Assembly of Face Decorated Cuboidal Cages into Ultraporous Structures with Hierarchical Porosity: Accessing MOFs with the Awaited <b>red-a</b> Topology

The rational design of ultraporous metal-organic frameworks (MOFs) with hierarchical pore systems is of great significance but remains highly challenging. MOFs based on the <b>reo</b>-<b>e</b> or <b>red</b> topologies offer such pore architectures through face-shared cuboidal, cuboctahedral, and rhombicuboctahedral cages. Although hypothesized and computationally explored over the past two decades, these solids had not been experimentally realized. Here, we report the first MOFs based on the long-awaited <b>red</b>-<b>a</b> net, denoted as M-<b>red</b>-MOF-1 (M = Fe, Cr). Combining the nearly square yet rectangularly connected 4-c organic linker 4,4',″,4‴-([1,1':4',1″-terphenyl]-3,3'',5,5''-tetrayltetrakis(ethyne-2,1-diyl))tetrabenzoic acid, denoted as H<sub>4</sub>TCEPT, with FeCl<sub>3</sub>·6H<sub>2</sub>O under solvothermal conditions yielded Fe-<b>red</b>-MOF-1 as cubic-like single crystals. Extensive characterization using SCXRD, PXRD, SEM, TEM, gas sorption, TGA, and in-silico structure modeling, confirmed the <b>red</b>-<b>a</b> topology. Argon sorption at 87 K revealed three distinct S-type steps, consistent with the hierarchical pore network and demonstrated an ultrahigh pore volume (3.56 cm<sup>3</sup> g<sup>-1</sup>) and BET area (5081 m<sup>2</sup> g<sup>-1</sup>). Owing to its hierarchical porosity, Fe-<b>red</b>-MOF-1 exhibits excellent hydrogen storage performance with high gravimetric (13.5 wt %) and volumetric (39.5 g·L<sup>-1</sup>) working capacities under temperature and pressure swing conditions (77 K/100 bar → 160 K/5 bar), placing it among the top-performing MOFs. The isostructural Cr-<b>red</b>-MOF-1, obtained postsynthetically, showed a remarkable water uptake of 2.81 g g<sup>-1</sup> at 298 K, surpassing the current top-ranking Cr-<b>soc</b>-MOF-1 (1.95 g g<sup>-1</sup>). Isoreticular analogues, denoted as M-<b>red</b>-MOF-2 (M = Fe, Cr), were also synthesized using the anthracene-based linker H<sub>4</sub>TEBDA. The present work opens new directions for designing ultraporous, hierarchical MOFs based on the <b>red</b>-<b>a</b> net.

Authors

Institutions

Publication Details

Journal
Journal of the American Chemical Society
Published
2025-12-18
DOI
https://doi.org/10.1021/jacs.5c16581
Primary Topic
Metal-Organic Frameworks: Synthesis and Applications
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Assembly of Face Decorated Cuboidal Cages into Ultraporous Structures with Hierarchical Porosity: Accessing MOFs with the Awaited red-a Topology

Christos Tampaxis, George E. Froudakis, Georgia Charalambopoulou, Pantelis N. Trikalitis et al.
Journal of the American Chemical Society
Metal-Organic Frameworks: Synthesis and Applications
article

Assembly of Face Decorated Cuboidal Cages into Ultraporous Structures with Hierarchical Porosity: Accessing MOFs with the Awaited red-a Topology

Christos Tampaxis, George E. Froudakis, Georgia Charalambopoulou, Pantelis N. Trikalitis, Konstantinos G. Froudas, Emmanuel Klontzas, Theodore Steriotis, Constantinos Tsangarakis, Tamsyn Montagnon, Charalampos Livas
article en

Abstract

The rational design of ultraporous metal-organic frameworks (MOFs) with hierarchical pore systems is of great significance but remains highly challenging. MOFs based on the <b>reo</b>-<b>e</b> or <b>red</b> topologies offer such pore architectures through face-shared cuboidal, cuboctahedral, and rhombicuboctahedral cages. Although hypothesized and computationally explored over the past two decades, these solids had not been experimentally realized. Here, we report the first MOFs based on the long-awaited <b>red</b>-<b>a</b> net, denoted as M-<b>red</b>-MOF-1 (M = Fe, Cr). Combining the nearly square yet rectangularly connected 4-c organic linker 4,4',″,4‴-([1,1':4',1″-terphenyl]-3,3'',5,5''-tetrayltetrakis(ethyne-2,1-diyl))tetrabenzoic acid, denoted as H<sub>4</sub>TCEPT, with FeCl<sub>3</sub>·6H<sub>2</sub>O under solvothermal conditions yielded Fe-<b>red</b>-MOF-1 as cubic-like single crystals. Extensive characterization using SCXRD, PXRD, SEM, TEM, gas sorption, TGA, and in-silico structure modeling, confirmed the <b>red</b>-<b>a</b> topology. Argon sorption at 87 K revealed three distinct S-type steps, consistent with the hierarchical pore network and demonstrated an ultrahigh pore volume (3.56 cm<sup>3</sup> g<sup>-1</sup>) and BET area (5081 m<sup>2</sup> g<sup>-1</sup>). Owing to its hierarchical porosity, Fe-<b>red</b>-MOF-1 exhibits excellent hydrogen storage performance with high gravimetric (13.5 wt %) and volumetric (39.5 g·L<sup>-1</sup>) working capacities under temperature and pressure swing conditions (77 K/100 bar → 160 K/5 bar), placing it among the top-performing MOFs. The isostructural Cr-<b>red</b>-MOF-1, obtained postsynthetically, showed a remarkable water uptake of 2.81 g g<sup>-1</sup> at 298 K, surpassing the current top-ranking Cr-<b>soc</b>-MOF-1 (1.95 g g<sup>-1</sup>). Isoreticular analogues, denoted as M-<b>red</b>-MOF-2 (M = Fe, Cr), were also synthesized using the anthracene-based linker H<sub>4</sub>TEBDA. The present work opens new directions for designing ultraporous, hierarchical MOFs based on the <b>red</b>-<b>a</b> net.

Journal of the American Chemical SocietyVol. 147(52)
University of Crete (GR), National Centre of Scientific Research "Demokritos" (GR), National Hellenic Research Foundation (GR)
Openalex Percentile: Top 65%
Metal-Organic Frameworks: Synthesis and Applications
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.