Two expanded pyridinium-based compounds 1 and 2 were studied by cyclic voltammetry in two different environments. The nonaqueous solution suppresses the adsorption of the compounds on the electrode surface. Adsorption process in aqueous environment was confirmed by typical shape of the curve as well as by the linear dependence of peak current on the scan rate. The shift of standard redox potential in aqueous solution compared to nonaqueous environment toward more negative potential indicates the adsorption of reactant on the electrode surface. Larger shift observed for flat conjugated molecule 1 confirms its stronger adsorption than for the second molecule
The electrochemical properties of branched extended pyridinium cations depend strongly on the struct...
In this work, a new electrochemical detection method was developed with the ability to determine a ...
In this work, a new electrochemical detection method was developed with the ability to determine a ...
Adsorption properties of a series of redox-active expanded pyridinium molecules were studied at an e...
This paper gives a brief review of our efforts to describe adsorption of organic molecules at gold a...
We examine the electrochemical behavior of pyridine (py) and pyridinium ion (pyrH<sup>+</sup>) on go...
PhDAnalytical chemistryUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://de...
The major factors determining the potential-driven phase changes of the films of 4-pyridyl terminate...
The major factors determining the potential-driven phase changes of the films of 4-pyridyl terminate...
Ph.D.Analytical chemistryUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://...
The electrochemical reduction of aqueous hexamminecobalt(III) is studied using cyclic voltammetry, o...
The electroadsorption on columnar Au electrodes (substrate) of pyridine from x M pyridine + 0.1 M HC...
The cathodic stripping voltammetric behaviour of pyridine-2-thiol and some related heterocyclic thio...
Electrochemical reduction of organic compounds is elegant methods of preparative organic chemistry a...
The adsorption behaviour of the bifunctional molecule 2-(2'-thienyl)pyridine (TP) on Au(111) was cha...
The electrochemical properties of branched extended pyridinium cations depend strongly on the struct...
In this work, a new electrochemical detection method was developed with the ability to determine a ...
In this work, a new electrochemical detection method was developed with the ability to determine a ...
Adsorption properties of a series of redox-active expanded pyridinium molecules were studied at an e...
This paper gives a brief review of our efforts to describe adsorption of organic molecules at gold a...
We examine the electrochemical behavior of pyridine (py) and pyridinium ion (pyrH<sup>+</sup>) on go...
PhDAnalytical chemistryUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://de...
The major factors determining the potential-driven phase changes of the films of 4-pyridyl terminate...
The major factors determining the potential-driven phase changes of the films of 4-pyridyl terminate...
Ph.D.Analytical chemistryUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://...
The electrochemical reduction of aqueous hexamminecobalt(III) is studied using cyclic voltammetry, o...
The electroadsorption on columnar Au electrodes (substrate) of pyridine from x M pyridine + 0.1 M HC...
The cathodic stripping voltammetric behaviour of pyridine-2-thiol and some related heterocyclic thio...
Electrochemical reduction of organic compounds is elegant methods of preparative organic chemistry a...
The adsorption behaviour of the bifunctional molecule 2-(2'-thienyl)pyridine (TP) on Au(111) was cha...
The electrochemical properties of branched extended pyridinium cations depend strongly on the struct...
In this work, a new electrochemical detection method was developed with the ability to determine a ...
In this work, a new electrochemical detection method was developed with the ability to determine a ...
Add to ORKG