Related Experiment Video
Updated: Apr 1, 2026

Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology
Published on: March 12, 2015
One-step synthesis of 1,3- and 1,1'-diarylated ferrocenes toward main-chain metallomacrocycles
Wenjuan Li1, Yuanping Li2, Yanting Shi2
1Henan Key Laboratory of Biomarker Detection and Diagnosis for Neurodegenerative Diseases, Shangqiu Normal University, Shangqiu, 476000, China. liult05@iccas.ac.cn.
Abstract:
An efficient one-step synthesis of 1,3- and 1,1'-diarylferrocenes was developed via the reaction of ferrocene with anilines. This practical method enables gram-scale preparation of diarylsubstituted ferrocene derivatives. Furthermore, the 1,1'-diarylferrocene served as a key building block for the concise construction of a main-chain ferrocene-based macrocycle (main-Fc[11]CPP) in only two additional steps. The structure of main-Fc[11]CPP was unambiguously confirmed by single-crystal X-ray diffraction, revealing a strained ellipsoidal geometry. Photophysical and electrochemical studies demonstrate that the macrocycle exhibits intramolecular charge-transfer behavior and possesses a lower strain energy compared to its side-chain analog.
More Related Videos
09:45Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
Published on: March 20, 2017
09:35Preparation of a Corannulene-functionalized Hexahelicene by CopperI-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
Related Concept Videos
Cycloaddition Reactions: Overview
Diels–Alder Reaction Forming Cyclic Products: Stereochemistry
Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
Thermal and Photochemical Electrocyclic Reactions: Overview
Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction