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Voltage Stimulated Anion Binding of Metalloporphyrin‐induced Crystalline 2D Nanoflakes
Author(s) -
Mrinalini Madoori,
Pathak Sushil Swaroop,
Achary B. Shivaprasad,
Panchakarla Leela S.,
Prasanthkumar Seelam
Publication year - 2019
Publication title -
chemistry – an asian journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.18
H-Index - 106
eISSN - 1861-471X
pISSN - 1861-4728
DOI - 10.1002/asia.201801794
Subject(s) - amorphous solid , stacking , protonation , ion , chemistry , ferrocene , materials science , nanotechnology , electrochemistry , crystallography , electrode , organic chemistry
Voltage‐stimulated redox‐active materials have received significant attention in the field of organic electronics and sensor technology. Such stimuli‐responsive materials trigger the formation of crystalline nanostructures and facilitate the design of efficient smart devices hitherto unknown. Herein, we report that free‐base and metallo‐tetratolylporphyrin‐linked ferrocene derivatives ( H 2 TTP ‐ Fc and ZnTTP ‐ Fc ) undergo distinct proton/anion binding mechanism in CHCl 3 during bulk electrolysis at applied voltage of 1.4 V to give [ H 4 TTP ‐ Fc] + Cl − and H + [ (Cl)ZnTTP ‐ Fc] − followed by nanospheres and crystalline 2D nanoflakes formation, confirmed by SEM and TEM images, by methanol vapor diffusion (MVD) approach. Moreover, X‐ray diffraction analysis suggest that protonated H 2 TTP ‐ Fc aggregates exhibit amorphous nature, whereas H + [ (Cl)ZnTTP ‐ Fc] − depict crystalline nature from layer‐by‐layer arrangement of nanoflakes assisted by π–π stacking and ion‐dipole interactions.