Two
helical ligands (L
1
and L
2
) containing a pyridine-2,6-dicarboxamide
skeleton were synthesized, and the crystal structures indicated racemic
configurations with equal amounts of P- and M-helicity. Eight one-dimensional coordination polymers
(CPs), {[ZnL
1
Cl2]·2CH3OH}
n
(1), [HgL
1
I2]
n
(2), {[AgL
1
NO3]·CHCl3}
n
(3), {[Cd(L
1
)2Cl2]·2DMF}
n
(4), {[Co(L
1
)2Cl2]·2DMF}
n
(5), {[ZnL
2
I2]·2DMF·H2O}
n
(6), [HgL
2
Cl2]
n
(7), and {[Hg2(L
2
)2Br4]·2CH3OH}
n
(8), were synthesized
from the reaction of the two ligands with a series of transition metal
ions. The crystal structures showed that the chiral self-assembly
process of these ligands resulted in homochiral complexes (CP 1, 3, and 6), heterochiral complexes
(CP 2, 4, 5, and 7), or the coexistence of homochiral and heterochiral complexes (CP 8). The gas adsorption/desorption experiments were investigated
at room temperature, which showed that all the CPs exhibited good
selective adsorption capacities (24.6–62.5 cm3/g)
toward methanol vapor over other gas. Furthermore, CP 3, 5, and 6 were selected for the recyclable
methanol vapor adsorption experiments, and the results showed that
all three CPs can be recycled as good adsorbents for methanol vapor.