Evidence map›Paper›PMID 26416382›Full record

ArticleScientific reports2015

Flower-like supramolecular self-assembly of phosphonic acid appended naphthalene diimide and melamine.

Rajesh S Bhosale, Mohammad Al Kobaisi, Sidhanath V Bhosale, Suresh Bhargava, Sheshanath V Bhosale

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
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  11. Article
  12. Phosphonic acid: preparation and applications.Beilstein journal of organic chemistry · 2017
    Review
  13. Article
  14. 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

5 authors.

Rajesh S BhosaleRMIT-IICT Research Centre, CSIR-Indian Institute of Chemical Technology, Hyderabad- 500 007, Telangana, India.
Mohammad Al KobaisiSchool of Applied Sciences, RMIT University, GPO Box 2476, Melbourne, Vic. 3001, Australia.
Sidhanath V BhosalePolymers and Functional Materials Division, CSIR-Indian Institute of Chemical Technology, Hyderabad-500 007, Telangana, India.
Suresh BhargavaSchool of Applied Sciences, RMIT University, GPO Box 2476, Melbourne, Vic. 3001, Australia.
Sheshanath V BhosaleSchool of Applied Sciences, RMIT University, GPO Box 2476, Melbourne, Vic. 3001, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diverse supramolecular assemblies ranging from nanometres to micrometers of small aromatic π-conjugated functional molecules have attracted enormous research interest in light of their applications in optoelectronics, chemosensors, nanotechnology, biotechnology and biomedicines. Here we study the mechanism of the formation of a flower-shaped supramolecular structure of phosphonic acid appended naphthalene diimide with melamine. The flower-shaped assembly formation was visualised by scanning electron microscope (SEM) and transmission electron microscopy (TEM) imaging, furthermore, XRD and DLS used to determined mode of aggregation. Characteristically, phosphonic acid-substituted at imide position of NDIs possess two important properties resulting in the formation of controlled flower-like nanostructures: (i) the aromatic core of the NDI which is designed to optimize the dispersive interactions (π-π stacking and van der Waals interactions) between the cores within a construct and (ii) phosphonic acid of NDI interact with malamine through molecular recognition i.e. strong hydrogen-bonding (H-bonding). We believe such arrangements prevent crystallization and favour the directional growth of flower-like nanostructure in 3D fashion. These works demonstrate that complex self-assembly can indeed be attained through hierarchical non-covalent interactions of two components. Furthermore, flower-like structures built from molecular recognition by these molecules indicate their potential in other fields if combined with other chemical entities.

Identifiers

PMID26416382
PMCPMC4586721

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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.