Strong π-stacking causes unusually large anisotropic thermal expansion and thermochromism

Abstract

π-stacking in ground-state dimers/trimers/tetramers of <i>N</i>-butoxyphenyl(naphthalene)diimide (BNDI) exceeds 50 kcal ⋅ mol^-1 in strength, drastically surpassing that for the ^*3[pyrene]₂ excimer (∼30 kcal ⋅ mol^-1; formal bond order = 1) and similar to other weak-to-moderate classical covalent bonds. Cooperative π-stacking in triclinic (BNDI-T) and monoclinic (BNDI-M) polymorphs effects unusually large linear thermal expansion coefficients (α _<i>a</i> , α _<i>b</i> , α _<i>c</i> , β) of (452, -16.8, -154, 273) × 10^-6 ⋅ K^-1 and (70.1, -44.7, 163, 177) × 10^-6 ⋅ K^-1, respectively. BNDI-T exhibits highly reversible thermochromism over a 300-K range, manifest by color changes from orange (ambient temperature) toward red (cryogenic temperatures) or yellow (375 K), with repeated thermal cycling sustained for over at least 2 y.