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Single model compounds have been widely used, but they give a quite simplified picture.
Various model compounds have been synthesized to investigate substituent effects on benzocyclobutene reactivity.
Model compounds have been used to investigate the curing behaviour of resole phenol formaldehyde resins.
Due to the diversity of organic compounds found in this aqueous fraction, model compounds have usually been used to study this mixture.
Mononuclear model compounds have been used to advance the knowledge base regarding the physical properties and reactivity of high-valent (MnIV or MnV) complexes.
Structural changes in the Brill transitions of Nylon 10/10 and its model compounds have been investigated by carrying out the temperature-dependent measurements of X-ray diffraction and infrared spectra along with the DSC measurement.
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The bonding of sodium ions by these polymers having PEO arms and with model compounds has been studied in anhydrous methanol solutions.
Some NOM model compounds had experimentally determined Langmuir maximum adsorption capacities (qmax−Langmuir) greater than those calculated based on external surface area measurements and the size of the NOM model compound, suggesting adsorption to internal as well as external sites at the GR-Cl surface for these compounds.
Huber, et al. [11] used model compounds having the same reactive groups towards O3 as 17α-ethinylestradiol in order to simplify the identification process of the OTPs of this estrogen.
The results indicate that the model compound has not DNA as a target molecule.
N-(4′-benzyl phenyl-1,2,3,6-tetrahydrophthalimide model compound has been synthesized and its thermal reaction mechanism studied.
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