Synthesis and crystal structure of cadmium(II) coordination polymers with 3- and 4-pyridylacrylic acids

Abstract

Four new cadmium(II) coordination polymers, [Cd 3(4-Hpya) 4(SCN) 6(H 2O) 2] ( 1), [Cd(4-pya)(SCN)(H 2O)]·H 2O ( 2), [Cd(3-Hpya) 2(SCN) 2] ( 3) and [Cd(3-pya) 2] ( 4), have been synthesized from appropriate Cd(II) salts and 4-pyridylacrylic acid (4-Hpya) or 3-pyridylacrylic acid (3-Hpya) in the presence of thiocyanate under similar hydrothermal conditions. The use of cadmium perchlorate as metal source leads to complexes ( 1 and 3) with 4-Hpya and 3-Hpya, while the use of cadmium acetate leads to complexes ( 2 and 4) with 4-pya - and 3-pya -. In 1 and 3, the protonated ligands act as monodentate terminal ligands and lead to different 1D coordination chains with alternating end-to-end and end-on-N thiocyanate bridges ( 1) or with uniform end-to-end thiocyanate bridges ( 3). While 3-Hpya is in the normal carboxylic acid form in 3, it is unusual and unprecedented that 4-Hpya in 1 takes the zwitterionic form with the proton attached to the pyridyl nitrogen. The proton in either compound plays an important role in assembling the chains into higher-dimensional networks via hydrogen bonds. On the other hand, the deprotonated ligands in 2 and 4 assume μ 2 and μ 3 multidentate bridging modes, respectively, and allow the formation of 2D layers with coexistent NCS − and 4-pya - bridges ( 2) or with only 3-pya - bridges ( 4).