Solid state NMR characterization of phenylphosphonic acid encapsulated in SBA-15 and aminopropyl-modified SBA-15

被引:24
作者
Aiello, Daniela [1 ,2 ]
Folliet, Nicolas [1 ,2 ]
Laurent, Guillaume [1 ,2 ]
Testa, Flaviano [3 ]
Gervais, Christel [1 ,2 ]
Babonneau, Florence [1 ,2 ]
Azais, Thierry [1 ,2 ]
机构
[1] UPMC Univ Paris 06, F-75005 Paris, France
[2] Coll France, CNRS, UMR 7574, F-75005 Paris, France
[3] Univ Calabria, CR INSTM, Dept Chem Engn & Mat, Arcavacata Di Rende, CS, Italy
关键词
Mesoporous materials; Silica; Encapsulation; Phosphonic acid; Solid state NMR; NUCLEAR-MAGNETIC-RESONANCE; ORDERED MESOPOROUS SILICA; DRUG-DELIVERY RATE; CONTROLLED-RELEASE; MCM-41; IBUPROFEN; SPECTROSCOPY; CONFINEMENT; PROPERTY; MATRICES;
D O I
10.1016/j.micromeso.2012.04.028
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
We present in this communication that phenyl phosphonic acid can be efficiently loaded in mesoporous SBA-15 and aminopropyl-modified SBA powdered samples through the incipient wetness impregnation method. High amount of phosphonic acid can be reach up to 380 mg/g of sample. We use multinuclear solid state NMR as a method of choice for the indeep characterization of the samples. Thus we demonstrate that phosphonic acid molecules do not crystallize inside the pores. The molecules are highly mobile in SBA-15 because they are submitted to a confinement effect due to the mesoscopic size of the pores and consequently they exhibit a weak interaction with the silica walls. In the case of aminopropyl-modified SBA material, we show that the molecules are rigid and that they are in strong interaction with the aminopropyl groups. Moreover, a 2D double quantum H-1 NMR experiment recorded at high field and high spinning speed permit to propose a model of the phosphonate-aminopropyl interaction. The increase in spectral resolution due to the combination of high magnetic field and fast MAS rate allows also the assignment of H-1 resonances in aminopropyl-modified SBA matrix and notably allows the assignment of the protons resonance of the amino group. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:109 / 116
页数:8
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