New materials capable of storing and processing information at the level of a single molecule (atom) will contribute to the development of digital technologies. This type of molecules has to possess the property of bistability—the ability of molecules to exist in two stable spin states, for example, spin-crossover. In recent decades, there has been a growing interest in control over spin states of coordinative compounds based on Fe(III) cations because of their potential application in fields like molecular spintronics, memory and electronic devices, switches, and sensors [1].
The rational design of molecular building blocks allows researchers to manage the coordination sphere of the metal, and hence magnetic properties can be controlled [2]. Due to the possibility of wide functionalization, calix[4]arenes are extremely attractive for the design of pre-organized ligands. Moreover, the modification of calix[4]arene makes it possible to tune the structure of the complexes as well as to control their size and geometry. Disubstituted derivatives of calix[4]arenes allow the fine-tuning of the metal environment by varying the length of the alkyl spacer and the nature of the substituent in the coordinating fragment. It is particularly attractive to obtain salen-type ligands possessing N,O-coordinating chelate fragments.
In this work, we report on the synthesis of new Fe(III)-complexes based on polydentate lower rim disubstituted calix[4]arenes ligands, displaying a salen-type coordination pocket. The structures of prepared coordination compounds were studied by means of X-ray diffraction analysis, IR and 57Fe Mössbauer spectroscopy, and HR-ESI mass spectrometry. The structure–property correlation is also discussed.
- Kaushik, S. Mehta, M. Das, S. Ghosh, S. Kamilya, A. Mondal. Chem. Com. 2023. 59(88), 13107-13124.
- J. Harding, P. Harding, W. Phonsri. Coord. Chem. Rev. 2016, 313, 38-61.
