Hirabayashi Shinichi, Yamada Koichi M T
National Institute of Advanced Industrial Science and Technology (AIST), Research Institute for Environmental Management Technology (EMTech), AIST Tsukuba-West, Japan.
J Chem Phys. 2005 Jun 22;122(24):244501. doi: 10.1063/1.1943948.
The infrared absorption spectra of the water molecules and small water clusters, (H(2)O)(n) with n = 2-6, trapped in solid argon, krypton, and xenon matrices have been investigated. The infrared bands of the water clusters with n = 5 and 6 in krypton and n = 3, 4, 5, and 6 in xenon matrices have been identified for the first time in the bonded OH stretching region. The frequency shifts in the bonded OH stretching band of the water dimer and trimer in xenon matrices show fairly large deviations to the red from the empirical correlation between the matrix shifts and the square root of the critical temperatures of the matrix material. The observed anomalous shifts suggest that the water dimer and trimer in solid xenon are trapped in multiple sites, and that the structures of the preferential trapping sites are different from those in argon and krypton matrices.
对捕获在固态氩、氪和氙基质中的水分子以及小水簇((n = 2 - 6) 的 ((H_2O)_n))的红外吸收光谱进行了研究。首次在氪基质中鉴定出 (n = 5) 和 (6) 的水簇以及在氙基质中 (n = 3)、(4)、(5) 和 (6) 的水簇在氢键合 (OH) 伸缩区域的红外谱带。氙基质中水分子二聚体和三聚体的氢键合 (OH) 伸缩带的频率位移相对于基质位移与基质材料临界温度平方根之间的经验相关性,向红端显示出相当大的偏差。观察到的异常位移表明,固态氙中的水分子二聚体和三聚体被困在多个位置,并且优先捕获位置的结构与氩和氪基质中的不同。