ArticleACS omega2020
Cross-Linked Polyamide Chains Enhanced the Fluorescence of Polymer Carbon Dots.
Article in ACS omega, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
6 citing papers in PubMed.
- A Review on Polymer-Quantum Dots Nanocomposite Membrane and Its Multifunctional Applications.Chemical record (New York, N.Y.) · 2026Review
- Heteroatom-doped magneto-fluorescent carbon dots, a potent agent for multimodal imaging.Scientific reports · 2024Article
- Green Preparation of S, N Co-Doped Low-Dimensional C Nanoribbon/C Dot Composites and Their Optoelectronic Response Properties in the Visible and NIR Regions.Materials (Basel, Switzerland) · 2024Article
- Article
- Chiral carbon dots: synthesis, optical properties, and emerging applications.Light, science & applications · 2022Review
- Carbon Dots: An Emerging Smart Material for Analytical Applications.Micromachines · 2021Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Carbon dots (CDs) have attracted tremendous attention for their outstanding advantages in luminescence. Here, α-amino-substituted lysine derivatives with the determined chemical structure were employed as precursors to obtain bright and highly stable fluorescent CDs through a facile hydrothermal route. The relationships among the chemical structure of precursors, CD fluorescence, and particle size were investigated. The results indicated that increased numbers of functional groups in precursors could promote the degree of cross-linking and lead to a smaller size, better fluorescent properties, and stronger stability of CDs. The C-CDs that were prepared from lysine derivatives with most functional groups showed excitation-dependent dual excitation and dual emission (DE
Identifiers
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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.