Evidence map›Paper›PMID 36234781›Full record

ArticleMolecules (Basel, Switzerland)2022

Density Functional Method Study on the Cooperativity of Intermolecular H-bonding and π-π

Yanni Wang, Chaowu Dai, Wei Huang, Tingting Ni, Jianping Cao, Jiangmei Pang, Huining Wei, Chaojie Wang

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Yanni WangThe Third Affiliated Hospital of Wenzhou Medical University, The Pharmacy Department of Ruian People's Hospital, Wenzhou 325000, China.
Chaowu DaiThe Third Affiliated Hospital of Wenzhou Medical University, The Pharmacy Department of Ruian People's Hospital, Wenzhou 325000, China.
Wei HuangThe Pharmacy Department of Ruian Hospital of Traditional Chinese Medicine, Wenzhou 325000, China.
Tingting NiSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325035, China.
Jianping CaoSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325035, China.
Jiangmei PangSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325035, China.
Huining WeiSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325035, China.
Chaojie WangSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325035, China.

Funding

the National Natural Science Foundation of China 21177098the National Science Foundation of Zhejiang Province Project LY16B070006
6 · The paper itself

Abstract

The exploration of the ionic liquids’ mechanism of action on nucleobase’s structure and properties is still limited. In this work, the binding model of the 1-alkyl-3-methylimidazolium bromide ([Cnmim]Br, n = 2, 4, 6, 8, 10) ionic liquids to the thymine (T) was studied in a water environment (PCM) and a microhydrated surroundings (PCM + wH2O). Geometries of the mono-, di-, tri-, and tetra-ionic thymine (T-wH2O-y[Cnmim]+-xBr−, w = 5~1 and x + y = 0~4) complexes were optimized at the M06-2X/6-311++G(2d, p) level. The IR and UV-Vis spectra, QTAIM, and NBO analysis for the most stable T-4H2O-Br−-1, T-3H2O-[Cnmim]+-Br−-1, T-2H2O-[Cnmim]+-2Br−-1, and T-1H2O-2[Cnmim]+-2Br−-1 hydrates were presented in great detail. The results show that the order of the arrangement stability of thymine with the cations (T-[Cnmim]+) by PCM is stacking > perpendicular > coplanar, and with the anion (T-Br−) is front > top. The stability order for the different microhydrates is following T-5H2O-1 < T-4H2O-Br−-1 < T-3H2O-[Cnmim]+-Br−-1 < T-2H2O-[Cnmim]+-2Br−-1 < T-1H2O-2[Cnmim]+-2Br−-1. A good linear relationship between binding EB values and the increasing number (x + y) of ions has been found, which indicates that the cooperativity of interactions for the H-bonding and π-π+ stacking is varying incrementally in the growing ionic clusters. The stacking model between thymine and [Cnmim]+ cations is accompanied by weaker hydrogen bonds which are always much less favorable than those in T-xBr− complexes; the same trend holds when the clusters in size grow and the length of alkyl chains in the imidazolium cations increase. QTAIM and NBO analytical methods support the existence of mutually reinforcing hydrogen bonds and π-π cooperativity in the systems.

Indexed as

Ionic LiquidsAnionsBromidesCationsImidazolesThymineWaterAnionsBromidesCationsImidazolesIonic LiquidsThymineWatercooperativityH-bondingionic liquidsthymineπ-π+ stacking

Identifiers

PMID36234781
PMCPMC9572290

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.