Reactions were carried out under nitrogen atmosphere using standard Schlenk techniques. Thin-layer chromatography (TLC) was performed using glass plates pre-coated with silica gel impregnated with a fluorescent indicator (Merck, #1.15685.0001). Silica gel column chromatography was performed as described by Still, et al., 1 employing (Davisil, 60 Å, 40-63 micron) purchased from Sigma-Aldrich.
Energy conversion by water flowing over graphene is a promising mode of energy harvesting. However, the mechanism, energy-conversion efficiency, and quantification of power density for this mode of interfacial electricity generation remain unknown. Quantification of the output performance for the flow-induced electricity generation using graphene is presented in this work. The output performance per unit contact area between water and graphene is found to be proportional to the flow speed, with an electromotive force density of 0.0025 [μV/mm2/mm/s] for the conditions used in this work. The ability to quantify output density will help to construct guidelines for future applications of this form of electricity generation.
Sulfur‐embedded polycyclic aromatic compounds have been used as building blocks for numerous organic semiconductors over the past few decades. While the success is based on thiophene‐containing compounds, aromatic compounds that contain thiepine, a sulfur‐containing seven‐membered‐ring arene, has been less well investigated. Here we report the synthesis and properties of π‐extended pyrrole‐fused heteropine compounds such as thiepine and oxepine. A π‐extended pyrrole‐fused thiepine exhibited a “pitched π‐stacking” structure in the crystal, and exhibited a high charge carrier mobility of up to 1.0 cm2 V−1 s−1 in single‐crystal field‐effect transistors.
Heteroatom-embedded buckybowl molecules provide a fundamental molecular framework that has potential applications in various research fields. However, selective introduction of heteroatoms into buckybowls is challenging, and thus, studies investigating the effect of introduced heteroatoms have been limited. Here, we report the synthesis of pyridine-fused azacorannulene molecules. The influence of nitrogen atoms introduced into the peripheral positions on the structural, electronic, and optical properties is discussed.
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