ArticleChemical science2024
Rational design of CT-coupled J-aggregation platform based on Aza-BODIPY for highly efficient phototherapy.
Article in Chemical science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 51 citations in OpenAlex.
- π-π-Coupled J-Aggregates Synergized With Hydrogen Bonding via Molecular Planarity Engineering for Second Near-Infrared Imaging and Phototherapy.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026Article
- Article
- Intermolecular hydrogen-bonded associates of BODIPYs drive controllable aggregates and enhanced NIR phototherapeutic performance.Smart molecules : open access · 2026Article
- Resonator-based add-drop filters enabled by flexible polymorphic crystals with TADF-RTP motifs.Chemical science · 2026Article
- Architecting NIR-II metal supramolecular dyes-illuminating the path to precision medicine.Chemical science · 2026Review
- Fluorinated Hypoxia-Responsive Aza-BODIPY for NIR-II FL/Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Article
- Influence of Chlorine Substitution on the Structures and Photophysical Properties of 9,10-Distyrylanthracene (DSA).Journal of fluorescence · 2026Article
- Enhancing Near-Infrared Two-Photon Absorption of Aza-Boron-Dipyrromethene Compounds Through Intramolecular Charge Transfer Via Electron Donating Substitution.ChemPlusChem · 2025Article
- Electrostatic Co-Assembly of Cyanine Pair for Augmented Photoacoustic Imaging and Photothermal Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
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Authors and funding
9 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Supramolecular engineering is exceptionally appealing in the design of functional materials, and J-aggregates resulting from noncovalent interactions offer intriguing features. However, building J-aggregation platforms remains a significant challenge. Herein, we report 3,5-dithienyl Aza-BODIPYs with a donor-acceptor-donor (D-A-D) architecture as the first charge transfer (CT)-coupled J-aggregation BODIPY-type platform. The core acceptor moieties in one molecule interact with donor units in neighboring molecules to generate slip-stacked packing motifs, resulting in CT-coupled J-aggregation with a redshifted wavelength up to 886 nm and an absorption tail over 1100 nm. The J-aggregates show significant photoacoustic signals and high photothermal conversion efficiency of 66%. The results obtained
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.