<?xml version="1.0" encoding="UTF-8" standalone="yes"?><add><doc><field name="objectKind">mycoreobject</field><field name="id">rosdok_disshab_0000003118</field><field name="returnId">rosdok_disshab_0000003118</field><field name="objectProject">rosdok</field><field name="objectType">disshab</field><field name="link">rosdok_derivate_0000219198</field><field name="modified">2024-02-13T11:00:00.996Z</field><field name="created">2024-02-12T10:57:56.089Z</field><field name="modifiedby">MCRJANITOR</field><field name="createdby">editorMS</field><field name="state">published</field><field name="derCount">1</field><field name="derivates">rosdok_derivate_0000219198</field><field name="worldReadable">true</field><field name="worldReadableComplete">true</field><field name="category">derivate_types:fulltext</field><field name="allMeta">Volltext</field><field name="allMeta">fulltext</field><field name="allMeta">wf_edit_epub wf_register_epub</field><field name="category">state:published</field><field name="category.top">state:published</field><field name="allMeta">veröffentlicht</field><field name="allMeta">published</field><field name="allMeta">rosdok/id00004535</field><field name="allMeta">1880511576</field><field name="allMeta">Oau</field><field name="allMeta">2024-02-12</field><field name="allMeta">2024-02-12T11:23:14Z</field><field name="allMeta">rda</field><field name="allMeta">Converted from PICA to MODS using Pica2MODS XSLT Transformer 2.8 [SCM: "0dd72eb2002cd5e1d4341cacf34e92f44f7894b4" "v2.8" "2023-10-12T16:45:19+0200"] with mode 'DEFAULT'.</field><field name="allMeta">Dissertation</field><field name="allMeta">Hochschulschrift</field><field name="allMeta">Selective synthesis of 1,5-pentanediol from furfural derivatives over stable nickel-based catalysts</field><field name="allMeta">Reduced Ni on highly basic lanthanide supports in isopropanol (2-PrOH) was proved to be an efficient catalyst and an economically viable alternative to modified noble metal catalytic systems for the direct hydrogenolysis of tetrahydrofurfuryl alcohol (THFA) and furfural to 1,5-pentanediol (1,5-PeD). For the first time, a continuous catalytic transfer hydrogenolysis (CTH) process for the selective hydrogenolysis of THFA to 1,5-PeD was developed using Ni-La(R) in 2-PrOH. A maximum 1,5-PeD yield of 73% with an productivity of 1.4 mmol g(cat)-1 h-1 was achieved under continuous CTH conditions.</field><field name="allMeta">Ni(0) auf basischen, hydroxidischen Lanthanoid-Trägern in Isopropanol erwies sich als effizienter Katalysator und als wirtschaftlich tragfähige Alternative zu modifizierten Edelmetallkatalysatoren für die Hydrogenolyse von Tetrahydrofurfurylalkohol und Furfural zu 1,5-Pentandiol. Somit wurde zum ersten Mal ein kontinuierlicher CTH-Prozess für die selektive Hydrogenolyse von THFA zu 1,5-PeD unter Verwendung von Ni-La(R) in Isopropanol entwickelt. Unter kontinuierlichen CTH-Bedingungen wurde eine maximale 1,5-PeD-Ausbeute von 73 % und eine Produktivität von 1,4 mmol g(cat)-1 h-1 erreicht.</field><field name="allMeta">Mohammed Abdullah Ahmed</field><field name="allMeta">Al-Yusufi</field><field name="allMeta">1991 -</field><field name="allMeta">VerfasserIn</field><field name="allMeta">aut</field><field name="allMeta">1280442492</field><field name="allMeta">0000-0003-2471-9995</field><field name="allMeta">Thomas</field><field name="allMeta">Werner</field><field name="allMeta">1973 -</field><field name="allMeta">AkademischeR BetreuerIn</field><field name="allMeta">dgs</field><field name="allMeta">129483605</field><field name="allMeta">0000-0001-9025-3244</field><field name="allMeta">Leibniz-Institut für Katalyse e.V. 