In recent years, the design and construction of crystalline coordination complexes by the assembly of metal ions with multitopic ligands have attracted considerable attention because of the unique architectures and potential applications of these compounds. Two new coordination polymers, namely poly[[μ-trans-1-(2-aminopyridin-3-yl)-2-(pyridin-4-yl)ethene-κ2
N:N′](μ3-5-methylisophthalato-κ4
O
1,O
1′:O
3:O
3′)cadmium(II)], [Cd(C9H6O4)(C12H11N3)]
n
or [Cd(5-Me-ip)(2-NH2-3,4-bpe)]
n
, (I), and poly[[μ-trans-1-(2-aminopyridin-3-yl)-2-(pyridin-4-yl)ethene-κ2
N:N′](μ2-5-hydroxyisophthalato-κ4
O
1,O
1′:O
3:O
5)cadmium(II)], [Cd(C8H4O5)(C12H11N3)]
n
or [Cd(5-HO-ip)(2-NH2-3,4-bpe)]
n
, (II), have been prepared hydrothermally by the self-assembly of Cd(NO3)2·4H2O and trans-1-(2-aminopyridin-3-yl)-2-(pyridin-4-yl)ethene (2-NH2-3,4-bpe) with two similar dicarboxylic acids, i.e. 5-methylisophthalic acid (5-Me-H2ip) and 5-hydroxyisophthalic acid (5-HO-H2ip). The coordination network of (I) is a two-dimensional sql net parallel to (101). Adjacent sql nets are further linked to form a three-dimensional supramolecular framework via hydrogen-bonding interactions. Compound (II) is a two-dimensional (3,5)-connected coordination network parallel to (010) with the point symbol (63)(55647). As the other reactants and reaction conditions are the same, the structural differences between (I) and (II) are undoubtedly determined by the different substituent groups in the 5-position of isophthalic acid. Both (I) and (II) exhibit good thermal stabilities and photoluminescence properties.
A versatile strategy towards non-covalent functionalization of graphene by surface-confined supramolecular self-assembly of Janus tectons