ArticleChem2025
Electrochemical sequencing of sequence-defined ferrocene-containing oligourethanes.
Article in Chem, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 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
2 citing papers in PubMed.
- Highly robust molecular information carriers for traceability of plastic materials.Nature communications · 2026Article
- Ferrocene-Based Sensors for Green Analytical Applications in Environmental, Biomedical, Industrial, and Food Monitoring.ChemistryOpen · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
Abstract
The growing demand for data storage has driven research into alternative storage media. Although DNA has proven effective, synthetic sequence-defined polymers (SDPs) offer tailored information-encoding potential. Despite advances in SDP chemodiversity, sequencing methods remain limited, primarily relying on tandem mass spectrometry. To address this, we developed an electrochemical sequencing technique for sequence-defined oligourethanes (SDOs), incorporating four ferrocene-based monomers. Our method combines controlled chain-end degradation with differential pulse voltammetry (DPV) to yield unique voltammograms specific to each sequence. Coupled with kinetic modeling and principal component analysis (PCA), this approach enables accurate sequence identification. We automated this process with a Python program that decodes sequences by comparing experimental DPV data to predicted profiles and thereby successfully demonstrated the encoding and decoding of an 11-character password. The technique expands the toolbox for sequencing SDPs and opens new possibilities for molecular data storage.
Identifiers
What OpenQuestion holds
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.