Journal
JOURNAL OF CHEMICAL PHYSICS
Volume 155, Issue 17, Pages -Publisher
AIP Publishing
DOI: 10.1063/5.0067404
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This study investigates the molecular dynamics of imidacloprid using dielectric spectroscopy, oscillatory shear rheology, and calorimetry, revealing that the molecular dynamics in its glassy state strongly depends on its thermal history. The research shows that different methods predict different relaxation times, indicating the complexity of imidacloprid's behavior in technological applications.
Employing dielectric spectroscopy, oscillatory shear rheology, and calorimetry, the present work explores the molecular dynamics of the widely used insecticide imidacloprid above and below its glass transition temperature. In its supercooled liquid regime, the applied techniques yield good agreement regarding the characteristic structural (alpha) relaxation times of this material. In addition, the generalized Gemant-DiMarzio-Bishop model provides a good conversion between the frequency-dependent dielectric and shear mechanical responses in its viscous state, allowing for an assessment of imidacloprid's molecular hydrodynamic radius. In order to characterize the molecular dynamics in its glassy regime, we employ several approaches. These include the application of frequency-temperature superposition (FTS) to its isostructural dielectric and rheological responses as well as use of dielectric and calorimetric physical aging and the Adam-Gibbs-Vogel model. While the latter approach and dielectric FTS provide relaxation times that are close to each other, the other methods predict notably longer times that are closer to those reflecting a complete recovery of ergodicity. This seemingly conflicting dissimilarity demonstrates that the molecular dynamics of glassy imidacloprid strongly depends on its thermal history, with high relevance for the use of this insecticide as an active ingredient in technological applications.
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