Abstract

Fullerenes were synthesized to form sulfonated fullerenes by novel less cost-effective manner using diethyl ether as solvent. The synthesized sulfonated fullerene was extensively characterized by UV–Vis, FT-IR, FT-RAMAN, XRD, SEM HRTEM, XPS, EPR and VSM. FT-IR characterization reveals the presence of functional SO3H groups and FT-Raman characterization confirms the symmetry of the molecule. UV–Vis spectral analysis endorses red shifting of absorption peak. EPR spectrum, at room temperature with g-factor values, indicates the paramagnetic nature and magnetic ion sites of the samples. Structural changes, in sulfonated fullerene, are observed through Scanning electron microscope (SEM) and High-resolution transmission electron microscope (HRTEM). HRTEM micrographs showed that the sulfonation improves the good dispersion of fullerene in water. X-ray photoelectron spectroscopy (XPS) and energy dispersive spectroscopy (EDX) confirm the presence of carbon, sulphur and oxygen element in the molecule. Magnetization studies were measured using a vibrating sample magnetometer (VSM). The sulfonated fullerene exhibited superparamagnetic (SPM) behaviour at 5 K with saturation magnetization value (ms = 0.14 emu/g). The zero-field cooled (ZFC) curve exhibited a blocking temperature Tb which is close to 5 K. Such superparamagnetic studies attempted for the first time in this work for sulfonated fullerene and the result displays potential applications in the field of magnetically guided drug delivery and can be envisaged as a good agent for various biomedical and engineering purposes in future.

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.