{"id":{"repo_id":"rice","oai_identifier":"oai:repository.rice.edu:1911/16443"},"canonical_url":"https://search.dev.ndltd.org/etd/rice/oai:repository.rice.edu:1911/16443","repository":{"repo_id":"rice","name":"Rice University","base_url":"https://repository.rice.edu/server/oai/request"},"display":{"title":"Part I. Spin-state isomerism in crystalline (trifluoromethanesulfonato)(meso-tetraphenylporphinato)iron(III). Part II. Toward refined model compounds for the cytochrome c oxidase active site: A new picket-fence porphyrin with short imidazole pickets","abstract":"Part I. The unsolvated porphyrin compound (Fe$\\sp{\\rm III}$(TPP)(OSO$\\sb2$CF$\\sb3$)) has been structurally characterized by single-crystal X-ray diffraction in a monoclinic phase at 293 K and in a triclinic phase at 293, 188 and 103 K. While only one type of molecular site is found in the monoclinic phase, the temperature-dependent structural parameters and magnetic susceptibility data (5.82 $\\mu\\sb{\\rm B}$ at 293 K; 4.86 $\\mu\\sb{\\rm B}$ at 20 K) together indicate the existence of two crystallographically and magnetically distinct spin-admixed crystal lattice sites in the triclinic phase. One site (molecule 1) is unique in that its structure is temperature dependent, whereas the second site (molecule 2) has a structure which is essentially independent of temperature. This distinct site assignment has been further investigated by Mossbauer and EPR spectroscopies which suggest different spin ground states for molecules 1 and 2. This triclinic phase is also the first report of molecule pairs of the same porphyrin complex interacting in very different ways in the same crystal lattice in that molecule 1 pairs form $\\pi$-$\\pi$ dimers, whereas molecule 2 pairs do not. Part II. A new binucleating picket-fence porphyrin ligand, 5,10,15,20-Tetrakis (o-4-methylimidazole-5-ethylcarboxyl-2-oxy)phenyl) porphyrin, N$\\sb4$-PH$\\sb2$, has been synthesized and characterized to be used eventually as a vehicle to study the structure, function and reactivity patterns of the active site of cytochrome c oxidase. The enzyme itself contains an (Fe(porphyrin)$\\cdots$Cu) binuclear active site of unknown structure. The properties which set N$\\sb4$-PH$\\sb2$ apart from other binucleating picket-fence porphyrin ligands previously prepared as active site ligating molecules are the four authentic imidazole nitrogen donor atoms in the potential binding site for the Cu center and a separation between potential metal binding sites of only 3.5 to 4.0 A, made possible by the ligand&apos;s exceptionally &quot;short&quot; picket-fence arms derived from imidazole-ether linkages.","abstract_html":"Part I. The unsolvated porphyrin compound (Fe$\\sp{\\rm III}$(TPP)(OSO$\\sb2$CF$\\sb3$)) has been structurally characterized by single-crystal X-ray diffraction in a monoclinic phase at 293 K and in a triclinic phase at 293, 188 and 103 K. While only one type of molecular site is found in the monoclinic phase, the temperature-dependent structural parameters and magnetic susceptibility data (5.82 <span class=\"etd-inline-math\">&mu;\\sb{\\rm B}</span> at 293 K; 4.86 <span class=\"etd-inline-math\">&mu;\\sb{\\rm B}</span> at 20 K) together indicate the existence of two crystallographically and magnetically distinct spin-admixed crystal lattice sites in the triclinic phase. One site (molecule 1) is unique in that its structure is temperature dependent, whereas the second site (molecule 2) has a structure which is essentially independent of temperature. This distinct site assignment has been further investigated by Mossbauer and EPR spectroscopies which suggest different spin ground states for molecules 1 and 2. This triclinic phase is also the first report of molecule pairs of the same porphyrin complex interacting in very different ways in the same crystal lattice in that molecule 1 pairs form <span class=\"etd-inline-math\">&pi;</span>-<span class=\"etd-inline-math\">&pi;</span> dimers, whereas molecule 2 pairs do not. Part II. A new binucleating picket-fence porphyrin ligand, 5,10,15,20-Tetrakis (o-4-methylimidazole-5-ethylcarboxyl-2-oxy)phenyl) porphyrin, N$\\sb4$-PH$\\sb2$, has been synthesized and characterized to be used eventually as a vehicle to study the structure, function and reactivity patterns of the active site of cytochrome c oxidase. The enzyme itself contains an (Fe(porphyrin)$\\cdots$Cu) binuclear active site of unknown structure. The properties which set N$\\sb4$-PH$\\sb2$ apart from other binucleating picket-fence porphyrin ligands previously prepared as active site ligating molecules are the four authentic imidazole nitrogen donor atoms in the potential binding site for the Cu center and a separation between potential metal binding sites of only 3.5 to 4.0 A, made possible by the ligand&amp;apos;s exceptionally &amp;quot;short&amp;quot; picket-fence arms derived from imidazole-ether linkages.","abstract_has_math":true,"creators":["Gonzalez, Jorge Alberto"],"institution":"Rice University","degree_name":"Doctor of Philosophy","degree_level":"Doctoral","degree_discipline":"Natural Sciences","degree_department":null,"school":null,"contributors":[],"advisors":["Wilson, Lon J."],"committee_chairs":[],"committee_members":[],"year":1991,"date_issued":"1991","date_published":"1991","updated_at":"2026-07-24T04:10:17Z","subjects":["Inorganic chemistry","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/1911/16443","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Wilson, Lon J."]