Revisiting the TCNQF 4 0 / 1 - / 2 - ${{\bf TCNQF}_{\bf 4}^{{\bf 0/1 - /2 - }} }$ Catalysis Mechanism for the F e C N 6 3 - / 4 - ${\left[ {{\bf Fe}\left( {{\bf CN}} \right)_{\bf 6} } \right]^{{\bf 3 - /4 - }} }$ - S 2 O 6 2 - ${{\bf S}_{\bf 2} {\bf O}_{\bf 6}^{{\bf 2 - }} }$ / S 4 O 6 2 - ${{\bf S}_{\bf 4} {\bf O}_{\bf 6}^{{\bf 2 - }} }$ Redox Reaction.
Copyright policy ) Anbrah E, Alzubidi; Alan M, Bond; Lisandra L, Martin;
Revisiting the TCNQF 4 0 / 1 - / 2 - ${{\bf TCNQF}_{\bf 4}^{{\bf 0/1 - /2 - }} }$ Catalysis Mechanism for the F e C N 6 3 - / 4 - ${\left[ {{\bf Fe}\left( {{\bf CN}} \right)_{\bf 6} } \right]^{{\bf 3 - /4 - }} }$ - S 2 O 6 2 - ${{\bf S}_{\bf 2} {\bf O}_{\bf 6}^{{\bf 2 - }} }$ / S 4 O 6 2 - ${{\bf S}_{\bf 4} {\bf O}_{\bf 6}^{{\bf 2 - }} }$ Redox Reaction.
The front cover artwork was done by Michelle Farrelly, a member of the Martin group at Monash University. The image represents a perspective of a cuvette in which the catalysis of the thiosulfate-ferricyanide reaction was achieved by a TCNQF4 -based redox reaction in aqueous solution. The primary method used to monitor these reactions was spectrophotometry. Read the full text of the Research Article at 10.1002/cphc.202200942.
- Monash University Australia
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