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Mechanistic Insight into the Heterogeneous Hydrogenation of Furan Derivatives with the use of Parahydrogen Full article

Journal ChemCatChem
ISSN: 1867-3880
Output data Year: 2017, Volume: 10, Number: 5, Pages: 1178-1183 Pages count : 6 DOI: 10.1002/cctc.201701653
Authors Salnikov Oleg G. 1,2 , Kovtunova Larisa M. 3,2 , Skovpin Ivan V. 1,2 , Bukhtiyarov Valerii I. 3,2 , Kovtunov Kirill V. 1,2 , Koptyug Igor V. 1,2
Affiliations
1 Laboratory of Magnetic Resonance Microimaging, International Tomography Center, SB RAS, 3A Institutskaya st., Novosibirsk, 630090 Russia
2 Novosibirsk State University, 2 Pirogova st., Novosibirsk, 630090 Russia
3 Laboratory of Surface Science, Boreskov Institute of Catalysis, SB RAS, 5 Acad. Lavrentiev pr., Novosibirsk, 630090 Russia

Abstract: Parahydrogen-induced polarization (PHIP) was shown to be a useful and unique technique to study the mechanisms of catalytic reactions involving hydrogen. In this paper, PHIP was utilized for mechanistic investigation of the gas-phase hydrogenation of furan, 2,3-dihydrofuran, and 2,5-dihydrofuran over titania-supported Rh, Pd, and Pt catalysts. In the hydrogenation of all three substrates over the Rh/TiO2 catalyst, the PHIP technique revealed the possibility of pairwise addition of two H atoms from the same H2 molecule with the formation of tetrahydrofuran molecules while retaining spin correlation between the added protons. In the hydrogenation of 2,3-dihydrofuran over the Rh/TiO2 catalyst, PHIP effects were detected not only for tetrahydrofuran but also for the reactant (2,3-dihydrofuran) at positions 2 and 3 of the heterocyclic ring. Such unexpected results are direct evidence for the pairwise replacement of the hydrogen atoms in 2,3-dihydorfuran. A probable mechanism for this pairwise replacement includes sequential steps of addition and elimination of hydrogen atoms. In contrast, if the hydrogenation of 2,5-dihydrofuran was performed over Rh/TiO2, PHIP effects were detected for all protons of 2,3-dihydrofuran, implying that 2,3-dihydrofuran could be formed from 2,5-dihydrofuran not only through isomerization of the C=C bond but also through dehydrogenation of 2,5-dihydrofuran to furan with subsequent semihydrogenation.
Cite: Salnikov O.G. , Kovtunova L.M. , Skovpin I.V. , Bukhtiyarov V.I. , Kovtunov K.V. , Koptyug I.V.
Mechanistic Insight into the Heterogeneous Hydrogenation of Furan Derivatives with the use of Parahydrogen
ChemCatChem. 2017. V.10. N5. P.1178-1183. DOI: 10.1002/cctc.201701653 WOS Scopus
Dates:
Published print: Mar 7, 2018
Identifiers:
Web of science: WOS:000426844600042
Scopus: 2-s2.0-85041602872
Citing:
DB Citing
Scopus 20
Web of science 19
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