Evidence map›Paper›PMID 21611989›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2011

Self-assembled arene-ruthenium-based rectangles for the selective sensing of multi-carboxylate anions.

Vaishali Vajpayee, Young Ho Song, Min Hyung Lee, Hyunuk Kim, Ming Wang, Peter J Stang, Ki-Whan Chi

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

18 citing papers in PubMed, 85 citations in OpenAlex.

  1. Article
  2. Tailored charge-neutral self-assembled LBeilstein journal of organic chemistry · 2024
    Article
  3. Article
  4. Self-assembled ruthenium (II) metallacycles and metallacages with imidazole-based ligands and their in vitro anticancer activity.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  5. Article
  6. Article
  7. Review
  8. Coordination-driven self-assembly of discrete RuBeilstein journal of organic chemistry · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
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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 at 3 institutions in 2 countries.

Vaishali VajpayeeDepartment of Chemistry, University of Ulsan, Ulsan 680-749, Republic of Korea.
Young Ho Song
Min Hyung Lee
Hyunuk Kim
Ming Wang
Peter J Stang
Ki-Whan Chi
University of Ulsan · KRUniversity of Utah · USPohang University of Science and Technology · KR

Funding

POLYVALENT IODINE AND DERIVED CHEMISTRYR01GM057052 · NIGMS · UNIVERSITY OF UTAH · PI STANG, PETER J · 1998 to 2012
$3.3M
NIGMS NIH HHS GM-57052NIGMS NIH HHS R01 GM057052
6 · The paper itself

Abstract

Novel arene-ruthenium [2+2] metalla-rectangles 4 and 5 have been synthesized by self-assembly using dipyridyl amide ligand 3 and arene-ruthenium acceptors (arene: benzoquinone (1), naphthacenedione (2)) and characterized by NMR spectroscopy and ESI-MS. The solid-state structure of 5 was determined by X-ray diffraction and shows encapsulated diethyl ether molecule in the rectangular cavity of 5. The luminescent 5 was further used for anion sensing with the amidic linkage serving as a hydrogen-bond donor site for anions and the ruthenium moiety serving as a signaling unit. A UV/Vis titration study demonstrated that although 5 interacts very weakly with common monoanions as well as with flexible dicarboxylate anions such as malonate and succinate, it displays significant binding affinity (K>10(3) in MeOH) for rigid multi-carboxylate anions such as oxalate, citrate, and tartrate, exhibiting a 1:1 stoichiometry. It has been suggested that 1:1 bidentate hydrogen bonding assisted by appropriate geometrical complementarity is mainly responsible for the increased affinity of 5 towards such anions. A fluorescence titration study revealed a large fluorescence enhancement of 5 upon binding to multi-carboxylate anions, which can be attributed to the blocking of the photoinduced electron-transfer process from the arene-Ru moiety to the amidic donor in 5 as a result of hydrogen bonding between the donor and the anion.

Indexed as

AmidesAnionsCarboxylic AcidsHydrogen BondingMolecular StructureNuclear Magnetic Resonance, BiomolecularRutheniumAmidesAnionsCarboxylic AcidsRuthenium

Identifiers

PMID21611989
PMCPMC3358929
OpenAlexW2104095118

What OpenQuestion holds

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Read underepoch 390

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.