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Relating Excited States to the Dynamics of Macroscopic Strain in Photoresponsive Crystals Full article

Journal Inorganic Chemistry
ISSN: 0020-1669 , E-ISSN: 1520-510X
Output data Year: 2022, Volume: 61, Number: 8, Pages: 3573–3585 Pages count : 13 DOI: 10.1021/acs.inorgchem.1c03607
Tags Ammonia; Dynamics; Irradiation; Isomerization; Isomers; Photochemical reactions; Single crystals
Authors Ahmed Ejaz 1 , Chizhik Stanislav 2,3 , Sidelnikov Anatoly 2 , Boldyreva Elena 3,4 , Naumov Pance 1
Affiliations
1 Smart Materials Lab, New York University, 808 Abu Dhabi, Abu Dhabi 51133, U.A.E.
2 Institute of Solid State Chemistry and Mechanochemistry SB RAS, Novosibirsk 630128
3 Novosibirsk State University, Novosibirsk, 630090, Russian Federation
4 Boreskov Institute of Catalysis SB RAS, Novosibirsk 630090, Russian Federation

Funding (3)

1 Ministry of Science and Higher Education of the Russian Federation 0239-2021-0002
2 New York University Abu Dhabi
3 Ministry of Science and Higher Education of the Russian Federation 075-00521-21-00 (121032500059-4) (FWUS-2021-0001)

Abstract: Exposure of a photoreactive single crystal to light with a wavelength offset from its absorption maximum can have two distinct effects. The first is the “direct” effect, wherein the excited state generated in individual chemical species is influenced. The second is the “indirect” effect, which describes the penetration of light into the crystal and hence the spatial propagation and completeness of transformation. We illustrate using the nitro−nitrito isomerization of [Co(NH3)5NO2]Cl(NO3) as an example that the direct and indirect effects can be independently determined. This is achieved by comparing the dynamics of macroscopic crystal deformation (bending curvature and crystal elongation) induced by the photochemical reaction when irradiating a crystal at the absorption maximum and at different band edges (above or below the maximum) of the same band. Quantitative description of the macroscopic strain dynamics in comparison with experiments allowed us to suggest that irradiation at different tails of the same absorption band causes isomerization to proceed via different excited states and an additional photochemical reaction (presumably, reverse nitrito−nitro isomerization) can occur on irradiation at the ligand-field band edges.
Cite: Ahmed E. , Chizhik S. , Sidelnikov A. , Boldyreva E. , Naumov P.
Relating Excited States to the Dynamics of Macroscopic Strain in Photoresponsive Crystals
Inorganic Chemistry. 2022. V.61. N8. P.3573–3585. DOI: 10.1021/acs.inorgchem.1c03607 WOS Scopus РИНЦ ANCAN PMID OpenAlex
Dates:
Submitted: Nov 18, 2021
Published online: Feb 16, 2022
Published print: Feb 28, 2022
Identifiers:
Web of science: WOS:000790015500023
Scopus: 2-s2.0-85125370146
Elibrary: 48186106
Chemical Abstracts: 2022:356010
Chemical Abstracts (print): 182:79873
PMID: 35170305
OpenAlex: W4213367860
Citing:
DB Citing
Scopus 20
Elibrary 22
Web of science 20
OpenAlex 19
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