Electrochemistry of Redox Active Centres Encapsulated by Non-Covalent Methods

2010 ◽  
Vol 63 (2) ◽  
pp. 184 ◽  
Author(s):  
Suresh Gadde ◽  
Elizabeth K. Batchelor ◽  
Angel E. Kaifer

This manuscript presents a summary of recent research work on the electrochemical behaviour of redox active guests fully or almost fully encapsulated by suitable molecular receptors or molecular capsules. From the standpoint of their voltammetric behaviour the cyclodextrins have been shown to be very dynamic hosts, which hamper the observation of direct electron transfer to/from their inclusion complexes. Therefore, this Review is essentially concerned with research work on cucurbituril and cavitand-type hosts, which was mostly done in the author’s laboratory. In general terms, the observed voltammetric behaviour for encapsulated guests covers a wide range of possibilities. Cucurbituril and cavitand-type hosts afford more kinetically stable complexes, whose direct electrochemical behaviour is observable and tends to be kinetically slower than that of the free guests. However, the degree of kinetic attenuation varies over a wide range and, in some cases, challenges our ability to rationalize the data. Clearly, more variation in the host structures and more research work are required to improve our understanding of encapsulation effects on these electron transfer reactions.

2021 ◽  
Author(s):  
Dai Oyama ◽  
Takatoshi Kanno ◽  
Tsugiko Takase

Quinone derivatives and their metal complexes are well-known molecules that participate in electron-transfer reactions relevant to diverse fields. However, the fundamental knowledge on the unique reactivity of redox-active quinone complexes...


1988 ◽  
Vol 43 (4) ◽  
pp. 382-388 ◽  
Author(s):  
K. Bütje ◽  
W. Preetz

AbstractThe first two complete series of all 10 possible linkage and geometric isomers of the general formula [Os(NCS)n(SCN)6-n]3-/2- have been obtained. The Os(III) complexes, some of which have been previously known, are prepared from the reactions of K2[OsX6], X = Cl. Br. I, and K2[OsO2(OH)4] with excess aqueous or methanolic KSCN solution and subsequent chromato­graphic separation on DEAE cellulose. Oxidation with Ce(IV) in acetone or methanol yields the corresponding Os(IV) compounds without changes in the ligand sphere except for n = 0, but pure salts of [Os(SCN)6]2“ are isolated by repeated recrystallization. S-bonding is less favoured in Os(IV) than in Os(III), proving that Os(IV) is the harder Lewis acid. Cyclic voltammograms of all isomers show two waves, a mainly irreversible Os(II)/Os(III) couple and a reversible Os(III)/Os(IV) couple. Characteristic shifts of the half-wave potentials of both electron transfer reactions within the series give strong evidence of π-back donation to -NCS.


2005 ◽  
Vol 67 (1) ◽  
pp. 115-124 ◽  
Author(s):  
Sergey Shleev ◽  
Anna Jarosz-Wilkolazka ◽  
Anna Khalunina ◽  
Olga Morozova ◽  
Alexander Yaropolov ◽  
...  

2009 ◽  
Vol 76 (1-2) ◽  
pp. 34-41 ◽  
Author(s):  
Karolina Haberska ◽  
Cristina Vaz-Domínguez ◽  
Antonio L. De Lacey ◽  
Marius Dagys ◽  
Curt T. Reimann ◽  
...  

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