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020 ▼a 9780438047488
035 ▼a (MiAaPQ)AAI10811290
035 ▼a (MiAaPQ)princeton:12496
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0820 ▼a 540
1001 ▼a Gao, Hongxin.
24510 ▼a Highly Reactive Metal Porphyrazines.
260 ▼a [S.l.] : ▼b Princeton University., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 249 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 79-10(E), Section: B.
500 ▼a Adviser: John T. Groves.
5021 ▼a Thesis (Ph.D.)--Princeton University, 2018.
520 ▼a Nature has evolved a variety of different metalloenzymes for the selective oxygenation of C--H bonds. Cytochrome P450s, for example, are heme proteins that use an oxoiron(IV)-porphyrin pi-radical cation to break strong C--H bonds. Lipoxygenases,
520 ▼a Chapters 2 and 3 concentrate on a highly reactive hydroxo iron(III) porphyrazine complex, (PyPz)FeIII--OH (PyPz = tetramethyl-2,3-pyridino porphyrazine). Fe(II) and Fe(III) porphyrazines were synthesized and characterized. Electrochemical analys
520 ▼a In chapter 4, I report the first example of a fully characterized mononuclear CoIII--OH complex which can abstract benzylic C--H bonds as strong as 82 kcal/mol. This Co(III) porphyrazine was also determined to react with hydrocarbon substrates t
520 ▼a In the final chapter, I extend my research to manganese porphyrazine. (PyPz)Mn has more complicated oxidation states and redox properties. It can catalytically generate chlorine dioxide from chlorite at extremely fast rates with relatively high
590 ▼a School code: 0181.
650 4 ▼a Chemistry.
690 ▼a 0485
71020 ▼a Princeton University. ▼b Chemistry.
7730 ▼t Dissertation Abstracts International ▼g 79-10B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0181
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T14997969 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자