Evidence map›Paper›PMID 25706758›Full record

ArticleMolecules (Basel, Switzerland)2015

Divinyl sulfone cross-linked cyclodextrin-based polymeric materials: synthesis and applications as sorbents and encapsulating agents.

Julia Morales-Sanfrutos, Francisco Javier Lopez-Jaramillo, Mahmoud A A Elremaily, Fernando Hernández-Mateo, Francisco Santoyo-Gonzalez

Abstract 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Photoresponsive Slide-Ring Gels Enable Modulation of Sliding Dynamics.Angewandte Chemie (International ed. in English) · 2025
    Article
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  5. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Julia Morales-SanfrutosDepartamento de Química Orgánica, Facultad de Ciencias, Instituto de Biotecnología, Universidad de Granada, E1871 Granada, Spain. juliams@ugr.es.
Francisco Javier Lopez-JaramilloDepartamento de Química Orgánica, Facultad de Ciencias, Instituto de Biotecnología, Universidad de Granada, E1871 Granada, Spain. fjljara@ugr.es.
Mahmoud A A ElremailyDepartamento de Química Orgánica, Facultad de Ciencias, Instituto de Biotecnología, Universidad de Granada, E1871 Granada, Spain. msremaily@yahoo.com.
Fernando Hernández-MateoDepartamento de Química Orgánica, Facultad de Ciencias, Instituto de Biotecnología, Universidad de Granada, E1871 Granada, Spain. fhmateo@ugr.es.
Francisco Santoyo-GonzalezDepartamento de Química Orgánica, Facultad de Ciencias, Instituto de Biotecnología, Universidad de Granada, E1871 Granada, Spain. fsantoyo@ugr.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to evaluate the crosslinking abilities of divinyl sulfone (DVS) for the preparation of novel water-insoluble cyclodextrin-based polymers (CDPs) capable of forming inclusion complexes with different guest molecules. Reaction of DVS with native α-cyclodextrin (α-CD), β-cyclodextrin (β-CD) and/or starch generates a variety of homo- and hetero-CDPs with different degrees of crosslinking as a function of the reactants' stoichiometric ratio. The novel materials were characterized by powder X-ray diffraction, electron microscopy and for their sorption of phenol and 4-nitrophenol. They were further evaluated as sorbents with phenolic pollutants (bisphenol A and β-naphthol) and bioactive compounds (the hormone progesterone and curcumin). Data obtained from the inclusion experiments show that the degree of cross-linking has a minor influence on the yield of inclusion complex formation and highlight the important role of the CDs, supporting a sorption process based on the formation of inclusion complexes. In general, the inclusion processes are better described by a Freundlich isotherm although an important number of them can also be fitted to the Langmuir isotherm with R2 ≥ 0.9, suggesting a sorption onto a monolayer of homogeneous sites.

Indexed as

AdsorptionBenzhydryl CompoundsBisphenol A CompoundsCross-Linking ReagentsCurcuminCyclodextrinsHydrogen-Ion ConcentrationNaphtholsNitrophenolsPhenolsPolymersProgesteroneStarchSulfonesX-Ray Diffraction2-naphthol4-nitrophenolBenzhydryl Compoundsbisphenol ABisphenol A CompoundsCross-Linking ReagentsCurcuminCyclodextrinsdivinyl sulfoneNaphtholsNitrophenolsPhenolsPolymersProgesteroneStarchSulfones

Identifiers

PMID25706758
PMCPMC6272569

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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.