RT info:eu-repo/semantics/article
T1 Striking ligand-disproportionative Cl/aryl scrambling in a simple Au(iii) system. Solvent role, driving forces and mechanisms
A1 Fernández Moyano, Sara
A1 Peñas de Frutos, Marconi Nicolás
A1 Bartolomé Albistegui, María del Camino
A1 Espinet Rubio, Pablo
K1 Termodinámica
K1 Thermodynamic
K1 2210 Química Física
AB Aryl rearrangements triggered by Cl− extraction from trans-[AuIII(Rf)2Cl2]− (Rf = C6F3Cl2-3,5), led quickly to a mixture of [Au(Rf)3(solv)], cis-[Au(Rf)2Cl(solv)] and [Au(Rf)Cl2(solv)] (solv = OEt2, OH2). 19F NMR and X-ray diffraction studies led us to identify the species present in solution and the role of the solvent in their formation, while DFT calculations confirm the thermodynamic basis of their evolution. Very different Rf–Rf coupling rates are found from (μ-Cl)2[cis-Au(Rf)2]2 or cis-[Au(Rf)2ClL] species (L = OEt2, NCMe, Cl−) depending on the coordination strength of the ligand or solvent in the fourth position.
PB Royal Society of Chemistry
SN 1359-7345
YR 2021
FD 2021
LK http://uvadoc.uva.es/handle/10324/45391
UL http://uvadoc.uva.es/handle/10324/45391
LA eng
NO Chemical Communications, 2021, 57, 125-128
NO Producción Científica
DS UVaDOC
RD 07-ago-2024