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Abstract In this manuscript, we report the first demonstration of controlled helicity in extended graphene nanoribbons (GNRs). We present a wealth of new graphene nanoribbons that are a direct consequence of the high‐yielding and robust synthetic method revealed in this study. We created a series of defect‐free, ultralong, chiral cove‐edged graphene nanoribbons where helical twisting of the graphene nanoribbon backbone is tuned through functionalization with chiral side chains.S‐configured point chiral centers in the side chains transfer their chiral information to induce a helically chiral, right‐handed twist in the graphene nanoribbon. As the backbone is extended, these helically twisted graphene nanoribbons exhibit a substantial increase in their circular dichroic response. The longest variant synthesized consists of an average of 268 linearly fused rings, reaching 65 nm in average length with nearly 10 full end‐to‐end helical rotations. The structure exhibits an extraordinary |Δε| value of 6780 M⁻¹cm⁻¹at 550 nm—the highest recorded for an organic molecule in the visible wavelength range. This new chiroptic material acts as room‐temperature spin filters in thin films due to its chirality‐induced spin selectivity. 

Creating new chiral molecular and macromolecular systems that can polarize the spin of electrons has the dual promise of both applications in spintronics and a fundamental understanding of their origins. Here, we put forward two optically active helical ladder dimers from perylene diimide-based twistacenes and helicenes. We detail a scalable method to separate the helices for each of these systems and methods to functionalize them with thiol groups that allow for self-assembled monolayer formation on metal surfaces. We probed these monolayers with conductive atomic force microscopy, revealing that they are highly conductive. If the substrate is magnetized, then the current we measure with conductive atomic force microscopy is controlled by the handedness of the helices used to form the monolayers. Furthermore, helices of the same handedness for either the twistacene or helicene (right-handed helices vs left-handed helices) produce high (or low) currents in devices with the same magnetization. Importantly, we find a correlation between the magnetic field dependence of the conductivity and the helicity of the molecules, suggesting a link between these two properties, independent of the sign of their electronic circular dichroism. 

This manuscript describes a simple and effective method to cyclodehydrogenate arenes using liquid alkali metals. Direct reaction between molten potassium and arenes forms 6-membered rings and zigzag edged structures within polyarenes. The approach is extended to integration of pyridinic nitrogen and 5-membered rings to arene structures and synthesis of larger, open-shell nanographenes. 

Pseudocapacitors offer a unique strategy to combine the rapid charging rates of capacitors with the high energy density of batteries, potentially offering a unique solution to energy storage challenges. Bending and twisting aromatic building blocks to form contorted aromatics have emerged as a new strategy to create organic materials with unique and tunable properties. This paper studies the union between these two concepts: molecular contortion and organic pseudocapacitors. The recent development of fully organic pseudocapacitors, including high-performing devices based on perylene diimide organic redox units, introduces the added benefit of low cost, synthetic tunability, and increased flexibility. We synthesize a series of polymers by joining perylene diimide with various linkers that incorporate a helical moiety from [4]helicene to [6]helicene into the molecular backbone. We prepare three new electroactive polymers that incorporate benzene, naphthalene, and anthracene linkers and study their pseudocapacitive performance to infer key design principles for organic pseudocapacitors. Our results show that the naphthalene linker results in the most strongly coupled redox centers and displays the highest pseudocapacitance of 292 ± 47 F/g at 0.5 A/g. To understand the pseudocapacitive behavior, we synthesized dimer model compounds to further probe the electronic structure of these materials through electronic absorption spectroscopy and first-principles calculations. Our results suggest that the identity of the aromatic linker influences the contortion between neighboring perylene diimide units, the coupling between redox centers, and their relative angles and distances. We find that competing molecular design factors must be carefully optimized to generate high-performance devices. Overall, this study provides key insights into molecular design strategies for generating high-performing organic pseudocapacitor materials. 

Abstract Molecular clusters can function as nanoscale atoms/superatoms, assembling into superatomic solids, a new class of solid‐state materials with designable properties through modifications on superatoms. To explore possibilities on diversifying building blocks, here we thoroughly studied one representative superatom, Co₆Se₈(PEt₃)₆. We probed its structural, electronic, and magnetic properties and revealed its detailed electronic structure as valence electrons delocalize over inorganic [Co₆Se₈] core while ligands function as an insulated shell.⁵⁹Co SSNMR measurements on the core and³¹P,¹³C on the ligands show that the neutral Co₆Se₈(PEt₃)₆is diamagnetic and symmetric, with all ligands magnetically equivalent. Quantum computations cross‐validate NMR results and reveal degenerate delocalized HOMO orbitals, indicating aromaticity. Ligand substitution keeps the inorganic core nearly intact. After losing one electron, the unpaired electron in [Co₆Se₈(PEt₃)₆]⁺¹is delocalized, causing paramagnetism and a delocalized electron spin. Notably, this feature of electron/spin delocalization over a large cluster is attractive for special single‐electron devices.