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Manifestations of Weak O–H···F Hydrogen Bonding in M(H2O)n(B12F12) Salt Hydrates: Unusually Sharp Fourier Transform Infrared ν(OH) Bands and Latent Porosity (M = Mg–Ba, Co, Ni, Zn)

化学 氢键 八面体 结晶学 盐(化学) 分子 红外光谱学 傅里叶变换红外光谱 晶体结构 水合物 物理化学 量子力学 物理 有机化学
作者
Matthew R. Lacroix,Eric V. Bukovsky,Matic Lozinšek,Travis C. Folsom,Brooke Newell,Yong Liu,Dmitry V. Peryshkov,Steven H. Strauss
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:57 (23): 14983-15000 被引量:13
标识
DOI:10.1021/acs.inorgchem.8b02786
摘要

Eight M(H2O) n(Z) salt hydrates were characterized by single-crystal X-ray diffraction (Z2- = B12F122-): M = Ca, Sr, n = 7; M = Mg, Co, Ni, Zn, n = 6; M = Ba, n = 4, 5. Weak O-H···F hydrogen bonding between the M(H2O) n2+ cations and Z2- resulted in room-temperature Fourier transform infrared (FTIR) spectra having sharp ν(OH) bands, with full widths at half max of 10-30 cm-1, which are much more narrow than ν(OH) bands in room temperature FTIR spectra of most salt hydrates. Clearly resolved νasym(OH/OD) and νsym(OH/OD) bands with Δν(OH) as small as 17 cm-1 and Δν(OD) as small as 11 cm-1 were observed (Δν(OX) = νasym(OX) - νsym(OX)). The isomorphic hexahydrates ( R3̅) have two fac-(H2O)3 sets of H2O ligands and nearly octahedral coordination spheres. They exhibited four resolvable ν(OH) bands, one νasym(OH)/νsym(OH) pair for H2O ligands with longer O(H)···F distances and one νasym(OH)/νsym(OH) pair for H2O ligands with shorter O(H)···F distances. The ν(OH) bands for the three H2O molecules with shorter, slightly stronger O(H)···F hydrogen bonds were broader, more intense, and red-shifted by ca. 25 cm-1 relative to the bands for the three other H2O molecules, the first time that such small differences in relatively weak O(H)···F hydrogen bonds in the same crystalline hexahydrate have resulted in observable IR spectroscopic differences at room temperature. For the first time room temperature ν(OH) values for salt hexahydrates showed the monotonic progression Mg2+ > Co2+ > Ni2+ > Zn2+, essentially the same progression as the p Ka values for these metal ions in aqueous solution. A further manifestation of the weak O-H···F hydrogen bonding in these hydrates is the latent porosity exhibited by Ba(H2O)5,8(Z), Sr(H2O) n,m(Z), and Ca(H2O)4,6(Z). Finally, the H2O/D2O exchange reaction Co(D2O)6(Z) → Co(H2O)6(Z) was ca. 50% complete in 1 h at 50 °C in N2/17 Torr H2O( g).
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