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Department of Physics and Chemistry
Asymmetric Organic Synthesis and Drug Synthesis Laboratory
1. Journal Articles
Synthesis of secondary and tertiary amine-containing MOFs: C-N bond cleavage during MOF synthesis
Hahm, Hyungwoo
;
Ha, Hyeonbin
;
Kim, Seongmin
;
Jung, Byunghyuck
;
Park, Myung Hwan
;
Kim, Youngjo
;
Heo, Jungseok
;
Kim, Min
Department of Physics and Chemistry
Asymmetric Organic Synthesis and Drug Synthesis Laboratory
1. Journal Articles
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Title
Synthesis of secondary and tertiary amine-containing MOFs: C-N bond cleavage during MOF synthesis
Issued Date
2015-08
Citation
Hahm, Hyungwoo. (2015-08). Synthesis of secondary and tertiary amine-containing MOFs: C-N bond cleavage during MOF synthesis. CrystEngComm, 17(30), 5644–5650. doi: 10.1039/c5ce00674k
Type
Article
Keywords
METAL-ORGANIC FRAMEWORK
;
ALKYLATION
;
OXIDATION
;
SULFONAMIDES
;
DEALKYLATION
;
SERIES
;
ACIDS
ISSN
1466-8033
Abstract
Secondary and tertiary amine-containing metal-organic frameworks (MOFs) have been synthesized, and unprecedented C-N bond cleavage phenomena were observed during MOF formation. Utilizing the secondary amine-containing ligand (BDC-NHMe), three new MOFs have been prepared, two of which are zinc(ii)-based, IRMOF-NHMe (IRMOF = isoreticular MOF) and DMOF-1-NHMe (DMOF = dabco MOF), in addition to the zirconium(iv)-based UiO-66-NHMe (UiO = University of Oslo). The tertiary amine-containing ligand (BDC-NMe
2
) was converted to the secondary amine-containing ligand (BDC-NHMe) under both IRMOF and UiO-66 synthesis conditions, indicating an in situ C-N bond cleavage of ligand during MOF formation. In contrast, the tertiary amine-containing DMOF-1-NMe
2
was successfully synthesized and studied for CO
2
adsorption experiments. © The Royal Society of Chemistry 2015.
URI
http://hdl.handle.net/20.500.11750/5226
DOI
10.1039/c5ce00674k
Publisher
Royal Society of Chemistry
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Jung, Byunghyuck
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