硫酸及其与水配合物的红外基质分离研究

A. Givan, L. A. Larsen, A. Loewenschuss, C. Nielsen
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引用次数: 41

摘要

H2SO4(也包括H2O和SO3)的红外光谱被捕获在氩气基体中。建立了H2SO4单体的振动赋值,并为(H2SO4)2、(H2O)·(H2SO4)和(H2O)2·(H2SO4)三种物质分配了额外的谱带。对于(H2O)·(H2SO4)配合物,存在几种异构体,其中最稳定的是H2O·HOSO2OH。与三聚体(H2O)3配合物类似,讨论了后一种配合物若干波段的温度可逆变化。分散在氩气固体中的H2O和H2SO4分子不影响混合(H2O)m·(SO3)n络合物的稳定性。在所调查的基质样品中没有发现质子转移引起的离子化物质的光谱证据。
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Infrared matrix isolation study of H2SO4 and its complexes with H2O
Infrared spectra of H2SO4 vapors, which also include H2O and SO3, were trapped in argon matrices. Vibrational assignments for monomeric H2SO4 were established and additional bands were assigned to the (H2SO4)2, (H2O)·(H2SO4) and (H2O)2·(H2SO4) species. For the (H2O)·(H2SO4) complex, several isomers are shown to exist, the most stable being H2O·HOSO2OH. Temperature reversible changes in several bands of the latter complex are discussed in analogy to the trimeric (H2O)3 complex. The H2O and H2SO4 molecules dispersed in the argon solid do not affect the stabilization of a mixed (H2O)m·(SO3)n complex. No spectral evidence for ionized species due to proton transfer was found in the matrix samples investigated.
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