{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/84101"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/84101","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Part I: Self-Assembling Dendrimers Using the Dda-Aad Hydrogen Bonding Motif. Part II: Supramolecular Discotic Liquid Crystals Through Hydrogen Bond Mediated Self-Assembly","abstract":"In part II, the ability of this heterocyclic unit to generate a self-assembled structure in bulk was tested by attachment of a 3,4,5-tris-dodecyloxybenzyl group to the 8-amino group and evaluating the mesomorphic properties of the resulting derivative. Cumulative solution studies by 1H NMR, SEC and DLS indicate the formation of a hydrogen bonded cyclic hexamer in apolar solvents. The studies by differential scanning calorimetry (DSC), polarized light microscopy (PLM) and X-ray diffraction (XRD) indicate that the hexameric disks can stack in bulk to form thermotropic columnar mesophases. The mesophases exist across a large temperature range (>248&deg;C).","abstract_html":"In part II, the ability of this heterocyclic unit to generate a self-assembled structure in bulk was tested by attachment of a 3,4,5-tris-dodecyloxybenzyl group to the 8-amino group and evaluating the mesomorphic properties of the resulting derivative. Cumulative solution studies by 1H NMR, SEC and DLS indicate the formation of a hydrogen bonded cyclic hexamer in apolar solvents. The studies by differential scanning calorimetry (DSC), polarized light microscopy (PLM) and X-ray diffraction (XRD) indicate that the hexameric disks can stack in bulk to form thermotropic columnar mesophases. The mesophases exist across a large temperature range (&gt;248&amp;deg;C).","abstract_has_math":false,"creators":["Ma, Yuguo"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":["Zimmerman, Steven C."],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2015,"date_issued":"2015-09-25T22:12:55Z","date_published":"2015-09-25T22:12:55Z","updated_at":"2026-07-22T22:26:22Z","subjects":["Engineering, Materials Science"],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["(MiAaPQ)AAI3086129"],"render_values":[{"text":"(MiAaPQ)AAI3086129","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/2142/84101","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Zimmerman, Steven C."]},{"key":"dc:creator","label":"Author","values":["Ma, Yuguo"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2015-09-25T22:12:55Z","10000-01-01","2003"]},{"key":"dc:type","label":"Dc Type","values":["text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Chemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Ph.D."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Illinois at Urbana-Champaign"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Engineering, Materials Science"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["eng"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/2142/84101","(MiAaPQ)AAI3086129"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["In part II, the ability of this heterocyclic unit to generate a self-assembled structure in bulk was tested by attachment of a 3,4,5-tris-dodecyloxybenzyl group to the 8-amino group and evaluating the mesomorphic properties of the resulting derivative. Cumulative solution studies by 1H NMR, SEC and DLS indicate the formation of a hydrogen bonded cyclic hexamer in apolar solvents. The studies by differential scanning calorimetry (DSC), polarized light microscopy (PLM) and X-ray diffraction (XRD) indicate that the hexameric disks can stack in bulk to form thermotropic columnar mesophases. The mesophases exist across a large temperature range (>248&deg;C).","Made available in DSpace on 2015-09-25T22:12:55Z (GMT). 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Part II: Supramolecular Discotic Liquid Crystals Through Hydrogen Bond Mediated Self-Assembly"]}]}],"canonical_facts":{"dc:contributor":["Zimmerman, Steven C."],"dc:creator":["Ma, Yuguo"],"dc:date":["2015-09-25T22:12:55Z","10000-01-01","2003"],"dc:description":["In part II, the ability of this heterocyclic unit to generate a self-assembled structure in bulk was tested by attachment of a 3,4,5-tris-dodecyloxybenzyl group to the 8-amino group and evaluating the mesomorphic properties of the resulting derivative. Cumulative solution studies by 1H NMR, SEC and DLS indicate the formation of a hydrogen bonded cyclic hexamer in apolar solvents. The studies by differential scanning calorimetry (DSC), polarized light microscopy (PLM) and X-ray diffraction (XRD) indicate that the hexameric disks can stack in bulk to form thermotropic columnar mesophases. The mesophases exist across a large temperature range (>248&deg;C).","Made available in DSpace on 2015-09-25T22:12:55Z (GMT). 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