What is it about?

Pterins (2-amino-4-oxopteridines) are important in a wide range of biological functions including a large number of metal–containing enzymes (e.g., Fe, Mo, W) . The redox noninnocent nature of the pterin ring is associated with the ability of its pyrazine ring to exist in a number of oxidation states . In the above enzymes, this redox capability of the pterin moiety is matched by the ability of the metal centres to display multiple oxidation states . This aspect has catalysed research work on the coordination chemistry of pteridines in general and pterins in particular .

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Why is it important?

like the NAD+/NADH couple where NAD+ can be reduced nonezymatically by the reducing agents like Na2S2O4 or NaBH4. NADH can in turn be nonenzymatically reoxidized with K3[Fe(CN)6], but it is not oxidized directly by molecular O2 .Here we observe that the reaction possibility also follows the principle of single electron transfer. A comparison of the kinetic parameters is quite instructive; the raction with K3[Fe(CN)6] involving an electron transfer process is quite faster as compared to the other two group transfer processes.

Perspectives

Here we studied the reactivity of synthetic W(IV) pterin complexs and provides with the impetus for the present endeavour using 2–pivaloylamino–6–acetonyl–isoxanthopterin (1, H2L) . Its 1´´-pivaloyl group plays a crucial role in enhancing solubility of the unsubtituted pterin and facilitating the synthetic and purification steps . Here (1) acts as a reducing agent towards the tungsten(VI) starting material Na2WO4.2H2O leading to the formation of the present tungsten (IV) complexes (2), (3) and (4). Their characterization aspects, spectroscopic analysis and reactivity studies towards biologically relevant substrates are delineated here

Mr Siddhartha S Baisya
University of North Bengal

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This page is a summary of: Synthesis, Characterization of New Tungsten(IV)?Pterin Complexes and their Reactivity Studies towards Trimethylamine N-Oxide, Sodium Borohydride and Potassium Ferricyanide, Journal of Chromatography & Separation Techniques, January 2013, OMICS Publishing Group,
DOI: 10.4172/2157-7064.1000198.
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