Evidence map›Paper›PMID 35559172›Full record

ArticleACS omega2022

Functional, Aromatic, and Fluorinated Monothiosemicarbazones: Investigations into Their Structures and Activity toward the Gallium-68 Incorporation by Microwave Irradiation.

Sophia Sarpaki, Fernando Cortezon-Tamarit, Rüdiger Maria Exner, Kexin Song, Sara Raquel Mota Merelo de Aguiar, Haobo Ge, Charareh Pourzand, Stephen James Paisey, Gabriele Kociok-Köhn, Jonathan Robin Dilworth and 2 more

Abstract read
In one paragraph

Article in ACS omega, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Sophia SarpakiDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.ORCID https://orcid.org/0000-0003-4323-3165
Fernando Cortezon-TamaritDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.ORCID https://orcid.org/0000-0002-2871-7965
Rüdiger Maria ExnerDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.ORCID https://orcid.org/0000-0002-9415-382X
Kexin SongDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
Sara Raquel Mota Merelo de AguiarDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
Haobo GeDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
Charareh PourzandDepartment of Pharmacy and Pharmacology, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
Stephen James PaiseyWales Research and Diagnostic PET Imaging Centre, School of Medicine, University of Cardiff, Cardiff CF10 3AT, United Kingdom.ORCID https://orcid.org/0000-0002-2274-3708
Gabriele Kociok-KöhnDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.ORCID https://orcid.org/0000-0002-7186-1399
Jonathan Robin DilworthDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
Laurence CarrollDepartment of Medicine, Imperial College, Du Cane Road, London W12 0NN, United Kingdom.
Sofia Ioana PascuDepartment of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.ORCID https://orcid.org/0000-0001-6385-4650

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report on the synthesis and spectroscopic characterization of a new series of coordinating monothiosemicarbazones incorporating aromatic backbones, featuring O/N/S donor centers monosubstituted with different aliphatic, aromatic, fluorinated, and amine-functionalized groups at their N centers. Their ability to bind metal ions such as Zn(II) and Ga(III) was explored, and the formation of two different coordination isomers of the Zn(II) complex was demonstrated by X-ray diffraction studies using synchrotron radiation. These studies showed the planar geometry for the coordinated mono(thiosemicarbazone) ligand and that the metal center can adopt either a heavily distorted tetrahedral Zn center (placed in an N/S/S/N environment, with CN = 4) or a pseudo-octahedral geometry, where the Zn(II) center is in the O/N/S/S/N/O environment, and CN = 6. Furthermore, 2-(4,5-dimethyl-2-thiazolyl)-3,5-diphenyl-2

Identifiers

PMID35559172
PMCPMC9088960

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Registered trials

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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.