Cd(C4H4N2)(H2 O)2MoO2F4 (C4H4N2 = pyrazine, pyz) was synthesized via hydro(solvato)thermal methods and characterized by single-crystal x-ray diffraction methods (P3221, no. 154, Z = 3, a = 7.4328(7) Å, c = 16.376(2) Å). Both of the known M(pyz)(H2O)2MoO2F4 (M = Zn, Cd) compounds are comprised of trans-M(pyz)2(OH2)2F2 and cis-MoO2F4 octahedra that share fluoride vertices to form helical chains along the 3-fold screw axes. Individual chains are bridged to six symmetry-equivalent helices through metal-pyrazine and OH2⋯F and OH2⋯O hydrogen bonds. Structural comparisons of similar oxyfluoride chains demonstrate that they can be varied from linear to helical through (1) the replacement of pyridine or pyrazine by H2O molecules and (2) the substitution of cisdirecting MoO2F42- anions in place of trans-directing WO2F42- or TiF62- anions. Infrared absorption (IR) measurements for M = Cd show two distinct O-H stretches corresponding to hydrogen-bonded O-H⋯F and O-H⋯O groups. Contrastingly for M = Zn, IR measurements exhibit O-H stretches for averaged hydrogen-bonded O-H⋯(O/F) groups, free (unbound) O-H groups, and higher energy Mo-F stretches. The IR data suggest a small fraction of the O-H⋯F hydrogen bonds are broken in the M = Zn analogue as a result of the racemic twinning. Both compounds exhibit nonlinear optical behavior, with second harmonic generation (SHG) intensities, relative to SiO2, of ∼0.25 (〈dijk2ω〉 = 0.28 pm/V) for the racemically twinned Zn(pyz)(H2O)2MoO2F4 and ∼1.0 (〈dijk2ω〉 = 0.55 pm/V) for the enantiopure Cd(pyz)(H2O)2MoO2F4.
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Inorganic Chemistry