Premium
The Supramolecular Structural Chemistry of Pentafluorosulfanyl and Tetrafluorosulfanylene Compounds
Author(s) -
Liebing Phil,
Pitts Cody Ross,
Reimann Marc,
Trapp Nils,
Rombach David,
Bornemann Dustin,
Kaupp Martin,
Togni Antonio
Publication year - 2021
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202100163
Subject(s) - chemistry , van der waals force , substituent , supramolecular chemistry , molecule , fluorine , crystal structure , crystallography , hydrogen bond , crystal (programming language) , halogen , atom (system on chip) , stereochemistry , computational chemistry , organic chemistry , alkyl , computer science , programming language , embedded system
The analysis of crystal structures of SF 5 ‐ or SF 4 ‐containing molecules revealed that these groups are often surrounded by hydrogen or other fluorine atoms. Even though fluorine prefers F⋅⋅⋅H over F⋅⋅⋅F contacts, the latter appeared to be important in many compounds. In a significant number of datasets, the closest F⋅⋅⋅F contacts are below 95 % of the van der Waals distance of two F atoms. Moreover, a number of repeating structural motifs formed by contacts between SF 5 groups was identified, including different supramolecular dimers and infinite chains. Among SF 4 ‐containing molecules, the study focused on SF 4 Cl compounds, including the first solid‐state structure analyses of these reactive species. Additionally, electrostatic potential surfaces of a series of Ph‐SF 5 derivatives were calculated, pointing out the substituent influence on the ability of F⋅⋅⋅X contact formation (X=F or other electronegative atom). Interaction energies were calculated for different dimeric arrangements of Ph‐SF 5 , which were extracted from experimental crystal structure determinations.