The squaric acid aggregate in mordenite investigated by Raman spectroscopy

被引:25
作者
Lopes, JGS
de Oliveira, LFC
Santos, PS [1 ]
机构
[1] Univ Sao Paulo, Inst Quim, Dept Quim Fundamental, BR-05508900 Sao Paulo, Brazil
[2] Univ Fed Juiz de Fora, Inst Ciencias Exatas, Dept Quim, Juiz De Fora, MG, Brazil
基金
巴西圣保罗研究基金会;
关键词
D O I
10.1016/S1386-1425(00)00399-1
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
A more detailed investigation of the squaric acid aggregate within mordenite was undertaken with the use of Raman spectroscopy. The previous reported investigation was limited to the carbonyl stretching region in the IR. In the present work the entire region from 500 to 2000 cm(-1) was investigated, revealing rather substantial vibrational shifts of the oxocarbon ring modes in the aggregate. Comparison of such shifts with those observed for the squaric acid (H(2)Sq)/4,4'-bipyridine (Bipy) charge transfer (CT) complex reveals that the interaction is much stronger in the aggregate, a clear effect of the restrict geometry. On the other hand, the shifts observed for the CO stretching modes are rather modest. The comparison of the ring modes present in the Raman spectra of squaric acid, potassium hydrogen squarate, potassium squarate, H(2)sq/Bipy and squaric acid aggregate in mordenite strongly suggests that in the latter hydrogen bonded species are present. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:399 / 404
页数:6
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