Retraction: Aqueous aerobic oxidation of alkyl arenes and alcohols catalyzed by copper(II) phthalocyanine supported on three-dimensional nitrogen-doped graphene at room temperature.

Retraction of 'Aqueous aerobic oxidation of alkyl arenes and alcohols catalyzed by copper(II) phthalocyanine supported on three-dimensional nitrogen-doped graphene at room temperature' by Mojtaba Mahyari et al., Chem. Commun., 2014, 50, 7855-7857, https://doi.org/10.1039/C4CC01406E.

Correction: Gold nanoparticles supported on supramolecular ionic liquid grafted graphene: a bifunctional catalyst for the selective aerobic oxidation of alcohols.

[This corrects the article DOI: 10.1039/C3RA44696D.].

Copper on chitosan-modified cellulose filter paper as an efficient dip catalyst for ATRP of MMA.

Achieving an efficient catalyst in the ATRP system with a simple design, preparation from available materials, and high recyclability is a significant challenging issue. To attain the goal, herein, we used chitosan (CS)-modified cellulose filter paper (FP) as a green support for the synthesis of dip catalyst. The preparation of this catalyst involved surface treatment of the FP strips by CS coating through a dipping method, which increased the affinity of the substrate for adsorbing copper ions in the next step. The Cu@CS-FP catalyst was prepared without the requirement of any ligands. The synthesized dip-catalyst, in the form of the strips, was employed for the first time in the ATRP reaction of methyl methacrylate to assay catalytic activity. Catalytic insertion/ removal (ON/OFF) experiments were carried out during the polymerization. A reasonable control over the molecular weight with high conversion (68%) and polydispersity index of 1.32 under mild reaction conditions were obtained. Significantly, because of the facile separation of the catalyst, the amount of copper that remained in the polymer was very low (2.7 ppm). Also, the recyclability of the catalyst was investigated for five runs. The conversion in the final run was 64% without a loss of catalyst efficiency.

Chemical-resistant ammonia sensor based on polyaniline/CuO nanoparticles supported on three-dimensional nitrogen-doped graphene-based framework nanocomposites.

A novel ammonia (NH3) chemical sensor is presented with ultra-high response, good selectivity, fast response, and long-term stability using detecting layer of polyaniline/cupric oxide nanoparticles supported on three-dimensional nitrogen-doped graphene-based frameworks (PANI/CuO@3D-NGF) nanocomposite. The NH3 gas sensing response of the PANI/CuO@3D-NGF nanocomposite was studied by resistivity method in low concentration range of 50 ppb-100 ppm at room temperature. The PANI/CuO@3D-NGF nanocomposite was prepared through in situ polymerization of PANI on the CuO@3D-NGF with a high surface area. Morphological and structural analysis revealed that the ultrathin 3D interconnected graphene substrate maximizes the surface area. It is also shown that the CuO nanoparticles offer active adsorption sites for free NH3 molecule. The PANI/CuO@3D-NGF nanocomposite gas sensor shows the response of 930% to 100 ppm NH3 with an outstanding low detection limit of 50 ppb and an average response time of 30 s at room temperature. The excellent sensing performance of the PANI/CuO@3D-NGF nanocomposite was attributed to 3D interconnected porous structure, remarkable enhancement of charge carriers as a result of CuO@3D-NGF, and modified π-interactions between molecules. Graphical abstract.

High sensitivity ammonia detection using metal nanoparticles decorated on graphene macroporous frameworks/polyaniline hybrid.

In this paper, we presented the fabrication and properties of new ammonia (NH3) sensors with sensitive layer of nickel nanoparticles decorated on three-dimensional nitrogen-doped graphene-based frameworks/polyaniline (NiNPs@3D-(N)GFs/PANI) hybrid. The hybrid are synthesized through in-situ oxidative polymerization on flexible thin substrate. Synergetic behavior between both components manifested outstanding sensitivity (750.2 at 1000 ppm NH3) and quick response (95 s) and recovery (25 s) times and a lower limit of detection (~ 45 ppb) at room temperature. The sensitivity of NiNPs@3D-(N)GFs/PANI hybrid sensor was shown to be about 14 times more than its of pure PANI sensor at 1000 ppm of NH3. The excellent sensitivity of the as-prepared hybrid is mainly originated from the substantial rise of hole-like carriers by NiNPs@3D-(N)GFs as well as improved inter-molecule interactions via π- π electron networks. The obtained results revealed significant advantages for the synthesized hybrid sensor, making it a suitable choice for real-world applications of NH3 detection.

Evaluation of sulfated maltodextrin as a novel anionic chiral selector for the enantioseparation of basic chiral drugs by capillary electrophoresis.

Introducing a new class of chiral selectors is an interesting work and this issue is still one of the hot topics in separation science and chirality. In this study, for the first time, sulfated maltodextrin (MD) was synthesized as a new anionic chiral selector and then it was successfully applied for the enantioseparation of five basic drugs (amlodipine, hydroxyzine, fluoxetine, tolterodine, and tramadol) as model chiral compounds using CE. This chiral selector has two recognition sites: a helical structure and a sulfated group which contribute to three corresponding driving forces; inclusion complexation, electrostatic interaction, and hydrogen binding. Under the optimized condition (buffer solution: 50 mM phosphate (pH 3.0) and 2% w/v sulfated MD; applied voltage: 18 kV; temperature: 20°C), baseline enantioseparation was observed for all mentioned chiral drugs. When instead of sulfated MD neutral MD was used under the same condition, no enantioseparation was observed which means the resolution power of sulfated MD is higher than neutral MD due to the electrostatic interaction between sulfated groups and protonated chiral drugs. Also, the countercurrent mobility of negatively charged MD (sulfated MD) allows more interactions between the chiral selector and chiral drugs and this in turn results in a successful resolution for the enantiomers. Furthermore, a higher concentration of neutral MD (approximately five times) is necessary to achieve the equivalent resolution compared with the negatively charged MD.

