Coordination polymers with external stimuli-responsive
structural
transformation acquired paramount importance in the advanced material
research field due to their eye-catching application to deal with
the existing challenging issue, and Co(II) metal complex with d7 electronic configuration is a renowned candidate for kinetic
accountability and has the potentiality of structural transformation.
Bearing these factors in mind, here, a Co(II) congener of a previously
reported high hydrogen-adsorbing Cu(II)-based coordination polymer
(CP), {[Cu(4-bpe)(2-ntp)]}
n
[where 2-ntp2– = 2-nitroterephthalate and 4-bpe = 1,2-bis-(4-pyridyl)ethane],
has been synthesized to study the metal change impact on hydrogen
adsorption and solvent-induced structural transformation with their
impact on hydrogen uptake. This modified framework has a 2D + 2D →
3D inclined polycatenated framework as comparable to our previously
published Cu(II) framework. Here, on the variation of different solvents,
the labile Co(II)-containing framework exhibits a structural change
through single-crystal to single-crystal (SC–SC) structural
transformation and results in three new framework structures. All
four frameworks are structurally characterized by elemental analysis,
IR, PXRD, TGA, and single-crystal X-ray diffraction. The desolvated
parent framework with exposed metal centers exhibits excellent results
of H2 adsorption of 1.3 wt % (145 cc/g) at 77 K and pressure
of 1 bar with structural sustainability and CO2 uptake
of 130 cc/g at 195 K and 1 bar. For the other three solvent-mediated
structural derivatives, H2 and CO2 adsorption
have been studied, and the results are correlated with their structure.