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Comparative Study on Temperature-Dependent CO 2 Sorption Behaviors of Two Isostructural N-Oxide-Functionalized 3D Dynamic Microporous MOFs.

Authors :
Zhang WQ
Wang RD
Wu ZB
Kang YF
Fan YP
Liang XQ
Liu P
Wang YY
Source :
Inorganic chemistry [Inorg Chem] 2018 Feb 05; Vol. 57 (3), pp. 1455-1463. Date of Electronic Publication: 2018 Jan 08.
Publication Year :
2018

Abstract

By functionalization of the achiral carboxylate-based pyridine-N ligand 2,2'-bipyridine-3,3'-dicarboxylate (H <subscript>2</subscript> bpda) with N-oxide groups, the axially chiral ligand 2,2'-bipyridine-3,3'-dicarboxylate 1,1'-dioxide (H <subscript>2</subscript> bpdado) has been obtained. On the basis of H <subscript>2</subscript> bpdado and auxiliary N-donor ligands, two isostructural 3D dynamic porous Cu(II) metal-organic frameworks (MOFs), {[Cu <subscript>0.5</subscript> (bpdado) <subscript>0.5</subscript> (L) <subscript>0.5</subscript> ]·3H <subscript>2</subscript> O} <subscript>n</subscript> (L = 1,2-bis(4-pyridyl)ethane (bpa), trans-1,2-bis(4-pyridyl)ethene (bpe) for 1 and 2, respectively), have been synthesized, which contain N-oxide "open donor sites" (ODSs) and carboxyl sites on the pore surfaces. The modification of pyridine-N into the N-oxide group not only transforms the nonporous structure into a porous framework but also endows the N-oxide group with unique charge-separated plus electron-rich character, which may provide an enhanced affinity toward CO <subscript>2</subscript> molecules. Interestingly, both 1 and 2 present reversible structural transformation upon dehydration and rehydration. The adsorption properties of 1 and 2 have been investigated by N <subscript>2</subscript> , H <subscript>2</subscript> , CH <subscript>4</subscript> , and CO <subscript>2</subscript> gases, and they reveal evident adsorption for CO <subscript>2</subscript> and CH <subscript>4</subscript> . Both MOFs have high CO <subscript>2</subscript> uptake, CO <subscript>2</subscript> sorption affinity, and sorption selectivities of CO <subscript>2</subscript> over CH <subscript>4</subscript> and N <subscript>2</subscript> . Remarkably, 1' and 2' exhibit intriguingly comparable temperature-dependent CO <subscript>2</subscript> sorption behaviors that can probably be attributed to the difference in bpa and bpe. First, at 195 K, 1' and 2' exhibit stepwise adsorption and hysteretic desorption behavior for CO <subscript>2</subscript> , but in the second step, the isotherms of 2' display a starting pressure greater than that of 1'. Then, at 298 K, their CO <subscript>2</subscript> isotherms all show nonclassical type I adsorption, while peculiarly, at 273 K, the CO <subscript>2</subscript> isotherm of 1' still exhibits uncommon stepwise adsorption but that of 2' does not. Thus, these temperature-dependent CO <subscript>2</subscript> sorption behaviors indicate that there exist different threshold temperatures and pressures of channel expansion for 1' and 2'.

Details

Language :
English
ISSN :
1520-510X
Volume :
57
Issue :
3
Database :
MEDLINE
Journal :
Inorganic chemistry
Publication Type :
Academic Journal
Accession number :
29308885
Full Text :
https://doi.org/10.1021/acs.inorgchem.7b02844