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Ketone" ORDER="1" CONTENTIDS="urn:nbn:de:hbz:468-20200730-123636-3"><mets:fptr FILEID="PDF_3552819"/><mets:fptr FILEID="IMG_TEASER_3904635"/><mets:div ID="log3904652" TYPE="section" LABEL="2.1  Übersicht zur Photochemie der Ketone" ORDER="1"><mets:div ID="log3904656" TYPE="section" LABEL="2.1.2  Norrish-Typ-I-Reaktion  -  alpha-Spaltung" ORDER="1"/><mets:div ID="log3904658" TYPE="section" LABEL="2.1.3  Norrish-Typ-II-Reaktion und Yang-Cyclisierung (Norrish-Yang-Reaktion)" ORDER="2"/><mets:div ID="log3904660" TYPE="section" LABEL="2.1.4  Paternó-Büchi-Reaktion mit Oxetanbildung" ORDER="3"/><mets:div ID="log3904662" TYPE="section" LABEL="2.1.5  Photoenolisierung von ortho-Alkyl-substituierten Phenylketonen" ORDER="4"/><mets:div ID="log3904664" TYPE="section" LABEL="2.1.6  Energie-Transfer" ORDER="5"/><mets:div ID="log3904666" TYPE="section" LABEL="2.1.7  Photoinduzierter Elektron-Transfer" ORDER="6"/><mets:div ID="log3904668" TYPE="section" LABEL="2.2.1  Photochemie von Butyrophenon" ORDER="7"/><mets:div ID="log3904670" TYPE="section" LABEL="2.2.2  Photochemische Bildung von 1,2-Dibenzoylethan aus Butyrophenon" ORDER="8"/><mets:div ID="log3904672" TYPE="section" LABEL="2.2.3  Photochemie von Acetophenon" ORDER="9"/><mets:div ID="log3904674" TYPE="section" LABEL="2.2.4  Photoreaktionen von Aceton in flüssiger Phase" ORDER="10"/><mets:div ID="log3904677" TYPE="section" LABEL="2.2.5  Denkbare Reaktionsmöglichkeiten im Butyrophenon-System" ORDER="11"><mets:div ID="log3904678" TYPE="section" LABEL="Die Komponenten des Butyrophenon-Systems könnten involviert sein in verschiedene denkbare Additions-, HAT- und Rekombinationsschritte (zweiseitiges Schema 11).  In die Betrachtung sind u.a. in der Literatur berichtete Reaktionsmöglichkeiten des Aceton..." ORDER="1"/><mets:div ID="log3904680" TYPE="section" LABEL="Anregung, Norrish-Typ-II-Prozess und Tautomerie:" ORDER="2"/><mets:div ID="log3904681" TYPE="section" LABEL="- Weg 1: Nach photochemischer Anregung und ISC liegen die T1-Keton-Spezies als 1,2-Biradikale aufgefasst vor [1,8,19,24,130]." ORDER="3"/><mets:div ID="log3904682" TYPE="section" LABEL="- Weg 2: Die T1-1,2-Biradikal-Situation kann via Energietransfer auf Grundzustands-Ketone übertragen werden [8,19,21,87] (vgl. auch Anhang S.247)." ORDER="4"/><mets:div ID="log3904683" TYPE="section" LABEL="- Weg 3: Der geschilderte Norrish-Typ-II-Prozess führt zur Bildung von ACP-Enol und Ethen (Hauptprodukte) bzw. 1-Phenylcyclobutanol. Das Butyrophenon-1,2-Biradikal fungiert dabei als intramolekularer reaktiver HAT-Akzeptor [1–3,5–12,15]." ORDER="5"/><mets:div ID="log3904684" TYPE="section" LABEL="- Weg 4: Enolformen können thermisch ketonisieren [19,58,94,131,132]." ORDER="6"/><mets:div ID="log3904685" TYPE="section" LABEL="HAT-Schritte:" ORDER="7"/><mets:div ID="log3904686" TYPE="section" LABEL="- Weg 5: Keton-1,2-Biradikale könnten als sehr reaktive HAT-Akzeptoren fungieren, wobei sie in Ketylradikale