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Properties of metastable linkage NO isomers in Na2[Fe(CN)5NO]·2H2O incorporated in mesopores of silica xerogels
Author(s) -
Z. Tahri,
Robert Lepski,
KuanYing Hsieh,
ElEulmi Bendeif,
Sébastien Pillet,
Pierrick Durand,
Theo Woike,
Dominik Schaniel
Publication year - 2012
Publication title -
physical chemistry chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.053
H-Index - 239
eISSN - 1463-9084
pISSN - 1463-9076
DOI - 10.1039/c2cp23607a
Subject(s) - metastability , linkage isomerism , absorption spectroscopy , infrared spectroscopy , spectroscopy , absorption (acoustics) , particle size , molecule , chemistry , particle (ecology) , mesoporous material , analytical chemistry (journal) , materials science , crystallography , metal , organic chemistry , physics , oceanography , quantum mechanics , composite material , geology , catalysis
We study the properties of photoinduced metal-nitrosyl linkage isomers in sodium nitroprusside (SNP) as a function of particle size. By embedding the molecular complex at various concentrations into mesopores of silica xerogels the size of the particles can be adjusted. The ground state is characterized by X-ray diffraction, absorption and infrared spectroscopy. The physical properties of the photoswitched molecules were analysed by steady-state low-temperature absorption, infrared spectroscopy and by nanosecond transient absorption spectroscopy. The electronic structure as well as the activation energies of the metastable linkage isomers are independent of the particle size down to single isolated molecules, indicating that the SNP complexes are quasi-free inside the pores of the gel.

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