volume 56 issue 20 pages 12379-12388

Luminescence Mechanochromism Induced by Cluster Isomerization

Brendan Huitorel 1
Hani El Moll 2
Marie Odile Cordier 3
Alexandre Fargues 4
Alain Garcia 4
Florian Massuyeau 5
Thierry Gacoin 1
1
 
Laboratoire de Physique de la Matière Condensée
2
 
Institut de Chimie de Strasbourg
3
 
Laboratoire de chimie moléculaire
4
 
Institut de Chimie de la Matière Condensée de Bordeaux, CNRS, 87 Avenue du Docteur A. Schweitzer, 33608 Pessac Cedex, France
7
 
CEMHTI-CNRS, UPR 3079, 1D Avenue de la Recherche Scientifique, 45071 Orléans Cedex 2, France
Publication typeJournal Article
Publication date2017-09-26
scimago Q1
wos Q1
SJR0.958
CiteScore7.4
Impact factor4.7
ISSN00201669, 1520510X
Inorganic Chemistry
Physical and Theoretical Chemistry
Abstract
Luminescent mechanochromic materials exhibiting reversible changes of their emissive properties in response to external mechanical forces are currently emerging as an important class of stimuli-responsive materials because of promising technological applications. Here, we report on the luminescence mechanochromic properties of a [Cu4I4(PPh3)4] copper iodide cluster presenting a chair geometry, being an isomer of the most common cubane form. This molecular cluster formulated [Cu4I4(PPh3)4]·2CHCl3 (1) exhibits a highly contrasted emission response to manual grinding, and, interestingly, the optical properties of the ground phase present striking similarities with those of the cubane isomer. In order to understand the underlying mechanism, a comparison with two related compounds has been conducted. The first one is a pseudopolymorph of 1 formulated as [Cu4I4(PPh3)4]·CH2Cl2 (2), which exhibits luminescent mechanochromic properties as well. The other one is also a chair compound but with a slightly different phosphine ligand, namely, [Cu4I4(PPh2C6H4CO2H)4] (3), lacking mechanochromic properties. Structural and optical characterizations of the clusters have been analyzed in light of previous electronic structure calculations. The results suggest an unpreceded mechanochromism phenomenon based on a solid-state chair → cubane isomer conversion. This study shows that polynuclear copper iodide compounds are particularly relevant for the development of luminescent mechanochromic materials.
Found 
Found 

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GOST Copy
Huitorel B. et al. Luminescence Mechanochromism Induced by Cluster Isomerization // Inorganic Chemistry. 2017. Vol. 56. No. 20. pp. 12379-12388.
GOST all authors (up to 50) Copy
Huitorel B., Moll H. E., Cordier M. O., Fargues A., Garcia A., Massuyeau F., Martineau Corcos C., Gacoin T., Perruchas S. Luminescence Mechanochromism Induced by Cluster Isomerization // Inorganic Chemistry. 2017. Vol. 56. No. 20. pp. 12379-12388.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1021/acs.inorgchem.7b01870
UR - https://doi.org/10.1021/acs.inorgchem.7b01870
TI - Luminescence Mechanochromism Induced by Cluster Isomerization
T2 - Inorganic Chemistry
AU - Huitorel, Brendan
AU - Moll, Hani El
AU - Cordier, Marie Odile
AU - Fargues, Alexandre
AU - Garcia, Alain
AU - Massuyeau, Florian
AU - Martineau Corcos, Charlotte
AU - Gacoin, Thierry
AU - Perruchas, Sandrine
PY - 2017
DA - 2017/09/26
PB - American Chemical Society (ACS)
SP - 12379-12388
IS - 20
VL - 56
PMID - 28949130
SN - 0020-1669
SN - 1520-510X
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2017_Huitorel,
author = {Brendan Huitorel and Hani El Moll and Marie Odile Cordier and Alexandre Fargues and Alain Garcia and Florian Massuyeau and Charlotte Martineau Corcos and Thierry Gacoin and Sandrine Perruchas},
title = {Luminescence Mechanochromism Induced by Cluster Isomerization},
journal = {Inorganic Chemistry},
year = {2017},
volume = {56},
publisher = {American Chemical Society (ACS)},
month = {sep},
url = {https://doi.org/10.1021/acs.inorgchem.7b01870},
number = {20},
pages = {12379--12388},
doi = {10.1021/acs.inorgchem.7b01870}
}
MLA
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Huitorel, Brendan, et al. “Luminescence Mechanochromism Induced by Cluster Isomerization.” Inorganic Chemistry, vol. 56, no. 20, Sep. 2017, pp. 12379-12388. https://doi.org/10.1021/acs.inorgchem.7b01870.