The atypical 1:2 complexation between an electron-rich crown ether host and electron-deficient naphthalene diimide-based guests led to the formation of alternative donor-acceptor (ADA) stacks. The ADA stacks can be expediently obtained in high yield as polycrystalline aggregates from solution. More remarkably, the high degree of organization has also been realized in a simple solid-to-solid mechanical grinding process. The solid-state structures have been verified by solid-state NMR spectroscopy, single crystal, and powder X-ray diffraction analysis. The current findings not only provide convenient ways of obtaining novel donor-acceptor stacks involving a macrocyclic host but also represent an important step in transferring electroactive host-guest systems from solution to the solid state.

Download full-text PDF

Source
http://dx.doi.org/10.1021/ja809088vDOI Listing

Publication Analysis

Top Keywords

alternative donor-acceptor
8
donor-acceptor stacks
8
solution solid
8
solid state
8
ada stacks
8
stacks
4
stacks crown
4
crown ethers
4
ethers naphthalene
4
naphthalene diimide
4

Similar Publications

Photodynamic therapy (PDT) using oxygen-dependent type II photosensitizers is frequently limited by the hypoxic microenvironment of solid tumors. Type I photosensitizers show oxygen-independent reactive oxygen species (ROS) generation upon light irradiation but still face the challenges of aggregation-caused quenching (ACQ) and low efficiency to produce ROS. Herein, we first prepare an efficient type I photosensitizer from a perylene derivative via intramolecular donor-acceptor binding and sulfur substitution, which significantly enhance intersystem crossing between singlet and triplet states and electron transfer capability.

View Article and Find Full Text PDF

Computing Excited States of Very Large Systems with Range-Separated Hybrid Functionals and the Exact Integral Simplified Time-Dependent Density Functional Theory (XsTD-DFT).

J Phys Chem Lett

December 2024

Theoretical Chemistry Group, Molecular Chemistry, Materials and Catalysis Division (MOST), Institute of Condensed Matter and Nanosciences, Université Catholique de Louvain, Place Louis Pasteur 1, B-1348 Louvain-la-Neuve, Belgium.

Simplified quantum chemistry (sQC) methods can routinely compute excited states for very large systems in an "all-atom" fashion. They are viable alternatives to regular multiscale schemes. sQC methods have the advantage of accounting explicitly for all of the environment at a quantum mechanical (QM) level.

View Article and Find Full Text PDF

An Organic EnT Photocatalyst 4CzMeBN and the Application in the Synthesis of cis-Fused Azetidines.

Chemistry

December 2024

Nuclear Medicine and Molecular Imaging Key Laboratory of Sichuan Province, School of Pharmacy, Southwest Medical University, Luzhou, 646000, China.

A powerful EnT photocatalyst 4CzMeBN has been developed and utilized in the synthesis of cis-fused azetidines via dearomative [2+2] cycloaddition under visible light. The photocatalyst 4CzMeBN is a donor-acceptor cyanoarene and features high triplet state energy and long lifetime of triplet state, which would be an alternative to widely used EnT photocatalyst Ir[dF(CF)ppy](dtbbpy)PF. The photochemical [2+2] cycloaddition provides a facile method to synthesize valuable dihydroisoquinolone-fused azetidines with high efficiency.

View Article and Find Full Text PDF

Atomic Zn-N Site-Regulated Donor-Acceptor Catalyst for Boosting Photocatalytic Bactericidal Activity.

Nano Lett

December 2024

Department of Materials Science and Engineering, Jiangsu University, Zhenjiang, Jiangsu 212013, China.

Reactive oxygen species (ROS)-mediated photocatalytic antibacterial materials are emerging as promising alternatives for the antibiotic-free therapy of drug-resistant bacterial infections. However, the overall efficiency of photocatalytic sterilization is restricted by the rapid recombination of the charge carriers. Herein, we design an in-plane π-conjugated donor-acceptor (D-A) system (g-CN-Zn-NC), comprising graphitic carbon nitride (g-CN) as the donor and Zn single-atom anchored nitrogen-doped carbon (Zn-NC) as the acceptor.

View Article and Find Full Text PDF

New intrinsically unsymmetric aromatic donors (D) and acceptors (A) were designed to simplify the incorporation of a single reactive group. Naphthalene diimide (NDI) was desymmetrized by replacing one of the imide units with two nitro groups to yield 3,6-dinitronaphthalene monoimide (NMI(NO)); likewise, 3,6-dimethoxycarbazole (CBZ(OMe)) was designed as a 3-ring aromatic donor. Different derivatives of naphthalene monoimide (NMI) and carbazole (CBZ) were prepared, and charge-transfer complex formation between them was studied using NMR and UV-visible titrations; the estimated association constants () were compared with the common pair, NDI, and 1,5-dialkoxy naphthalene (DAN).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!