High-Field 17O MAS NMR Investigation of Phosphonic Acid Monolayers on Titania
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Brodard-Severac, Florence
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Univ Montpellier 2, Inst Charles Gerhardt Montpellier, CNRS,UMR 5253, ENSCM,UM1,UM2, F-34095 Montpellier, FranceUniv Paris 06, Lab Chim Mat Condensee Paris, UMR 7574, F-75005 Paris 06, France
Brodard-Severac, Florence
[2
]
Guerrero, Gilles
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Univ Montpellier 2, Inst Charles Gerhardt Montpellier, CNRS,UMR 5253, ENSCM,UM1,UM2, F-34095 Montpellier, FranceUniv Paris 06, Lab Chim Mat Condensee Paris, UMR 7574, F-75005 Paris 06, France
Guerrero, Gilles
[2
]
Maquet, Jocelyne
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Univ Paris 06, Lab Chim Mat Condensee Paris, UMR 7574, F-75005 Paris 06, FranceUniv Paris 06, Lab Chim Mat Condensee Paris, UMR 7574, F-75005 Paris 06, France
Maquet, Jocelyne
[1
]
Florian, Pierre
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CNRS, CRMHT, F-45071 Orleans 2, FranceUniv Paris 06, Lab Chim Mat Condensee Paris, UMR 7574, F-75005 Paris 06, France
Florian, Pierre
[3
]
Gervais, Christel
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Univ Paris 06, Lab Chim Mat Condensee Paris, UMR 7574, F-75005 Paris 06, FranceUniv Paris 06, Lab Chim Mat Condensee Paris, UMR 7574, F-75005 Paris 06, France
Gervais, Christel
[1
]
Mutin, P. Hubert
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Univ Montpellier 2, Inst Charles Gerhardt Montpellier, CNRS,UMR 5253, ENSCM,UM1,UM2, F-34095 Montpellier, FranceUniv Paris 06, Lab Chim Mat Condensee Paris, UMR 7574, F-75005 Paris 06, France
Mutin, P. Hubert
[2
]
机构:
[1] Univ Paris 06, Lab Chim Mat Condensee Paris, UMR 7574, F-75005 Paris 06, France
[2] Univ Montpellier 2, Inst Charles Gerhardt Montpellier, CNRS,UMR 5253, ENSCM,UM1,UM2, F-34095 Montpellier, France
High-field O-17 MAS NMR was used to investigate the binding of self-assembled monolayers of O-17- enriched phosphonic acids deposited on a titania anatase support. The spectra were recorded at two different magnetic fields (9.4 and 17.6 T), to improve the reliability of the simulations of the different resonances. The spectra recorded at 17.6 T offer an excellent resolution between the different oxygen sites, P=O, P-O-H, and P-O-Ti, thus greatly facilitating their quantification. The data reported here give direct evidence of the extensive formation of Ti-O-P bonds in the surface modification of titania by phosphonic acids. The presence of residual P=O and P-O-H sites indicates the presence of several different binding modes in phosphonic acid monolayers. The chemical shift of P-O-Ti sites is consistent with bridging (as opposed to chelating) modes.