überführt werden [8,16,23,24,58,61,108,133,134]." ORDER="8"/><mets:div ID="log3904687" TYPE="section" LABEL="- Weg 6: Grundzustands-Ketone könnten als C-HAT-Donatoren fungieren, wobei sie in PAR überführt würden [17,18,23,111,121,122,126,135]." ORDER="9"/><mets:div ID="log3904688" TYPE="section" LABEL="Für die Abstrahierbarkeit des α-C-H-Atoms spricht die „allylische“ Delokalisierbarkeit des gebildeten Radikals [111], dagegen spricht die Delokalisation zum elektronegativen O-Atomrumpf. Im Aceton-System [23] ist die α-C-H-Abstraktion von Grundzustand..." ORDER="10"/><mets:div ID="log3904689" TYPE="section" LABEL="Überlegungen zur α-C-Substitution der aromatischen Ketone des Butyrophenon-Systems: Das Acetophenon-System kann als ein Maß für die Effizienz der α-C-H-Abstraktion im Fall ohne Alkyl-Substitution betrachtet werden. Im ethyl-substituierten Butyrophenon..." ORDER="11"/><mets:div ID="log3904691" TYPE="section" LABEL="- Weg 7: Enolformen könnten als O-HAT-Donatoren fungieren, wobei sie in PAR überführt würden [16,97,99,135,139]." ORDER="12"/><mets:div ID="log3904692" TYPE="section" LABEL="Becker postulierte die Hypothese [16], dass die photochemische Disproportionierung von Acetophenon zu 1,2-Dibenzoylethan (via PAR) und ACP-Pinakol (via Ketylradikale) erst durch phenol-katalysierte Bildung des O-HAT-Donators ACP-Enol effizient ablaufe..." ORDER="13"/><mets:div ID="log3904693" TYPE="section" LABEL="- Weg 8: PAR könnten als HAT-Akzeptoren wirken, wobei Grundzustands-Ketone gebildet würden [23,113,114,116,117,121,122]." ORDER="14"/><mets:div ID="log3904694" TYPE="section" LABEL="- Weg 9: Ketylradikale könnten als HAT-Akzeptoren wirken und zur Alkoholstufe reduziert werden, wobei Hydrole bzw. 1-Phenylbutanol und 1-Phenylethanol gebildet würden [19,24,57–59,61,121,122,141,142]." ORDER="15"/><mets:div ID="log3904695" TYPE="section" LABEL="- Weg 10: Ketylradikale könnten als O-HAT-Donatoren agieren, wodurch Grundzustands-Ketone gebildet würden [8,56]." ORDER="16"/><mets:div ID="log3904696" TYPE="section" LABEL="- Weg 11: Ketylradikale könnten als C-HAT-Donatoren agieren, wodurch Enolformen gebildet würden (Analogieschluss) [8,23,57–59]. Zwei Ketylradikale könnten disproportionieren („Dismutation“) [127,135].  Acetophenon läge im thermodynamischen Gleichgewic..." ORDER="17"/><mets:div ID="log3904699" TYPE="section" LABEL="Beim Butyrophenon-System ist Letzteres a priori betrachtet möglicherweise nicht ganz identisch, da der Ethylrest an der α-Position sowohl die α-C-H-Bindung destabilisieren bzw. radikalisch abstrahierbar machen könnte als auch eine eventuell gebildete ..." ORDER="18"/><mets:div ID="log3904701" TYPE="section" LABEL="- Weg 12: BTP-1,4-Biradikale könnten an der 4-Position als HAT-Akzeptoren beteiligt sein, wobei sie in Ketylradikale überführt würden." ORDER="19"/><mets:div ID="log3904702" TYPE="section" LABEL="- Weg 13: Hydrole bzw. Alkohole könnten als HAT-Donatoren fungieren, wobei sie wieder in Ketylradikale konvertiert