Abstract
The magnetic properties of a Mn12 single-molecule magnet with a loop structure are characterized by a computational study based on density functional theory. A study of the two reported crystal structures of such a complex correctly reproduces the experimental spin ground state. We have analyzed the effect of the choice of spin configurations employed for the calculations, as well as the influence of the inclusion of the next-nearest neighbor interactions on the calculated exchange coupling constants. Quantum Monte Carlo simulations performed with the calculated exchange coupling constants show that the best agreement with the experimental susceptibility curve is achieved by using the hybrid B3LYP functional.
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.
