TY - JOUR
T1 - Methane reacts with heteropolyacids chemisorbed on silica to produce acetic acid under soft conditions
AU - Sun, Miao
AU - Abou-Hamad, Edy
AU - Rossini, Aaron J.
AU - Zhang, Jizhe
AU - Lesage, Anne
AU - Zhu, Haibo
AU - Pelletier, Jeremie
AU - Emsley, Lyndon
AU - Caps, Valerie
AU - Basset, Jean-Marie
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: The authors acknowledge KAUST Nuclear Magnetic Resonance Core Lab and technical assistance of Dr. Kazuo Yamauchi (NMR). The authors also wish to thank Dr. Aram Amassian, Mr. Ahmed E. Mansour, and Mr. Guy Olivier NGONGANG NDJAWA for their kind help in XPS measurements. M.S. acknowledges support from Dr. Xin Liu in HPA structure drawing. A.J.R acknowledges support from an EU Marie-Curie IIF fellowship (PIIF-GA-2010-274574). This work was supported by funds from King Abdullah University of Science and Technology and SABIC (Saudi Basic Industries Corporation) company.
PY - 2013/1/3
Y1 - 2013/1/3
N2 - Selective functionalization of methane at moderate temperature is of crucial economic, environmental, and scientific importance. Here, we report that methane reacts with heteropolyacids (HPAs) chemisorbed on silica to produce acetic acid under soft conditions. Specially, when chemisorbed on silica, H 4SiW12O40, H3PW12O 40, H4SiMo12O40, and H 3PMo12O40 activate the primary C-H bond of methane at room temperature and atmospheric pressure. With these systems, acetic acid is produced directly from methane, in a single step, in the absence of Pd and without adding CO. Extensive surface characterization by solid-state NMR spectroscopy, IR spectroscopy, cyclic voltammetry, and X-ray photoelectron spectroscopy suggests that C-H activation of methane is triggered by the protons in the HPA-silica interface with concerted reduction of the Keggin cage, leading to water formation and hydration of the interface. This is the simplest and mildest way reported to date to functionalize methane. © 2012 American Chemical Society.
AB - Selective functionalization of methane at moderate temperature is of crucial economic, environmental, and scientific importance. Here, we report that methane reacts with heteropolyacids (HPAs) chemisorbed on silica to produce acetic acid under soft conditions. Specially, when chemisorbed on silica, H 4SiW12O40, H3PW12O 40, H4SiMo12O40, and H 3PMo12O40 activate the primary C-H bond of methane at room temperature and atmospheric pressure. With these systems, acetic acid is produced directly from methane, in a single step, in the absence of Pd and without adding CO. Extensive surface characterization by solid-state NMR spectroscopy, IR spectroscopy, cyclic voltammetry, and X-ray photoelectron spectroscopy suggests that C-H activation of methane is triggered by the protons in the HPA-silica interface with concerted reduction of the Keggin cage, leading to water formation and hydration of the interface. This is the simplest and mildest way reported to date to functionalize methane. © 2012 American Chemical Society.
UR - http://hdl.handle.net/10754/562614
UR - https://pubs.acs.org/doi/10.1021/ja309966j
UR - http://www.scopus.com/inward/record.url?scp=84872580901&partnerID=8YFLogxK
U2 - 10.1021/ja309966j
DO - 10.1021/ja309966j
M3 - Article
C2 - 23268596
SN - 0002-7863
VL - 135
SP - 804
EP - 810
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 2
ER -