Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/19283
Title: Promotion of phosphoester hydrolysis by the Zr-IV-based metal-organic framework UiO-67
Author: Nunes, Patrique
Gomes, Ana C.
Pillinger, Martyn
Goncalves, Isabel S.
Abrantes, Marta
Keywords: CHEMICAL WARFARE AGENTS
BIMETALLIC TETRABENZIMIDAZOLE COMPLEXES
ORGANOPHOSPHATE NERVE AGENTS
MODEL PHOSPHODIESTER
ESTER HYDROLYSIS
SULFUR MUSTARD
DEGRADATION
PHOSPHATE
STABILITY
PHOSPHOTRIESTERASE
Issue Date: 2015
Publisher: ELSEVIER SCIENCE BV
Abstract: The Zr-IV-based metal-organic framework (MOF) UiO-67 has been examined as a promoter of the hydrolysis of phosphoester bonds by using sodium para-nitrophenylphosphate (pNPP) as a model substrate. The reactions were followed by H-1 NMR spectroscopy and performed under mild conditions using 2-100 mol% of the MOF relative to pNPP. All of the systems studied promoted the hydrolysis of pNPP to give para-nitrophenol (pNPh) and inorganic phosphate. A reaction half-life of ca. 30 min was achieved using 17 mol% of UiO-67 at 55 degrees C and 30 mol% at ambient temperature; >= 98% removal of pNPP was reached within 1 h for both reaction temperatures. H-1 NMR spectra of the reaction solutions, together with powder X-ray diffraction, FT-IR spectroscopy and solid-state NMR data for the recovered MOF, revealed that (i) pNPP was encapsulated and then converted to pNPh within the cavities of UiO-67, (ii) both pNPh and inorganic phosphate were retained in the solid promoter, and (iii) the MOF suffered partial structural breakdown into the components Zr6O4(OH)(4) and 4,4'-biphenyldicarboxylate, with partial release of the latter into solution. These structural changes eventually compromized the recyclability of the promoter, although the material could be recovered and reused in a second cycle without loss of activity. (C) 2015 Elsevier Inc. All rights reserved.
Peer review: yes
URI: http://hdl.handle.net/10773/19283
DOI: 10.1016/j.micromeso.2015.01.016
ISSN: 1387-1811
Publisher Version: 10.1016/j.micromeso.2015.01.016
Appears in Collections:CICECO - Artigos



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