Evidence map›Paper›PMID 26389866›Full record

ArticleMolecules (Basel, Switzerland)2015

Quantification of CH-π Interactions Using Calix[4]pyrrole Receptors as Model Systems.

Gemma Aragay, Daniel Hernández, Begoña Verdejo, Eduardo C Escudero-Adán, Marta Martínez, Pablo Ballester

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
5.7field-weighted citation impact, top 5% 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

5 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Molecular recognition of pyrazineChemical science · 2020
    Article
  4. Article
  5. Host-guest complexes of conformationally flexibleBeilstein journal of organic chemistry · 2018
    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

6 authors at 1 institution in 1 country.

Gemma AragayInstitute of Chemical Research of Catalonia (ICIQ), Avgda. Països Catalans 16, Tarragona 43007, Spain. garagay@iciq.es.
Daniel HernándezInstitute of Chemical Research of Catalonia (ICIQ), Avgda. Països Catalans 16, Tarragona 43007, Spain. dhernandez@iciq.es.
Begoña VerdejoInstitute of Chemical Research of Catalonia (ICIQ), Avgda. Països Catalans 16, Tarragona 43007, Spain. begona.verdejo@uv.es.
Eduardo C Escudero-AdánInstitute of Chemical Research of Catalonia (ICIQ), Avgda. Països Catalans 16, Tarragona 43007, Spain. eescudero@iciq.es.
Marta MartínezInstitute of Chemical Research of Catalonia (ICIQ), Avgda. Països Catalans 16, Tarragona 43007, Spain. mmartinez@iciq.es.
Pablo BallesterInstitute of Chemical Research of Catalonia (ICIQ), Avgda. Països Catalans 16, Tarragona 43007, Spain. pballester@iciq.es.
Institut Català d'Investigació Química · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe the use of two series of aryl-extended calix[4]pyrrole receptors bearing two and four electronically tunable phenyl groups, respectively, in their meso-positions as model systems for the quantification of CH-π interactions in solution. The "four-wall" and the "two-wall" receptors formed thermodynamically stable 1:1 complexes in acetonitrile solution with both trimethylamine N-oxide and trimethylphosphine P-oxide as guests. The complexes were mainly stabilized by the formation of four convergent hydrogen bonds between the oxygen atom of the guests and the pyrrole NHs of the host. In general, the N-oxide produced thermodynamically more stable hydrogen bonding interactions than the P-oxide. Upon guest binding, the receptors adopted the cone conformation and the methyl groups of the included guests engaged in CH-π interactions with the aromatic walls. We show that the modification of the electronic properties of the aromatic surfaces, in any of the receptor series, did not have a significant impact in the measured binding affinities for a given guest. However, the larger binding affinities determined for the "four-wall" receptors in comparison to the "two-wall" counterparts supported the importance of CH-π interactions on guest complexation. The strength of the CH-π interactions present in the inclusion complexes was quantified employing the octamethyl calix[4]pyrrole as reference. We determined an average magnitude of ~1 kcal·mol(-1) for each CH-π interaction. The CH-π interactions featured a reduced electrostatic nature and thus dispersion forces were assigned as main contributors of their strength.

Indexed as

Models, MolecularQuantum TheoryCalixarenesHydrogen BondingMolecular StructurePorphyrinsThermodynamicscalix(4)pyrroleCalixarenesPorphyrinscalix[4]pyrroleCH-π interactionsdispersion forceselectrostatic forcestrimethylamine oxidetrimethylphosphine oxide

Identifiers

PMID26389866
PMCPMC6332063
OpenAlexW1708672294

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.