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• W2891834864 abstract "We investigated the aggregation behavior of the donor–acceptor molecules p-DTS(FBTTh2)2 (T1) and p-SIDT(FBTTh2)2 (H1) in MTHF solutions. Using optical spectroscopy, we found that T1 forms aggregates in solution while H1 aggregates only when processed as a thin film, but not in solution. Free energy molecular dynamics (MD) simulations based on force fields derived from quantum-mechanical density functional theory fully reproduce this difference. Our simulations reveal that this difference is not due to the lengthy carbon side chains. Rather, the molecular symmetry of T1 allows for an aggregated state in which the central donor units are spatially well-separated while a similar configuration is sterically impossible for H1. As a consequence, any aggregation of H1 necessarily involves aggregation of the central donors which requires, as a first step, stripping the central donor of its protective MTHF solvation shell. This unfavorable process leads to a significant kinetic hindrance for aggregation and explains the strongly differing aggregation behavior of T1/H1 in MTHF despite their otherwise similar structures." @default.
• W2891834864 created "2018-09-27" @default.
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• W2891834864 date "2018-09-11" @default.
• W2891834864 modified "2023-09-25" @default.
• W2891834864 title "Elucidating Aggregation Pathways in the Donor–Acceptor Type Molecules p-DTS(FBTTh₂)₂ and p-SIDT(FBTTh₂)₂" @default.
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• W2891834864 doi "https://doi.org/10.1021/acs.jpcb.8b06283" @default.
• W2891834864 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30204437" @default.
• W2891834864 hasPublicationYear "2018" @default.
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