},{"key":"dc:creator","label":"Author","values":["Gonzalez, Jorge Alberto"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2009-06-04T00:24:00Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2009-06-04T00:24:00Z"]},{"key":"dc:date.issued","label":"Date","values":["1991"]},{"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":["Inorganic chemistry","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/1911/16443"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Part I. The unsolvated porphyrin compound (Fe$\\sp{\\rm III}$(TPP)(OSO$\\sb2$CF$\\sb3$)) has been structurally characterized by single-crystal X-ray diffraction in a monoclinic phase at 293 K and in a triclinic phase at 293, 188 and 103 K. While only one type of molecular site is found in the monoclinic phase, the temperature-dependent structural parameters and magnetic susceptibility data (5.82 $\\mu\\sb{\\rm B}$ at 293 K; 4.86 $\\mu\\sb{\\rm B}$ at 20 K) together indicate the existence of two crystallographically and magnetically distinct spin-admixed crystal lattice sites in the triclinic phase. One site (molecule 1) is unique in that its structure is temperature dependent, whereas the second site (molecule 2) has a structure which is essentially independent of temperature. This distinct site assignment has been further investigated by Mossbauer and EPR spectroscopies which suggest different spin ground states for molecules 1 and 2. This triclinic phase is also the first report of molecule pairs of the same porphyrin complex interacting in very different ways in the same crystal lattice in that molecule 1 pairs form $\\pi$-$\\pi$ dimers, whereas molecule 2 pairs do not. Part II. A new binucleating picket-fence porphyrin ligand, 5,10,15,20-Tetrakis (o-4-methylimidazole-5-ethylcarboxyl-2-oxy)phenyl) porphyrin, N$\\sb4$-PH$\\sb2$, has been synthesized and characterized to be used eventually as a vehicle to study the structure, function and reactivity patterns of the active site of cytochrome c oxidase. The enzyme itself contains an (Fe(porphyrin)$\\cdots$Cu) binuclear active site of unknown structure. The properties which set N$\\sb4$-PH$\\sb2$ apart from other binucleating picket-fence porphyrin ligands previously prepared as active site ligating molecules are the four authentic imidazole nitrogen donor atoms in the potential binding site for the Cu center and a separation between potential metal binding sites of only 3.5 to 4.0 A, made possible by the ligand&apos;s exceptionally &quot;short&quot; picket-fence arms derived from imidazole-ether linkages."]},{"key":"dc:format.mimetype","label":"Dc Format Mimetype","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["Part I. Spin-state isomerism in crystalline (trifluoromethanesulfonato)(meso-tetraphenylporphinato)iron(III). Part II. Toward refined model compounds for the cytochrome c oxidase active site: A new picket-fence porphyrin with short imidazole pickets"]}]}],"canonical_facts":{"dc:contributor.advisor":["Wilson, Lon J."],"dc:creator":["Gonzalez, Jorge Alberto"],"dc:date.accessioned":["2009-06-04T00:24:00Z"],"dc:date.available":["2009-06-04T00:24:00Z"],"dc:date.issued":["1991"],"dc:description.abstract":["Part I. The unsolvated porphyrin compound (Fe$\\sp{\\rm III}$(TPP)(OSO$\\sb2$CF$\\sb3$)) has been structurally characterized by single-crystal X-ray diffraction in a monoclinic phase at 293 K and in a triclinic phase at 293, 188 and 103 K. While only one type of molecular site is found in the monoclinic phase, the temperature-dependent structural parameters and magnetic susceptibility data (5.82 $\\mu\\sb{\\rm B}$ at 293 K; 4.86 $\\mu\\sb{\\rm B}$ at 20 K) together indicate the existence of two crystallographically and magnetically distinct spin-admixed crystal lattice sites in the triclinic phase. One site (molecule 1) is unique in that its structure is temperature dependent, whereas the second site (molecule 2) has a structure which is essentially independent of temperature. This distinct site assignment has been further investigated by Mossbauer and EPR spectroscopies which suggest different spin ground states for molecules 1 and 2. This triclinic phase is also the first report of molecule pairs of the same porphyrin complex interacting in very different ways in the same crystal lattice in that molecule 1 pairs form $\\pi$-$\\pi$ dimers, whereas molecule 2 pairs do not. Part II. A new binucleating picket-fence porphyrin ligand, 5,10,15,20-Tetrakis (o-4-methylimidazole-5-ethylcarboxyl-2-oxy)phenyl) porphyrin, N$\\sb4$-PH$\\sb2$, has been synthesized and characterized to be used eventually as a vehicle to study the structure, function and reactivity patterns of the active site of cytochrome c oxidase. The enzyme itself contains an (Fe(porphyrin)$\\cdots$Cu) binuclear active site of unknown structure. The properties which set N$\\sb4$-PH$\\sb2$ apart from other binucleating picket-fence porphyrin ligands previously prepared as active site ligating molecules are the four authentic imidazole nitrogen donor atoms in the potential binding site for the Cu center and a separation between potential metal binding sites of only 3.5 to 4.0 A, made possible by the ligand&apos;s exceptionally &quot;short&quot; picket-fence arms derived from imidazole-ether linkages."],"dc:format.mimetype":["application/pdf"],"dc:identifier.uri":["https://hdl.handle.net/1911/16443"],"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":["Inorganic chemistry","Organic chemistry"],"dc:title":["Part I. Spin-state isomerism in crystalline (trifluoromethanesulfonato)(meso-tetraphenylporphinato)iron(III). Part II. Toward refined model compounds for the cytochrome c oxidase active site: A new picket-fence porphyrin with short imidazole pickets"],"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":"2026-07-24T04:10:17Z"}