| Literature DB >> 27992421 |
Ji Woong Yoon1, Hyunju Chang1, Seung-Joon Lee2, Young Kyu Hwang1, Do-Young Hong1, Su-Kyung Lee1, Ji Sun Lee1, Seunghun Jang1, Tae-Ung Yoon2, Kijeong Kwac3, Yousung Jung3, Renjith S Pillai4, Florian Faucher5, Alexandre Vimont5, Marco Daturi5, Gérard Férey6, Christian Serre6,7, Guillaume Maurin4, Youn-Sang Bae2, Jong-San Chang1,8.
Abstract
Selective dinitrogen binding to transition metal ions mainly covers two strategic domains: biological nitrogen fixation catalysed by metalloenzyme nitrogenases, and adsorptive purification of natural gas and air. Many transition metal-dinitrogen complexes have been envisaged for biomimetic nitrogen fixation to produce ammonia. Inspired by this concept, here we report mesoporous metal-organic framework materials containing accessible Cr(III) sites, able to thermodynamically capture N2 over CH4 and O2. This fundamental study integrating advanced experimental and computational tools confirmed that the separation mechanism for both N2/CH4 and N2/O2 gas mixtures is driven by the presence of these unsaturated Cr(III) sites that allows a much stronger binding of N2 over the two other gases. Besides the potential breakthrough in adsorption-based technologies, this proof of concept could open new horizons to address several challenges in chemistry, including the design of heterogeneous biomimetic catalysts through nitrogen fixation.Entities:
Year: 2016 PMID: 27992421 DOI: 10.1038/nmat4825
Source DB: PubMed Journal: Nat Mater ISSN: 1476-1122 Impact factor: 43.841