Fritz-Haber-Institut der Max-Planck-Gesellschaft, Faradayweg 4-6, D-14195 Berlin, Germany.
J Am Chem Soc. 2010 Jun 2;132(21):7398-404. doi: 10.1021/ja1011806.
Infrared photodissociation spectra of buffer-gas-cooled MgNO(3)(H(2)O)(n) complexes with n = 1-4 are measured in the O-H stretching region. The observed bands are assigned to the excitation of the symmetric and antisymmetric stretching modes of the water molecules. The structural assignment of the spectra is aided by density functional theory calculations (B3LYP/6-311+G(d,p)) on energetically low-lying isomers, including the calculation of harmonic and anharmonic vibrational frequencies, as well as dissociation energies. The nitrate anion binds to the Mg dication in a bidentate fashion, occupying two coordination sites. The water molecules fill the remaining binding sites of the Mg cation, completing the first coordination shell at n = 4 and forming a stable six-fold-coordinated complex, the structure of which persists up to room temperature.
用缓冲气体冷却的 MgNO(3)(H(2)O)(n) 配合物(n = 1-4)的红外光解光谱在 O-H 伸缩区域中进行了测量。观察到的谱带被分配到水分子的对称和反对称伸缩模式的激发。通过对低能异构体的密度泛函理论计算(B3LYP/6-311+G(d,p)),包括计算调和和非调和振动频率以及离解能,辅助了光谱的结构分配。硝酸根阴离子以双齿配位的方式与 Mg 二价阳离子结合,占据两个配位位。水分子填充 Mg 阳离子的剩余配位位,在 n = 4 时完成第一个配位壳层,并形成稳定的六配位配合物,其结构一直持续到室温。