Computational Study of Ion-Molecule Interactions

P, Priya and Mallik, Bhabani Shankar (2015) Computational Study of Ion-Molecule Interactions. Masters thesis, Indian Institute of Technology Hyderabad.

[img]
Preview
Text
CY13M1012.pdf - Submitted Version

Download (4MB) | Preview

Abstract

The interaction of ions with neutral molecules was studied by computational methods in this project. Two types of systems were studied; the first one being triethyloxonium ion with water molecules and the second one is N-methylacetamide (NMA) with alkyl ammonium ions and carboxylate ions in the presence of water molecule. It was found that the interaction energy of first two water molecules to oxonium ion Et3O+ is mainly contributed by hydrophobic interactions. With the addition of more water molecules, the interaction energy was found to be increasing and it comes from the stability gained due to H-bonds among water molecules. The lowest energy isomers of the clusters for 3, 4 and 5 water molecules, are found to have cyclic structures of water molecules. The cyclic water tetramer also stabilizes the clusters with more water molecules, indicating that it is the most stable cyclic structure of water molecules. Et3O+ ion is found to be stabilized in basic medium, and got destabilized in acidic medium. When compared for the hydrophobic nature, Et3O+ is found to be slightly more hydrophobic than its analogous carbon counterpart Et3C+. NMA, being amide, has nucleophilic as well as electrophilic centre. So, it can interact with charged and neutral chemical entities. Based on the interactions of NMA with protonated amines, carboxylates and water molecules, it was found that NMA can interact more with electrophiles than nucleophiles. Transfer of two protons took place, when protonated amine and carboxylate interacted with NMA simultaneously. One proton transfer took place from protonated amine to NMA, and second one from NMA to carboxylate ion. When these cations and anions were made to interact separately with NMA in the presence of water molecule, the cations and anions didn’t undergo proton transfer. This finding can be exploited in stabilizing the peptides as well as proteins by using suitable ion- pairs in aqueous solution.

[error in script]
IITH Creators:
IITH CreatorsORCiD
Mallik, Bhabani Shankarhttp://orcid.org/0000-0001-9657-1497
Item Type: Thesis (Masters)
Uncontrolled Keywords: Oxonium Ion, Triethyloxonium IOn, N-methylacutamide (NMA), Water; TD336
Subjects: ?? sub5.8 ??
Divisions: Department of Chemistry
Depositing User: Library Staff
Date Deposited: 28 Apr 2015 06:15
Last Modified: 21 May 2019 11:06
URI: http://raiithold.iith.ac.in/id/eprint/1461
Publisher URL:
Related URLs:

Actions (login required)

View Item View Item
Statistics for RAIITH ePrint 1461 Statistics for this ePrint Item