Improved Syntheses of Halogenated Benzene-1,2,3,4-Tetracarboxylic Diimides.

The preparation of halogenated benzene-1,2,3,4-tetracarboxylic diimide derivatives is challenging because of the possibility of competitive incorrect cyclizations and SNAr reactivity. Here, we demonstrate that bypassing traditional cyclic anhydrides and instead directly reacting dihalobenzene-1,2,3,4-tetracarboxylic acids with primary amines in acetic acid solvent successfully provides a range of desirable ortho-diimide products in good yields. Furthermore, we demonstrate that sterically challenging N-derivatizations can be readily achieved under microwave reactor conditions. The halogenated diimides described here are attractive building blocks for organic materials chemistry.

Modulating Polymerization Thermodynamics of Thiolactones Through Substituent and Heteroatom Incorporation.

A central challenge in the development of next-generation sustainable materials is to design polymers that can easily revert back to their monomeric starting material through chemical recycling to monomer (CRM). An emerging monomer class that displays efficient CRM are thiolactones, which exhibit rapid rates of polymerization and depolymerization. This report details the polymerization thermodynamics for a series of thiolactone monomers through systematic changes to substitution patterns and sulfur heteroatom incorporation. Additionally, computational studies highlight the importance of conformation in modulating the enthalpy of polymerization, leading to monomers that display high conversions to polymer at near-ambient temperatures, while maintaining low ceiling temperatures (Tc). Specifically, the combination of a highly negative enthalpy (-19.3 kJ/mol) and entropy (-58.4 J/(mol·K)) of polymerization allows for a monomer whose equilibrium polymerization conversion is very sensitive to temperature.

Toward Recyclable Polymers: Ring-Opening Polymerization Enthalpy from First-Principles.

Ring-opening polymerization (ROP) enthalpy ΔHROP is an important thermodynamic property controlling the polymerization of cyclic monomers. While ΔHROP can be measured, computing ΔHROP for realistic polymer systems with an error of ≃5-10 kJ/mol is critical for designing new monomer systems for depolymerizable polymers. We have developed a first-principles computational scheme in which multiple challenges in computing ΔHROP are resolved definitively including extensive exploration of conformational states and adequately addressing finite size effects. This scheme is validated on a diverse benchmark set of 42 ROP polymers for which reliable experimental values of ΔHROP are available. For this set, the ΔHROP root-mean-square error is ≃7 kJ/mol, about 3-times smaller than conventional approaches. This development opens up new pathways to build up a high-quality database of ΔHROP for downstream predictive machine-learning models and ultimately to accelerate the design of depolymerizable polymers with desired properties.

Redox-Active Heteroacene Chromophores Derived from a Nonlinear Aromatic Diimide.

This work describes a three-step chromatography-free protocol for the synthesis of a novel organic materials building block, dichlorinated mellophanic diimide (MDI), that is shown to undergo nucleophilic substitution with a variety of ortho disubstituted benzenes to yield a series of chromophores. Furthermore, 1,2,4,5-tetrasubstituted benzenes can be used to synthesize tetraimide heteropentacene derivatives endcapped by MDI motifs. The fine-tuning effects of heteroatom identity were investigated by UV-vis and fluorescence spectroscopy, cyclic and differential pulse voltammetries, and density functional theory calculations. Oxidation of diamino MDI derivatives yields di- and tetraimide functionalized azaacenes with significantly lowered LUMO levels (down to -4.49 eV), narrowed band gaps (down to 1.81 eV), and high molar absorptivities (up to 84,000 M-1 cm-1).