂ norm is established theoretically for both nominal and robust controller design. Copyright © 2014 John Wiley & Sons, Ltd.     

Photooxidation of triarylphosphines under aerobic conditions in the presence of a gold(iii) complex on cellulose extracted from Carthamus tinctorius immobilized on nanofibrous phosphosilicate

Triarylphosphines were converted to the corresponding oxides via photooxidation as a novel method. In this study, cellulose was extracted from the Carthamus tinctorius plant and then oxidized by sodium metaperiodate. A gold complex was supported on this natural cellulose. Then, a gold complex on natural cellulose supported on FPS (FPS/Au(iii)) was synthesized for the reduction of phosphine oxides to corresponding phosphines with remarkable chemoselectivity. The morphology of FPS led to higher catalytic activity. FPS/Au(iii) NPs were thoroughly characterized using TEM, FESEM, FTIR, TGA, and BET.

Triarylphosphines were converted to the corresponding oxides via photooxidation as a novel method.     

Green synthesis of PbCrO4 nanostructures using gum of ferula assa-foetida for enhancement of visible-light photocatalytic activity

Photocatalytic selective oxidation has attracted considerable attention as an environmentally friendly strategy for organic transformations. Some methods have been reported for the photocatalytic oxidation of sulfides into sulfoxides in recent years. However, the practical application of these processes is undermined by several challenges, such as low selectivity, sluggish reaction rates, requirement of UV-light irradiation, use of additives, and instability of the photocatalyst. Pure monoclinic lead chromate nanoparticles were prepared via a new simple way as Pb and Cr sources. PbCrO₄ NPs were synthesized via a green method in the presence of gum of ferula assa-foetida from Pb(NO₃)₂ and CrCl₃ as lead and chromium resources, respectively. The structural analysis of the samples confirmed the formation of PbCrO₄ nanostructures in the range of 30 ± 5 nm. The PbCrO₄ nanocatalyst was thoroughly characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive X-ray spectroscopy (EDX) study. Considering the large ionic internal character and high mechanical and thermal stability as well as long-term colloidal stability, this system can be considered as a perfect nanocatalyst by using the host–guest approach. A green and ecofriendly method for oxidation of sulfides to sulfones in the presence of O₂ as an oxidant was examined for the synthesised PbCrO₄ NPs. The easy and applied reusability of the catalyst was observed after the completion of the reaction under visible-light irradiation.

Photocatalytic selective oxidation has attracted considerable attention as an environmentally friendly strategy for organic transformations.     

Synthesis of benzimidazolones by immobilized gold nanoparticles on chitosan extracted from shrimp shells supported on fibrous phosphosilicate

Here we demonstrate the synthesis of benzimidazolones from o-phenylenediamines and carbon dioxide in the presence of gold nanoparticles supported on a composite material based on microcrystalline chitosan from shrimp shells and fibrous phosphosilicate (CS–FPS/Au). The results showed that the gold nanoparticles were stable with the P, N and O atoms of CS–FPS. The morphology and structure of FPS leads to a higher catalytic activity. The CS–FPS/Au NPs were thoroughly characterized using TEM, FESEM, TGA, FTIR, and BET.

We demonstrate the synthesis of benzimidazolones from o-phenylenediamines and CO₂ in the presence of gold nanoparticles supported on a composite material based on microcrystalline chitosan from shrimp shells and fibrous phosphosilicate.