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Mathematisch-Naturwissenschaftliche Fakultät</field><field name="allMeta">Mathematisch-Natur-&lt;br /&gt;wissenschaftliche Fakultät</field><field name="allMeta">Uni.Rostock.Fakultaet.MNF</field><field name="allMeta">http://d-nb.info/gnd/2147083-2</field><field name="category">licenseinfo:work</field><field name="category.top">licenseinfo:work</field><field name="allMeta">Werk</field><field name="allMeta">work</field><field name="category">licenseinfo:work.rightsreserved</field><field name="category.top">licenseinfo:work.rightsreserved</field><field name="allMeta">alle Rechte vorbehalten</field><field name="allMeta">all rights reserved</field><field name="allMeta">/creativecommons/r/reserved/0.9/88x31.png</field><field name="allMeta">[DE-28]Urheberrechtsschutz 1.0$gRights Statements$uhttp://rightsstatements.org/vocab/InC/1.0/</field><field name="allMeta">http://rightsstatements.org/vocab/InC/1.0/</field><field name="allMeta">http://rightsstatements.org/vocab/InC/1.0/</field><field 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name="category">accesscondition:openaccess</field><field name="category.top">accesscondition:openaccess</field><field name="allMeta">frei zugänglich (Open Access)</field><field name="allMeta">open access</field><field name="allMeta">http://purl.org/coar/access_right/c_abf2</field><field name="allMeta">OA</field><field name="allMeta">free</field><field name="allMeta">info:eu-repo/semantics/openAccess</field><field name="allMeta">[DE-28]Open Access$gControlled Vocabulary for Access Rights$uhttp://purl.org/coar/access_right/c_abf2</field><field name="category">rfc5646:en</field><field name="category.top">rfc5646:en</field><field name="allMeta">Englisch</field><field name="allMeta">English</field><field name="allMeta">eng</field><field name="allMeta">eng</field><field name="mods.title">Selective synthesis of 1,5-pentanediol from furfural derivatives over stable nickel-based catalysts</field><field name="mods.title.main">Selective synthesis of 1,5-pentanediol from furfural derivatives over stable nickel-based catalysts</field><field name="mods.title.subtitle"></field><field name="mods.nameIdentifier">gnd:1280442492</field><field name="mods.nameIdentifier">orcid:0000-0003-2471-9995</field><field name="mods.nameIdentifier">gnd:129483605</field><field name="mods.nameIdentifier">orcid:0000-0001-9025-3244</field><field name="mods.nameIdentifier">gnd:1211348113</field><field name="mods.nameIdentifier">orcid:0000-0002-9271-7425</field><field name="mods.nameIdentifier">gnd:38329-6</field><field name="mods.nameIdentifier">gnd:2147083-2</field><field name="mods.nameIdentifier.top">gnd:1280442492</field><field name="mods.nameIdentifier.top">orcid:0000-0003-2471-9995</field><field name="mods.nameIdentifier.top">gnd:129483605</field><field name="mods.nameIdentifier.top">orcid:0000-0001-9025-3244</field><field name="mods.nameIdentifier.top">gnd:1211348113</field><field name="mods.nameIdentifier.top">orcid:0000-0002-9271-7425</field><field name="mods.nameIdentifier.top">gnd:38329-6</field><field name="mods.nameIdentifier.top">gnd:2147083-2</field><doc><field name="id">rosdok_disshab_0000003118-d1280071e54</field><field name="mods.nameIdentifier">gnd:1280442492</field><field name="mods.nameIdentifier">orcid:0000-0003-2471-9995</field><field