Conjugated ladder polymers (CLPs) are difficult yet captivating synthetic targets due to their fully unsaturated fused backbones. Inherent challenges associated with their synthesis often lead to low yields, structural defects, and insoluble products. Here a new method to form CLPs is demonstrated, utilizing a high-yielding dimerization of annulated zirconacyclopentadienes to form cyclooctatetraene (COT) monomer units. The resulting COT-containing polymers form rapidly in a single ladderization step from the bis-zirconacyclopentadiene precursors and display up to 29.7 kg mol. The polymers represent rare examples of CLPs with negatively curved rings, resulting in the observation of unusual properties. The rigid tub-shaped COT units embedded in the backbone imbue the polymers with microporosity, exhibiting BET surface areas up to 555 m g. Additionally, the remarkable solubility of these CLPs in organic solvents enables the fabrication of thin films showcasing high dielectric performance with a discharged energy density as high as 6.54 J cm at 650 MV m.
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http://dx.doi.org/10.1039/d4sc06902a | DOI Listing |
Molecules
November 2024
The Institute of Computational Chemistry and Catalysis and Department of Chemistry, University of Girona, C/M.A. Capmany 69, 17003 Girona, Spain.
Poly-CPDTBT, as typical low-band gap copolymers, have potential applications in organic bulk heterojunction solar cells. To have a clear picture of its excited-state processes, the first task is to understand their excited states, in particular, electronic character and relevant optical absorption. Herein, the low-lying singlet excited states of Poly-CPDTBT oligomers were investigated via Algebraic Diagrammatic Construction Second Order (ADC(2)) and time-dependent density functional theory (TDDFT) method with several functionals.
View Article and Find Full Text PDFChem Sci
December 2024
Department of Chemistry, University of California Berkeley California 94720 USA
Conjugated ladder polymers (CLPs) are difficult yet captivating synthetic targets due to their fully unsaturated fused backbones. Inherent challenges associated with their synthesis often lead to low yields, structural defects, and insoluble products. Here a new method to form CLPs is demonstrated, utilizing a high-yielding dimerization of annulated zirconacyclopentadienes to form cyclooctatetraene (COT) monomer units.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
State Key Laboratory of Applied Organic Chemistry (SKLAOC), Key Laboratory of Special Function Materials and Structure Design (MOE), College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, 730000, China.
Chem Commun (Camb)
November 2024
Department of Chemistry and Institute for Soft Matter Synthesis and Metrology, Georgetown University, 37th and O St, NW, Washington DC, USA.
Pendant alkyl chains are widely used to successfully obtain a wide variety of soluble linear 1D π-conjugated polymers. Over the past several decades, a wide variety of π-conjugated polymers have been synthesized to realize the desired properties and improve the performance of organic electronic devices. However, this strategy is not suitable for generating soluble 2D-π-conjugated materials, including ladder polymers, nanoribbons, and 2D-π-conjugated polymers, due to strong van der Waals interactions between the ribbons and sheets.
View Article and Find Full Text PDFJ Am Chem Soc
November 2024
Fukui Institute for Fundamental Chemistry, Kyoto University, Sakyo-ku, Kyoto 606-8103, Japan.
Dividing orbital interactions into through-space (TS) and through-bond (TB) modes is valuable for understanding various molecular properties. In this paper, we elucidate how the quantum interference phenomenon known as σ interference in electron transport through σ systems arises from TS and TB interactions. We performed electron transport calculations using a combination of density functional theory and nonequilibrium Green's function methods, focusing on ethylenediamine, a classical molecule that effectively highlights the contrast between TS and TB interactions.
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