Seven novel coordination
polymers based on 2,2′-phosphinico-dibenzoic
acid (H3L), namely, {[Zn3L2(H2O)4]·2H2O}
n
(1), [Zn3L2(4,4′-bipy)2]
n
(2), [Zn(HL)(2,2′-bipy)(H2O)]
n
(3), {[Cd9L6(H2O)8]·4H2O}
n
(4), [Cd8L4(OH)2(OAc)2(4,4′-bipy)]
n
(5), [Mn3L2(4,4′-bipy)(EtOH)(H2O)2]
n
(6), and [Mn(HL)(2,2′-bipy)(H2O)]
n
(7), were synthesized
under hydro(solvo)thermal conditions. These compounds crystallize
in the triclinic P1̅ space group for 1, 4, 5, and 6, the
monoclinic space group C2/c for 2, and the monoclinic P21/c space group for 3 and 7. The
L3– ligand displays versatile binding modes in 1–7. Compound 1 is a one-dimensional
(1-D) chain coordination polymer with a three-dimensional (3-D) supramolecular
framework. Compound 2 is a 3-D porous metal–organic
framework (MOF) with two different 4,4′-bipyridine linkers.
Compounds 3 and 7 show 1-D zigzag chain
structures. Compound 4 exhibits a sophisticated 3-D MOF
constructed from two types of Cd8 clusters and one Cd2 dimer, which is the first example exhibiting the coexistence
of four coordination modes of L3– ligands and four
geometries of Cd(II) ions in one network. Compound 5 displays
a two-dimensional (2-D) network containing a ring-like Cd8 cluster. Compound 6 shows a 2-D layered network with
4,4′-bipyridine linker. Their luminescence and variable-temperature
magnetic property were investigated, which indicated ligand-centered
emission in 1–5 and weak antiferromagnetic
coupling between Mn(II) ions in 6 and 7.