Some results on the annihilator graph of a commutative ring

Let R be a commutative ring. The annihilator graph of R, denoted by AG(R), is the undirected graph with all nonzero zero-divisors of R as vertex set, and two distinct vertices x and y are adjacent if and only if ann _R (xy) ≠ ann _R (x) ∪ ann _R (y), where for z ∈ R, ann _R (z) = {r ∈ R: rz = 0}. In this paper, we characterize all finite commutative rings R with planar or outerplanar or ring-graph annihilator graphs. We characterize all finite commutative rings R whose annihilator graphs have clique number 1, 2 or 3. Also, we investigate some properties of the annihilator graph under the extension of R to polynomial rings and rings of fractions. For instance, we show that the graphs AG(R) and AG(T(R)) are isomorphic, where T(R) is the total quotient ring of R. Moreover, we investigate some properties of the annihilator graph of the ring of integers modulo n, where n ? 1.     

Analytic Analysis for Oil Recovery During Counter-Current Imbibition in Strongly Water-Wet Systems

We study counter-current imbibition, where a strongly wetting phase (water) displaces non-wetting phase spontaneously under the influence of capillary forces such that the non-wetting phase moves in the opposite direction to the water. We use an approximate analytical approach to derive an expression for saturation profile when the viscosity of the non-wetting phase is non-negligible. This makes the approach applicable to water flooding in hydrocarbon reservoirs, or the displacement of non-aqueous phase liquid (NAPL) by water. We find the recovery of non-wetting phase as a function of time for one-dimensional flow. We compare our predictions with experimental results in the literature. Our formulation reproduces experimental data accurately and is superior to previously proposed empirical models.     

Antioxidant and antimicrobial study of Schefflera vinosa leaves crude extracts against rice pathogens

Plant extracts are one of the best possible sources of bioactive molecules, and are being used globally as an antioxidants and natural antimicrobial compounds. In current study, Schefflera vinosa leaves extract was prepared through Soxhlet extraction procedure using methanol and chloroform as solvents. The extract was investigated for total antioxidant, phenolic and flavonoid contents, free radical scavenging and antimicrobial activities. The free radical scavenging activities were evaluated through 2,2- diphenyl-1-picrylhydrazyl (DPPH), 2,2′-azino-bis-3-ethylbenzotiazolin-6-sulfonic acid (ABTS) and Ferric-reducing/ antioxidant power (FRAP) assay. The antimicrobial activity of extract was determined through poisoned food method. The methanolic extract has exhibited high antioxidant, phenolic, and flavonoid activities compared to chloroform extract. Similarly, free radical scavenging activities (ABTS, DPPH and FRAP) were higher in methanolic extract. Further, Fourier-Transform Infrared Spectroscopy (FTIR) used to determine the functional group and Gas chromatography-mass spectrometry (GC–MS) to elucidate volatile composition of the crude extract. Different functional group like N-H, O-H, C-O, C-N, C-H, C=O, C≡C and C-O-H presence indicate the existence of many metabolites in the extracts. GC–MS study identified 61 compounds and subsequently, these molecules were screened virtually using DockThor. Furthermore, antimicrobial study was confirmed against rice pathogens like Magnaporthe oryzae (M. oryzae) and Xanthomonas oryzae pv. oryzae (Xoo). Molecular docking study further suggested that phytomolecules (3-Isopropoxy-1,1,1,7,7,7-hexamethyl-3,5,5-tris (trimethylsiloxy) tetrasiloxane, and 2-Methoxy-5-methylthiophene) targets Histone Deacetylase (HDAC) of M. oryzae and Peptide Deformylase (PDF) of Xoo, which could inhibit their growth. Hence, this study indicated that Schefflera vinosa extracts could be an important ingredient as an antioxidant as well as antimicrobial agent against rice pathogens.     

N‐heterocyclic carbene–palladium(II) complex supported on magnetic mesoporous silica for Heck cross‐coupling reaction

