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dc.contributor.authorAw, Hong Wai
dc.contributor.authorBurns, Dennis H.
dc.date.accessioned2012-12-12T14:50:20Z
dc.date.available2012-12-12T14:50:20Z
dc.date.issued2010-03-25
dc.identifier.urihttp://hdl.handle.net/10057/5468
dc.descriptionThe project completed at the Wichita State University Department of Chemistry. Presented at the 7th Annual Capitol Graduate Research Summit, Topeka, KS, 2010en_US
dc.description.abstractThe determination of anion binding constants using 1H NMR and Isothermal Titration Calorimetric (ITC) reveals the occurrence of several specific and unspecific binding steps. In general, ITC reports on all specific and unspecific binding processes of the whole system, whereas a typical NMR probe details the thermodynamic properties associated with the binding of the anion to the receptor. For example, the (α, α, α, α)-5,10,15,20-tetrakis (2-(4-fluorophenylurea)phenyl) porphyrin binds strongly (K(M-1)>104) to chloride anion, and close to 2-3 orders of magnitude less to acetate anion, in DMSO-d6 as revealed by 1H NMR titration studies. However, acetate anion showed stronger binding than chloride anion when ITC analyses were done. Thus, the binding studies’ results vary with the use of instrumental method. Other significant differences observed in the behavior of anion binding with the porphyrin receptor when using the two probes will also be addressed in this report.en_US
dc.language.isoen_USen_US
dc.titleComparative binding studies with a tetraurea picket porphyrin receptor using 1H NMR and isothermal titration calorimetryen_US
dc.typeAbstract


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