Category

Poster - Basic

Description

Organometallic semiconductors have emerged as pivotal components driving technological innovations in recent years. With a rich history in chemistry, organometallic compounds have gained prominence for their semiconductive properties, leading to significant advancements in fields such as optoelectronics and materials science. This study focuses on streamlining the synthesis of 5,6-fused ring pyridazines, a critical organic building block for cutting-edge organometallic semiconductor technologies. Pyridazines, characterized by a six-membered aromatic ring with adjacent nitrogen atoms, exhibit remarkable stability and have diverse applications in optoelectronics and pharmaceuticals. The primary objective of this research is to develop a more efficient process for the synthesis of 5,6-fused ring pyridazines from phenyl fulvene and hydrazine, intended for use in organometallic semiconductor research. This endeavor seeks to optimize the production of this crucial building block, facilitating advancements in the field. The experimental design for this research project is organized in two phases: 1. Synthesis and Isolation. 2. Analysis. The synthesis of the 5,6-fused ring pyridazine was accomplished by reacting phenyl fulvene with excess hydrazine. The synthesized product was then separated and extracted using separatory funnel procedures with an associated magnesium sulfate drying agent. The product was then isolated using a simple distillation procedure followed by trituration. The product was then analyzed using several analytic techniques: percent yield, IR spectroscopy, melting point analysis, thin-layer chromatography (TLC), and NMR spectroscopy. The results and conclusions of this research project are yet to be determined as research is still in progress. There is also a possibility for an additional inorganic reaction to be conducted with the product and thallium to produce the desired organometallic semiconductor.

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Undergraduate

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Apr 17th, 1:00 PM

Efficient Synthesis of 5,6-Fused Ring Pyridazines for Advanced Organometallic Semiconductor Applications

Poster - Basic

Organometallic semiconductors have emerged as pivotal components driving technological innovations in recent years. With a rich history in chemistry, organometallic compounds have gained prominence for their semiconductive properties, leading to significant advancements in fields such as optoelectronics and materials science. This study focuses on streamlining the synthesis of 5,6-fused ring pyridazines, a critical organic building block for cutting-edge organometallic semiconductor technologies. Pyridazines, characterized by a six-membered aromatic ring with adjacent nitrogen atoms, exhibit remarkable stability and have diverse applications in optoelectronics and pharmaceuticals. The primary objective of this research is to develop a more efficient process for the synthesis of 5,6-fused ring pyridazines from phenyl fulvene and hydrazine, intended for use in organometallic semiconductor research. This endeavor seeks to optimize the production of this crucial building block, facilitating advancements in the field. The experimental design for this research project is organized in two phases: 1. Synthesis and Isolation. 2. Analysis. The synthesis of the 5,6-fused ring pyridazine was accomplished by reacting phenyl fulvene with excess hydrazine. The synthesized product was then separated and extracted using separatory funnel procedures with an associated magnesium sulfate drying agent. The product was then isolated using a simple distillation procedure followed by trituration. The product was then analyzed using several analytic techniques: percent yield, IR spectroscopy, melting point analysis, thin-layer chromatography (TLC), and NMR spectroscopy. The results and conclusions of this research project are yet to be determined as research is still in progress. There is also a possibility for an additional inorganic reaction to be conducted with the product and thallium to produce the desired organometallic semiconductor.

 

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