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Crystalline fibers of the hydrogen-bonded framework bis(guanidinium) naphthalene-1,5-disulfonate, (G)2(1,5-NDS), with ethanol guest molecules twist as they grow when deposited from solution under conditions that favor low nucleation densities and high branching rates. Spherulites comprising helicoidal fibers with a pitch of 3.4 ± 0.5 μm display rhythmic concentric variations in interference colors between crossed polarizers. Tightly packed fibers and platelets, systematically change orientations between flat-on and edge-on crystallites with respect to the substrate surface. Mueller matrix imaging reveals periodic oscillations in the absolute magnitude of the linear retardance and an associated bisignate circular retardance. Single-crystal X-ray diffraction data demonstrates that the twisted (G)2(1,5-NDS)⊃EtOH crystals adopt a bilayer packing motif with ethanol as guest molecules (space group P1 ̅). When the banded spherulite films were subsequently heated at 130°C, the solvated phase was converted to a guest-free crystalline phase (space group P21/c). This transition resulted in loss of linear retardance. 

Abstract A great proportion of molecular crystals can be made to grow as twisted fibrils. Typically, this requires high crystallization driving forces that lead to spherulitic textures. Here, it is shown how micron size channels fabricated from poly(dimethylsiloxane) (PDMS) serve to collimate the circular polycrystalline growth fronts of optically banded spherulites of twisted crystals of three compounds, coumarin, 2,5‐bis(3‐dodecyl‐2‐thienyl)‐thiazolo[5,4‐d]thiazole, and tetrathiafulvalene. The relationships between helicoidal pitch, growth front coherence, and channel width are measured. As channels spill into open spaces, collimated crystals “diffract” via small angle branching. On the other hand, crystals grown together from separate channels whose bands are out of phase ultimately become a single in‐phase bundle of fibrils by a cooperative mechanism yet unknown. The isolation of a single twist sense in individual channels is described. We forecast that such chiral molecular crystalline channels may function as chiral optical wave guides. 

Abstract Optoelectronic properties of anisotropic crystals vary with direction requiring that the orientation of molecular organic semiconductor crystals is controlled in optoelectronic device active layers to achieve optimal performance. Here, a generalizable strategy to introduce periodic variations in the out‐of‐plane orientations of 5,11‐bis(triisopropylsilylethynyl)anthradithiophene (TIPS ADT) crystals is presented. TIPS ADT crystallized from the melt in the presence of 16 wt.% polyethylene (PE) forms banded spherulites of crystalline fibrils that twist in concert about the radial growth direction. These spherulites exhibit band‐dependent light absorption, photoluminescence, and Raman scattering depending on the local orientation of crystals. Mueller matrix imaging reveals strong circular extinction (CE), with TIPS ADT banded spherulites exhibiting domains of positive or negative CE signal depending on the crystal twisting sense. Furthermore, orientation‐dependent enhancement in charge injection and extraction in films of twisted TIPS ADT crystals compared to films of straight crystals is visualized in local conductive atomic force microscopy maps. This enhancement leads to 3.3‐ and 6.2‐times larger photocurrents and external quantum efficiencies, respectively, in photodetectors comprising twisted crystals than those comprising straight crystals.