Some of these crystals also represent problem cases as the ensuing crystals are generally small and extremely prone for different kinds of twinning. Still, a first classification of such systems seems to be feasible. Results of these investigations will be reported concurrently. It is often stated that the penetration of so-called pervasive computing in society depends on the availability of cheap, even disposable, electronics for RFID tags, sensors, flexible displays and matching backplane circuits. Organic field effect transistors (OFETs) are expected to be the building block for these devices, but have been hampered by their low mobility. The performance of organic field effect transistors is seriously compromised by trapping and scattering sites that may comprise structural defects and grain boundaries. Thus, it is crucial to control the formation of such sites, minimizing their occurrence frequency in the completed device, preferably as an integral part of facile processing, i.e. by self-assembly. Research has to a large degree focused on device models based on spin-coated thin films, but in practice, real devices will be manufactured by printing techniques. It is therefore important to determine the process of self-organization of organic molecules using either industrial, or simulated industrial deposition methods. Examples are inkjet or coating methods using molecules in solution. It is well established that texture can be induced by crystallisation from solvent in confined geometries with substantial impact on the charge transport properties of organic semiconductors [1]. We present two cases that may be regarded as laboratory equivalents of the "slot die" and the "immersion/dip coating" techniques of the coating industry, and demonstrate the self-organization effect of these techniques. The first example uses the zone-casting technique [2] which is closely related to the roll-to-roll slotdie coating method. With this method, we demonstrate thinfilm deposition of large area (several mm 2 ) crystalline monodomains of the small-molecule organic semiconductor, pentacene [3]. The second example employs the dip-coating method with a high-mobility conjugated copolymer, cyclopentadithiophenebenzothiadiazole, which shows a doubling of the charge mobility in the processed device because of crystalline texture [4]. The thin film crystalline texture was in both cases determined by comparing grazing incidence X-ray diffraction data with simulations [5]. The well-known supramolecular building block p-sulfonatocalix [4]arene (mostly occurring in its anionic form) crystallizes in a variety of different packing arrangements, depending on the co-crystallized components. It has especially attracted attention when it crystallizes in large, spherical arrangements of twelve calixarene anions residing on the vertices of an icosahedron or cuboctahedron, respectively, the former mimicking the geometry of the many viruses [1,2]. Here we report a variety of novel arrangements of the p-sulfonatocalix [4]arene anion some of which ...