基态
吸收(声学)
基体隔离
氩
材料科学
基质(化学分析)
变形(气象学)
原子物理学
物理
复合材料
作者
Marilyn E. Jacox,Dolphus E. Milligan
标识
DOI:10.1016/0022-2852(73)90116-1
摘要
Studies of the reaction with NO in an argon or a nitrogen matrix at 4° or 14°K of H and D atoms produced either photolytically or in a microwave discharge have confirmed the previous identification of the ground-state NO stretching fundamental of HNO and of DNO but have dictated a reassignment of the deformation fundamental of these two species. An absorption at 1153 cm−1 has been assigned as the deformation fundamental of DNO, and evidence is presented suggesting that the deformation fundamental of HNO lies very close to 1500 cm−1. The assignment of an absorption at 2717 cm−1 as the NH stretching fundamental of HNO and of an absorption at 2043 cm−1 as the corresponding fundamental of DNO is consistent with the previous report of an exceptionally long NH bond for ground-state HNO. Detailed isotopic studies support this revised vibrational assignment, which is shown to be consistent with previous gas-phase studies. The force constants and thermodynamic properties of ground-state HNO derived from the matrix data are presented.
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