Structural and Adsorption Effects of Some Thiopurine and Thiopyrimidine Derivatives on their Catalytic Activity at the Mercury Electrode

1994 ◽  
Vol 59 (7) ◽  
pp. 1472-1482 ◽  
Author(s):  
Mohamed Sayed Ibrahim

6-Thiopurine, 6-thiopurine riboside, 6-thioguanine, 6-thioguanosine, 8-thioguanosine, 2-thiouracil, 4-thiouridine, 2-thiocytosine and 2-thiocytidine are investigated by means of DC polarography and coulometry. In acid medium they give a typical catalytic hydrogen discharge wave, as shown by its parameters and the regeneration of the depolarizer during the electrode process. At pH values above 4.2 a second catalytic wave appears. Both catalytic waves possess pronounced surface characteristics, most likely due to adsorption of the molecules with differing orientations on the electrode surface. The catalytic wave overlaps the reduction wave, which is placed in evidence under conditions where the catalytic effect is absent. Under the same conditions, 2-thiouracil was found to be catalytically inactive, but it induces catalytic hydrogen evolution in Co(II)-containing ammonia buffer. The present results indicate that the position of thio group yields also such distinct change in the catalytic activity of the investigated compounds.

2000 ◽  
Vol 65 (6) ◽  
pp. 995-1013 ◽  
Author(s):  
Florinel G. Banica ◽  
Ana Ion

The catalytic hydrogen evolution on the dropping mercury electrode in the presence of Ni(II) and D-penicillamine (Pen) at pH around 6 yields a catalytic hydrogen prewave (CHP) with E1/2 = -1.21 V vs SCE. This wave is similar to the CHP produced by selenocysteine and cysteine described previously. The occurrence of the CHP depends on the formation of the mono(D-penicillamine-N,S)nickel(II) complex whereas bis(D-penicillamine-N,S)nickel(II) complex is inert and has no influence on the CHP electrode process. Although the analogous bis(cysteine) complex is labile, there is strong evidence that it does not take part directly in the CHP process in the Ni(II)-cysteine system. The actual proton donor in the CHP electrode process is the hydronium ion and not the acid component of the buffer. A tentative reaction mechanism was formulated with emphasis on the state of the intermediate hydrogen species. The characteristic pH, nickel ion involvement and the structure of the ligand make the CHP process an attractive model for hydrogen redox reactions catalyzed by [NiFe] hydrogenase.


2019 ◽  
Vol 7 (39) ◽  
pp. 22571-22578 ◽  
Author(s):  
In Hye Kwak ◽  
Ik Seon Kwon ◽  
Tekalign Terfa Debela ◽  
Jaemin Seo ◽  
Jae-Pyoung Ahn ◽  
...  

Two-dimensional MoS2–melamine hybrid nanostructures exhibit excellent catalytic activity toward the hydrogen evolution reaction.


2017 ◽  
Vol 53 (5) ◽  
pp. 846-849 ◽  
Author(s):  
Naoto Kuwamura ◽  
Yoshinari Kurioka ◽  
Takumi Konno

Stepwise construction of a 1D heterotrimetallic coordination polymer containing all three group 10 metal ions and its heterogeneous catalytic activity for electrochemical hydrogen evolution are reported.


1983 ◽  
Vol 48 (2) ◽  
pp. 544-549 ◽  
Author(s):  
Jorge Alfredo Bolzan ◽  
Robert Tokoro

The electroreduction of cobalt(II) in aqueous thiocyanate solutions at the dropping mercury electrode depends on the thiocyanate concentration. At [SCN-] = 0.3 mol/l the intermediate cobalt(I)-thiocyanate complex does exist electrokinetically and may be responsible for the appearance of a peaked catalytic wave. The predecessor species of this intermediate may be CoSCN+ and Co(SCN)2 in similarity to the behaviour of cobalt(II) with cyanide and azide ions.


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