Masters Theses
Date of Award
8-2008
Degree Type
Thesis
Degree Name
Master of Science
Major
Chemistry
Major Professor
George Schweitzer
Committee Members
George Kabalka, Jamie Adcock
Abstract
Due to their chemical and thermodynamic stability, fullerenes could play an important role in encapsulation of radionuclides for applications in radio-immunotherapy. In this thesis, we report the first synthesis of actinium endohedral fullerenes. The alpha-emitter Actinium-225 (225Ac, t1/2 =10 d) was trapped in fullerenes by the direct current (D.C) arc discharge-catcher method in a He atmosphere. Endohedral 225Ac and the bulk of fullerene C60 was dissolved from the catcher electrode (a Pt disk covered with a thin layer of C60) in toluene under N2, and converted to the malonic ester derivative. Repeated washing of the organic phase with dilute HNO3 demonstrated that a small fraction of 225Ac (1.0 %) could not be removed from the organic phase and presumably was inside the fullerenes. The Fr- 221 (the α-decay daughter of 225Ac), however, was observed to be leaking from the cage probably as a result of nuclear recoil. The cage stability was enhanced significantly by coupling the fullerene surface with organic adducts. After repetitive extractions, a 45% fraction of original activity was still retained in the cage. The radioactivity distribution coefficients {Kd = (225Ac radioactivity in aqueous- phase)/ (225Ac radioactivity in organic phase)} were investigated. We propose that, if Kd and back to back extractions, collectively are to be study in timely manner, the rate in which 225Ac@C60 dissociate into individual components would be obtained.
Recommended Citation
Mwakisege, Jofa Gideon, "The synthesis and stability of endohedral actinium-225(225Ac@C60). " Master's Thesis, University of Tennessee, 2008.
https://trace.tennessee.edu/utk_gradthes/3685