دورية أكاديمية
Mechanistic Investigation of C—C Bond Activation of Phosphaalkynes with Pt(0) Complexes
| العنوان: | Mechanistic Investigation of C—C Bond Activation of Phosphaalkynes with Pt(0) Complexes |
|---|---|
| المؤلفون: | Escobar, Roberto M., AteÅŸin, Abdurrahman C., Müller, Christian, Jones, William D., AteÅŸin, Tülay |
| المصدر: | Research Symposium |
| بيانات النشر: | ScholarWorks @ UTRGV |
| سنة النشر: | 2024 |
| مصطلحات موضوعية: | Carbon–carbon (C–C) bond activation, homogeneous transition-metal catalysts, phosphaalkynes, Density Functional Theory, Pt(0)-mediated C–CP bond activation, reductive elimination pathway, energetics, metal complexes, reaction intermediates, reaction pathways, polar solvent (tetrahydrofuran), mesityl and phenyl groups, Pt(0) and Ni(0), transition state energies, C–CN bond activation, benzonitriles, transition-metal-catalyzed reactions, pharmaceutical synthesis, catalysis, pharmaceutical industry, drug synthesis, therapeutic agents, Computational Chemistry, Data Science, Heterocyclic Compounds, Inorganic Chemistry, Medicinal and Pharmaceutical Chemistry, Medicine and Health Sciences, Numerical Analysis and Scientific Computing, Organic Chemistry |
| الوصف: | Carbon–carbon (C–C) bond activation has gained increased attention as a direct method for the synthesis of pharmaceuticals. Due to the thermodynamic stability and kinetic inaccessibility of the C–C bonds, however, activation of C–C bonds by homogeneous transition-metal catalysts under mild homogeneous conditions is still a challenge. Most of the systems in which the activation occurs either have aromatization or relief of ring strain as the primary driving force. The activation of unstrained C–C bonds of phosphaalkynes does not have this advantage. This study employs Density Functional Theory (DFT) calculations to elucidate Pt(0)-mediated C–CP bond activation mechanisms in phosphaalkynes. Investigating the thermal reductive elimination pathway from the C–CP bond activation product, we present energetics of resulting metal complexes, potential reaction intermediates, and reaction pathways leading to product formation in polar solvent (tetrahydrofuran). Additionally, comparisons between mesityl and phenyl groups, Pt(0) and Ni(0), and ligand-substituent variations reveal nuanced influences on product stability and transition state energies. Parallels with C–CN bond activation in benzonitriles with the Ni(0) fragment provide additional context, advancing understanding not only of C–C bond activation but also offering insights into broader transition-metal-catalyzed reactions. This study, encapsulating the intricacies of C–C bond activation in phosphaalkynes and its implications, contributes to the evolving landscape of pharmaceutical synthesis and catalysis. For example, the application of Pt(0)-mediated C–CP bond activation in the pharmaceutical industry offers innovative routes for drug synthesis, potentially leading to production of novel therapeutic agents with enhanced biological activities. |
| نوع الوثيقة: | text |
| وصف الملف: | application/pdf |
| اللغة: | unknown |
| العلاقة: | https://scholarworks.utrgv.edu/somrs/2024/posters/46Test; https://scholarworks.utrgv.edu/context/somrs/article/1417/viewcontent/auto_convert.pdfTest |
| الإتاحة: | https://scholarworks.utrgv.edu/somrs/2024/posters/46Test https://scholarworks.utrgv.edu/context/somrs/article/1417/viewcontent/auto_convert.pdfTest |
| رقم الانضمام: | edsbas.EFB22FDD |
| قاعدة البيانات: | BASE |
| الوصف غير متاح. |