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Metal Coordination and Isomerization of a Hydrazone Switch
Author(s) -
Croteau Molly L.,
Su Xin,
Wilcox Dean E.,
Aprahamian Ivan
Publication year - 2014
Publication title -
chempluschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.801
H-Index - 61
ISSN - 2192-6506
DOI - 10.1002/cplu.201402134
Subject(s) - isomerization , chemistry , hydrazone , molecular switch , counterion , metal , isothermal titration calorimetry , stoichiometry , coordination complex , metal ions in aqueous solution , inorganic chemistry , photochemistry , ion , computational chemistry , stereochemistry , molecule , catalysis , organic chemistry
Metal coordination and isomerization of a hydrazone‐based molecular switch ( 1 ) was investigated with isothermal titration calorimetry (ITC) and UV/Vis spectroscopy. Three equilibria—initial binding, ligand redistribution, and isomerization ( 1 → 1′ )—are required to characterize the interaction of metal ions with the molecular switch. The stoichiometry of the initial complex and the relative magnitudes of the three equilibria constants depend on the size and Lewis acidity of the metal ion and competition from the counterion. Strongly coordinating anions (e.g., Cl − ) suppress the formation of the initial metal–switch complex and isomerization. The thermodynamics for the equilibrium M 2+ +2 1 ⇌M( 1′ ) 2 2+ have been determined for Zn 2+ , Cd 2+ , and Hg 2+ from the ITC data.