Vermeeren, Pascal and Wolters, Lando P. and Paragi, Gábor and Fonseca Guerra, Celia (2021) Cooperative Self-Assembly in Linear ChainsBased on Halogen Bonds. CHEMPLUSCHEM, 86 (6). pp. 812-819. ISSN 2192-6506
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Abstract
Cooperative properties of halogen bonds were investigated with computational experiments based on dispersion-corrected relativistic density functional theory. The bonding mechanism in linear chains of cyanogen halide (X-CN), halocyanoacetylene (X-CC-CN), and 4-halobenzonitrile (X-C6H4-CN) were examined for X = H, Cl, Br, and I. Our energy decomposition and Kohn-Sham molecular-orbital analyses revealed the bonding mechanism of the studied systems. Cyanogen halide and halocyanoacetylene chains possess an extra stabilizing effect with increasing chain size, whereas the 4-halobenzonitrile chains do not. This cooperativity can be traced back to charge separation within the sigma-electronic system by charge-transfer between the lone-pair orbital of the nitrogen (sigma(HOMO)) on one unit and the acceptor orbital of the C-X (sigma*(LUMO)) on the adjacent unit. As such, the HOMO-LUMO gap in the sigma-system decreases, and the cooperativity increases with chain length revealing the similarity in the bonding mechanisms of hydrogen and halogen bonds.
| Item Type: | Article | 
|---|---|
| Uncontrolled Keywords: | COOPERATIVITY; COMPLEXES; Electrostatics; HYDROGEN-BONDS; MO theory; COVALENCY; Halogen bonding; energy decomposition analysis; activation strain model; BASE-PAIRS; | 
| Subjects: | Q Science / természettudomány > QD Chemistry / kémia | 
| SWORD Depositor: | MTMT SWORD | 
| Depositing User: | MTMT SWORD | 
| Date Deposited: | 14 Mar 2022 08:00 | 
| Last Modified: | 14 Mar 2022 08:00 | 
| URI: | http://real.mtak.hu/id/eprint/138805 | 
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