Evidence map›Paper›PMID 37265740›Full record

ArticleChemical science2023

Two-photon isomerization properties of donor-acceptor Stenhouse adducts.

Francisco A Reza-González, Emmanuel Villatoro, Mariana M Reza, Jesús Jara-Cortés, Héctor García-Ortega, Edgard F Blanco-Acuña, José G López-Cortés, Nuria Esturau-Escofet, Alan Aguirre-Soto, Jorge Peon

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2023. 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
1.1field-weighted citation impact, top 28% of its field
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, 11 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Francisco A Reza-GonzálezInstituto de Química, Universidad Nacional Autónoma de México Ciudad de México Mexico jpeon@unam.mx.ORCID https://orcid.org/0009-0003-0439-6006
Emmanuel VillatoroInstituto de Química, Universidad Nacional Autónoma de México Ciudad de México Mexico jpeon@unam.mx.ORCID https://orcid.org/0000-0002-3682-5077
Mariana M RezaInstituto de Química, Universidad Nacional Autónoma de México Ciudad de México Mexico jpeon@unam.mx.ORCID https://orcid.org/0000-0002-2698-9393
Jesús Jara-CortésUnidad Académica de Ciencias Básicas e Ingenierías, Universidad Autónoma de Nayarit Tepic 63155 Mexico.ORCID https://orcid.org/0000-0002-2296-6119
Héctor García-OrtegaFacultad de Química, Universidad Nacional Autónoma de México Ciudad de México Mexico.ORCID https://orcid.org/0000-0003-4262-4033
Edgard F Blanco-AcuñaFacultad de Química, Universidad Nacional Autónoma de México Ciudad de México Mexico.ORCID https://orcid.org/0000-0002-1031-4375
José G López-CortésInstituto de Química, Universidad Nacional Autónoma de México Ciudad de México Mexico jpeon@unam.mx.ORCID https://orcid.org/0000-0002-4508-117X
Nuria Esturau-EscofetInstituto de Química, Universidad Nacional Autónoma de México Ciudad de México Mexico jpeon@unam.mx.ORCID https://orcid.org/0000-0002-0915-5346
Alan Aguirre-SotoSchool of Engineering and Sciences, Tecnologico de Monterrey Monterey Nuevo Leon Mexico.ORCID https://orcid.org/0000-0003-0455-5401
Jorge PeonInstituto de Química, Universidad Nacional Autónoma de México Ciudad de México Mexico jpeon@unam.mx.ORCID https://orcid.org/0000-0002-4571-5136
Universidad Nacional Autónoma de México · MXTecnológico de Monterrey · MXUniversidad Autónoma de Nayarit · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Donor-acceptor Stenhouse adducts (DASAs) are important photo-responsive molecules that undergo electrocyclic reactions after light absorption. From these properties, DASAs have received extensive attention as photo-switches with negative photochromism. Meanwhile, several photochemical applications require isomerization events to take place in highly localized volumes at variable depths. Such focused photoreactions can be achieved if the electronic excitation is induced through a non-linear optical process. In this contribution we describe DASAs substituted with extended donor groups which provide them with significant two-photon absorption properties. We characterized the photo-induced transformation of these DASAs from the open polymethinic form to their cyclopentenic isomer with the use of 800 nm femtosecond pulses. These studies verified that the biphotonic excitation produces equivalent photoreactions as linear absorbance. We also determined these DASAs' two-photon absorption cross sections from measurements of their photoconverted yield after biphotonic excitation. As we show, specific donor sections provide these systems with important biphotonic cross-sections as high as 615 GM units. Such properties make these DASAs among the most non-linearly active photo-switchable molecules. Calculations at the TDDFT level with the optimally tuned range-separated functional OT-CAM-B3LYP, together with quadratic response methods indicate that the non-linear photochemical properties in these molecules involve higher lying electronic states above the first excited singlet. This result is consistent with the observed relation between their two-photon chemistry and the onset of their short wavelength absorption features around 400 nm. This is the first report of the non-linear photochemistry of DASAs. The two-photon isomerization properties of DASAs extend their applications to 3D-photocontrol, non-linear lithography, variable depth birefringence, and localized drug delivery schemes.

Identifiers

PMID37265740
PMCPMC10231324
OpenAlexW4366956762

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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.