name="mods.name">Mohammed Abdullah Ahmed Al-Yusufi</field><field name="mods.name.top">Mohammed Abdullah Ahmed Al-Yusufi</field></doc><doc><field name="id">rosdok_disshab_0000003118-d1280071e70</field><field name="mods.nameIdentifier">gnd:129483605</field><field name="mods.nameIdentifier">orcid:0000-0001-9025-3244</field><field name="mods.name">Thomas Werner</field><field name="mods.name.top">Thomas Werner</field></doc><doc><field name="id">rosdok_disshab_0000003118-d1280071e87</field><field name="mods.nameIdentifier">gnd:1211348113</field><field name="mods.nameIdentifier">orcid:0000-0002-9271-7425</field><field name="mods.name">Tapio Salmi</field><field name="mods.name.top">Tapio Salmi</field></doc><doc><field name="id">rosdok_disshab_0000003118-d1280071e105</field><field name="mods.nameIdentifier">gnd:38329-6</field><field name="mods.name">Universität Rostock</field><field name="mods.name.top">Universität Rostock</field></doc><doc><field name="id">rosdok_disshab_0000003118-d1280071e116</field><field name="mods.nameIdentifier">gnd:2147083-2</field><field name="mods.name">Universität Rostock. Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.name.top">Universität Rostock. Mathematisch-Naturwissenschaftliche Fakultät</field></doc><field name="mods.name">Mohammed Abdullah Ahmed Al-Yusufi</field><field name="mods.name">Thomas Werner</field><field name="mods.name">Tapio Salmi</field><field name="mods.name">Universität Rostock</field><field name="mods.name">Universität Rostock. Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.name.top">Mohammed Abdullah Ahmed Al-Yusufi</field><field name="mods.name.top">Thomas Werner</field><field name="mods.name.top">Tapio Salmi</field><field name="mods.name.top">Universität Rostock</field><field name="mods.name.top">Universität Rostock. Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.author">Mohammed Abdullah Ahmed Al-Yusufi</field><field name="mods.place">Rostock</field><field name="mods.publisher">Universität Rostock</field><field name="mods.genre">epub.dissertation</field><field name="mods.identifier">https://purl.uni-rostock.de/rosdok/id00004535</field><field name="mods.identifier">urn:nbn:de:gbv:28-rosdok_id00004535-9</field><field name="mods.identifier">10.18453/rosdok_id00004535</field><field name="mods.abstract">Reduced Ni on highly basic lanthanide supports in isopropanol (2-PrOH) was proved to be an efficient catalyst and an economically viable alternative to modified noble metal catalytic systems for the direct hydrogenolysis of tetrahydrofurfuryl alcohol (THFA) and furfural to 1,5-pentanediol (1,5-PeD). For the first time, a continuous catalytic transfer hydrogenolysis (CTH) process for the selective hydrogenolysis of THFA to 1,5-PeD was developed using Ni-La(R) in 2-PrOH. A maximum 1,5-PeD yield of 73% with an productivity of 1.4 mmol g(cat)-1 h-1 was achieved under continuous CTH conditions.</field><field name="mods.abstract">Ni(0) auf basischen, hydroxidischen Lanthanoid-Trägern in Isopropanol erwies sich als effizienter Katalysator und als wirtschaftlich tragfähige Alternative zu modifizierten Edelmetallkatalysatoren für die Hydrogenolyse von Tetrahydrofurfurylalkohol und Furfural zu 1,5-Pentandiol. Somit wurde zum ersten Mal ein kontinuierlicher CTH-Prozess für die selektive Hydrogenolyse von THFA zu 1,5-PeD unter Verwendung von Ni-La(R) in Isopropanol entwickelt. Unter kontinuierlichen CTH-Bedingungen wurde eine maximale 1,5-PeD-Ausbeute von 73 % und eine Produktivität von 1,4 mmol g(cat)-1 h-1 erreicht.