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- W4309175931 endingPage "7938" @default.
- W4309175931 startingPage "7938" @default.
- W4309175931 abstract "Intermolecular complexes with calixarenes are intriguing because of multiple possibilities of noncovalent binding for both polar and nonpolar molecules, including docking in the calixarene cavity. In this contribution calix[6]arenes interacting with amino acids are studied with an additional aim to show that tools such as symmetry-adapted perturbation theory (SAPT), functional-group SAPT (F-SAPT), and systematic molecular fragmentation (SMF) methods may provide explanations for different numbers of noncovalent bonds and of their varying strength for various calixarene conformers and guest molecules. The partitioning of the interaction energy provides an easy way to identify hydrogen bonds, including those with unconventional hydrogen acceptors, as well as other noncovalent bonds, and to find repulsive destabilizing interactions between functional groups. Various other features can be explained by energy partitioning, such as the red shift of an IR stretching frequency for some hydroxy groups, which arises from their attraction to the phenyl ring of calixarene. Pairs of hydrogen bonds and other noncovalent bonds of similar magnitude found by F-SAPT explain an increase in the stability of both inclusion and outer complexes." @default.
- W4309175931 created "2022-11-24" @default.
- W4309175931 creator A5032972680 @default.
- W4309175931 creator A5039203160 @default.
- W4309175931 creator A5044439398 @default.
- W4309175931 creator A5087657079 @default.
- W4309175931 date "2022-11-16" @default.
- W4309175931 modified "2023-10-17" @default.
- W4309175931 title "Association Complexes of Calix[6]arenes with Amino Acids Explained by Energy-Partitioning Methods" @default.
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