würden [2,8,19,22,24,59,60,63,108–110,145–147]." ORDER="20"/><mets:div ID="log3904703" TYPE="section" LABEL="HAT von Ketylradikalen zu Grundzustands-Ketonen („Ketylradikal-Transfer“):" ORDER="21"/><mets:div ID="log3904704" TYPE="section" LABEL="Additionen:" ORDER="22"/><mets:div ID="log3904706" TYPE="section" LABEL="- Weg 15: Keton-1,2-Biradikale könnten an Enolformen via Paternó-Büchi-Reaktion addieren, so dass Oxetanbildung auftritt [23,58,78,119–121,148]." ORDER="23"/><mets:div ID="log3904707" TYPE="section" LABEL="- Weg 16: PAR könnten an die elektronenreichen Doppelbindungen von Enolformen addieren, analog zur radikalischen Polymerisation von Styrol [41,149] 11F  (Acetophenon-Enol kann als 1-Hydroxystyrol aufgefasst werden [132].) bzw. zur allgemeinen Reaktion..." ORDER="24"/><mets:div ID="log3904708" TYPE="section" LABEL="- Weg 17: Ketylradikale könnten an Enolformen bzw. Olefinfunktionen addieren [154–159]. Das entstandene Ketylradikal könnte auf einem der beschriebenen Wege in die Ketoform umwandeln, so dass „gemischte Rekombinationsprodukte“ entstünden." ORDER="25"/><mets:div ID="log3904709" TYPE="section" LABEL="Rekombinationen:" ORDER="26"/><mets:div ID="log3904710" TYPE="section" LABEL="- Weg 18: Zwei PAR könnten zu 1,2-Dibenzoylethanen rekombinieren. Für die Dimerisierung zweier Acetophenon-PAR zu 1,2-Dibenzoylethan sind mehrere literaturbekannte Beispiele beschrieben  [16,112–116], und die Entsprechung wurde auch beim Aceton-System..." ORDER="27"/><mets:div ID="log3904711" TYPE="section" LABEL="- Weg 19: Zwei Ketylradikale könnten zu Pinakolen rekombinieren [2,8,16,19,21–24,60,63,109,110,133]." ORDER="28"/><mets:div ID="log3904712" TYPE="section" LABEL="- Weg 20: PAR könnte mit Ketylradikalen zu „gemischten Rekombinationsprodukten“ reagieren [23,121,122]. Gemischte Rekombinationsprodukte könnten auch thermisch aus gebildeten Oxetanen entstehen, die geminale O-Atome aufweisen [23] (nicht gezeigt). Bec..." ORDER="29"/><mets:div ID="log3904713" TYPE="section" LABEL="Weg via substituierte 1,2-Dibenzoylethane:" ORDER="30"/><mets:div ID="log3904714" TYPE="section" LABEL="- Weg 21: Ethyl-substituierte 1,2-Dibenzoylethane (3,4-Dibenzoylhexan und 1,2-Dibenzoylbutan) könnten via Norrish-Typ-II-Reaktion Ethen abspalten, wodurch nach Tautomerisierung 1,2-Dibenzoylethan gebildet würde [8,9,19,24]. Jedoch sind auch andere Rea..." ORDER="31"/></mets:div><mets:div ID="log3904715" TYPE="section" LABEL="2.2.6  Reaktionsverlauf bei Enolisierung von Acetophenon durch alkoholische Katalyse" ORDER="12"/><mets:div ID="log3904719" TYPE="section" LABEL="2.2.7  Denkbarer Kupplungsweg via Light Absorbing Transients" ORDER="13"><mets:div ID="log3904720" TYPE="section" LABEL="- Weg L3: Der gleiche Analogieschluss zum Acetophenon- und Benzophenon-Themenkreis gilt für die Bildung von intermolekularen LATs. Im Acetophenon-System ist davon auszugehen, dass es durch Bestrahlung zu einer (geringen) Bildung von Ketylradikalen und..." ORDER="1"/></mets:div><mets:div