ArticleSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy2016
Characterization of novel perylene diimides containing aromatic amino acid side chains.
Article in Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
5 citing papers in PubMed, 27 citations in OpenAlex.
- Chiral coronene diimide assemblies with strong chiroptical properties in solution and thin-films.Chemical science · 2026Article
- A Bis-Perylene Diimide Macrocycle Chiroptical Switch.Angewandte Chemie (International ed. in English) · 2025Article
- Supramolecular Nanostructures Based on Perylene Diimide Bioconjugates: From Self-Assembly to Applications.Nanomaterials (Basel, Switzerland) · 2022Review
- A Turn off-on Fluorescent Chemosensor for Sequential Determination of Mercury and Biothiols.Journal of fluorescence · 2018Article
- Design and synthesis of N-substituted perylene diimide based low band gap polymers for organic solar cell applications.RSC advances · 2018Article
Corrections and comments
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
Abstract
Perylene diimide derivatives have attracted initial interest as industrial dyes. Recently, much attention has been focused on their strong π-π stacks resulting from the large PDI aromatic core. These PDI stacks have distinct optical properties, and provide informative models that could mimic light-harvesting systems and initial charge transfer typical of photosynthetic systems. The absorption property of PDI derivatives may be tuned from visible to near-infrared region by peripheral substitution. We have studied a new class of PDI derivatives with aryl substituents derived from the side chains of aromatic aminoacids (Tyrosine, Tryptophan and Phenylalanine). We have investigated their absorption and the fluorescence properties in a set of organic solvents and established their different tendencies to aggregate in solution despite their solubility. Most aggregation appears to be unordered. One PDI analogue (the one formed from Tyr) in Methanol, however, appears to form J-type aggregates. Based on our results the compounds appear to be promising for future investigations regarding the interaction of these dyes with biomolecules.
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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.