A series of guest-binding Cu-parallel to coordination polymers, {[Cu(bpetha)(2)(acetone)(2)]center dot 2PF(6)}(n) (bpetha = 1,2-bis(4-pyridyl)ethane) (1), {[Cu(bpetha)(2)(DMF)(2)]center dot 2PF(6)}(n) (2), {[Cu(bpetha)(2)(MeCN)(2)]center dot 2PF(6)center dot 2MeCN}(n) (3), {[Cu(bpetha)(2)(H2O)(2)]center dot 2PF(6)center dot 3THF center dot 2H(2)O}(n) (4), {[Cu(bpetha)(2)(H2O)(2)]center dot 2PF(6)center dot 3dioxane}(n) (5), and {[Cu(bpetha)(2)(H2O)(2)]center dot 2PF(6)center dot 2-PrOH center dot 2H(2)O}(n) ( 6), have been synthesized and crystallographically characterized. Their framework stabilities and guest-exchange properties have also been investigated. All compounds form a similar framework motif, a "double chain", in which the bpetha ligands bridge Cu-parallel to centers to form 1-D [Cu(bpetha)(2)](n) double chains. A variety of Lewis base guest molecules, such as H2O, acetone, DMF, MeCN, THF, dioxane, and 2-PrOH, are incorporated into the assembly of the 1-D double chains. These chains flexibly change their forms of assembly in a guest-dependent manner. Interestingly, acetone, DMF, and MeCN guests with a carbonyl or cyanide group coordinate directly to the axial sites of the Cu-parallel to centers; in contrast, THF, dioxane, and 2-PrOH guests with an ether or alcohol group are incorporated into the frameworks not via coordination bonds but via weak interactions (hydrogen bonds and van der Waals forces). This selectivity is probably due to steric effects at coordinated oxygen or nitrogen atoms of the guests. Crystal-to-crystal transformations triggered by guests are observed, during which guests coordinated to the Cu-parallel to axial sites are readily removed and replaced by other guests.