ID="log3904724" TYPE="section" LABEL="2.2.8  Denkbare Kupplungswege via photoinduzierte Elektronentransfer-Schritte" ORDER="14"/><mets:div ID="log3904731" TYPE="section" LABEL="3.1.1  Erarbeitung eines analytischen Trennsystems" ORDER="15"/><mets:div ID="log3904733" TYPE="section" LABEL="3.1.2  Erarbeitung eines präparativen Trennsystems" ORDER="16"/><mets:div ID="log3904735" TYPE="section" LABEL="3.1.3  2-Phenacylacetonitril (Fraktion P1)" ORDER="17"/><mets:div ID="log3904738" TYPE="section" LABEL="3.1.4  Pinakol-Komponenten (Fraktionen P4-P9)" ORDER="18"/><mets:div ID="log3904740" TYPE="section" LABEL="3.1.5  1,2-Dibenzoylethan (Fraktion P5)" ORDER="19"/><mets:div ID="log3904741" TYPE="section" LABEL="3.1.6  Komponenten in den Fraktionen P10 und P11" ORDER="20"/></mets:div><mets:div ID="log3904744" TYPE="section" LABEL="3.1.7  Massen- bzw. H-Atom-Bilanz der Komponenten" ORDER="2"><mets:div ID="log3904746" TYPE="section" LABEL="3.1.8  Untersuchung der Gasphase der Reaktionsmischung" ORDER="1"/></mets:div><mets:div ID="log3904748" TYPE="section" LABEL="3.2  Zeitlicher Verlauf der Komponentensignale" ORDER="3"><mets:div ID="log3904755" TYPE="section" LABEL="3.2.1  Untersuchung zum Vorliegen einer zeitlich verzögerten 1,2-Dibenzoylethan-Bildung" ORDER="1"/></mets:div><mets:div ID="log3904758" TYPE="section" LABEL="3.3  Variation der Reaktionsparameter der photochemischen Umsetzung des Butyrophenon-Systems" ORDER="4"><mets:div ID="log3904760" TYPE="section" LABEL="3.3.1  Variation der Edukt-Konzentration" ORDER="1"/><mets:div ID="log3904762" TYPE="section" LABEL="3.3.2  Tabellarische Aufstellung der Parameter-Variationsexperimente und Clusteranalyse" ORDER="2"/><mets:div ID="log3904765" TYPE="section" LABEL="3.3.3  Temperaturabhängigkeit" ORDER="3"/><mets:div ID="log3904767" TYPE="section" LABEL="3.3.4  Untersuchungen zum Wassergehalt des Lösemittels" ORDER="4"><mets:div ID="log3904768" TYPE="section" LABEL="Die meisten Experimente dieser Arbeit wurden aufgrund pragmatischer Überlegungen bzw. finanzieller und zeitlicher Rahmenbedingungen in Acetonitril der Qualität für die Chromatographie (Spezifikation: ≥ 99,9%, H2O ≤ 0,02%, „Normalfall“) durchgeführt, u..." ORDER="1"/><mets:div ID="log3904770" TYPE="section" LABEL="- „Wasserfreier Acetonitril“ (Spezifikation: 99,8%, max. 0,001% (w/w) H2O), kommerziell erworben)." ORDER="2"/><mets:div ID="log3904771" TYPE="section" LABEL="- „Drastische Wasser-Anwesenheit“ (1:1-(v/v)-Mischung aus ACN und H2O)." ORDER="3"/><mets:div ID="log3904772" TYPE="section" LABEL="Beim Vergleich (normal vs. H2O-frei, jew. UVB) bei jeweils identischen Temperaturen (Clusteranalyse-Eintrag 12 vs. 15 bzw. 13 vs. 16) findet der Umsatz jeweils rascher statt und weniger 1,2-Dibenzoyl-ethan entsteht. Bezieht man jeweils die kürzere Ums..." ORDER="4"/><mets:div ID="log3904773" TYPE="section" LABEL="Beim Vergleich der „H2O-freien“-Experimente untereinander (Einträge 15 vs. 16, jew. UVB) zeigt sich bei Variation der