Evidence map›Paper›PMID 29046861›Full record

ArticleChemistryOpen2017

Quinoline-Derived Two-Photon-Sensitive Octupolar Probes.

Petra Dunkel, Morgane Petit, Hamid Dhimane, Mireille Blanchard-Desce, David Ogden, Peter I Dalko

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in ChemistryOpen, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Breaking Bonds by Light: The Absorbance-Fragmentation Paradox.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025
    Article
  3. 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.

Petra DunkelLaboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques Université Paris Descartes 45, rue des Saints-Pères 75270 Paris Cedex 06 France.
Morgane PetitLaboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques Université Paris Descartes 45, rue des Saints-Pères 75270 Paris Cedex 06 France.
Hamid DhimaneLaboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques Université Paris Descartes 45, rue des Saints-Pères 75270 Paris Cedex 06 France.
Mireille Blanchard-DesceUniversité de Bordeaux ISM (CNRS UMR5255) Bâtiment A12, 351, Cours de la Libération 33405 Talence Cedex France.
David OgdenLaboratoire de Physiologie Cérébrale Université Paris Descartes 45, rue des Saints-Pères 75270 Paris Cedex 06 France.
Peter I DalkoLaboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques Université Paris Descartes 45, rue des Saints-Pères 75270 Paris Cedex 06 France.ORCID 0000-0003-2294-3643

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A systematic study on quinoline-derived light sensitive probes, having third-order rotational symmetry is presented. The electronically linked octupolar structures show considerably improved linear and nonlinear photophysical properties under one- and two-photon irradiation conditions compared to the corresponding monomers. Photolysis of the three acetate derivatives shows strong structure dependency: whereas irradiation of the 6- and 7-aminoquinoline derivatives resulted in fast intramolecular cyclization and only trace amounts of fragmentation products, the 8-aminoquinoline derivative afforded clean and selective photolysis, with a sequential release of their acetate groups (

Indexed as

caged compoundsnonlinear opticsphotolysisprotecting groupsreactive intermediates

Identifiers

PMID29046861
PMCPMC5641908

What OpenQuestion holds

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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.