A family of propeller-shaped donor-acceptor hexapyrrolylbenzenes (HPBs) were designed and synthesized by sequential nucleophilic substitution of hexafluorobenzene with π-extended pyrroles. In particular, four hybrids were obtained, containing various combinations of electron-rich and electron-poor acenaphthylene-fused pyrroles. Additionally, to probe the efficiency of ortho transfer interactions, a system was designed containing unique donor and acceptor subunits spatially separated with four unfunctionalized pyrroles.
View Article and Find Full Text PDFA novel approach to detect and decode direct-part-marked, low-contrast data matrix codes on polymer-based selective laser sintering manufactured parts, which is able to work on lightweight devices, is presented. Direct-part marking is a concept for labeling parts directly, which can be carried out during the additive manufacturing's design process. Because of low contrast in polymer-based selective laser sintering manufactured parts, it is a challenging task to detect and read codes on unicolored parts.
View Article and Find Full Text PDFπ-Extended acenaphtho[1,2-d][1,2,3]triazoles, the unsubstituted Anta-H and its di-tert-butyl derivative Dibanta-H, as well as 5,6,7,8-tetrahydro-1H-naphtho[2,3-d][1,2,3]triazole Cybta-H were obtained in concise syntheses. In the solid state, Dibanta-H forms an unprecedented hydrogen-bonded cyclic tetrad, stabilized by dispersion interactions of the bulky tBu substituents, whereas a cyclic triad was found in the crystal structure of Anta-H. These cyclic assemblies form infinite slipped stacks in the crystals.
View Article and Find Full Text PDF