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Chameleonic Photo- and Mechanoluminescence in Pyrazolate-Bridged NHC Cyclometalated Platinum Complexes

[Image: see text] DFT investigations on the ground (GS) and the first triplet (T(1)) excited state potential energy surfaces (PES) were performed on a new series of platinum-butterfly complexes, [{Pt(C(∧)C*)(μ-Rpz)}(2)] (Rpz: pz, 1; 4-Mepz, 2; 3,5-dmpz, 3; 3,5-dppz, 4), containing a cyclometalated N...

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Autores principales: Sicilia, Violeta, Arnal, Lorenzo, Escudero, Daniel, Fuertes, Sara, Martin, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892954/
https://www.ncbi.nlm.nih.gov/pubmed/34339189
http://dx.doi.org/10.1021/acs.inorgchem.1c01470
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author Sicilia, Violeta
Arnal, Lorenzo
Escudero, Daniel
Fuertes, Sara
Martin, Antonio
author_facet Sicilia, Violeta
Arnal, Lorenzo
Escudero, Daniel
Fuertes, Sara
Martin, Antonio
author_sort Sicilia, Violeta
collection PubMed
description [Image: see text] DFT investigations on the ground (GS) and the first triplet (T(1)) excited state potential energy surfaces (PES) were performed on a new series of platinum-butterfly complexes, [{Pt(C(∧)C*)(μ-Rpz)}(2)] (Rpz: pz, 1; 4-Mepz, 2; 3,5-dmpz, 3; 3,5-dppz, 4), containing a cyclometalated NHC in their wings. The geometries of two close-lying local minima corresponding to butterfly spread conformers, 1s–4s, and butterfly folded ones, 1f–4f, with long and short Pt–Pt separations, respectively, were optimized in the GS and T(1) PES. A comparison of the GS and T(1) energy profiles revealed that an opposite trend is obtained in the relative stability of folded and spread conformers, the latter being more stabilized in their GS. Small ΔG (s/f) along with small-energy barriers in the GS support the coexistence of both kinds of conformers, which influence the photo- and mechanoluminescence of these complexes. In 5 wt % doped PMMA films in the air, these complexes exhibit intense sky-blue emissions (PLQY: 72.0–85.9%) upon excitation at λ ≤ 380 nm arising from (3)IL/MLCT excited states, corresponding to the predominant 1s–4s conformers. Upon excitation at longer wavelengths (up to 450 nm), the minor 1f–4f conformers afford a blue emission as well, with PLQY still significant (40%–60%). In the solid state, the as-prepared powder of 4 exhibits a greenish-blue emission with QY ∼ 29%, mainly due to (3)IL/(3)MLCT excited states of butterfly spread molecules, 4s. Mechanical grinding resulted in an enhanced and yellowish-green emission (QY ∼ 51%) due to the (3)MMLCT excited states of butterfly folded molecules, 4f, in such a way that the mechanoluminescence has been associated with an intramolecular structural change induced by mechanical grinding.
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spelling pubmed-88929542022-03-04 Chameleonic Photo- and Mechanoluminescence in Pyrazolate-Bridged NHC Cyclometalated Platinum Complexes Sicilia, Violeta Arnal, Lorenzo Escudero, Daniel Fuertes, Sara Martin, Antonio Inorg Chem [Image: see text] DFT investigations on the ground (GS) and the first triplet (T(1)) excited state potential energy surfaces (PES) were performed on a new series of platinum-butterfly complexes, [{Pt(C(∧)C*)(μ-Rpz)}(2)] (Rpz: pz, 1; 4-Mepz, 2; 3,5-dmpz, 3; 3,5-dppz, 4), containing a cyclometalated NHC in their wings. The geometries of two close-lying local minima corresponding to butterfly spread conformers, 1s–4s, and butterfly folded ones, 1f–4f, with long and short Pt–Pt separations, respectively, were optimized in the GS and T(1) PES. A comparison of the GS and T(1) energy profiles revealed that an opposite trend is obtained in the relative stability of folded and spread conformers, the latter being more stabilized in their GS. Small ΔG (s/f) along with small-energy barriers in the GS support the coexistence of both kinds of conformers, which influence the photo- and mechanoluminescence of these complexes. In 5 wt % doped PMMA films in the air, these complexes exhibit intense sky-blue emissions (PLQY: 72.0–85.9%) upon excitation at λ ≤ 380 nm arising from (3)IL/MLCT excited states, corresponding to the predominant 1s–4s conformers. Upon excitation at longer wavelengths (up to 450 nm), the minor 1f–4f conformers afford a blue emission as well, with PLQY still significant (40%–60%). In the solid state, the as-prepared powder of 4 exhibits a greenish-blue emission with QY ∼ 29%, mainly due to (3)IL/(3)MLCT excited states of butterfly spread molecules, 4s. Mechanical grinding resulted in an enhanced and yellowish-green emission (QY ∼ 51%) due to the (3)MMLCT excited states of butterfly folded molecules, 4f, in such a way that the mechanoluminescence has been associated with an intramolecular structural change induced by mechanical grinding. American Chemical Society 2021-08-02 2021-08-16 /pmc/articles/PMC8892954/ /pubmed/34339189 http://dx.doi.org/10.1021/acs.inorgchem.1c01470 Text en © 2021 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Sicilia, Violeta
Arnal, Lorenzo
Escudero, Daniel
Fuertes, Sara
Martin, Antonio
Chameleonic Photo- and Mechanoluminescence in Pyrazolate-Bridged NHC Cyclometalated Platinum Complexes
title Chameleonic Photo- and Mechanoluminescence in Pyrazolate-Bridged NHC Cyclometalated Platinum Complexes
title_full Chameleonic Photo- and Mechanoluminescence in Pyrazolate-Bridged NHC Cyclometalated Platinum Complexes
title_fullStr Chameleonic Photo- and Mechanoluminescence in Pyrazolate-Bridged NHC Cyclometalated Platinum Complexes
title_full_unstemmed Chameleonic Photo- and Mechanoluminescence in Pyrazolate-Bridged NHC Cyclometalated Platinum Complexes
title_short Chameleonic Photo- and Mechanoluminescence in Pyrazolate-Bridged NHC Cyclometalated Platinum Complexes
title_sort chameleonic photo- and mechanoluminescence in pyrazolate-bridged nhc cyclometalated platinum complexes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892954/
https://www.ncbi.nlm.nih.gov/pubmed/34339189
http://dx.doi.org/10.1021/acs.inorgchem.1c01470
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