Abstract

Ferrocenylamine complexes have found increasing applications in the fields of catalysis in various organic reactions, industry, medical treatments and enzyme–activity determinations. Therefore, information related to the thermal and thermo-oxidative stability of these compounds is important for such applications; however, this information is currently limited. Twenty previously prepared palladium and platinum ferrocenylamine complexes with systematic structural variations are examined for their thermal (under nitrogen) and thermo-oxidation stability (under atmospheric air) using thermogravimetry (TG), differential thermal analysis (DTG), and differential scanning calorimetry (DSC) techniques. Degradation products are identified by comparing thermogravimetric analysis and theoretical calculations. Structure–stability studies are also discussed. The results show that all the compounds have high thermal and thermo-oxidative stabilities of up to 265 and 173 °C, respectively. Electron–donating substituents enhance the thermal and thermo-oxidative stabilities of the palladium complexes ( t-Bu, selenide electrophiles and dielectrophiles), while those with destabilizing effects are aromatic substituents (Ph and tolyl). Most platinum ferrocenylamine sulfides and selenides show higher thermal and thermo-oxidative stabilities than their corresponding palladium analogs. All the prepared compounds show high thermal and thermo-oxidative stability which reinforces their catalytic and industrial applications. However, their thermal stability is higher than their thermo-oxidative stability.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.