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020 ▼a 9780438349568
035 ▼a (MiAaPQ)AAI10842910
035 ▼a (MiAaPQ)unc:18077
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0491 ▼f DP
0820 ▼a 540
1001 ▼a Smith, Jacob B.
24510 ▼a Roles of Cation-macrocycle Interactions in Modulating the Reactivity of Transition Metal Pincer-crown Ether Complexes.
260 ▼a [S.l.] : ▼b The University of North Carolina at Chapel Hill., ▼c 2018
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2018
300 ▼a 191 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 80-01(E), Section: B.
500 ▼a Adviser: Alexander J M Miller.
5021 ▼a Thesis (Ph.D.)--The University of North Carolina at Chapel Hill, 2018.
520 ▼a Pincer-crown ether ligands were designed to exhibit hemilability and also support cation- macrocycle interactions. These ligands feature strong phosphine and phenyl donors, and a pendent aza-crown ether group that provides hemilabile donors that
520 ▼a In chapter 2, nickel catalysts supported by diethylamine- or aza-crown ether-containing aminophosphinite (NCOP) pincer ligands catalyze the insertion of benzaldehyde into a C--H bond of acetonitrile. Neutral tert -butoxide precatalysts are activ
520 ▼a In Chapter 3, the thermochemistry of cation--macrocycle interactions in nickel pincer complexes bearing a hemilabile aza-15-crown-5 or aza-18-crown-6 macrocycle is investigated and applied to cation-controlled reversible ligand binding. Cation-c
520 ▼a In Chapter 4, the impact of post-macrocyclization modification of 1-aza-15-crown 5 through synthetic organic and organometallic tuning is discussed. Binding affinities for Li+ and Na+ salts are reduced substantially moving from the simple organi
590 ▼a School code: 0153.
650 4 ▼a Chemistry.
690 ▼a 0485
71020 ▼a The University of North Carolina at Chapel Hill. ▼b Chemistry.
7730 ▼t Dissertation Abstracts International ▼g 80-01B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0153
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T14999881 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자 ▼b 관리자