New copper compounds, [Cu(C14H8O6)(C10H8N2)(H2O)] (1), [Cu(C14H8O6)(C10H8N2)(H2O)]·(C3H7ON)2 (2), [Cu(C14H8O6)(C10H8N2)(H2O)2]·(C3H7ON)
(3), [Cu(C14H8O6)(C10H8N4)] (4), and [Cu(C14H8O6)(C10H8N4)]·(H2O) (5), were prepared employing
2,5-bis(prop-2-yn-1-yloxy)terephthalic acid (2,5-BPTA) as the primary
ligand and 4,4′-bipyridine (1–3) and 4,4′-azopyridine (4–5) as the secondary ligands. Single-crystal studies indicated that
compounds 1–4 have two-dimensional
layer structures and compound 5 has a three-dimensional
structure. Compounds 1–3 were isolated
from the same reaction mixture but by varying the time of reaction.
The framework structures of compounds 1–3 are similar and may be considered as polymorphic structures.
Compounds 4 and 5 can also be considered
polymorphic with a change in dimensionality of the structure. Compounds 1–3 can be formed through a single-crystal-to-single-crystal
transformation under a suitable solvent mixture. The Cu center was
explored for the Lewis acid-catalyzed cycloaddition reaction of epoxide
and CO2 under ambient conditions in a solventless condition
and also for the synthesis of propargylamine derivatives by three-component
coupling reactions (A3 coupling) in a DCM medium. The Lewis
basic functionality of the MOF (–NN– group)
has been explored for the Henry reaction (aldol condensation) in a
solventless condition. In all of the catalytic reactions, good yields
and recyclability were observed. The magnetic studies indicated that
compounds 1 and 4 have antiferromagnetic
interactions and compound 5 has ferromagnetic interactions.
The present studies illustrated the rich diversity that the copper-containing
compounds exhibit in extended framework structures.