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- W2531405841 abstract "Among recent advances toward efficient semiconducting materials, rational design guidelines have emerged focusing on the synergy between various intermolecular interactions to improve the solid-state order of π-conjugated molecules in organic electronic devices. Herein, we focus our attention on halogen bonding (XB) interactions and the crucial role of electron withdrawing substituents (e.g., nitro and fluoro) toward influencing solid-state properties via secondary interactions. Employing iodoethynyl benzene derivatives (F2BAI and (NO2)2BAI) and thiophene/furan-based building blocks equipped with pyridyl groups as self-assembling domains (PyrTF and PyrT2), co-crystals driven by XB and π-stacking interactions were formed and studied. Spectroscopic and thermal analysis of 1:1 mixtures provide initial evidence of co-crystallization. X-ray crystallography affords the inherent solid-state packing motifs within each assembly. Computational studies support experimental observations, revealing the dominant interactions and contribution of each substituent group toward increasing the stability of the resulting assemblies." @default.
- W2531405841 created "2016-10-21" @default.
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- W2531405841 date "2016-10-24" @default.
- W2531405841 modified "2023-09-30" @default.
- W2531405841 title "Elucidating the Effects of Fluoro and Nitro Substituents on Halogen Bond Driven Assemblies of Pyridyl-Capped π-Conjugated Molecules" @default.
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- W2531405841 doi "https://doi.org/10.1021/acs.cgd.6b01321" @default.
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