Temperatur, dass bei 20 C (Eintrag 15) der vollständige Umsatz überraschender-weise und aus unbekannten Gründen früher auftritt als b..." ORDER="5"/><mets:div ID="log3904774" TYPE="section" LABEL="Beim Vergleich der „H2O-freien“-Experimente untereinander (Einträge 10, UVA-LED vs. 16, UVB) führt längerwelliges bzw. intensiveres Licht bei vergleichbarer Umsatzdauer scheinbar zu einer höheren 1,2-Dibenzoylethan-Bildung. Es ist nicht klar schlussfo..." ORDER="6"/></mets:div><mets:div ID="log3904775" TYPE="section" LABEL="3.3.5  Strahlungsintensitäts-Abhängigkeit der 1,2-Dibenzoylethan-Bildung" ORDER="5"><mets:div ID="log3904777" TYPE="section" LABEL="Bei geringer Strahlungsintensität: In einer zweiten Experimentalreihe wurde die Intensitäts-abhängigkeit in Richtung schwacher Intensitäten untersucht: Bei 20 C (Quarz-Kühlmantel) wurde die direkte Strecke zwischen einer UVB-Lampe und dem Quarz-Reakti..." ORDER="1"/></mets:div><mets:div ID="log3904779" TYPE="section" LABEL="3.3.6  Wellenlängenabhängigkeit der 1,2-Dibenzoylethan-Bildung" ORDER="6"/><mets:div ID="log3904781" TYPE="section" LABEL="3.3.7  Umsetzung von Butyrophenon in wasserfreiem Benzol" ORDER="7"/><mets:div ID="log3904784" TYPE="section" LABEL="3.3.8  Zusammenfassung der Ergebnisse zur Variation der Reaktionsparameter der photochemischen Umsetzung des Butyrophenon-Systems" ORDER="8"/></mets:div><mets:div ID="log3904786" TYPE="section" LABEL="3.4  Untersuchungen zu den Bildungswegen von 1,2-Dibenzoylethanen und der Pinakole" ORDER="5"><mets:div ID="log3904787" TYPE="section" LABEL="3.4.1  Untersuchung des reinen Acetophenon-Systems" ORDER="1"/><mets:div ID="log3904792" TYPE="section" LABEL="3.4.2  Untersuchung des reinen Propiophenon-Systems" ORDER="2"/><mets:div ID="log3904795" TYPE="section" LABEL="3.4.3  Untersuchungen zur Produktbildung in einem gemischten Butyrophenon-Propiophenon-System" ORDER="3"/><mets:div ID="log3904799" TYPE="section" LABEL="3.4.4  Untersuchung der Bildung von 1,2-Dibenzoylethan aus 3,4-Dibenzoylhexan und 1,2-Dibenzoylbutan" ORDER="4"/><mets:div ID="log3904805" TYPE="section" LABEL="3.4.5  Einbau-Experimente isotopenmarkierter exogener Grundkörper in gebildetes 1,2-Dibenzoylethan bzw. in gebildete Pinakole" ORDER="5"/><mets:div ID="log3904812" TYPE="section" LABEL="3.4.6  Experimente zur LAT-Hypothese" ORDER="6"/><mets:div ID="log3904815" TYPE="section" LABEL="3.4.7  Kreuzexperimente mit bekannten Komponenten des Butyrophenon-Systems und mit 1-Naphthol" ORDER="7"/><mets:div ID="log3904819" TYPE="section" LABEL="3.5.1  Aromatische Butyrophenon-Analoga" ORDER="8"/><mets:div ID="log3904821" TYPE="section" LABEL="3.5.2  Aliphatische Butyrophenon-Analoga" ORDER="9"/></mets:div><mets:div ID="log3904823" TYPE="section" LABEL="3.6  Experimente zur Photoreaktivität von 1,2-Dibenzoylethan" ORDER="6"><mets:div ID="log3904824" TYPE="section" LABEL="3.6.1  Bestrahlung von 1,2-Dibenzoylethan alleine ohne Reaktionspartner" ORDER="1"/><mets:div ID="log3904826" TYPE="section" LABEL="3.6.2  