{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/70269"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/70269","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Synthetic Iron Porphyrins as Models for Heme Proteins","abstract":"Various iron porphyrin complexes have been studied as models for the active sites of heme proteins. Spectroscopic studies of (FeTPP)(,2)N('+) (where TPP is the dianion of tetraphenylporphyrin) and (FeTPP)(,2)C indicate that these complexes contain iron(IV). This behavior can be contrasted with the isoelectronic complex (FeTPP)(,2)O('2+), which contains iron(III) and porphyrin pication radicals. (FePor)(,2)N('+) complexes (where Por can be one of several tetraarylporphyrins) can be further oxidized to yield (FePor)(,2)N('2+), a stable iron(IV) porphyrin pi-cation radical. The electronic structure of these species is dependent on the counterions and porphyrin substituents.","abstract_html":"Various iron porphyrin complexes have been studied as models for the active sites of heme proteins. Spectroscopic studies of (FeTPP)(,2)N('+) (where TPP is the dianion of tetraphenylporphyrin) and (FeTPP)(,2)C indicate that these complexes contain iron(IV). This behavior can be contrasted with the isoelectronic complex (FeTPP)(,2)O('2+), which contains iron(III) and porphyrin pication radicals. (FePor)(,2)N('+) complexes (where Por can be one of several tetraarylporphyrins) can be further oxidized to yield (FePor)(,2)N('2+), a stable iron(IV) porphyrin pi-cation radical. The electronic structure of these species is dependent on the counterions and porphyrin substituents.","abstract_has_math":false,"creators":["English, Daniel Roy"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2014,"date_issued":"2014-12-15T23:18:16Z","date_published":"2014-12-15T23:18:16Z","updated_at":"2026-07-22T22:26:02Z","subjects":["Chemistry, Inorganic"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["(UMI)AAI8502134"],"render_values":[{"text":"(UMI)AAI8502134","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/2142/70269","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["English, Daniel Roy"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2014-12-15T23:18:16Z","10000-01-01","1984"]},{"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":["Chemistry, Inorganic"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/2142/70269","(UMI)AAI8502134"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Various iron porphyrin complexes have been studied as models for the active sites of heme proteins. Spectroscopic studies of (FeTPP)(,2)N('+) (where TPP is the dianion of tetraphenylporphyrin) and (FeTPP)(,2)C indicate that these complexes contain iron(IV). This behavior can be contrasted with the isoelectronic complex (FeTPP)(,2)O('2+), which contains iron(III) and porphyrin pication radicals. (FePor)(,2)N('+) complexes (where Por can be one of several tetraarylporphyrins) can be further oxidized to yield (FePor)(,2)N('2+), a stable iron(IV) porphyrin pi-cation radical. The electronic structure of these species is dependent on the counterions and porphyrin substituents.","(FeTPP)(,2)N interacts with dioxygen in a polar frozen glass medium. This interaction is totally reversible. The optical spectrum of the oxygen adduct is equivalent to that of the unbound dimer; this indicates that the two iron atoms are inequivalent in the adduct while electron paramagnetic resonance data indicate a less anisotropic g tensor and appreciably diminished ('14)N and ('57)Fe hyperfine coupling relative to the nonadducted species. O(,2) titrations, as monitored by electron paramagnetic resonance, show that the adduct's stoichiometry is one O(,2) per dimer. All these data are consistent with a weak axial interaction of O(,2) with one side of the dimer.","To date, synthetic five-coordinate ferric porphyrin thiolates are all high-spin. Reaction of S(,8) and LiB(Et)(,3)H with Fe(TAP)Cl, where TAP is the dianion of p-methoxyphenylporphyrin, produces Fe(TAP)SH. Mossbauer, electron paramagnetic resonance, and nuclear magnetic resonance spectroscopic studies and magnetic susceptibility measurements indicate that the product is a low-spin ferric species. The stereochemistry of Fe(TAP)SH has been determined by a single-crystal x-ray structure. The average Fe-N(,por) distance of 2.01 (ANGSTROM) is indicative of a low-spin iron center.","Made available in DSpace on 2014-12-15T23:18:16Z (GMT). No. of bitstreams: 1 8502134.pdf: 5886343 bytes, checksum: d801fa099bc31b116e5945e42cecc307 (MD5) Previous issue date: 1984","Embargo set by: Seth Robbins for item 70435 Lift date: Forever Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","U of I Only","260 p.","Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1984."]},{"key":"dc:title","label":"Title","values":["Synthetic Iron Porphyrins as Models for Heme Proteins"]}]}],"canonical_facts":{"dc:creator":["English, Daniel Roy"],"dc:date":["2014-12-15T23:18:16Z","10000-01-01","1984"],"dc:description":["Various iron porphyrin complexes have been studied as models for the active sites of heme proteins. Spectroscopic studies of (FeTPP)(,2)N('+) (where TPP is the dianion of tetraphenylporphyrin) and (FeTPP)(,2)C indicate that these complexes contain iron(IV). This behavior can be contrasted with the isoelectronic complex (FeTPP)(,2)O('2+), which contains iron(III) and porphyrin pication radicals. (FePor)(,2)N('+) complexes (where Por can be one of several tetraarylporphyrins) can be further oxidized to yield (FePor)(,2)N('2+), a stable iron(IV) porphyrin pi-cation radical. The electronic structure of these species is dependent on the counterions and porphyrin substituents.","(FeTPP)(,2)N interacts with dioxygen in a polar frozen glass medium. This interaction is totally reversible. The optical spectrum of the oxygen adduct is equivalent to that of the unbound dimer; this indicates that the two iron atoms are inequivalent in the adduct while electron paramagnetic resonance data indicate a less anisotropic g tensor and appreciably diminished ('14)N and ('57)Fe hyperfine coupling relative to the nonadducted species. O(,2) titrations, as monitored by electron paramagnetic resonance, show that the adduct's stoichiometry is one O(,2) per dimer. All these data are consistent with a weak axial interaction of O(,2) with one side of the dimer.","To date, synthetic five-coordinate ferric porphyrin thiolates are all high-spin. Reaction of S(,8) and LiB(Et)(,3)H with Fe(TAP)Cl, where TAP is the dianion of p-methoxyphenylporphyrin, produces Fe(TAP)SH. Mossbauer, electron paramagnetic resonance, and nuclear magnetic resonance spectroscopic studies and magnetic susceptibility measurements indicate that the product is a low-spin ferric species. The stereochemistry of Fe(TAP)SH has been determined by a single-crystal x-ray structure. The average Fe-N(,por) distance of 2.01 (ANGSTROM) is indicative of a low-spin iron center.","Made available in DSpace on 2014-12-15T23:18:16Z (GMT). No. of bitstreams: 1 8502134.pdf: 5886343 bytes, checksum: d801fa099bc31b116e5945e42cecc307 (MD5) Previous issue date: 1984","Embargo set by: Seth Robbins for item 70435 Lift date: Forever Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","U of I Only","260 p.","Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1984."],"dc:identifier":["http://hdl.handle.net/2142/70269","(UMI)AAI8502134"],"dc:subject":["Chemistry, Inorganic"],"dc:title":["Synthetic Iron Porphyrins as Models for Heme Proteins"],"dc:type":["text"],"thesis:degree_discipline":["Chemistry"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Ph.D."],"thesis:institution_name":["University of Illinois at Urbana-Champaign"]},"updated_at":"2026-07-22T22:26:02Z"}