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분자활성 촉매반응 연구단
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Room-Temperature Ring-Opening of Quinoline, Isoquinoline, and Pyridine with Low-Valent Titanium

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Title
Room-Temperature Ring-Opening of Quinoline, Isoquinoline, and Pyridine with Low-Valent Titanium
Author(s)
Seung-yeol Baek; Takashi Kurogi; Dahye Kang; Masahiro Kamitani; Seongyeon Kwon; Douglas P. Solowey; Chun-Hsing Chen; Maren Pink; Patrick J. Carroll; Daniel J. Mindiola; Mu-Hyun Baik
Publication Date
2017-09
Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.139, no.36, pp.12804 - 12814
Publisher
AMER CHEMICAL SOC
Abstract
The complex (PNP)Ti=CHtBu(CH2 tBu) (PNP = N[2-PiPr2-4-methylphenyl]2 -) dehydrogenates cyclohexane to cyclohexene by forming a transient low-valent titanium-alkyl species, [(PNP)Ti(CH2 tBu)], which reacts with 2 equiv of quinoline (Q) at room temperature to form H3CtBu and a Ti(IV) species where the less hindered C2=N1 bond of Q is ruptured and coupled to another equivalent of Q. The product isolated from this reaction is an imide with a tethered cycloamide group, (PNP)Ti=N[C18H13N] (1). Under photolytic conditions, intramolecular C - H bond activation across the imide moiety in 1 occurs to form 2, and thermolysis reverses this process. The reaction of 2 equiv of isoquinoline (Iq) with intermediate [(PNP)Ti(CH2 tBu)] results in regioselective cleavage of the C1=N2 and C1 - H bonds, which eventually couple to form complex 3, a constitutional isomer of 1. Akin to 1, the transient [(PNP)Ti(CH2 tBu)] complex can ring-open and couple two pyridine molecules, to produce a close analogue of 1, complex (PNP)Ti=N[C10H9N] (4). Multinuclear and multidimensional NMR spectra confirm structures for complexes 1-4, whereas solid-state structural analysis reveals the structures of 2, 3, and 4. DFT calculations suggest an unprecedented mechanism for ring-opening of Q where the reactive intermediate in the low-spin manifold crosses over to the high-spin surface to access a low-energy transition state but returns to the low-spin surface immediately. This double spin-crossover constitutes a rare example of a two-state reactivity, which is key for enabling the reaction at room temperature. The regioselective behavior of Iq ring-opening is found to be due to electronic effects, where the aromatic resonance of the bicycle is maintained during the key C - C coupling event. © 2017 American Chemical Society
URI
https://pr.ibs.re.kr/handle/8788114/3953
ISSN
0002-7863
Appears in Collections:
Center for Catalytic Hydrocarbon Functionalizations(분자활성 촉매반응 연구단) > Journal Papers (저널논문)
Files in This Item:
124-SYB-DM-Quinoline (1).pdfDownload

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