The intention of the study is to find the nature of interactions that exist in inclusion complexes formed between the steroids, nandrolone, and testosterone with cucurbit[n]urnils (n = 7 and 8) host, using density functional theory incorporated with empirical dispersion correction. Upon encapsulation, nandrolone caused a larger geometrical distortion in cucurbituril geometry, while testosterone inclusion complex is formed with a larger number of intermolecular hydrogen bonds. The molecular electrostatic potential examination shows that the positive potential observed on the eight-membered ring in CB7 got reduced upon encapsulation, while on the nandrolone the negative potential on carbonyl unit has increased. AIM analysis shows that in inclusion complexes, the observed electron density are higher for the interactions between the oxygen atoms of carbonyl fringe of cucurbituril molecule and the steroid molecules. The NCI isosurface of nandrolone@CB7 has green patches in between the nandrolone and cucurbituril molecule, evenly distributed. In the testosterone@CB7, along with the green patches, red patches, due to the steric crowding between the testosterone and cucurbituril, were observed. The energy decomposition analysis parameters show that Pauli’s repulsive term was highest for nandrolone@CB7. When testosterone is the guest, repulsive energy was found to be larger than nandrolone guest. From the above interference, it can be confirmed that the steric hindrance that arises during the interaction of testosterone with CB7 reduces the stability of the complex, and the nandrolone best fit inside the CB7 cavity with the combination of hydrogen bonding and weak van der Waals bonding as intermolecular interactions.
|Number of pages||10|
|Journal||Journal of Inclusion Phenomena and Macrocyclic Chemistry|
|Publication status||Published - 2019 Apr 15|
- Inclusion complex
ASJC Scopus subject areas
- Food Science
- Condensed Matter Physics