An rht-type metal-organic framework (MOF) prepared from M(2)(carboxylate)(4) (M = Cu, Co) paddlewheel clusters and a flexible C(3)-symmetric hexacarboxylate ligand with acylamide groups exhibits larger CO(2) uptake, an enhanced heat of adsorption, and higher selectivity toward CO(2)/N(2) in comparison with what was previously observed for an analogous MOF with alkyne groups.
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http://dx.doi.org/10.1021/ja110042b | DOI Listing |
ACS Appl Mater Interfaces
January 2017
Laboratory of Analytical Chemistry, College of Chemistry, Jilin University, Changchun 130012, China.
The surface and interface could be designed to enhance properties of electrocatalysts, and they are regarded as the key characteristics. This report describes surface modification of a bifunctional rht-type metal-organic framework (MOF, Cu-TDPAT) with nanosized electrochemically reduced graphene oxide (n-ERGO). The hybrid strategy results in a Cu-TDPAT-n-ERGO sensor with sensitive and selective response toward hydrogen peroxide (HO).
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November 2016
State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116024, China.
The combination of carbon dioxide capture and chemical fixation in a one-pot process is attractive for both chemists and governments. The cycloaddition of carbon dioxide with epoxides to produce cyclic carbonates is an atomic economical reaction without any side products. By incorporating acylamide to enhance the binding affinity toward CO, new rht-type metal-organic frameworks (MOFs) with (3, 28) and (3, 24) connected units were constructed.
View Article and Find Full Text PDFChem Commun (Camb)
October 2016
State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing, 210023, China and State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing Tech University, Nanjing, 210009, China.
A new, highly porous acylamide-functionalized MOF with a (3,24)-connected rht-type network (HNUST-5) has been synthesized and structurally determined using powder X-ray diffraction. HNUST-5 exhibits a high BET surface area of 3643 m g, and a large CO uptake capability (38.9 mmol g under 36 bar) with an excellent selectivity of CO/CH (7.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
October 2015
Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, 21 Nanyang Link, 637371 (Singapore).
Three highly porous metal-organic frameworks (MOFs) with a uniform rht-type topological network but hierarchical pores were successfully constructed by the assembly of triazole-containing dendritic hexacarboxylate ligands with Zn(II) ions. These transparent MOF crystals present gradually increasing pore sizes upon extension of the length of the organic backbone, as clearly identified by structural analysis and gas-adsorption experiments. The inherent accessibility of the pores to large molecules endows these materials with unique properties for the uptake of large guest molecules.
View Article and Find Full Text PDFChem Commun (Camb)
June 2015
Department of Chemistry, University of South Florida, 4202 E. Flower Avenue, Tampa, Florida 33620, USA.
Two rht-type metal-organic frameworks (MOFs) based upon the tetrazolate moiety and pyrazolate moiety, respectively, have been investigated for carbon dioxide (CO2) adsorption and selective adsorption of CO2 over CH4, which shows that the rht-MOF featuring the pyrazolate moiety demonstrates superior performances compared to the rht-MOF based on the tetrazolate moiety. In spite of more exposed nitrogen atoms in the tetrazolate-based rht-MOF, the counter-intuitive observations of CO2 capture in the two rht-MOFs were interpreted by computational studies, which reveal that the local electric field favours more than the richness of exposed nitrogen atoms for the interactions with CO2 molecules.
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