Thermoreversible Diels-Alder reactions of fullerenes: Applications in polymers and materials |
Posted on:1998-08-01 | Degree:Ph.D | Type:Dissertation |
University:University of Massachusetts Amherst | Candidate:Nie, Bing | Full Text:PDF |
GTID:1461390014979028 | Subject:Organic Chemistry |
Abstract/Summary: | |
Diels-Alder cycloaddition reactions have played an essential role on chemical modification of fullerenes. The torsionally strained alkene system makes fullerenes excellent dienophiles, accommodating dienes which react in a reversible fashion. This research investigated the use of fullerene Diels-Alder methodology as a means to reversibly incorporate fullerenes into polymers, materials and also as building blocks of polymeric materials.;Furan-functionalized Merrifield's polymer resin was synthesized. HPLC analysis demonstrated that C;A thermal stress-resistant silicate-based material was also investigated in reacting with fullerenes. Cyclopentadiene-functionalized silica gel and methylcyclopentadiene-functionalized silica gel reacted with fullerene C;Fullerene-Diels-Alder methodology was also investigated as a means to create polymeric materials. Intermolecular Diels-Alder condensation of C... |
Keywords/Search Tags: | Diels-alder, Fullerenes, Materials |
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