</field><field name="mods.dateIssued">2022</field><field name="mods.yearIssued">2022</field><field name="mods.note.referee">Thomas Werner (Leibniz-Institut für Katalyse e.V. (LIKAT Rostock)) ; Tapio Salmi (Åbo Akademi University)</field><field name="mods.note.personal_details">[{"name":"Werner, Thomas","affil":"Leibniz-Institut für Katalyse e.V. (LIKAT Rostock)"},{"name":"Salmi, Tapio","affil":"Åbo Akademi University"}]</field><field name="mods.note.statement of responsibility">vorgelegt von Mohammed Abdullah Ahmed Al-Yusufi</field><field name="mods.type">epub.dissertation</field><field name="search_result_link_text">1
        Al-Yusufi_Dissertation_2024.pdf
        
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        rosdok/id000045351880511576Oau2024-02-122024-02-12T11:23:14ZrdaConverted from PICA to MODS using Pica2MODS XSLT Transformer 2.8 [SCM: "0dd72eb2002cd5e1d4341cacf34e92f44f7894b4" "v2.8" "2023-10-12T16:45:19+0200"] with mode 'DEFAULT'.DissertationHochschulschriftSelective synthesis of 1,5-pentanediol from furfural derivatives over stable nickel-based catalystsReduced Ni on highly basic lanthanide supports in isopropanol (2-PrOH) was proved to be an efficient catalyst and an economically viable alternative to modified noble metal catalytic systems for the direct hydrogenolysis of tetrahydrofurfuryl alcohol (THFA) and furfural to 1,5-pentanediol (1,5-PeD). For the first time, a continuous catalytic transfer hydrogenolysis (CTH) process for the selective hydrogenolysis of THFA to 1,5-PeD was developed using Ni-La(R) in 2-PrOH. A maximum 1,5-PeD yield of 73% with an productivity of 1.4 mmol g(cat)-1 h-1 was achieved under continuous CTH conditions.Ni(0) auf basischen, hydroxidischen Lanthanoid-Trägern in Isopropanol erwies sich als effizienter Katalysator und als wirtschaftlich tragfähige Alternative zu modifizierten Edelmetallkatalysatoren für die Hydrogenolyse von Tetrahydrofurfurylalkohol und Furfural zu 1,5-Pentandiol. Somit wurde zum ersten Mal ein kontinuierlicher CTH-Prozess für die selektive Hydrogenolyse von THFA zu 1,5-PeD unter Verwendung von Ni-La(R) in Isopropanol entwickelt. Unter kontinuierlichen CTH-Bedingungen wurde eine maximale 1,5-PeD-Ausbeute von 73 % und eine Produktivität von 1,4 mmol g(cat)-1 h-1 erreicht.Mohammed Abdullah AhmedAl-Yusufi1991 -VerfasserInaut12804424920000-0003-2471-9995ThomasWerner1973 -AkademischeR BetreuerIndgs1294836050000-0001-9025-3244Leibniz-Institut für Katalyse e.V. (LIKAT Rostock)TapioSalmi1957 -AkademischeR BetreuerIndgs12113481130000-0002-9271-7425Åbo Akademi University38329-6Universität Rostock1419 -Grad-verleihende Institutiondgg2147083-2Universität Rostock. Mathematisch-Naturwissenschaftliche FakultätGrad-verleihende Institutiondgghttps://purl.uni-rostock.de/rosdok/id00004535urn:nbn:de:gbv:28-rosdok_id00004535-910.18453/rosdok_id00004535540 Chemie660 Technische ChemieMathematisch-Naturwissenschaftliche Fakultätalle Rechte vorbehaltenNutzungsrechte erteiltLizenz Metadaten: CC0frei zugänglich (Open Access)en2022Universität RostockRostockmonographic202320222024Universitätsbibliothek RostockRostock2024Universitätsbibliothek Rostockhttps://purl.uni-rostock.de/rosdok/id00004535Thomas Werner (Leibniz-Institut für Katalyse e.V. (LIKAT Rostock)) ; Tapio Salmi (Åbo Akademi University)[{"name":"Werner, Thomas","affil":"Leibniz-Institut für Katalyse e.V. (LIKAT Rostock)"},{"name":"Salmi, Tapio","affil":"Åbo Akademi University"}]vorgelegt von Mohammed Abdullah Ahmed Al-Yusufi
              
