Molecular structure and selective theophylline complexation by conformational change of diethyl N,N′‐(1,3‐phenylene)dicarbamate

• Published in: Acta crystallographica. Section C, Crystal structure communications Vol. 80; no. 6; pp. 190 - 199
• Main Authors: González-González, Juan Saulo, Martínez-Santos, Alfonso, Emparán-Legaspi, María José, Pineda-Contreras, Armando, Martínez-Martínez, Francisco Javier, Flores-Alamo, Marcos, García-Ortega, Hector
• Format: Journal Article
• Language: English
• Published: 5 Abbey Square, Chester, Cheshire CH1 2HU, England International Union of Crystallography 01.06.2024; Wiley Subscription Services, Inc
• Subjects: Caffeine; conformational change; crystal structure; Ethyl carbamate; host‐guest complex; Hydrogen bonds; Infrared spectroscopy; IR spectroscopy; mechanochemistry; Molecular structure; NMR; Nuclear magnetic resonance; phenyl carbamate; Selective binding; Supramolecular compounds; Theophylline; X-ray diffraction; mechanochemistry; theophylline; crystal structure; host-guest complex; phenyl carbamate; conformational change; IR spectroscopy
• ISSN: 2053-2296; 0108-2701; 2053-2296; 1600-5759
• DOI: 10.1107/S2053229624003358

The receptor ability of diethyl N,N′‐(1,3‐phenylene)dicarbamate (1) to form host–guest complexes with theophylline (TEO) and caffeine (CAF) by mechanochemistry was evaluated. The formation of the 1–TEO complex (C12H16N2O4·C7H8N4O2) was preferred and involves the conformational change of one of the ethyl carbamate groups of 1 from the endo conformation to the exo conformation to allow the formation of intermolecular interactions. The formation of an N—H…O=C hydrogen bond between 1 and TEO triggers the conformational change of 1. CAF molecules are unable to form an N—H…O=C hydrogen bond with 1, making the conformational change and, therefore, the formation of the complex impossible. Conformational change and selective binding were monitored by IR spectroscopy, solid‐state 13C nuclear magnetic resonance and single‐crystal X‐ray diffraction. The 1–TEO complex was characterized by IR spectroscopy, solid‐state 13C nuclear magnetic resonance, powder X‐ray diffraction and single‐crystal X‐ray diffraction. The diethyl N,N′‐(1,3‐phenylene)dicarbamate–theophylline (1–TEO) complex was obtained by mechanochemistry involving the conformational change of one of the ethyl carbamate groups of 1 from the endo conformation to the exo conformation to allow the formation of intermolecular interactions.