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CHEM2019SCHMITT50258 CHEM

The Synthesis of Amaryllidaceae Alkaloid Analogs

Type: Undergraduate
Author(s): Nate Schmitt Chemistry & Biochemistry Adam Montoya Chemistry & Biochemistry
Advisor(s): David Minter Chemistry & Biochemistry
Location: Session: 2; 1st Floor; Table Number: 4

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Amaryllidaceae isoquinoline alkaloids as well as their analogs have long been of interest as lead compounds in drug discovery due to their range of biological activity. Many of these alkaloids are cytotoxic anti-tumor agents. Moreover, there have also been studies showing the effectiveness of these molecules against yellow fever and other diseases caused by RNA- containing flaviviruses. The study of these compounds as pharmaceutical agents is hampered by their low natural abundance, which necessitates the development of laboratory syntheses of these alkaloids and their analogs.
This project focuses on the total syntheses of the Pancratistatin-type natural products that contain the phenanthridone ring system. In stage one, model systems are being investigated to develop the methodology required to introduce requisite functionality found in natural systems. Previous research from this laboratory gives the basic phenanthridone skeleton with several different functional groups, but there are no reported methods for converting these functions into polyhydroxycyclohexenes with stereochemical control. Two of the problems under investigation involve the ring expansion of a spiro ring containing an epoxide and the production of a specific trihydroxycyclohexene with control of stereochemistry. In stage two, a specific phenanthridone alkaloid will be targeted for total synthesis that uses the new methodology developed in stage one.

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CHEM2019SCHWARTZ27386 CHEM

Synthesis and Characterization of N,N,N,-Copper Pincer Complexes

Type: Undergraduate
Author(s): Timothy Schwartz Chemistry & Biochemistry Marianne Burnett Chemistry & Biochemistry Akop Yepremyam Chemistry & Biochemistry
Advisor(s): Kayla Green Chemistry & Biochemistry
Location: Session: 2; 1st Floor; Table Number: 2

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Organometallic catalysts are useful in many organic reactions by exploiting the Lewis acidity of the metal complex. Most catalysts available rely on precious metals like platinum and rhenium. These catalysts pose a financial and environmental barrier to many scientists. Thus, there is a need for catalysts that use less expensive and toxic metals, such as copper. A library of copper catalysts with different electronic functionalities have been synthesized and characterized by cyclic voltammetry, UV-VIS, NMR, and X-ray crystallography. It was found that the complexes with electron donating groups better stabilize the copper center, when compared to the complexes with electron withdrawing groups. However, the planar characteristics of each ligand makes them unsuitable candidates for copper catalysis because they cannot bind to the tetrahedral geometry of reduced copper. This work warrants the complexation of these ligands with other metals, like nickel or cobalt, to determine their viability as applicable organometallic catalysts.

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CHEM2019TA53316 CHEM

DESIGNER SOLVENTS AND MATERIALS

Type: Undergraduate
Author(s): Daniel Ta Chemistry & Biochemistry Onofrio Annunziata Chemistry & Biochemistry Christian Chen Chemistry & Biochemistry
Advisor(s): Sergei Dzyuba Chemistry & Biochemistry
Location: Session: 2; 2nd Floor; Table Number: 8

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Room-temperature ionic liquids and deep-eutectic solvents have become unique and almost indispensible materials for various areas of sciences, medicine and engineering. The ability to engineer media with desired properties favorably distinguishes these solvents from traditionally used molecular solvents.

This poster will describe our ongoing efforts on designing various types of ionic, eutectic systems as well as approaches towards modulating their phase transitions. Studies related to controlling the self-assembly process of various solutes in this type of media will also be presented.

(Presentation is private)

CHEM2019WEGENER47813 CHEM

Can Whiskey have Terroir? Assessing sugar differences after mashing heirloom cereals for Bourbon production

Type: Undergraduate
Author(s): Kathleen Wegener Chemistry & Biochemistry
Advisor(s): Eric Simanek Chemistry & Biochemistry Rob Arnold Biology
Location: Session: 1; 1st Floor; Table Number: 7

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This project will entail assessing several varieties of common and heirloom corn from throughout Texas to identify sugar (and thus alcohol) content.
After obtaining cereal samples from a local distillery, the cereals will be processed by mashing and fermenting.
The resulting mashes will be measured for pH and S.G., then analyzed through chromatography using HPLC-RID. These samples of corn will be assessed for variations in sugar yield, both and composition and quantification. After fermentation, the HPLC-RID will be used for chromatographic analysis of ethanol concentration. Ultimately, this will provide information on the most promising corn varieties, and expose their potential as a future staples of this partner distillery.

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COSC2019BEEBE45127 COSC

DSound

Type: Undergraduate
Author(s): Emma Beebe Engineering Shane Mitchell Computer Science Wynn Pho Computer Science
Advisor(s): Liran Ma Computer Science
Location: Session: 1; 2nd Floor; Table Number: 7

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Hearing aids are costly, inconvenient, unappealing, and unfortunately are currently one of the only devices on the market for the hearing impaired. This explains why less than 30% of American adults with hearing impairment actually use hearing aids and in underdeveloped countries it is as low as 10%. With the abundance and accessibility of smartphones, an app that could substitute as a hearing aid could help people all over the world.

Due to technological advancement, smartphones have become powerful digital processing machines and are improved and refined constantly. It is the capability of processing sounds and playing the altered signal to the user that allows a smartphone to be used as a hearing aid. The teams before me have made an iOS app that can listen to the surrounding area and amplify sound in certain frequencies according to the user’s prescription.

This year our top priority is to pass Apple's latest requirements to put the iOS app on the App Store and add functionalities that allow it interact with the Apple Watch 4. We will then add more capabilities like developing a method to shift certain sounds from frequencies the patient cannot hear, as well to frequencies they can hear. Another new functionality would be for the app to have situational awareness so it plays the correct sound depending on the outside environment. In order to best achieve these goals, we will need some new technologies to meet Apple’s requirements and improve the performance of the app.

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