Mechanically induced polyamorphism in a one-dimensional coordination polymer

一维配位聚合物的机械诱导多晶型现象

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Abstract

We created different amorphous structures of a coordination polymer by applying mechanical shear forces. One-dimensional Cu(Tf(2)N)(2)(bip)(2) (1, Tf(2)N(-) = bis(trifluoromethanesulfonyl)imide, bip = 1,3-bis(1-imidazolyl)propane) melted at 245 °C and underwent a glass transition at -10 °C by a static cooling process. 1 formed another amorphous state with a distinct glass transition point of 70 °C under oscillatory shear stress. The difference of orientation in their structures was studied by X-ray absorption fine structure and small-angle X-ray scattering. The reversible transition between the two amorphous states was observed by dynamic mechanical analyses.

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