Atom transfer radical polymerization of methyl methacrylate using copper-based homogeneous and heterogeneous catalysts

This study aimed at polymerization of methyl methacrylate with novel catalysts in the atom transfer radical polymerization (ATRP) condition at 90 °C. This was accomplished using CuBr/N-(2-aminoethyl)-3-aminopropyltrimethoxysilane (CuBr–AEAPTMS) as a homogeneous catalyst and one time with CuBr@AEAPTMS/SBA-15 as a heterogeneous catalyst. Catalysts were characterized using TGA, FT-IR, and UV–Vis spectroscopy. The structural analysis of the polymer was carried out by ¹³C NMR spectroscopy and GPC. Three characteristic parts of polymer produced by ATRP method including the initiator, monomer units, and end group was shown in ¹³C NMR spectra. In addition, the presence of C–Br unit showed that the polymerization process is alive. The ¹H NMR analysis was used for kinetic investigation of methyl methacrylate polymerization with homogeneous and heterogeneous catalysts that showed high monomer conversion (98 and 90% after 35 min, respectively) and good control of molecular weight with a dispersity (Р= 1.5–1.7). In addition, the plot of ln ([monomer]₀/[monomer] _t ) versus time gave linear relationships indicating a constant concentration of the propagating species throughout the polymerization. Finally, the results of the polymerization using heterogeneous catalyst compared with homogeneous catalyst revealed that it was according to ATRP method.     

Annihilator Conditions on Polynomials over Modules

Let R be a ring with unity and M be a right R-module. The system M[x] forms a left near R[x]-module under addition and substitution operations. In this paper we extend the study of annihilator conditions on nearring of polynomials to left near R[x]-module M[x], when M is a reduced Baer module. Also, we give a characterization of reduced modules. As a corollary we obtain some results of Birkenmeier and Huang [3].     

Cluster Model Analysis of Pion Elastic and Inelastic Scattering from 12C

Angular distributions of differential cross sections for the ¹²C(π ^±, π ^±)¹²C and ¹²C(π ^±, π ^±)¹²C^* reactions at pion kinetic energy ranging from 50 to 260 MeV have been analyzed with the 3α-particle model of ¹²C. The model provides good fits to a wide range of data. Differential cross sections for inelastic transitions to the (2^?+?; 4.44 MeV) and (3^???; 9.64 MeV) states in ¹²C are computed and the deformation lengths δ ₂ and δ ₃ are extracted. It is found that the extracted deformation lengths are sensitive to the nuclear model used and similar to the corresponding values found with other probes and nuclear models.     

ZL-amenability and characters for the restricted direct products of finite groups

Let G   be a restricted direct product of finite groups _{Gi}i∈I${\{G_i\}}_{i\in I}$, and let Z?¹(G)${\mathrm{Z}?}^1(G)$ denote the centre of its group algebra. We show that Z?¹(G)${\mathrm{Z}?}^1(G)$ is amenable if and only if _Gi$G_i$ is abelian for all but finitely many i  , and characterize the maximal ideals of Z?¹(G)${\mathrm{Z}?}^1(G)$ which have bounded approximate identities. We also study when an algebra character of Z?¹(G)${\mathrm{Z}?}^1(G)$ belongs to _c0$c_0$ or ?^p${?}^p$ and provide a variety of examples.     

Novel isocyanide-based three-component reaction: a facile synthesis of substituted 1H-chromeno[2,3-d]pyrimidine-5-carboxamides

A mild and efficient method for the synthesis of 1H-chromeno[2,3-d]pyrimidine-5-carboxamide derivatives via a one-pot, three-component reaction of an isocyanide, barbituric acid, and a salicylaldehyde in the presence of acetic acid in ethanol/water mixture at 75 °C is reported. This high atom economy reaction led to the construction of one benzopyran ring, and one amide group in a single synthetic step.     

Levamizole enhances immune responsiveness to intra-dermal and intra-muscular hepatitis B vaccination in chronic hemodialysis patients

Background  

Hemodialysis patient are at high risk for hepatitis B virus (HBV) infection.     

Synthesis of pyrano[2,3-<Emphasis Type="Italic">c</Emphasis>]pyrazoles by ionic liquids under green and eco-safe conditions

Optimization of a green approach to the synthesis of pyrano[2,3-c]pyrazoles based on the one-pot, four-component condensation via a domino Knoevenagel/Michael/cyclization sequence was investigated. This method involved the evaluation of the activity of several ionic liquids (ILs) in various solvents. This one-pot, four-component reaction revealed simplicity, higher yield and lower toxicity advantages over a corresponding three-component method. The effect of reaction parameters including the type and amount of catalyst, type of solvent, reaction temperature and time were studied with respect to yield of pyrano[2,3-c]pyrazoles. Catalyst recyclability and time-saving aspects of the reaction suggest that this method presents real alternatives over conventional reaction protocols.     

Intramolecular cyclization of <Emphasis Type="Italic">N</Emphasis>-propargyl anilines: a new synthetic entry into highly substituted indoles

Indole derivatives are an important class of heterocycle found in a large number of natural products and synthetic pharmaceuticals. Given the low cost and easy availability of N-propargyl anilines, synthesis of indole cores from these versatile structural motifs has attracted a lot of attention in the past decade. In this review, we summarize the most representative and interesting reports on this rapidly advancing area, with special emphasis on mechanistic aspects of the reactions.     

Heat-resistant and soluble fluorinated poly(amide imide)s based on non-coplanar ortho-linked diimide-dicarboxylic acid

A series of novel fluorinated heat-resistant poly(amide imide)s (PAIS) based on non-coplanar diimide-diacid monomer (DIDA) were synthesized and characterized. The poly(amide imide)s were obtained in high yields and possessed inherent viscosities in the range of 0.47-0.91 dL g⁻¹. All of the polymers were amorphous in nature, showed outstanding solubility and could be readily soluble in common organic solvents such as N,N-dimethylacetamide, N-methyl-2-pyrrolidinoned, dimethyl sulfoxide, N,N-dimethylformamide, pyridine and tetrahydrofuran. Glass transition temperatures were in the range of 221-263 °C, as determined by differential scanning calorimetry. Degradation temperatures for 10% weight loss occurred all above 520 °C and char yields was more than 50% at 700 °C in nitrogen atmosphere. Moreover, these PAIs possessed low refractive indexes (n = 1.58-1.59), birefringence (Δn = 0.008-0.013), and dielectric constants (? ≈ 2.5) due to the trifluoromethyl pendent groups and ortho-catenated aromatic rings that interrupt chain packing and increase free volume.