                Werner, Thomas
                Leibniz-Institut für Katalyse e.V. (LIKAT Rostock)
              
              
                Salmi, Tapio
                Åbo Akademi University
              
            
      
    
  
  
    
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      {"identifier":"urn:nbn:de:gbv:28-rosdok_id00004535-9","type":"dnbUrn","additional":"","service":"RosDokURN","created":"2024-02-12T10:57:57.408Z","registered":"2024-02-13T10:02:04.717Z"}
      MCRJANITOR</field><field name="derivateLabel">fulltext</field><field name="ir.pdffulltext_url">file/rosdok_disshab_0000003118/rosdok_derivate_0000219198/Al-Yusufi_Dissertation_2024.pdf</field><field name="mods.title">Selective synthesis of 1,5-pentanediol from furfural derivatives over stable nickel-based catalysts</field><field name="mods.title.main">Selective synthesis of 1,5-pentanediol from furfural derivatives over stable nickel-based catalysts</field><field name="mods.title.subtitle"></field><field name="mods.nameIdentifier">gnd:1280442492</field><field name="mods.nameIdentifier">orcid:0000-0003-2471-9995</field><field name="mods.nameIdentifier">gnd:129483605</field><field name="mods.nameIdentifier">orcid:0000-0001-9025-3244</field><field name="mods.nameIdentifier">gnd:1211348113</field><field name="mods.nameIdentifier">orcid:0000-0002-9271-7425</field><field name="mods.nameIdentifier">gnd:38329-6</field><field name="mods.nameIdentifier">gnd:2147083-2</field><field name="mods.nameIdentifier.top">gnd:1280442492</field><field name="mods.nameIdentifier.top">orcid:0000-0003-2471-9995</field><field name="mods.nameIdentifier.top">gnd:129483605</field><field name="mods.nameIdentifier.top">orcid:0000-0001-9025-3244</field><field name="mods.nameIdentifier.top">gnd:1211348113</field><field name="mods.nameIdentifier.top">orcid:0000-0002-9271-7425</field><field name="mods.nameIdentifier.top">gnd:38329-6</field><field name="mods.nameIdentifier.top">gnd:2147083-2</field><doc><field name="id">rosdok_disshab_0000003118-d1280071e54</field><field name="mods.nameIdentifier">gnd:1280442492</field><field name="mods.nameIdentifier">orcid:0000-0003-2471-9995</field><field name="mods.name">Mohammed Abdullah Ahmed Al-Yusufi</field><field name="mods.name.top">Mohammed Abdullah Ahmed Al-Yusufi</field></doc><doc><field name="id">rosdok_disshab_0000003118-d1280071e70</field><field name="mods.nameIdentifier">gnd:129483605</field><field name="mods.nameIdentifier">orcid:0000-0001-9025-3244</field><field name="mods.name">Thomas Werner</field><field name="mods.name.top">Thomas Werner</field></doc><doc><field name="id">rosdok_disshab_0000003118-d1280071e87</field><field name="mods.nameIdentifier">gnd:1211348113</field><field name="mods.nameIdentifier">orcid:0000-0002-9271-7425</field><field name="mods.name">Tapio Salmi</field><field name="mods.name.top">Tapio Salmi</field></doc><doc><field name="id">rosdok_disshab_0000003118-d1280071e105</field><field name="mods.nameIdentifier">gnd:38329-6</field><field name="mods.name">Universität Rostock</field><field name="mods.name.top">Universität Rostock</field></doc><doc><field name="id">rosdok_disshab_0000003118-d1280071e116</field><field name="mods.nameIdentifier">gnd:2147083-2</field><field name="mods.name">Universität Rostock. Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.name.top">Universität Rostock. Mathematisch-Naturwissenschaftliche Fakultät</field></doc><field name="mods.name">Mohammed Abdullah Ahmed Al-Yusufi</field><field name="mods.name">Thomas Werner</field><field name="mods.name">Tapio Salmi</field><field name="mods.name">Universität Rostock</field><field name="mods.name">Universität Rostock. Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.name.top">Mohammed Abdullah Ahmed Al-Yusufi</field><field name="mods.name.top">Thomas Werner</field><field name="mods.name.top">Tapio Salmi</field><field name="mods.name.top">Universität Rostock</field><field name="mods.name.top">Universität Rostock. Mathematisch-Naturwissenschaftliche Fakultät</field><field name="mods.author">Mohammed Abdullah Ahmed Al-Yusufi</field><field name="mods.place">Rostock</field><field name="mods.publisher">Universität Rostock</field><field name="mods.genre">epub.dissertation</field><field name="mods.identifier">https://purl.uni-rostock.de/rosdok/id00004535</field><field name="mods.identifier">urn:nbn:de:gbv:28-rosdok_id00004535-9</field><field name="mods.identifier">10.18453/rosdok_id00004535</field><field name="mods.abstract">Reduced Ni on highly basic lanthanide supports in isopropanol (2-PrOH) was proved to be an efficient catalyst and an economically viable alternative to modified noble metal catalytic systems for the direct hydrogenolysis of tetrahydrofurfuryl alcohol (THFA) and furfural to 1,5-pentanediol (1,5-PeD). For the first time, a continuous catalytic transfer hydrogenolysis (CTH) process for the selective hydrogenolysis of THFA to 1,5-PeD was developed using Ni-La(R) in 2-PrOH. A maximum 1,5-PeD yield of 73% with an productivity of 1.4 mmol g(cat)-1 h-1 was achieved under continuous CTH conditions.</field><field name="mods.abstract">Ni(0) auf basischen, hydroxidischen Lanthanoid-Trägern in Isopropanol erwies sich als effizienter Katalysator und als wirtschaftlich tragfähige Alternative zu modifizierten Edelmetallkatalysatoren für die Hydrogenolyse von Tetrahydrofurfurylalkohol und Furfural zu 1,5-Pentandiol. Somit wurde zum ersten Mal ein kontinuierlicher CTH-Prozess für die selektive Hydrogenolyse von THFA zu 1,5-PeD unter Verwendung von Ni-La(R) in Isopropanol entwickelt. Unter kontinuierlichen CTH-Bedingungen wurde eine maximale 1,5-PeD-Ausbeute von 73 % und eine Produktivität von 1,4 mmol g(cat)-1 h-1 erreicht.</field><field name="mods.dateIssued">2022</field><field name="mods.yearIssued">2022</field><field name="mods.note.referee">Thomas Werner (Leibniz-Institut für Katalyse e.V. (LIKAT Rostock)) ; Tapio Salmi (Åbo Akademi University)</field><field name="mods.note.personal_details">[{"name":"Werner, Thomas","affil":"Leibniz-Institut für Katalyse e.V. (LIKAT Rostock)"},{"name":"Salmi, Tapio","affil":"Åbo Akademi University"}]</field><field name="mods.note.statement of responsibility">vorgelegt von Mohammed Abdullah Ahmed Al-Yusufi</field><field name="ir.identifier">[xslt]Saxon</field><field name="recordIdentifier">rosdok/id00004535</field><field name="purl">https://purl.uni-rostock.de/rosdok/id00004535</field><field name="ppn">1880511576</field><field name="doi">10.18453/rosdok_id00004535</field><field name="urn">urn:nbn:de:gbv:28-rosdok_id00004535-9</field><field name="ir.creator.result">Mohammed Abdullah Ahmed Al-Yusufi</field><field name="ir.creator.sort">Al-Yusufi Mohammed Abdullah Ahmed</field><field name="ir.title.result">Selective synthesis of 1,5-pentanediol from furfural derivatives over stable nickel-based catalysts</field><field name="ir.doctype.result">Dissertation</field><field name="ir.doctype_en.result">doctoral thesis</field><field name="ir.originInfo.result">Universität Rostock, 2022</field><field name="ir.abstract300.result">Reduced Ni on highly basic lanthanide supports in isopropanol (2-PrOH) was proved to be an efficient catalyst and an economically viable alternative to modified noble metal catalytic systems for the direct hydrogenolysis of tetrahydrofurfuryl alcohol (THFA) and furfural to 1,5-pentanediol (1,5-PeD).