Monitoring of trace amounts of heavy metals in different food and water samples by flame atomic absorption spectrophotometer after preconcentration by amine-functionalized graphene nanosheet.

We are introducing graphene oxide modified with amine groups as a new solid phase for extraction of heavy metal ions including cadmium(II), copper(II), nickel(II), zinc(II), and lead(II). Effects of pH value, flow rates, type, concentration, and volume of the eluent, breakthrough volume, and the effect of potentially interfering ions were studied. Under optimized conditions, the extraction efficiency is >97 %, the limit of detections are 0.03, 0.05, 0.2, 0.1, and 1 µg L(-1) for the ions of cadmium, copper, nickel, zinc, and lead, respectively, and the adsorption capacities for these ions are 178, 142, 110, 125, and 210 mg g(-1). The amino-functionalized graphene oxide was characterized by thermogravimetric analysis, transmission electron microscopy, scanning electron microscopy, and Fourier transform infrared spectrometry. The proposed method was successfully applied in the analysis of environmental water and food samples. Good spiked recoveries over the range of 95.8-100.0 % were obtained. This work not only proposes a useful method for sample preconcentration but also reveals the great potential of modified graphene as an excellent sorbent material in analytical processes.

Aqueous aerobic oxidation of alkyl arenes and alcohols catalyzed by copper(II) phthalocyanine supported on three-dimensional nitrogen-doped graphene at room temperature.

Copper(ii) tetrasulfophthalocyanine supported on three-dimensional nitrogen-doped graphene-based frameworks was synthesized and introduced as a bifunctional catalyst for selective aerobic oxidation of alkyl arenes and alcohols to the corresponding carbonyl compounds. The ease of catalyst separation, high turnover, low catalyst loading and recyclability could potentially render it applicable in industrial setting.

Ordered carbohydrate-derived porous carbons immobilized gold nanoparticles as a new electrode material for electrocatalytical oxidation and determination of nicotinamide adenine dinucleotide.

The ordered carbohydrate-derived porous carbons (OC-DPCs) were first functionalized with thiol groups (-SH) and then immobilized with gold nanoparticles (AuNPs). The Au-SH-OC-DPCs were characterized by CHN analysis, transmission electron microscopy (TEM), fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and x-ray diffraction (XRD). The Au-SH-OC-DPCs were applied for the fabrication of a new electrochemical sensor. The electrocatalytic capabilities of the new sensor were tested by the oxidation of nicotinamide adenine dinucleotide (NADH) in a 0.1 M Robinson buffer solution (pH 7.0) using cyclic voltammetry (CV), linear sweep voltammetry (LSV), and differential pulse voltammetry (DPV). The Au-SH-OC-DPCs showed a good voltammetric performance in the electrochemical detection of NADH with a low detection limit (1.0 nM), high sensitivity (4.934 µA/µM), and wide linear concentration range (5.0 nM-10 µM).

A novel bioelectrochemical sensing platform based on covalently attachment of cobalt phthalocyanine to graphene oxide.

Graphene oxide-cobalt phthalocyanine (GO-PcCo) hybrid material as a new electrocatalyst was synthesized and used successfully to fabrication of new biosensor for the electrooxidation of l-cysteine (CSH) in aqueous media. Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), and transmission electron microscopy (TEM) images revealed that cobalt phthalocyanine is covalently attachment on graphene oxide sheets as single layers GO-PcCo. Cyclic voltammetric studies showed that the GO-PcCo/glassy carbon electrode (GO-PcCo/GCE) improves electrochemical behavior of CSH oxidation, as compared to the GO and PcCo. In addition, the results indicated that GO and PcCo have a synergic effect in the electrooxidation of CSH. The catalytic oxidation responses were studied and the reaction mechanisms were discussed. The electrocatalytic behavior is further developed as a new detection scheme for CSH by chronoamperometry method and under optimized conditions, excellent analytical features, including high sensitivity and selectivity, low detection limit and satisfactory dynamic range, were achieved.

A passerini-type condensation: a carboxylic acid-free approach for the synthesis of the α-acyloxycarboxamides.

A Passerini-type condensation for the synthesis of α-acyloxycarboxamides starting from simple and readily available inputs, including an isocyanide, aldehydes and water in the presence of trimethylsilyl azide as a catalyst under reflux conditions in toluene in good yields, is described.

Novel syntheses of tetrahydrobenzodiazepines and dihydropyrazines via isocyanide-based multicomponent reactions of diamines.

In this work, two novel isocyanide-based multicomponent reactions of 1,2-diamine compounds with diketene have been developed as efficient strategies for the synthesis of 2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepine-2-carboxamides with regiochemical control and 1,6-dihydropyrazine-2,3-dicarbonitriles in good to excellent yields at ambient temperature.