Bestrahlung von 1,2-Dibenzoylethan in Anwesenheit von 2-Propanol" ORDER="2"/><mets:div ID="log3904830" TYPE="section" LABEL="3.6.3  Bestrahlung von 1,2-Dibenzoylethan in Anwesenheit von Vinylacetat" ORDER="3"/></mets:div><mets:div ID="log3904833" TYPE="section" LABEL="3.7  Synthese und Photoumsetzung von 2-(2-Phenyloxiran-2-yl)-butyrophenon" ORDER="7"/><mets:div ID="log3904836" TYPE="section" LABEL="4  Diskussion" ORDER="8"><mets:div ID="log3904837" TYPE="section" LABEL="4.1  Bildungsmechanismus der Photoredox-Kupplungsprodukte" ORDER="1"><mets:div ID="log3904838" TYPE="section" LABEL="4.1.1  Ableitung des mechanistischen Bildungswegs aus den Ergebnissen" ORDER="1"/><mets:div ID="log3904845" TYPE="section" LABEL="4.1.2  Wahrscheinlichkeitsbetrachtung zu PET-Wegen" ORDER="2"/><mets:div ID="log3904848" TYPE="section" LABEL="4.1.3  Denkbare intermolekulare Schritte der Butyrophenon-1,4-Biradikale und von Folgespezies" ORDER="3"/><mets:div ID="log3904850" TYPE="section" LABEL="4.1.4  Abwesenheit von Oxetanen, Hydrolen und von gemischten Rekombinationsprodukten" ORDER="4"/><mets:div ID="log3904852" TYPE="section" LABEL="4.1.5  Weitere zum vorgeschlagenen mechanistischen Ablauf kongruente Aspekte" ORDER="5"/></mets:div><mets:div ID="log3904858" TYPE="section" LABEL="4.3  Experimente zur Photoumsetzung von 1,2-Dibenzoylethan" ORDER="2"/><mets:div ID="log3904860" TYPE="section" LABEL="4.4  Gesamtfazit zur Bildung von 1,2-Dibenzoylethan" ORDER="3"/></mets:div><mets:div ID="log3904863" TYPE="section" LABEL="5  Didaktischer Teil" ORDER="9"><mets:div ID="log3904864" TYPE="section" LABEL="5.1  Entwicklung eines Lehrkonzepts zur Erschließung von Prinzipien der Photochemie am Beispiel der Photochemie von Ketonen" ORDER="1"/><mets:div ID="log3904867" TYPE="section" LABEL="5.2  Teil 1 - Kostengünstiges Equipment als Basis der Integration von Photoreaktionen in die Lehre" ORDER="2"/><mets:div ID="log3904873" TYPE="section" LABEL="5.3  Teil 2 - Photoreduktion bzw. Photopinakolisierung von Benzophenon und Fluoreszenzlöschung von Aesculin - Modellreaktionen zur Vermittlung zentraler Prinzipien der Photochemie" ORDER="3"/><mets:div ID="log3904879" TYPE="section" LABEL="5.4  Teil 3 - Butyrophenon als Modellverbindung für durch Forschendes Lernen erschließbare weiterführende Konzepte der Photochemie - Radikalreaktionstypen und intra- vs. intermolekulare Konkurrenz" ORDER="4"><mets:div ID="log3904881" TYPE="section" LABEL="5.4.1  Didaktisch reduzierter Reaktionsmechanismus für den Einsatz an Hochschulen" ORDER="1"/><mets:div ID="log3904884" TYPE="section" LABEL="5.4.2  Experimente zur Photoumsetzung von Butyrophenon" ORDER="2"/><mets:div ID="log3904908" TYPE="section" LABEL="5.4.4  Didaktisch reduzierter Reaktionsmechanismus für den Einsatz in Gymnasien" ORDER="3"/></mets:div></mets:div><mets:div ID="log3904916" TYPE="section" LABEL="8  Experimenteller Teil" ORDER="10"><mets:div ID="log3904917" TYPE="section" LABEL="8.1  Analytik" ORDER="1"/><mets:div