{"id":{"repo_id":"wfu","oai_identifier":"oai:wakespace.lib.wfu.edu:10339/57160"},"canonical_url":"https://search.dev.ndltd.org/etd/wfu/oai:wakespace.lib.wfu.edu:10339/57160","repository":{"repo_id":"wfu","name":"Wake Forest University","base_url":"https://wakespace.lib.wfu.edu/oai/request"},"display":{"title":"Elucidation of Reactions in Organic Photochemistry","abstract":"Organic photochemistry is a unique discipline which allows for reactivity that is unavailable in the ground state. 1,2-Dialkoxy anthraquinones exhibit photochemistry which releases an alkane functional group from the 1-position and forms a dimer from the anthraquinone moiety. This reactivity is observed for a plethora of 1,2-dialkoxy-9,10-anthraquinones; however different products are observed for 1-ethoxy and 1-benzyloxy substituted anthraquinones which instead produce a 1-keto derivative.","abstract_html":"Organic photochemistry is a unique discipline which allows for reactivity that is unavailable in the ground state. 1,2-Dialkoxy anthraquinones exhibit photochemistry which releases an alkane functional group from the 1-position and forms a dimer from the anthraquinone moiety. This reactivity is observed for a plethora of 1,2-dialkoxy-9,10-anthraquinones; however different products are observed for 1-ethoxy and 1-benzyloxy substituted anthraquinones which instead produce a 1-keto derivative.","abstract_has_math":false,"creators":["Pifer, Jason Mark"],"institution":"Wake Forest University","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2015,"date_issued":"2015","date_published":"2015","updated_at":"2026-07-27T22:01:52Z","subjects":["Anthraquinones"],"languages":["en"],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/10339/57160","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Pifer, Jason Mark"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2015-06-23T08:35:55Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2016-06-22T08:30:09Z"]},{"key":"dc:date.issued","label":"Date","values":["2015"]},{"key":"dc:publisher","label":"Institution","values":["Wake Forest University"]},{"key":"dc:type","label":"Dc Type","values":["Dissertation"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Anthraquinones"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["en"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/10339/57160"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Organic photochemistry is a unique discipline which allows for reactivity that is unavailable in the ground state. 1,2-Dialkoxy anthraquinones exhibit photochemistry which releases an alkane functional group from the 1-position and forms a dimer from the anthraquinone moiety. This reactivity is observed for a plethora of 1,2-dialkoxy-9,10-anthraquinones; however different products are observed for 1-ethoxy and 1-benzyloxy substituted anthraquinones which instead produce a 1-keto derivative."]},{"key":"dc:title","label":"Title","values":["Elucidation of Reactions in Organic Photochemistry"]}]}],"canonical_facts":{"dc:creator":["Pifer, Jason Mark"],"dc:date.accessioned":["2015-06-23T08:35:55Z"],"dc:date.available":["2016-06-22T08:30:09Z"],"dc:date.issued":["2015"],"dc:description.abstract":["Organic photochemistry is a unique discipline which allows for reactivity that is unavailable in the ground state. 1,2-Dialkoxy anthraquinones exhibit photochemistry which releases an alkane functional group from the 1-position and forms a dimer from the anthraquinone moiety. This reactivity is observed for a plethora of 1,2-dialkoxy-9,10-anthraquinones; however different products are observed for 1-ethoxy and 1-benzyloxy substituted anthraquinones which instead produce a 1-keto derivative."],"dc:identifier.uri":["http://hdl.handle.net/10339/57160"],"dc:language.iso":["en"],"dc:publisher":["Wake Forest University"],"dc:subject":["Anthraquinones"],"dc:title":["Elucidation of Reactions in Organic Photochemistry"],"dc:type":["Dissertation"]},"updated_at":"2026-07-27T22:01:52Z"}