What is it about?
Coordination compounds of cobalt (III) [Co(NH3)5NO2]XY could undergo the isomerisation [Co(NH3)5NO2]XY -> [Co(NH3)5ONO]XY when irradiated by visible light. Photoisomerisation in such complexes lead to macroscopic mechanical effects, such as fragmentation of the crystal, bending or jumping. These phenomena were earlier called “photosalient effect” and “photomechanical effect”. Understanding its nature could help to develop molecular switches and other devices that could transform irradiation into mechanical work. It is well known that the rate of the photoisomerisation and photosalient effect in such complexes depend on the outer-sphere anions XY, because changing XY leads to changes in crystal structure.
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Why is it important?
Free space around NO2 group and hydrogen bonds play key role in solid-state reactivity. Therefore, it is important to compare corresponding parameters in different structures to better understand how changing the outer-sphere anions XY might affect crystal structure and photoisomerisation. We have compared two isostructural compounds [Co(NH3)5NO2]ClNO3 and [Co(NH3)5NO2]BrNO3, their crystal structures and the changes arising during the photoisomerisation. Crystal structures of the reaction products [Co(NH3)5ONO]ClNO3 and [Co(NH3)5ONO]BrNO3 also were compared. Mainly we concentrated on free space in those structures and hydrogen bonds. We found that substituting Cl for a larger Br anion in [Co(NH3)5NO2]XNO3 leads to the expansion of crystal structure and free space. Therefore, mechanical response becomes less pronounced.
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This page is a summary of: A comparison of the isostructural [Co(NH3)5NO2]XNO3 and [Co(NH3)5ONO]XNO3, X = Cl− or Br− in relation to nitro–nitrito linkage isome..., Acta Crystallographica Section B Structural Science Crystal Engineering and Materials, May 2024, International Union of Crystallography,
DOI: 10.1107/s2052520624002816.
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