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Vibrational spectra and structure of complexes containing the hydrogen dinitrate ion
Affiliation:1. Chimie Analytique et Chimie des Interfaces, Faculté des Sciences, Université libre de Bruxelles (ULB), Boulevard du Triomphe, 2, CP 255, B-1050 Bruxelles, Belgium;2. 4MAT, Ecole Polytechnique de Bruxelles, Université libre de Bruxelles (ULB), Avenue F.D. Roosevelt 50, CP165/63, B-1050 Bruxelles, Belgium
Abstract:Infrared and Raman spectra of solid hydrogen dinitrate complexes with K+, Rb+, Cs+, (CH3)4N+, trans-(Co py4Cl2)+, Ph4As+, Ph4P+, (C2H5)4N+ and (C4H9)N+ have been recorded and analyzed. The assignments were assisted by deuteration and, in the case of the Cs+, (CH3)4N+, and Ph4As+ complexes, by 15N substitution. Infrared spectra at 50 kbar of the (CH3)4N+ complex were also recorded. The salient features of the i.r. spectra are the lack of fundamental OH bands above 1800 cm−1 and the appearance of a strong absorption centered at about 600 cm−1, both indicating very strong hydrogen bonding. The i.r. and Raman spectra permit the differentiation between the planar and nonplanar types of the hydrogen dinitrate ion.
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