ID="log3904919" TYPE="section" LABEL="8.2  Materialien" ORDER="2"><mets:div ID="log3904920" TYPE="section" LABEL="8.2.1  Geräte" ORDER="1"/><mets:div ID="log3904923" TYPE="section" LABEL="8.2.2  Chemikalien und Labormaterialien" ORDER="2"/></mets:div><mets:div ID="log3904926" TYPE="section" LABEL="8.3  Methoden und Arbeitstechniken" ORDER="3"><mets:div ID="log3904927" TYPE="section" LABEL="8.3.1  Allgemeine Arbeitstechnik - Bestrahlung von präparativen Ansätzen" ORDER="1"/><mets:div ID="log3904929" TYPE="section" LABEL="8.3.2  Allgemeine Arbeitstechnik - Bestrahlung von Mikromaßstabsansätzen" ORDER="2"/><mets:div ID="log3904931" TYPE="section" LABEL="8.3.3  Bestrahlung und Probenvorbereitung von 2-Pentanon oder Aceton" ORDER="3"/><mets:div ID="log3904932" TYPE="section" LABEL="8.3.4  Analytisches HPLC-Trennsystem „für das 2-Pentanon-System“" ORDER="4"/><mets:div ID="log3904934" TYPE="section" LABEL="8.3.5  Analytisches HPLC-Trennsystem „für das Butyrophenon-System“" ORDER="5"/><mets:div ID="log3904935" TYPE="section" LABEL="8.3.6  „Anfängliches Butyrophenon-Trennsystem 1“" ORDER="6"/><mets:div ID="log3904937" TYPE="section" LABEL="8.3.7  „Anfängliches Butyrophenon-Trennsystem 2“" ORDER="7"/><mets:div ID="log3904938" TYPE="section" LABEL="8.3.8  Allgemein Arbeitstechnik - Aufstock-Methodik" ORDER="8"/></mets:div><mets:div ID="log3904939" TYPE="section" LABEL="8.4  Präparative photochemische Umsetzungen" ORDER="4"><mets:div ID="log3904940" TYPE="section" LABEL="8.4.1  Bestrahlung von Butyrophenon in Acetonitril („Butyrophenon-System“)" ORDER="1"/><mets:div ID="log3904943" TYPE="section" LABEL="8.4.1.1   2-Phenacylacetonitril (Fraktion P1)" ORDER="2"/><mets:div ID="log3904947" TYPE="section" LABEL="8.4.1.2   Acetophenon-Pinakol (Fraktionen P4 und P5)" ORDER="3"/><mets:div ID="log3904951" TYPE="section" LABEL="8.4.1.3   1,2-Dibenzoylethan (Fraktion P5)" ORDER="4"/><mets:div ID="log3904955" TYPE="section" LABEL="8.4.1.4   Acetophenon-Butyrophenon-Pinakol („gemischtes Pinakol“, Fraktionen P6 und P7)" ORDER="5"/><mets:div ID="log3904959" TYPE="section" LABEL="8.4.1.5   Butyrophenon-Pinakol (Fraktionen P8 und P9)" ORDER="6"/><mets:div ID="log3904963" TYPE="section" LABEL="8.4.1.6   3-Methyl-1,3,4-triphenyl-2,7-dioxabicyclo[2.2.1]heptan" ORDER="7"/><mets:div ID="log3904969" TYPE="section" LABEL="8.4.2  Photochemische Umsetzung von 1,2-Dibenzoylethan mit 2-Propanol" ORDER="8"/><mets:div ID="log3904971" TYPE="section" LABEL="8.4.2.1   1,4-Diphenyl-2,3-dioxabicyclo[2.2.0]hexan (Fraktion F3c)" ORDER="9"/><mets:div ID="log3904974" TYPE="section" LABEL="8.4.2.2   para-(2-Propanol-2-yl)-1,2-dibenzoylethan (Fraktion F3d)" ORDER="10"/><mets:div ID="log3904978" TYPE="section" LABEL="8.4.2.3   1-(4-(1-Hydroxy-4-oxo-1,4-diphenylbutyl)phenyl)-4-phenylbutan-1,4-dion" ORDER="11"/><mets:div ID="log3904980" TYPE="section" LABEL="und 2,3-Dihydronaphthalin-1,4-dion (beide möglicherweise, Fraktion F5)" ORDER="12"/><mets:div ID="log3904982" TYPE="section" LABEL="8.4.2.4   