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.
Various Co-loaded ZSM-5 zeolites (Co-ZSM-5) were prepared and the details of their structural, morphological and elemental properties characterized by different conventional methods.
Abstract Uric acid is mainly produced from metabolism of purine nucleotide in human body and have several medical importance in human system. It is therefore very imperative to develop a sensitive and accurate method of its detection. This study aimed to develop uric acid biosensor based on polydopamine/polypyrole (PDA/PPY) composite decorated on glassy carbon electrode. The conductive polymer PDA/PPY was electrochemically synthesized and casted on glassy carbon electrode (GCE). The synthesized PDA/PPY was characterized by fourier transform infrared spectroscopy, field emission scanning electron microscopy, electrochemical impedance spectroscopy, energy dispersive x‐ray spectroscopy and x‐ray photoelectron spectroscopy. PDA/PPY/GCE showed good response towards uric acid with low limit of detection (0.1 μM, S/N =3), good linearity (0.5‐40 μM) and high sensitivity (2.1 μAμMcm −2 ). It was also found to have stable response for uric acid unaffected by common interferents. Also, when used for uric acid detection in human serum and urine, it showed a good recovery of 90–110%. The developed PDA/PPY composite is proposed as a promising biosensor for uric acid for human health protection.
Due to its superior properties, erbium sesquioxide, Er2O3, is considered as an important material for applications in various fields such as corrosion-resistant coating, electrical insulating coating, in sensing membranes, semiconductor devices, as catalyst, and for applications in nuclear engineering. In the open literature there is a lack of information about the preparation of Er2O3 nanoparticles using the homogenous precipitation and subsequent calcination route. In this paper a facile method for the synthesis of Er2O3 nanoparticles is suggested. The fabrication was carried out by using the homogeneous precipitation of an erbium ions using sodium hydroxide followed by the calcination process. The influence of: (i) the pH value (9-12) during precipitation process, and (ii) the calcination temperature 300-700 °C on the structural and textural properties of the solids obtained will be addressed. The thermal events accompanying the heat treatment of the dried parent was monitored using thermogravimetric analysis (TGA). Various physicochemical techniques were used for investigating the structure and morphology of Er2O3 nanoparticles. These include X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectra, filed emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). Moreover, the electrical conductivity of the calcined samples with temperature was measured.
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.
This book titled Nanofiber Research - Reaching New Heights contains a number of latest research results on growth and developments on material fibers in nanoscale. It is a promising novel research area that has received a lot of interest in recent years. This book includes interesting reports on cutting-edge science and technology related to synthesis, morphology, control, self-assembly and prospective application of nanofibers. I hope that the book will lead to systematization of nanofiber science, creation of new nanofiber research field and further promotion of nanofiber technology. This potentially unique work offers various approaches on the implementation of nanofibers. As it is widely known, nanotechnology presents the control of matter at the nanoscale and nano-dimensions within few nanometers, whereas this exclusive phenomenon enables us to regulate and control novel applications with nanofibers. This book presents an overview of recent and current nanofibers fundamental, significant applications and implementation research worldwide. It examined the methods of nanofiber synthesis, types of fibers used and potential applications associated with nanofiber researches. It is an important booklet for research organizations, governmental research centers, academic libraries and R&D affianced in recent research and development of nanofibers.
A series of pyrazole containing Schiff bases were synthesized, by the reaction of 3,5-dimethyl-1-phenylpyrazole-4-carboxaldehyde and the corresponding active amines under microwave irradiation. The structures of the synthesized compounds were established by spectroscopic data (FT-IR, 1H NMR, 13C NMR and ESI-MS) and elemental analyses. The anti-bacterial activity of these compounds were tested in vitro by the disc diffusion assay against two Gram-positive and two Gram-negative bacteria, and then the minimum inhibitory concentration using chloramphenicol as reference drug. All the molecules were modeled and optimized by using density functional theory, DFT/B3LYP method. Calculated descriptors, the lower unoccupied molecular orbital and the density were used to interpret the antibacterial activity of the compounds. The results showed that compound 3 is better inhibitor of both types of test bacteria as compared to chloramphenicol.
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.
In the title compound, C20H18BrN3O2, the central carbonyl group forms amine-N—H...O and hydroxy-O—H...O hydrogen bonds, which lead to two fused S(6) rings. The N-bound phenyl ring is coplanar with the five-membered ring to which it is attached [dihedral angle = 5.22 (18)°], but the dihedral angle [33.87 (17)°] between the terminal phenyl and bromobenzene rings indicates an overall twist in the molecule. In the crystal packing, molecules assemble into dimeric aggregates via C—H...π interactions.
