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Full-Text Articles in Physical Sciences and Mathematics
Small Molecule Caspase Inhibitors Using Isatin And Oxindole Scaffolds And A Combinatorial Approach, Hagar Mahmoud Abdallah
Small Molecule Caspase Inhibitors Using Isatin And Oxindole Scaffolds And A Combinatorial Approach, Hagar Mahmoud Abdallah
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Quinolyl-valyl-O-methylaspartyl-[2,6-difluorophenoxy]-methyl ketone (Q-VD-OPh) is a next generation broad spectrum caspase inhibitor, the effectiveness and reduced toxicity of which can be partially attributable to the carboxyterminal O-phenoxy group as well as the amino terminal quinolyl groups. We seek to incorporate some of these unique recognition elements onto small molecule derived protease inhibitors with drug like properties. Specifically, heterocyclic scaffolds such as isatins and oxindoles. Thus, isatins bearing electron withdrawing groups on C-5 and 2,6-difluorobenzyl moieties have been prepared by analogy to the well studied N-substituted 5-pyrrololidinylsulfonyl isatins. Moreover, 3-benzylidene oxindole derivatives bearing these structural motifs have also been prepared and their …
Cationic Exchange Reactions Involving Dilithium Phthalocyanine, Morgan M. Hart
Cationic Exchange Reactions Involving Dilithium Phthalocyanine, Morgan M. Hart
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Dilithium phthalocyanine (Li2Pc) consists of an aromatic macrocycle possessing a doubly negative charge and two Li+ counterions. One Li+ ion is easily displaceable while the other remains coordinated to the phthalocyanine ring. The displaceable Li+ cation can be exchanged with other cations, such as a singly charged tetra-alkyl ammonium cation, by using several variations of a general procedure. It has been demonstrated that tetraalkylammonium lithium phthalocyanines (TAA-LiPcs) can be successfully and reproducibly synthesized with yields ranging from 54.5% up to 64.3%. All TAA-LiPcs demonstrated poor solubilities from approximately <0.2 mg/mL to 5 mg/ml in the solvents tested (with the exception of tetrapropylammonium lithium phthalocyanine and tetrahexylammonium lithium phthalocyanine). All of the TAA-LiPcs synthesized were dark-purple in color, with the exception of tetraheptylammonium lithium phthalocyanine and tetraoctylammonium lithium phthalocyanine. These two compounds were dark - blue in color. Melting points varied greatly from >370.4°C to 157.9°C and depended greatly upon …
Exploration Of Gradient-Type Poly(Arylene Ether)S Via An Abb' Monomer System, Alex V. Dolgov
Exploration Of Gradient-Type Poly(Arylene Ether)S Via An Abb' Monomer System, Alex V. Dolgov
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Evidence shows that a gradient like copolymer can be synthesized using nucleophilic aromatic substitution, NAS, chemistry. Using the 4-chloro-3-fluoro-4'hydroxydiphenylsulfone monomer, 5, it is possible to control the ratios of the leaving groups, in this case the fluorine and the chlorine, with the right solvent and temperature. Alternating the temperatures will alter the substitution of the leaving groups, thus forming a polymer backbone of gradient characteristics. Initial reactions to determine the relative rates of displacement of the chlorine and fluorine atoms were carried out using a model compound, 1, which possessed the chlorine and fluorine leaving groups, but not the phenol …
The Synthesis And Characterization Of Imidazolium Lithium Phthalocyanines, John J. Kelley
The Synthesis And Characterization Of Imidazolium Lithium Phthalocyanines, John J. Kelley
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A series of 1,3-di-substituted-imidazolium lithium phthalocyanines, in which the substituents on the imidazolium nitrogens were combinations of methyl, ethyl, pentyl, hexyl, isopropyl, adamantyl or 2,4,6-trimethylphenyl groups, was synthesized. The cation exchange of a single lithium ion of dilithium phthalocyanine for a 1,3-disubstituted-imidazolium ion was performed by mixing their salts in common organic solvents under ambient conditions. This afforded a number of imidazolium lithium phthalocyanines in moderate yields. They exhibited poor solubility in most solvents. Their composition and purity were initially verified by 1H and 13C-NMR and elemental analysis. The 1H-NMR spectra also indicated that the imidazolium and lithium phthalocyanine ions …
Tailoring Branching For Poly (Arylene Ether)S Via Reactivity Ratio Controlled Polymerizations, Amanda Ike
Tailoring Branching For Poly (Arylene Ether)S Via Reactivity Ratio Controlled Polymerizations, Amanda Ike
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The ability to control physical and mechanical properties of polymer systems has become an important aspect of polymer science. In order to tailor the branching in polymer systems, an understanding into the reactivity of the electrophilic sites in the monomer is important. Kinetic methods have been explored in order to determine the reactivity of monomers in preparing poly(arylene ether)s and to predict the degree of branching that will occur in a polymer of this kind. The reactivity of AB2 sulfones and phosphine oxides was explored, along with the reactivity of ABB'B'' sulfones. NMR spectroscopy was used as a probe into …