3-(Propiophenon-3-yl)-1,3,4-triphenyl-2,7-dioxabicyclo[2.2.1]heptan (Fraktionen F6a, F7, F10 und F11) und 3,3-Dimethyl-1,4-diphenyl-2,7-dioxabicyclo[2.2.1]heptan (möglicherw., Fraktionen F6a, F7 und F10)" ORDER="13"/><mets:div ID="log3904987" TYPE="section" LABEL="8.4.2.5   3-Methyl-1,3,4-triphenyl-2,7-dioxabicyclo[2.2.1]heptan (Fraktion F8)" ORDER="14"/><mets:div ID="log3904989" TYPE="section" LABEL="8.4.2.6   1,2-bis(1,3,4-Triphenyl-2,7-dioxabicyclo[2.2.1]heptan-3-yl)ethan  (möglicherw., Fraktion F12)" ORDER="15"/><mets:div ID="log3904990" TYPE="section" LABEL="8.4.3  Photochemische Umsetzung von 1,2-Dibenzoylethan mit Vinylacetat" ORDER="16"/><mets:div ID="log3904998" TYPE="section" LABEL="8.5.1  Darstellung von 3,4-Dibenzoylhexan und 1,2-Dibenzoylbutan" ORDER="17"/><mets:div ID="log3905003" TYPE="section" LABEL="8.5.2  Darstellung von 2-(13C)-Acetophenon, 1-(Phenyl-D5)-Acetophenon und 1-(Phenyl-D5)-Propiophenon" ORDER="18"/><mets:div ID="log3905008" TYPE="section" LABEL="8.5.3  Darstellung von 2-(2-Phenyloxiran-2-yl)-butyrophenon" ORDER="19"/></mets:div></mets:div><mets:div ID="log3905013" TYPE="section" LABEL="9  Verzeichnisse" ORDER="11"><mets:div ID="log3905014" TYPE="section" LABEL="9.1  Abbildungsverzeichnis" ORDER="1"/><mets:div ID="log3905019" TYPE="section" LABEL="9.2  Diagrammverzeichnis" ORDER="2"/><mets:div ID="log3905021" TYPE="section" LABEL="9.3  Schemataverzeichnis" ORDER="3"/><mets:div ID="log3905023" TYPE="section" LABEL="9.4  Tabellenverzeichnis" ORDER="4"/></mets:div><mets:div ID="log3905026" TYPE="section" LABEL="10  Anhang" ORDER="12"><mets:div ID="log3905027" TYPE="section" LABEL="10.1  Literaturinformationen zur Frage nach HAT-, PET-, PCET- und CT-Schritten bzw. zur Frage nach 3nπ*- und 3ππ*-Zuständen" ORDER="1"/><mets:div ID="log3905031" TYPE="section" LABEL="10.2  PET-Abschätzung zur Eingrenzung plausibler PET-Schritte" ORDER="2"/><mets:div ID="log3905036" TYPE="section" LABEL="10.3  Literaturinformationen zu kinetischen Daten und vorgenommene Abschätzungen zu betrachteten Schritten im Butyrophenon-System" ORDER="3"/><mets:div ID="log3905041" TYPE="section" LABEL="10.4  Daten in tabellarischer Form" ORDER="4"/></mets:div><mets:div ID="log3905051" TYPE="section" LABEL="11  Referenzen" ORDER="13"/></mets:div></mets:structMap><mets:structLink><mets:smLink xlink:from="log3552819" xlink:to="physroot"/><mets:smLink xlink:from="log3552819" xlink:to="phys3904635"/><mets:smLink xlink:from="log3552819" xlink:to="phys3904636"/><mets:smLink xlink:from="log3552819" xlink:to="phys3904637"/><mets:smLink xlink:from="log3552819" xlink:to="phys3904638"/><mets:smLink xlink:from="log3552819" xlink:to="phys3904639"/><mets:smLink xlink:from="log3552819" xlink:to="phys3904640"/><mets:smLink xlink:from="log3552819" xlink:to="phys3904641"/><mets:smLink xlink:from="log3552819" xlink:to="phys3904642"/><mets:smLink xlink:from="log3552819" xlink:to="phys3904643"/><mets:smLink 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