Related Experiment Video
Updated: Aug 20, 2026

Synthesis of a Water-soluble Metal–Organic Complex Array
Published on: October 8, 2016
Framework control by a metalloligand having multicoordination ability: new synthetic approach for crystal structures
Shin-Ichiro Noro1, Hitoshi Miyasaka, Susumu Kitagawa
1Supramolecular Science Laboratory, RIKEN (The Institute of Physical and Chemical Research), Hirosawa 2-1, Wako, Saitama 351-0198, Japan.
Abstract:
By utilizing the novel metalloligand l(Cu), [Cu(2,4-pydca)(2)](2)(-) (2,4-pydca(2)(-) = pyridine-2,4-dicarboxylate), which possesses two kinds of coordination groups, selective bond formation with the series of the first-period transition metal ions (Mn(ii), Fe(ii), Co(ii), Cu(ii), and Zn(ii)) has been accomplished. depending on the coordination mode of 4-carboxylate with Co(ii), Cu(ii), and Zn(ii) ions, L(Cu) forms a one-dimensional (1-d) assembly with a repeating motif of [-M-O(2)C-(py)N-Cu-N(py)-Co(2)-]: {[ZnL(Cu)(H(2)O)(3)(DMF)].DMF}(N)() (2), [ZnL(Cu)(H(2)O)(2)(MeOH)(2)](N)() (3), and {[ML(Cu)(H(2)O)(4)].2H(2)O}(N)() (M = Co (4), Cu (5), Zn (6)). the use of a terminal ligand of 2,2'-bipyridine (2,2'-bpy), in addition to the cu(ii) ion, gives a zigzag 1-d assembly with the similar repeating unit as 4-6: {[Cu(2,2'-bpy)L(Cu)].3H(2)O}(N)() (9). on the other hand, for Mn(ii) and Fe(ii) ions, L(Cu) shows a 2-carboxylate bridging mode to form an another 1-d assembly with a repeating motif of [-M-O-C-O-CU-O-C-O-]: [ML(Cu)(H(2)O)(4)](N)() (M = Mn (7), Fe (8)). this selectivity is related to the strength of lewis basicity and the electrostatic effect of L(Cu) and the irving-williams order on the present metal ions. according to their bridging modes, a variety of magnetic properties are obtained: 4, 5, and 9, which have the 4-carboxypyridinate bridge between magnetic centers, have weak antiferromagnetic interaction, whereas 7 and 8 with the carboxylate bridge between magnetic centers reveal 1-d ferromagnetic behavior (Cu(II)-M(II); M(II) = Mn(II), J/k(B) = 0.69 K for 7; M(II) = Fe(II), J/k(B) = 0.71 K for 8).
Related Concept Videos
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Metal-Ligand Bonds
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human eye.
Structural Isomerism
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can be...
Coordination Number and Geometry
Properties of Organometallic Compounds

