Resumen: We report a directed dynamic resolution process for an atropisomeric [Ag(NHC)2]+ complex, where stereochemical control is achieved through enantiomeric interconversion in solution before crystallization. Unlike conventional diastereomeric salt formation, our approach shifts the restricted interconversion between Ra and Sa atropisomers, allowing selective stabilization of one enantiomer via π–π interactions with enantiopure binaphthalene-based borate anions in solution. NMR spectroscopy reveals conformational locking and restricted dynamics preceding crystallization, which captures the resolved stereochemistry in highly crystalline salts. This study demonstrates that noncovalent interactions effectively modulate molecular conformational dynamics to achieve chiral resolution. Idioma: Inglés DOI: 10.1021/acs.inorgchem.5c03548 Año: 2025 Publicado en: Inorganic Chemistry (2025), [7 p.] ISSN: 0020-1669 Financiación: info:eu-repo/grantAgreement/ES/DGA/E05-23R Financiación: info:eu-repo/grantAgreement/ES/DGA/E42-23R Financiación: info:eu-repo/grantAgreement/ES/MCIU-AEI-FEDER/PID2021-122406NB-I00 Tipo y forma: Artículo (Versión definitiva) Área (Departamento): Área Química Inorgánica (Dpto. Química Inorgánica)