An article Rotational Signatures of Dispersive Stacking in the Formation of Aromatic Dimers WOS:000459709300025 published article about POTENTIAL-ENERGY SURFACE; BENZENE DIMER; CH/PI INTERACTION; WATER; SPECTROSCOPY; RECOGNITION; FLUORENE; RINGS in [Fatima, Mariyam; Steber, Amanda L.; Perez, Cristobal; Zinn, Sabrina; Schnell, Melanie] DESY, FS SMP, Notkestr 85, D-22607 Hamburg, Germany; [Fatima, Mariyam; Steber, Amanda L.; Perez, Cristobal; Zinn, Sabrina; Schnell, Melanie] Christian Albrechts Univ Kiel, Inst Phys Chem, Max Eyth Str 1, D-24118 Kiel, Germany; [Poblotzki, Anja] Univ Gottingen, Inst Phys Chem, Tammannstr 6, D-37077 Gottingen, Germany in 2019.0, Cited 45.0. Product Details of 101-84-8. The Name is Diphenyl oxide. Through research, I have a further understanding and discovery of 101-84-8
The aggregation of aromatic species is dictated by inter- and intramolecular forces. Not only is characterizing these forces in aromatic growth important for understanding grain formation in the interstellar medium, but it is also imperative to comprehend biological functions. We report a combined rotational spectroscopic and quantum-chemical study on three homo-dimers, comprising of diphenyl ether, dibenzofuran, and fluorene, to analyze the influence of structural flexibility and the presence of heteroatoms on dimer formation. The structural information obtained shows clear similarities between the dimers, despite their qualitatively different molecular interactions. All dimers are dominated by dispersion interactions, but the dibenzofuran dimer is also influenced by repulsion between the free electron pairs of the oxygen atoms and the pi-clouds. This study lays the groundwork for understanding the first steps of molecular aggregation in systems with aromatic residues.
About Diphenyl oxide, If you have any questions, you can contact Fatima, M; Steber, AL; Poblotzki, A; Perez, C; Zinn, S; Schnell, M or concate me.. Product Details of 101-84-8
Reference:
Ether – Wikipedia,
,Ether | (C2H5)2O – PubChem