Rational Design of Nonlinear Optical Materials Based on 2D Coordination Networks

Zinc(II) and cadmium(II) coordination networks with m -pyridinecarboxylate bridging ligands, Zn(nicotinate) 2, 1, Cd(nicotinate) 2, 2, Cd{3-[2-(4-pyridyl)ethenyl]benzoate} 2, 3, Zn 4 {3-[2-(4-pyridyl)ethenyl]benzoate} 8 ·{3-[2-(4-pyridyl)ethenyl]benzoic acid}·(H 2 O), 4, Zn{4-[2-(3-pyridyl)ethenyl]benzoate} 2 ·H 2 O, 5, and Zn{5-[2-(3-pyridyl)ethenyl]thiophene-2-carboxylate} 2, 6, have been synthesized under hydro(solvo)thermal conditions. With the exception of 5, these compounds adopt 2D grid structures. The use of unsymmetrical bent m -pyridinecarboxylate ligands leads to the formation of intrinsically acentric 2D grids which provide an interesting structural motif for the rational synthesis of polar solids. Compounds 1 and 3 − 5 are non-centrosymmetric and show significant powder second harmonic generation efficiencies. Compound 2 adopts a centrosymmetric structure due to the presence of a μ 2, η 3 -carboxylate bridge, while compound 6 adopts a centrosymmetric structure due to the presence of 2-fold interpenetration. The present work illustrates the potential of rational synthesis of nonlinear-optical-active acentric solids by exploiting the propensity of the formation of 2D coordination networks based on bent linking groups. Crystal data for 1: tetragonal space group P 4 3 2 1 2, a = 7.709(1) Å, b = 7.709(1) Å, c = 20.327 Å, and Z = 8. Crystal data for 2: monoclinic space group P 2 1 /n, a = 10.055(1) Å, b = 10.219(1) Å, c = 12.733(1) Å, β = 105.169(2) o, and Z = 4. Crystal data for 3: orthorhombic space group Fdd 2, a = 20.622(1) Å, b = 36.426(1) Å, c = 6.241(1) Å, and Z = 8. Crystal data for 4: monoclinic space group Cc, a = 21.875(2) Å, b = 15.158(1) Å, c = 32.863(2) Å, β = 102.997(1), and Z = 4. Crystal data for 5: orthorhombic space group P 2 1 2 1 2, a = 7.625(1) Å, b = 25.430(2) Å, c = 5.863(1) Å, and Z = 4. Crystal data for 6: orthorhombic space group Pcca, a = 17.150(2) Å, b = 9.966(1) Å, c = 12.108(2) Å, and Z = 8.