Aggregation Effects on Pigment Coatings: Pigment Red 179 as a Case Study.


Journal

ACS omega
ISSN: 2470-1343
Titre abrégé: ACS Omega
Pays: United States
ID NLM: 101691658

Informations de publication

Date de publication:
03 Dec 2019
Historique:
received: 31 08 2019
accepted: 04 11 2019
entrez: 10 12 2019
pubmed: 10 12 2019
medline: 10 12 2019
Statut: epublish

Résumé

Here, we have studied, with a combined experimental and computational approach, the effect of the crystal environment and aggregation on the electronic properties of Pigment Red 179, which affect both its color and optical energy gap. Spectra acquired in the near-infrared and visible range of energies suggest that this molecule is indeed a "cool" dye, which can be employed as a red pigment that provides effective color coverage to different substrates without contributing to their heating during light irradiation. Spectra acquired on different polymer mixtures at different pigment concentrations (i.e., 2.5-10 wt %) suggest that absorption features depend on chromophoric arrangements promoted by the strong intermolecular π-π interactions. Calculations, performed at the time-dependent density functional theory level, allowed to both attribute the nature of the electronic transitions causing the observed spectra involved and understand the effect of the environment. Indeed, the visible spectra of the pigment is dominated by two localized transitions, with negligible charge transfer for both a dye monomer and dimer either in vacuum or acetonitrile solution. Instead, models including the crystal environment of the pigment show the presence of a high-wavelength S

Identifiants

pubmed: 31815234
doi: 10.1021/acsomega.9b02819
pmc: PMC6893955
doi:

Types de publication

Journal Article

Langues

eng

Pagination

20315-20323

Informations de copyright

Copyright © 2019 American Chemical Society.

Déclaration de conflit d'intérêts

The authors declare no competing financial interest.

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Auteurs

Francesco Muniz-Miranda (F)

École Nationale Supérieure de Chimie de Paris and PSL Research University, CNRS, Institute of Chemistry for Life and Health Sciences (i-CLeHS), FRE 2027, 11, rue Pierre et Marie Curie, F-75005 Paris, France.

Pierpaolo Minei (P)

Deparment of Chemistry and Industrial Chemistry, University of Pisa, Via Giuseppe Moruzzi 13, 56124 Pisa, Italy.

Luca Contiero (L)

Cromology Italia S.P.A., Via 4 Novembre 4, 55016 Porcari, Lucca, Italy.

Frédéric Labat (F)

École Nationale Supérieure de Chimie de Paris and PSL Research University, CNRS, Institute of Chemistry for Life and Health Sciences (i-CLeHS), FRE 2027, 11, rue Pierre et Marie Curie, F-75005 Paris, France.

Ilaria Ciofini (I)

École Nationale Supérieure de Chimie de Paris and PSL Research University, CNRS, Institute of Chemistry for Life and Health Sciences (i-CLeHS), FRE 2027, 11, rue Pierre et Marie Curie, F-75005 Paris, France.

Carlo Adamo (C)

École Nationale Supérieure de Chimie de Paris and PSL Research University, CNRS, Institute of Chemistry for Life and Health Sciences (i-CLeHS), FRE 2027, 11, rue Pierre et Marie Curie, F-75005 Paris, France.

Fabio Bellina (F)

Deparment of Chemistry and Industrial Chemistry, University of Pisa, Via Giuseppe Moruzzi 13, 56124 Pisa, Italy.

Andrea Pucci (A)

Deparment of Chemistry and Industrial Chemistry, University of Pisa, Via Giuseppe Moruzzi 13, 56124 Pisa, Italy.

Classifications MeSH