Molecular structure of dimethyl sulfoxide in DMSO-intercalated kaolinites at 298 and 77 K

被引:37
作者
Frost, RL
Kristof, J
Horvath, E
Kloprogge, JT
机构
[1] Queensland Univ Technol, Ctr Instrumental & Dev Chem, Brisbane, Qld 4001, Australia
[2] Univ Veszprem, Dept Analyt Chem, H-8201 Veszprem, Hungary
[3] Hungarian Acad Sci, Res Grp Analyt Chem, H-8201 Veszprem, Hungary
关键词
D O I
10.1021/jp991763f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The molecular structure of dimethyl sulfoxide at liquid nitrogen temperature has been obtained from the Raman spectra of dimethyl sulfoxide intercalated kaolinites by the use of Raman microprobe and a low temperature thermal stage. Raman bands at 2917 and 2935 cm(-1) for the symmetric stretching and four bands at 2999, 3015, 3021, and 3029 cm(-1) for the antisymmetric stretching are observed at 298 K. At liquid nitrogen temperature, Eve symmetric stretching frequencies at 2882, 2907, 2917, 2920, and 2937 cm(-1) and six antisymmetric stretching frequencies at 2986, 2994, 3000, 3012, 3023, and 3032 cm(-1) are observed for the DMSO-intercalated low defect kaolinite. Differences in the position and number of bands are observed for DMSO between the DMSO-intercalated low and high defect kaolinites. The in-plane methyl-bending region shows two Raman bands at 1411 and 1430 cm(-1) at 298 K and 1411 and 1426 cm(-1) at 77 K. The S=O stretching region shows bands in the 298 K spectra at 1066, 1023, and 1010 cm(-1) and at 1010, 1023, and 1062 cm(-1) in the 77 K spectra. These bands are assigned to the free monomeric S=O group and two different polymeric S=O groups. The C-S vibrations also show increased complexity upon obtaining spectra at 77 KI The additional bands of DMSO are attributed to the different molecular structures of DMSO in the DMSO; intercalated kaolinites.
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页码:9654 / 9660
页数:7
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