Evidence map›Paper›PMID 31578331›Full record

ArticleNature communications2019

Hydrogen-bonded frameworks for molecular structure determination.

Yuantao Li, Sishuang Tang, Anna Yusov, James Rose, André Nyberg Borrfors, Chunhua T Hu, Michael D Ward

Abstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–field-weighted citation impact
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

30 citing papers in PubMed.

  1. Article
  2. Review
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  7. Article
  8. Hydrogen-bonded frameworks for conformational analysis of reactive substrates.Chemical communications (Cambridge, England) · 2024
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  9. Article
  10. Review
  11. Article
  12. Article
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  15. Article
  16. Steric and Geometrical Frustration Generate Two Higher-Order CuJournal of the American Chemical Society · 2024
    Article
  17. 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

7 authors.

Yuantao LiDepartment of Chemistry and Molecular Design Institute, New York University, 100 Washington Square East, Room 1001, New York, NY, 10003, USA.
Sishuang TangDepartment of Chemistry and Molecular Design Institute, New York University, 100 Washington Square East, Room 1001, New York, NY, 10003, USA.
Anna YusovDepartment of Chemistry and Molecular Design Institute, New York University, 100 Washington Square East, Room 1001, New York, NY, 10003, USA.
James RoseDepartment of Chemistry and Molecular Design Institute, New York University, 100 Washington Square East, Room 1001, New York, NY, 10003, USA.ORCID http://orcid.org/0000-0003-0607-2016
André Nyberg BorrforsDepartment of Chemistry and Molecular Design Institute, New York University, 100 Washington Square East, Room 1001, New York, NY, 10003, USA.
Chunhua T HuDepartment of Chemistry and Molecular Design Institute, New York University, 100 Washington Square East, Room 1001, New York, NY, 10003, USA. ch98@nyu.edu.
Michael D WardDepartment of Chemistry and Molecular Design Institute, New York University, 100 Washington Square East, Room 1001, New York, NY, 10003, USA. mdw3@nyu.edu.ORCID http://orcid.org/0000-0002-2090-781X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single crystal X-ray diffraction is arguably the most definitive method for molecular structure determination, but the inability to grow suitable single crystals can frustrate conventional X-ray diffraction analysis. We report herein an approach to molecular structure determination that relies on a versatile toolkit of guanidinium organosulfonate hydrogen-bonded host frameworks that form crystalline inclusion compounds with target molecules in a single-step crystallization, complementing the crystalline sponge method that relies on diffusion of the target into the cages of a metal-organic framework. The peculiar properties of the host frameworks enable rapid stoichiometric inclusion of a wide range of target molecules with full occupancy, typically without disorder and accompanying solvent, affording well-refined structures. Moreover, anomalous scattering by the framework sulfur atoms enables reliable assignment of absolute configuration of stereogenic centers. An ever-expanding library of organosulfonates provides a toolkit of frameworks for capturing specific target molecules for their structure determination.

Identifiers

PMID31578331
PMCPMC6775153

What OpenQuestion holds

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Registered trials

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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.