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The article 《Mechanically-tunable quantum interference in ferrocene-based single-molecule junctions》 also mentions many details about this compound(1273-73-0)Synthetic Route of C10BrFe, you can pay attention to it, because details determine success or failure

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: Bromoferrocene, is researched, Molecular C10BrFe, CAS is 1273-73-0, about Mechanically-tunable quantum interference in ferrocene-based single-molecule junctions.Synthetic Route of C10BrFe.

Ferrocenes are ubiquitous organometallic building blocks that comprise a Fe atom sandwiched between two cyclopentadienyl (Cp) rings that rotate freely at room temperature Of widespread interest in fundamental studies and real-world applications, they have also attracted some interest as functional elements of mol.-scale devices. Here, the impact of the configurational degrees of freedom of a ferrocene derivative on its single-mol. junction conductance is investigated. Measurements indicate that the conductance of the ferrocene derivative, which is suppressed by two orders of magnitude as compared to a fully conjugated analog, can be modulated by altering the junction configuration. Ab initio transport calculations show that the low conductance is a consequence of destructive quantum interference effects that arise from the hybridization of metal-based d-orbitals and the ligand-based π-system. By rotating the Cp rings, the hybridization, and thus the quantum interference, can be mech. controlled, resulting in a conductance modulation that is seen exptl.

The article 《Mechanically-tunable quantum interference in ferrocene-based single-molecule junctions》 also mentions many details about this compound(1273-73-0)Synthetic Route of C10BrFe, you can pay attention to it, because details determine success or failure

Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com