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Reduction Potential of Ferrocenoyl-Substituted Nucleobases. Experimental and Computational Study (CROSBI ID 250272)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Havaić, Valentina ; Djaković, Senka ; Lapić, Jasmina ; Weitner, Tin ; Šakić, Davor ; Vrček, Valerije Reduction Potential of Ferrocenoyl-Substituted Nucleobases. Experimental and Computational Study // Croatica chemica acta, 90 (2017), 4; 589-594. doi: 10.5562/cca3229

Podaci o odgovornosti

Havaić, Valentina ; Djaković, Senka ; Lapić, Jasmina ; Weitner, Tin ; Šakić, Davor ; Vrček, Valerije

engleski

Reduction Potential of Ferrocenoyl-Substituted Nucleobases. Experimental and Computational Study

Organometallic derivatives of nucleobases are characterized by distinctive biological and electrochemical properties. In this work, reduction potentials of ferrocenoyl-substituted nucleobases (uracil, 5-fluorouracil, and thymine) were measured by cyclic voltammetry and calculated by using density functional methods. Both experimental (281– 296 mV) and calculated (271–293 mV) values for reduction potential E°’ show that these conjugates are much better oxidants than the parent ferrocene system. In search for the computational model, which can successfully reproduce experimental results, the M06-2X functional appeared as the optimal method in terms of efficiency and accuracy.

redox potential ; ferrocene ; nucleobase ; cyclic voltammetry ; density functional

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Podaci o izdanju

90 (4)

2017.

589-594

objavljeno

0011-1643

1334-417X

10.5562/cca3229

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Kemija

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