Evidence map›Paper›PMID 29861969›Full record

ArticleChemical science2016

Cooperative duplex formation by synthetic H-bonding oligomers.

Alexander E Stross, Giulia Iadevaia, Christopher A Hunter

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Synthetically encoded complementary oligomers.Nature reviews. Chemistry · 2023
    Review
  3. Article
  4. Recognition-Encoded Synthetic Information Molecules.Accounts of chemical research · 2023
    Article
  5. H-Bond Templated Oligomer Synthesis Using a Covalent Primer.Journal of the American Chemical Society · 2022
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. H-Bonded Duplexes based on a Phenylacetylene Backbone.Journal of the American Chemical Society · 2018
    Article
  14. Article
  15. Sequence-Selective Formation of Synthetic H-Bonded Duplexes.Journal of the American Chemical Society · 2017
    Article
  16. Article
  17. H-Bond Self-Assembly: Folding versus Duplex Formation.Journal of the American Chemical Society · 2017
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Alexander E StrossDepartment of Chemistry , University of Cambridge , Lensfield Road , Cambridge CB2 1EW , UK . Email: herchelsmith.orgchem@ch.cam.ac.uk.
Giulia IadevaiaDepartment of Chemistry , University of Cambridge , Lensfield Road , Cambridge CB2 1EW , UK . Email: herchelsmith.orgchem@ch.cam.ac.uk.
Christopher A HunterDepartment of Chemistry , University of Cambridge , Lensfield Road , Cambridge CB2 1EW , UK . Email: herchelsmith.orgchem@ch.cam.ac.uk.
University of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of flexible oligomers equipped with phenol H-bond donors and phosphine oxide H-bond acceptors have been synthesised using reductive amination chemistry. H-bonding interactions between complementary oligomers leads to the formation of double-stranded complexes which were characterised using NMR titrations and thermal denaturation experiments. The stability of the duplex increases by one order of magnitude for every H-bonding group added to the chain. Similarly, the enthalpy change for duplex assembly and the melting temperature for duplex denaturation both increase with increasing chain length. These observations indicate that H-bond formation along the oligomers is cooperative despite the flexible backbone, and the effective molarity for intramolecular H-bond formation (14 mM) is sufficient to propagate the formation of longer duplexes using this approach. The product

Identifiers

PMID29861969
PMCPMC5950798
OpenAlexW2170324843

What OpenQuestion holds

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Registered trials

None linked

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.