…</field><field name="ir.creator_all">Mohammed Abdullah Ahmed Al-Yusufi</field><field name="ir.title_all">Selective synthesis of 1,5-pentanediol from furfural derivatives over stable nickel-based catalysts</field><field name="ir.location_all">Universitätsbibliothek Rostock</field><field name="ir.location_all">https://purl.uni-rostock.de/rosdok/id00004535</field><field name="ir.creator_all">Mohammed Abdullah Ahmed</field><field name="ir.creator_all">Al-Yusufi</field><field name="ir.creator_all">1991 -</field><field name="ir.creator_all"></field><field name="ir.creator_all">VerfasserIn</field><field name="ir.creator_all">aut</field><field name="ir.creator_all">1280442492</field><field name="ir.creator_all">0000-0003-2471-9995</field><field name="ir.creator_all">Thomas</field><field name="ir.creator_all">Werner</field><field name="ir.creator_all">1973 -</field><field name="ir.creator_all"></field><field name="ir.creator_all">AkademischeR BetreuerIn</field><field name="ir.creator_all">dgs</field><field name="ir.creator_all">129483605</field><field name="ir.creator_all">0000-0001-9025-3244</field><field name="ir.creator_all">Leibniz-Institut für Katalyse e.V. (LIKAT Rostock)</field><field name="ir.creator_all">Tapio</field><field name="ir.creator_all">Salmi</field><field name="ir.creator_all">1957 -</field><field name="ir.creator_all"></field><field name="ir.creator_all">AkademischeR BetreuerIn</field><field name="ir.creator_all">dgs</field><field name="ir.creator_all">1211348113</field><field name="ir.creator_all">0000-0002-9271-7425</field><field name="ir.creator_all">Åbo Akademi University</field><field name="ir.creator_all">38329-6</field><field name="ir.creator_all">Universität Rostock</field><field name="ir.creator_all">1419 -</field><field name="ir.creator_all"></field><field name="ir.creator_all">Grad-verleihende Institution</field><field name="ir.creator_all">dgg</field><field name="ir.creator_all">2147083-2</field><field name="ir.creator_all">Universität Rostock. Mathematisch-Naturwissenschaftliche Fakultät</field><field name="ir.creator_all"></field><field name="ir.creator_all">Grad-verleihende Institution</field><field name="ir.creator_all">dgg</field><field name="ir.identifier">[purl]https://purl.uni-rostock.de/rosdok/id00004535</field><field name="ir.identifier">[urn]urn:nbn:de:gbv:28-rosdok_id00004535-9</field><field name="ir.identifier">[doi]10.18453/rosdok_id00004535</field><field name="ir.oai.setspec.open_access">open_access</field><field name="ir.pubyear_start">2022</field><field name="ir.pubyear_end">2022</field><field name="ir.epoch_class.facet">epoch:21th_century</field><field name="ir.language_class.facet">rfc5646:en</field><field name="ir.doctype_class.facet">doctype:epub.dissertation</field><field name="ir.accesscondition_class.facet">accesscondition:openaccess</field><field name="ir.sdnb_class.facet">SDNB:540</field><field name="ir.sdnb_class.facet">SDNB:660</field><field name="ir.institution_class.facet">institution:unirostock.mnf</field><field name="ir.state_class.facet">state:published</field></doc></add>