Stacking interactions, also known as π-π or face-to-face interactions, occur between molecules whose
π bonds are in parallel planes. They are used to design self-assembling structures in nanotechnology,
influence organic reactions and are ubiquitous in nature.
The stacking interactions of substituted benzene heterodimers and substituted benzene-natural
nucleobase heterodimers are examined. Both electron-donating and withdrawing groups are studied
by varying their type, number and location around the benzene ring. The studies are done by carrying
out systematic scans of the potential energy surface at the MP2/6-31G*(0.25) level of theory. Charge
transfer interactions and extent of charge separation in the monomer are found to be dominant when
the difference in ESP between the monomers is large and small, respectively. Dipole-dipole
interactions are also found to affect stacking interactions. The results from MP2/6-31G*(0.25) are
checked against those at the CCSD(T)/CBS limit for select cases and are found to be within 81-
110%. / xii, 166 leaves : ill. ; 29 cm
| Identifer | oai:union.ndltd.org:LACETR/oai:collectionscanada.gc.ca:ALU.w.uleth.ca/dspace#10133/3234 |
| Date | January 2010 |
| Creators | Chhikara, Aditya |
| Contributors | Wetmore, Stacey |
| Publisher | Lethbridge, Alta. : University of Lethbridge, Dept. of Chemistry and Biochemistry, 2010, Arts and Science, Department of Chemistry and Biochemistry |
| Source Sets | Library and Archives Canada ETDs Repository / Centre d'archives des thèses électroniques de Bibliothèque et Archives Canada |
| Language | en_US |
| Detected Language | English |
| Type | Thesis |
| Relation | Thesis (University of Lethbridge. Faculty of Arts and Science) |
Page generated in 0.0018 seconds