Evidence map›Paper›PMID 24658327›Full record

ArticleScientific reports2014

Molecular structure-optical property relationships for a series of non-centrosymmetric two-photon absorbing push-pull triarylamine molecules.

Marcelo G Vivas, Daniel L Silva, Jérémy Malinge, Mohammed Boujtita, Robert Zaleśny, Wojciech Bartkowiak, Hans Ågren, Sylvio Canuto, Leonardo De Boni, Eléna Ishow and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

11 authors.

Marcelo G Vivas1] Instituto de Física de São Carlos, Universidade de São Paulo, Caixa Postal 369, 13560-970 São Carlos, SP, Brazil [2] Instituto de Ciência e Tecnologia, Universidade Federal de Alfenas, Cidade Universitária - BR 267 Km 533, 37715-400 Poços de Caldas, MG, Brazil.
Daniel L Silva1] Instituto de Física, Universidade de São Paulo, CP 66318, 05314-970, São Paulo, SP, Brazil [2] Departamento de Ciências da Natureza, Matemática e Educação, Universidade Federal de São Carlos, Rod. Anhanguera - Km 174, 13600-970 Araras, SP, Brazil.
Jérémy MalingePPSM-UMR CNRS 8531, ENS Cachan, 61 avenue du Président Wilson, 94235 Cachan, France.
Mohammed BoujtitaCEISAM-UMR CNRS 6230, Université de Nantes, 2 rue de la Houssinière, 44322 Nantes, France.
Robert ZaleśnyTheoretical Chemistry Group, Institute of Physical and Theoretical Chemistry, Wroclaw University of Technology, Wybrzeze Wyspianskiego 27, 50-370 Wroclaw, Poland.
Wojciech BartkowiakTheoretical Chemistry Group, Institute of Physical and Theoretical Chemistry, Wroclaw University of Technology, Wybrzeze Wyspianskiego 27, 50-370 Wroclaw, Poland.
Hans ÅgrenDepartment of Theoretical Chemistry and Biology, School of Biotechnology, Royal Institute of Technology, SE-106 91 Stockholm, Sweden.
Sylvio CanutoInstituto de Física, Universidade de São Paulo, CP 66318, 05314-970, São Paulo, SP, Brazil.
Leonardo De BoniInstituto de Física de São Carlos, Universidade de São Paulo, Caixa Postal 369, 13560-970 São Carlos, SP, Brazil.
Eléna Ishow1] PPSM-UMR CNRS 8531, ENS Cachan, 61 avenue du Président Wilson, 94235 Cachan, France [2] CEISAM-UMR CNRS 6230, Université de Nantes, 2 rue de la Houssinière, 44322 Nantes, France.
Cleber R MendoncaInstituto de Física de São Carlos, Universidade de São Paulo, Caixa Postal 369, 13560-970 São Carlos, SP, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This article reports on a comprehensive study of the two-photon absorption (2PA) properties of six novel push-pull octupolar triarylamine compounds as a function of the nature of the electron-withdrawing groups. These compounds present an octupolar structure consisting of a triarylamine core bearing two 3,3'-bis(trifluoromethyl)phenyl arms and a third group with varying electron-withdrawing strength (H < CN < CHO < NO2 < Cyet < Vin). The 2PA cross-sections, measured by using the femtosecond open-aperture Z-scan technique, showed significant enhancement from 45 up to 125 GM for the lowest energy band and from 95 up to 270 GM for the highest energy band. The results were elucidated based on the large changes in the transition and permanent dipole moments and in terms of (i) EWG strength, (ii) degree of donor-acceptor charge transfer and (iii) electronic coupling between the arms. The 2PA results were eventually supported and confronted with theoretical DFT calculations of the two-photon transition oscillator strengths.

Indexed as

ElectronsMolecular StructureAbsorptiometry, PhotonAbsorptionDiphenylamineFluorescent DyesOptics and PhotonicsPhotonsStructure-Activity RelationshipDiphenylamineFluorescent Dyes

Identifiers

PMID24658327
PMCPMC3963076

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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.