Abstract
AbstractSynthesis, structural organization, thermal, and magnetic properties of coordination polymers (OSS‐polymer‐Me) based on amphiphilic oligomeric silsesquioxanes (OSS) and transition metal ions (Co2+, Ni2+) are reported. The initial amphiphilic OSS containing various ratios of n‐octadecylurethane and carboxyl groups (OSS‐C18H37‐x‐COOH‐y) are characterized with two types of ordered phases. The first one is a supramolecular structure stabilized by hydrogen bonds and characterized with a specific endothermic transition on differential scanning calorimetry thermograms (Tm1). The second one is presented by crystalline domains of aliphatic chains with a melting transition peak (Tm2). Inclusion of metals has no effect on the magnitude of Tm2 while leading to a decrease in the value of the Tm1 in comparison to the same compounds without metal. Being located in the nodes of the irregular network structure of OSS‐polymer‐Me, metal ions form ≈2 nm clusters, which connect multifunctional molecules of OSS‐C18H37‐x‐COOH‐y in a supramolecular system similar to disordered metal‐organic framework. The OSS‐polymer‐Me nanocomposites display superparamagnetic properties determined by an adaptive behavior of the intermolecular network. The latter can be modified by the application of an external magnetic field and/or moderate heat.
Sign-in/Register to access full text options 
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 callDisclaimer: 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.
