Deciphering the Spatial Arrangement of Metals and Correlation to Reactivity in Multivariate Metal-Organic Frameworks

Qi Liu; Hengjiang Cong; Hexiang Deng

doi:10.1021/jacs.6b08724

Deciphering the Spatial Arrangement of Metals and Correlation to Reactivity in Multivariate Metal-Organic Frameworks

J Am Chem Soc. 2016 Oct 26;138(42):13822-13825. doi: 10.1021/jacs.6b08724. Epub 2016 Oct 13.

Authors

Qi Liu¹, Hengjiang Cong¹, Hexiang Deng¹

Affiliation

¹ Key Laboratory of Biomedical Polymers-Ministry of Education, College of Chemistry and Molecular Sciences and §The Institute for Advanced Studies, Wuhan University , Wuhan 430072, China.

PMID: 27701854
DOI: 10.1021/jacs.6b08724

Abstract

Thirty-six porphyrin-based metal-organic frameworks (MOFs) with composition of (M₃O)₂(TCPP-M)₃ and M₃O trigonal SBUs of various metals, Mg₃O, Mn₃O, Co₃O, Ni₃O, and Fe₃O including mixed-metal SBUs, Mn_xFe_3-xO, Ni_xFe_3-xO, Co_xNi_3-xO, Mn_xCo_3-xO, Mn_xMg_3-xO, and Mn_xNi_3-xO were synthesized and characterized. These multivariate MOFs (MTV-MOFs) were examined by X-ray photoelectron spectroscopy, UV-vis diffuse reflectance spectra, and for the first time, their metal spatial arrangement deciphered and were found to exist in the form of either domains or well-mixed. We find that MTV-MOFs with well-mixed metals in their SBUs, rather than the SBUs having one kind of metal but different from one SBU to another, perform better than the sum of their parts in the test reaction involving the photo-oxidation of 1,5-dihydroxynaphthalene.