Synthesis, Spectroscopic and Thermal Studies of Zinc(II) Complexes with the Symmetrical Bidentate Schiff-Base Ligand (2,3-MeO-ba)2en: Crystal Structure of Zn((2,3-MeO-ba)2en)I2

Abstract  

Two zinc(II) complexes [ZnI₂((2,3-MeO-ba)₂en)] (1) and [ZnCl₂((2,3-MeO-ba)₂en)] (2), with the symmetrical bidentate Schiff-base ligand (2,3-MeO-ba)₂en [N,N′-bis(2,3-dimethoxybenzylidene)-1,2-diaminoethane] have been synthesized and characterized by elemental analyses (CHN), FT-IR and ¹H-NMR spectroscopy. The thermal behaviors of these complexes were studied using thermogravimetry in order to evaluate their thermal stability and thermal decomposition pathways. The crystal structure of [ZnI₂((2,3-MeO-ba)₂en)] (1) was determined from single-crystal X-ray diffraction. The coordination polyhedron about the zinc(II) center in the complex 1 is best described as a distorted tetrahedron.     

On finite groups whose every proper normal subgroup is a union of a given number of conjugacy classes

Let G be a finite group andA be a normal subgroup ofG. We denote by ncc(A) the number ofG-conjugacy classes ofA andA is calledn-decomposable, if ncc(A)= n. SetK _G = {ncc(A)|A ⊲ G}. LetX be a non-empty subset of positive integers. A groupG is calledX-decomposable, ifK _G =X. Ashrafi and his co-authors [1-5] have characterized theX-decomposable non-perfect finite groups forX = {1, n} andn ≤ 10. In this paper, we continue this problem and investigate the structure ofX-decomposable non-perfect finite groups, forX = {1, 2, 3}. We prove that such a group is isomorphic to Z₆, D₈, Q₈, S₄, SmallGroup(20, 3), SmallGroup(24, 3), where SmallGroup(m, n) denotes the mth group of ordern in the small group library of GAP [11].     

MicroRNA-499a-5p Promotes Differentiation of Human Bone Marrow-Derived Mesenchymal Stem Cells to Cardiomyocytes

Since the adult mammalian heart has limited regenerative capacity, cardiac trauma, disease, and aging cause permanent loss of contractile tissue. This has fueled the development of stem cell-based strategies to provide the damaged heart with new cardiomyocytes. Bone marrow-derived mesenchymal stem cells (BM-MSCs) are capable of self-renewal and differentiation into cardiomyocytes, albeit inefficiently. MicroRNAs (miRNAs, miRs) are non-coding RNAs that have the potential to control stem cell fate decisions and are employed in cardiac regeneration and repair. In this study, we tested the hypothesis that overexpression of miR-499a induces cardiomyogenic differentiation in BM-MSCs. Human BM-MSCs (hBM-MSCs) were transduced with lentiviral vectors encoding miR-499a-3p or miR-499a-5p and analyzed by immunostaining and western blotting methods 14 days post-transduction. MiR-499a-5p-transduced cells adopted a polygonal/rod-shaped (myocyte-like) phenotype and showed an increase in the expression of the cardiomyocyte markers α-actinin and cTnI, as cardiogenic differentiation markers. These results indicate that miR-499a-5p overexpression promotes the cardiomyogenic differentiation of hBM-MSCs and may thereby increase their therapeutic efficiency in cardiac regeneration.     

Analysis of Microscopic Displacement Mechanisms of a MIOR Process in Porous Media with Different Wettability

Transport in Porous Media - The wettability of the reservoir rock has an important effect on the displacement of fluids on a microscopic scale in all EOR processes, especially in the microbial...     

Fragmentation pathways of O-alkyl methylphosphonothionocyanidates in the gas phase: Toward unambiguous structural characterization of chemicals in the Chemical Weapons Convention framework

The electron-impact (EI) mass spectra of a series of O-alkyl methylphosphonothionocyanidates were studied for Chemical Weapons Convention (CWC) purposes. General EI fragmentation pathways were constructed and discussed, and collision-induced dissociation studies of the major EI ions were performed to confirm proposed fragment structures by analyzing fragment ions of deuterated analogs and by use of density functional theory (DFT) calculations. Thiono–thiolo rearrangement, McLafferty-type rearrangement, and a previously unknown intramolecular electrophilic aromatic substitution reaction were observed and confirmed. The study also focused on differentiation of isomeric compounds. Retention indices for all compounds, and an electrophilicity index for several compounds, are reported and interpreted.     

Synthesis,Characterization and X‐ray Crystal Structures of [Cu(ncaen)2]ClO4 and [Cu(nca2en)(PPh3)2]BPh4 Complexes

A novel ligand, N,N′‐Bis‐[3‐(2‐nitrophenyl)‐allylidene]‐ethane‐1,2‐diamine (nca₂en), and their corresponding copper(I) complexes, [Cu(ncaen)₂]ClO₄ ( 1 ), and [Cu(nca₂en)(PPh₃)₂]BPh₄ ( 2 ), have been synthesized and characterized by CHN analyses, ¹H and ¹³C‐NMR, IR, and UV‐Vis spectroscopy. The crystal and molecular structures of [Cu(ncaen)₂]ClO₄ ( 1 ), and [Cu(nca₂en)(PPh₃)₂]BPh₄ ( 2 ), were determined by X‐ray crystallography from single‐crystal data. The coordination polyhedron about the copper(I) atom in the two complexes is best described as a distorted tetrahedron. A quasireversible redox behavior is observed for complex 1 and 2 (E_1/2 = 0.55 and 0.95 V, respectively).     

New upper bounds for Estrada index of bipartite graphs

Suppose G is a graph and λ₁,λ₂,…,λ_n are the eigenvalues of G. The Estrada index EE(G) of G is defined as the sum of e^λ_i, 1≤i≤n. In this paper some new upper bounds for the Estrada index of bipartite graphs are presented. We apply our result on a (4,6)-fullerene to improve our bound given in an earlier paper.