{"id":{"repo_id":"rice","oai_identifier":"oai:repository.rice.edu:1911/19579"},"canonical_url":"https://search.dev.ndltd.org/etd/rice/oai:repository.rice.edu:1911/19579","repository":{"repo_id":"rice","name":"Rice University","base_url":"https://repository.rice.edu/server/oai/request"},"display":{"title":"A study of the isomers of the higher fullerenes and the synthesis and study of fullerene hydrides","abstract":"Isomers of the higher fullerenes were analyzed using 3He NMR spectroscopy. Structures have been assigned to isomers for C76, C78 and C84. Several fullerene hydrides, C60H n (n = 2, 4, 6, 8, 18, 36), have been synthesized using a novel hydrazine reduction. Other fullerene hydrides, C60Hn (n = 38, 40, 42, 48), were synthesized via the Birch reduction of the hydrazine reduction products. Seven of eight isomers for C60H4 have been observed in the proton NMR spectra. 3He NMR spectra were obtained for 3He C60H4, 3He C 60H18 and 3He C60H36. These spectra revealed six isomers for C60H4, one isomer for C60H18 and two isomers for C60H 36. The most intense signal in the 3He spectrum for C 60H36 was assigned to the isomer of D3d' symmetry based on the 3He NMR chemical shift value. High field proton NMR analyses (750 MHz) of C60H2 and C60H4 in 1:1 solutions of CS2:C 6D6 gave spectra with signals which showed unexpected additional fine structure as a result of an alignment effect caused by the orientation of benzene in a strong magnetic field.","abstract_html":"Isomers of the higher fullerenes were analyzed using 3He NMR spectroscopy. Structures have been assigned to isomers for C76, C78 and C84. Several fullerene hydrides, C60H n (n = 2, 4, 6, 8, 18, 36), have been synthesized using a novel hydrazine reduction. Other fullerene hydrides, C60Hn (n = 38, 40, 42, 48), were synthesized via the Birch reduction of the hydrazine reduction products. Seven of eight isomers for C60H4 have been observed in the proton NMR spectra. 3He NMR spectra were obtained for 3He C60H4, 3He C 60H18 and 3He C60H36. These spectra revealed six isomers for C60H4, one isomer for C60H18 and two isomers for C60H 36. The most intense signal in the 3He spectrum for C 60H36 was assigned to the isomer of D3d' symmetry based on the 3He NMR chemical shift value. High field proton NMR analyses (750 MHz) of C60H2 and C60H4 in 1:1 solutions of CS2:C 6D6 gave spectra with signals which showed unexpected additional fine structure as a result of an alignment effect caused by the orientation of benzene in a strong magnetic field.","abstract_has_math":false,"creators":["Gonzalez, Alexander"],"institution":"Rice University","degree_name":"Doctor of Philosophy","degree_level":"Doctoral","degree_discipline":"Natural Sciences","degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1997,"date_issued":"1997","date_published":"1997","updated_at":"2026-07-24T04:10:15Z","subjects":["Organic chemistry"],"languages":["eng"],"rights":["Copyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder."],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://hdl.handle.net/1911/19579","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Gonzalez, Alexander"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2007-08-21T02:10:13Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2007-08-21T02:10:13Z"]},{"key":"dc:date.issued","label":"Date","values":["1997"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Natural Sciences"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Doctoral"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Doctor of Philosophy"]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["Rice University"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Organic chemistry"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["eng"]},{"key":"dc:rights","label":"Dc Rights","values":["Copyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder."]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["https://hdl.handle.net/1911/19579"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Isomers of the higher fullerenes were analyzed using 3He NMR spectroscopy. Structures have been assigned to isomers for C76, C78 and C84. Several fullerene hydrides, C60H n (n = 2, 4, 6, 8, 18, 36), have been synthesized using a novel hydrazine reduction. Other fullerene hydrides, C60Hn (n = 38, 40, 42, 48), were synthesized via the Birch reduction of the hydrazine reduction products. Seven of eight isomers for C60H4 have been observed in the proton NMR spectra. 3He NMR spectra were obtained for 3He C60H4, 3He C 60H18 and 3He C60H36. These spectra revealed six isomers for C60H4, one isomer for C60H18 and two isomers for C60H 36. The most intense signal in the 3He spectrum for C 60H36 was assigned to the isomer of D3d' symmetry based on the 3He NMR chemical shift value. High field proton NMR analyses (750 MHz) of C60H2 and C60H4 in 1:1 solutions of CS2:C 6D6 gave spectra with signals which showed unexpected additional fine structure as a result of an alignment effect caused by the orientation of benzene in a strong magnetic field."]},{"key":"dc:format.mimetype","label":"Dc Format Mimetype","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["A study of the isomers of the higher fullerenes and the synthesis and study of fullerene hydrides"]}]}],"canonical_facts":{"dc:creator":["Gonzalez, Alexander"],"dc:date.accessioned":["2007-08-21T02:10:13Z"],"dc:date.available":["2007-08-21T02:10:13Z"],"dc:date.issued":["1997"],"dc:description.abstract":["Isomers of the higher fullerenes were analyzed using 3He NMR spectroscopy. Structures have been assigned to isomers for C76, C78 and C84. Several fullerene hydrides, C60H n (n = 2, 4, 6, 8, 18, 36), have been synthesized using a novel hydrazine reduction. Other fullerene hydrides, C60Hn (n = 38, 40, 42, 48), were synthesized via the Birch reduction of the hydrazine reduction products. Seven of eight isomers for C60H4 have been observed in the proton NMR spectra. 3He NMR spectra were obtained for 3He C60H4, 3He C 60H18 and 3He C60H36. These spectra revealed six isomers for C60H4, one isomer for C60H18 and two isomers for C60H 36. The most intense signal in the 3He spectrum for C 60H36 was assigned to the isomer of D3d' symmetry based on the 3He NMR chemical shift value. High field proton NMR analyses (750 MHz) of C60H2 and C60H4 in 1:1 solutions of CS2:C 6D6 gave spectra with signals which showed unexpected additional fine structure as a result of an alignment effect caused by the orientation of benzene in a strong magnetic field."],"dc:format.mimetype":["application/pdf"],"dc:identifier.uri":["https://hdl.handle.net/1911/19579"],"dc:language.iso":["eng"],"dc:rights":["Copyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder."],"dc:subject":["Organic chemistry"],"dc:title":["A study of the isomers of the higher fullerenes and the synthesis and study of fullerene hydrides"],"dc:type":["Thesis"],"thesis:degree_discipline":["Natural Sciences"],"thesis:degree_level":["Doctoral"],"thesis:degree_name":["Doctor of Philosophy"],"thesis:institution_name":["Rice University"]},"updated_at":"2026-07-24T04:10:15Z"}