Publications

Herein, the detection of aspartic acid by doped Co₃O₄-ZnO nanorod materials was proposed using differential pulse voltammetry. The nano-composite metal oxide was synthesized by the wet precipitation method in basic media. Aspartic acid is a non-essential amino acid naturally synthesized in the body with lot of health significance, including as a biomarker for several health deficiencies. The synthesized composite Co₃O₄-ZnO nanorod was well-investigated by using FESEM, XRD, XPS, FTIR, UV/vis., EIS, and CV. The synthesized composite exhibited a low limit of detection (0.03 µM, high sensitivity (0.0014 µA µM^-1 cm^-2) and wide linear range (0.05-50 µM) for aspartic acid. The substrate, the Co₃O₄-ZnO nanorod, enhanced the electro-catalytic oxidation of aspartic acid as a result of its catalytic and conductivity properties. The developed sensor based on Co₃O₄-ZnO has a repeatable, reproducible and stable current response for aspartic acid. Additionally, other electroactive compounds did not interfere with the sensor's current response. The suitability of the developed sensor for real sample analysis was also established. Therefore, this study proposed the potential use of Co₃O₄-ZnO nanorod material in healthcare management for the maintenance of human well-being.

In the title compound, [Fe(C5H5)(C8H11N4S)], the cyclo-penta-dienyl (Cp) rings of the ferrocene unit are close to being eclipsed. They are inclined to one another at an angle of 1.95 (2)° and lie 3.309 (2)Å away from each other. The ethyl-idene-thio-carbonohydrazide fragment is planar, with an r.m.s. deviation of 0.0347 (2) Å from the mean plane of its eight non-H atoms, and makes dihedral angles of 21.78 (1) and 19.97 (1)° with respect to the two Cp rings. The mol-ecule adopts a trans geometry about the C=N double bond. In the crystal, N-H⋯(N/S) and C-H⋯S inter-actions stack the mol-ecules in an inverse fashion along the b axis.

The synthesis of room-temperature stable ionic liquids was obtained via metathesis reaction, which was accomplished by the reaction 1,10-Phenanthroline monohydrate hydrochloride with lithium-bis(trifluoromethane)sulfonamide in water (shortly, 1,10-PhenanNTf2). The prepared 1,10-PhenanNTf2 was characterized in details with various conventional methods. Finally, it was mixed with conducting binders and deposited on flat-silver electrode (AgE) to result in a sensor that has a fast response to bisphenol A (BPA) in the phosphate buffer phase (PBP). Features include high sensitivity, low-sample volume, reliability, reproducibility, ease of integration, long-term stability, and enhanced electrochemical responses. The calibration plot is linear (r2 = 0.9789) over the 0.1 nM–0.1 mM BPA concentration range. The sensitivity is ∼1.485 μA μM cm−2, and the detection limit is 0.09 ± 0.01 nM (at a signal-to-noise-ratio, SNR of 3). We believe that the developed approach significantly opens up a simple, fast, highly sensitive, and environment-friendly path to fabricate ionic liquid based chemical sensors with broad application prospects.

An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.

The asymmetric unit of the 5:3 title co-crystal of 2-amino-4-phenyl-5,6-dihydro-benzo[h]quinoline-3-carbonitrile and 3-amino-1-phenyl-9,10-dihydro-phenanthrene-2,4-dicarbonitrile, 0.625C(20)H(15)N(3).0.375C(22)H(15)N(3), has the atoms of the fused-ring system and those of the amino, cyano and phenyl substitutents overlapped. The fused-ring system is buckled owing to the ethyl-ene linkage in the central ring, the two flanking aromatic rings being twisted by 20.1 (1)°. This ethyl-ene portion is disordered over two positions in a 1:1 ratio. The phenyl ring is twisted by 69.5 (1)° relative to the amino- and cyano-bearing aromatic ring. In the crystal, two mol-ecules are linked by an N-H⋯N hydrogen bond, generating a a helical chain along [010].

In this paper, we report a facile one-pot route to prepare core-shell Ag2S@MSN mesoporous silica nanospheres with near-infrared (NIR) photoluminescent properties. The Ag2S@MSN nanospheres have uniform core-shell structures with single monoclinic α-Ag2S nanocrystal core (∼17 nm), ordered mesoporous silica shell (the thickness of ∼20 nm), very high surface area (∼909 m2 g−1), and uniform pore size (∼2.6 nm). The core-shell Ag2S@MSN nanospheres show NIR emission at around 1275 nm excited by a 648 nm laser diode, which can be observed in a wide range of concentration (0.2∼3.2 mg mL−1). The stability of the NIR photoluminescence for the core-shell Ag2S@MSN nanospheres is greatly improved compared to the bare Ag2S nanocrystals. The NIR emission intensity could be enhanced after the hydrothermal treatment with the increase of crystallinity of the silver sulfide cores. The thickness of mesoporous silica shell could be tuned by adjusting the amount of silica source. Furthermore, the core-shell Ag2S@MSN nanocomposites with several small Ag2S nanoparticles in one mesoporous silica shell could also be obtained, which may be a good candidate for bioimaging and biolabeling.

Abstract Starting from readily available 2-naphthol, aldehydes, aryl and alkylamines, a variety of Betti bases were efficiently synthesized utilizing a catalytic amount of cerium (IV) ammonium nitrate (CAN) at room temperature. This protocol has advantages of high yield, mild reaction conditions, no environmental pollution, diversity of reactants and simple work up procedure.