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Full-Text Articles in Physical Sciences and Mathematics
Synthesis, Characterization And Cell Viability Of Novel Tripodal Amines, Kinsley Lupton
Synthesis, Characterization And Cell Viability Of Novel Tripodal Amines, Kinsley Lupton
Honors College Theses
Cancer, over the years, has become a much more prevalent focus for the scientific community. Organizations and laboratories all over the world have spent countless hours searching for a cure, trying to learn more about what makes cancer so powerful and what is the best way to stop its growth. Iron-chelation drugs were already on the market, and it was shown that they did have the ability to act as both iron-chelators and anticancer drugs. Most of these iron-chelating drugs are not as effective at killing cancer cells as the medical field desires. Novel iron-chelating tris-indolyl derivatives, GSO2, GSO4 and …
Pyridyl Bis-Urea Macrocycles As Supramolecular Synthons And The Design And Synthesis Of Small Molecule Pharmaceuticals Targeting Ly6k, Devan D. Buchanan
Pyridyl Bis-Urea Macrocycles As Supramolecular Synthons And The Design And Synthesis Of Small Molecule Pharmaceuticals Targeting Ly6k, Devan D. Buchanan
Theses and Dissertations
Assembled pyridyl bis-urea macrocycles have been utilized as 1D supramolecular synthons to construct hierarchical assemblies. These macrocycles have both urea and pyridyl functional groups and can form non-covalent interactions with hydrogen or halogen bond donors through symmetric, ditopic acceptor motifs. Bis-urea macrocycles offer interesting capabilities as synthons to organize donors into well-defined crystal structures. In part, this is due to the urea motifs’ propensity to assemble through hydrogen bonding. New, asymmetric pyridyl macrocycles were synthesized, crystallized, and experimentally probed to determine how symmetry affects their assembly and utility as supramolecular synthons.
The Uphadhyay group identified small molecules, including NSC11150, …
The Development Of Dipyrrin Platforms For Oxygen Reduction, Myles Steed
The Development Of Dipyrrin Platforms For Oxygen Reduction, Myles Steed
Student Symposium
A redox-active ligand scaffold, dipyrrin, was synthesized in the interest of activating oxygen. The synthesis of the scaffold was modified from previous pathways. The original pathway used a Negishi-coupling followed by condensation with a benzaldehyde using pyrrole and di-tert-butyl anisole before being demethylated using either boron tribromide or a thiolate. The modified synthesis constructs the scaffold with a Negishi-coupling followed by a condensation with a benzaldehyde using pyrrole and a silyl protected di-methyl-phenol before being deprotected using triethylamine trihydrofluoride. The new pathway provides the opportunity limit toxic reagents and improve the overall efficiency of the synthesis. The dipyrrin scaffold was …
Design And Synthesis Of Hoogsteen-Binding Peptide Nucleic Acid Monomers With Extended Linkers For Triple Helical U-A Recognition In Rna, Angelina B. Giglio-Tos, Tristan L. Mabee, James A. Mackay
Design And Synthesis Of Hoogsteen-Binding Peptide Nucleic Acid Monomers With Extended Linkers For Triple Helical U-A Recognition In Rna, Angelina B. Giglio-Tos, Tristan L. Mabee, James A. Mackay
Summer Scholarship, Creative Arts and Research Projects (SCARP)
RNA provides many functions within biological systems. For example, noncoding RNA (ncRNA), a form of RNA that is not part of transcription or translation, serves a variety of unique roles, such as catalysis or gene regulation. ncRNA generally forms double helical motifs that are ripe for molecular recognition. Sequence selective recognition of double helical RNA (dhRNA) can be achieved using Peptide Nucleic Acids (PNA) through triple helical formation by Hoogsteen hydrogen bonding of PNA nucleobases in the major groove of dhRNA. However, strong, and selective recognition is typically limited to polypurine strands and pyrimidine recognition remains an unsolved problem. A …
Gene Vectors With Fluorescence Tracking Capabilities, Sophia Despina Angelopoulos
Gene Vectors With Fluorescence Tracking Capabilities, Sophia Despina Angelopoulos
Browse all Theses and Dissertations
This project focuses on the optimization of benzothiazole-based chromophores to utilize them as fluorescent tags functionalized onto stimuli-responsive, or “smart,” polymers as non-viral gene delivery vectors for gene therapy applications. Blue-fluorescent emissive chromophores will allow tracking capabilities for the transfection pathway of the vector to be monitored as it delivers the DNA payload within intercellular space. The most appropriate chromophore must be covalently bound to a free amine within the vector, which is accomplished through NAS chemistry from fluorophenyl-benzothiazoles (F-BTZ-CBz) derivatives to amidated hyperbranched poly(ethyleneimine)(HPEI-IBAm0.61). HPEI is considered to be a synthetic polycation, which promotes tunable solubility through characteristics of …
Covalent Attachment Of Tadf Chromophores To Thermally Stable Poly(Arylene Ether)S, Samuel Farrar
Covalent Attachment Of Tadf Chromophores To Thermally Stable Poly(Arylene Ether)S, Samuel Farrar
Browse all Theses and Dissertations
The covalent attachment of a blue emitting, benzothiazole based TADF chromophore into poly(arylene ether) backbone polymers was explored. A benzothiazole derivative, 2-(2,4-difluorophenyl)-benzothiazole (2,4-diF-BTZ), was synthesized to form the electrophilic component of the host polymer. Two polymers were synthesized to have chromophore incorporated, using 2,4-diFBTZ and 4,4-dihydroxydiphenyl ether (DPE) or 4,4’-biphenol (BP). The chromophore was covalently incorporated at a 10% molar ratio into the polymer backbone by copolymerization with 2,4-diF-BTZ and BP, utilizing nucleophilic aromatic substitution (NAS). Structural characterization was provided via NMR spectroscopy and GC/MS analysis. The polymer syntheses provided high molecular weight materials that were able to be cast …