Magnetic mesoporous silica was prepared via embedding magnetite nanoparticles between channels of mesoporous silica (SBA‐15). The prepared composite (Fe₃O₄@SiO₂‐SBA) was then reacted with 3‐chloropropyltriethoxysilane, sodium imidazolide and 2‐bromopyridine to give 3‐(pyridin‐2‐yl)‐1H‐imidazol‐3‐iumpropyl‐functionalized Fe₃O₄@SiO₂‐SBA as a supported pincer ligand for Pd(II). The functionalized magnetic mesoporous silica was further reacted with [PdCl₂(SMe₂)₂] to produce a supported N‐heterocyclic carbene–Pd(II) complex. The obtained catalyst was characterized using Fourier transform infrared spectroscopy, scanning electron microscopy, energy‐dispersive X‐ray analysis, vibrating sample magnetometry, Brunauer–Emmett–Teller surface area measurement and X‐ray diffraction. The amount of the loaded complex was 80.3 mg g^?1, as calculated through thermogravimetric analysis. The formation of the ordered mesoporous structure of SBA‐15 was confirmed using low‐angle X‐ray diffraction and transmission electron microscopy. Also, X‐ray photoelectron spectroscopy confirmed the presence of the Pd(II) complex on the magnetic support. The prepared magnetic catalyst was then effectively used in the coupling reaction of olefins with aryl halides, i.e. the Heck reaction, in the presence of a base. The reaction parameters, such as solvent, base, temperature, amount of catalyst and reactant ratio, were optimized by choosing the coupling reaction of 1‐bromonaphthalene and styrene as a model Heck reaction. N‐Methylpyrrolidone as solvent, 0.25 mol% catalyst, K₂CO₃ as base, reaction temperature of 120°C and ultrasonication of the catalyst for 10 min before use provided the best conditions for the Heck cross‐coupling reaction. The best results were observed for aryl bromides and iodides while aryl chlorides were found to be less reactive. The catalyst exhibited noticeable stability and reusability.     

Isatin‐SO3H coated on amino propyl modified magnetic nanoparticles (Fe3O4@APTES@isatin‐SO3H) as a recyclable magnetic nanoparticle for the simple and rapid synthesis of pyrano[2,3‐d] pyrimidines derivatives

Isatin‐SO₃H coated on amino propyl modified magnetic nanoparticles (Fe₃O₄@APTES@isatin‐SO₃H) is found to be a novel, efficient, and reusable magnetic nanocatalyst, and characterized by FT‐IR, SEM, TEM, XRD, EDX, VSM, and TGA analysis. The magnetic nanocatalyst demonstrated outstanding performance in synthesis of pyrano[2,3‐d] pyrimidines derivatives via one‐pot three‐component reaction of various aromatic aldehydes 1, malononitrile 2, and barbituric acid 3 under reflux conditions in mixture of H₂O:EtOH (1:1) as solvent. Easy workup procedure, short reaction time, high yield, simple preparation and easy recovery of the catalyst, mild reaction conditions are some advantages of this work.     

Ultrasonic synthesis,crystal structure,luminescent, and magnetic properties of a new metal–organic complex based on Ce(IV)–Sr(II)

Research on Chemical Intermediates - This paper presents the sonochemical synthesis of a new hetero-metallic inorganic complex, formulated as [(Sr(OH2)5Ce(dipic)3Sr(OH2)6][Ce(dipic)3]·6H2O...     

Synthesis and characterization of functionalized NaP Zeolite@CoFe2O4 hybrid materials: a micro–meso-structure catalyst for aldol condensation

Research on Chemical Intermediates - In this work, magnetic nanocomposite of NaP Zeolite and CoFe2O4 as magnetic nanoparticles (MNP’s) with different ratios were prepared and in the second...     

Preparation and electromagnetic wave absorption properties of polymer nanocomposites based on new functionalized graphene oxide iron pentacarbonyl and ionic liquid

Research on Chemical Intermediates - This paper presents the preparation of a new epoxy nanocomposite of functionalized graphene oxide (FGO) and iron pentacarbonyl [Fe(CO)5] (IPC) as...     

Determination of <Superscript>68</Superscript>Ga production parameters by different reactions using ALICE and TALYS codes

Gallium-68 (T _1/2 = 68 min, I _β+ = 89%) is an important positron-emitting radionuclide for positron emission tomography and used in nuclear medicine for diagnosing tumours. This study gives a suitable reaction to produce ⁶⁸Ga. Gallium-68 excitation function via ⁶⁸Zn(p, n)⁶⁸Ga, ⁶⁸Zn(d, 2n)⁶⁸Ga, ⁷⁰Zn(p, 3n)⁶⁸Ga and ⁶⁵Cu(α, n)⁶⁸Ga reactions were calculated by ALICE-91 and TALYS-1.0 codes. The calculated excitation function of ⁶⁸Zn(p, n)⁶⁸Ga reaction was compared with the reported measurement and evaluations. Requisite thickness of the targets was obtained by SRIM code for each reaction. The ⁶⁸Ga production yield was evaluated using excitation function and stopping power.