Evidence map›Paper›PMID 36686943›Full record

ArticleRSC advances2023

Solution- and gas-phase study of binding of ammonium and bisammonium hydrocarbons to oxacalix[4]arene carboxylate.

Anna Cowart, Mari-Liis Brük, Nikita Žoglo, Helena Roithmeyer, Merle Uudsemaa, Aleksander Trummal, Kaspar Selke, Riina Aav, Elina Kalenius, Jasper Adamson

Abstract read
In one paragraph

Article in RSC advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Anna CowartLaboratory of Chemical Physics, National Institute of Chemical Physics and Biophysics Akadeemia Tee 23 12618 Tallinn Estonia jasper.adamson@kbfi.ee.
Mari-Liis BrükLaboratory of Chemical Physics, National Institute of Chemical Physics and Biophysics Akadeemia Tee 23 12618 Tallinn Estonia jasper.adamson@kbfi.ee.ORCID https://orcid.org/0000-0002-2159-5539
Nikita ŽogloLaboratory of Chemical Physics, National Institute of Chemical Physics and Biophysics Akadeemia Tee 23 12618 Tallinn Estonia jasper.adamson@kbfi.ee.ORCID https://orcid.org/0000-0002-6006-1636
Helena RoithmeyerLaboratory of Chemical Physics, National Institute of Chemical Physics and Biophysics Akadeemia Tee 23 12618 Tallinn Estonia jasper.adamson@kbfi.ee.ORCID https://orcid.org/0000-0002-6585-5953
Merle UudsemaaLaboratory of Chemical Physics, National Institute of Chemical Physics and Biophysics Akadeemia Tee 23 12618 Tallinn Estonia jasper.adamson@kbfi.ee.ORCID https://orcid.org/0000-0001-9486-4632
Aleksander TrummalLaboratory of Chemical Physics, National Institute of Chemical Physics and Biophysics Akadeemia Tee 23 12618 Tallinn Estonia jasper.adamson@kbfi.ee.ORCID https://orcid.org/0000-0002-2943-6129
Kaspar SelkeLaboratory of Chemical Physics, National Institute of Chemical Physics and Biophysics Akadeemia Tee 23 12618 Tallinn Estonia jasper.adamson@kbfi.ee.
Riina AavDepartment of Chemistry and Biotechnology, Tallinn University of Technology Akadeemia Tee 15 12618 Tallinn Estonia.ORCID https://orcid.org/0000-0001-6571-7596
Elina KaleniusDepartment of Chemistry, NanoScience Center, University of Jyväskylä Survontie 9B FI-40014 JY Finland.ORCID https://orcid.org/0000-0001-8038-1314
Jasper AdamsonLaboratory of Chemical Physics, National Institute of Chemical Physics and Biophysics Akadeemia Tee 23 12618 Tallinn Estonia jasper.adamson@kbfi.ee.ORCID https://orcid.org/0000-0002-9853-7353

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxacalixarenes represent a distinctive class of macrocyclic compounds, which are closely related to the parent calixarene family, offering binding motifs characteristic of calixarenes and crown ethers. Nevertheless, they still lack extensive characterization in terms of molecular recognition properties and the subsequent practical applicability. We present here the results of binding studies of an oxacalix[4]arene carboxylate macrocycle toward a variety of organic ammonium cationic species. Our results show that the substituents attached to the guest ammonium compound largely influence the binding strengths of the host. Furthermore, we show that the characteristic binding pattern changes upon transition from the gas phase to solution in terms of the governing intermolecular interactions. We identify the key factors affecting host-guest binding efficacy and suggest rules for the important molecular structural motifs of the interacting parts of ammonium guest species and the macrocycle to facilitate sensing of ammonium cations.

Identifiers

PMID36686943
PMCPMC9812018

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.