Synthesis and reactivity of bioinspired superoxocopper(II) complexes
End-on superoxocopper(II) are evidenced to be active oxidants in a number of copper-containing oxygenase enzymes which are responsible for catalysing the stereoselective oxidation of moderate strength C─H bonds at ambient temperatures. Presently, there are over twenty synthetic biomimetic end-on sup...
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sg-ntu-dr.10356-1549602023-02-28T23:38:48Z Synthesis and reactivity of bioinspired superoxocopper(II) complexes Laxmi, Shoba Mihaiela Stuparu School of Physical and Mathematical Sciences Jason England mstuparu@ntu.edu.sg Science::Chemistry End-on superoxocopper(II) are evidenced to be active oxidants in a number of copper-containing oxygenase enzymes which are responsible for catalysing the stereoselective oxidation of moderate strength C─H bonds at ambient temperatures. Presently, there are over twenty synthetic biomimetic end-on superoxocopper(II) complexes which have played an invaluable role in understanding the factors that govern dioxygen activation and substrate reaction mechanisms. However, most of them are only stable at cryogenic temperatures and exhibit limited reactivity with exogenous substrates. The England group recently reported three end-on superoxocopper(II) complexes, [CuII(η1-O2•−)(Ar3-TMPA)]+ (Ar = tpb, dpb and dtbpb), that are fully stable against dimerization at all temperatures. However, the reactivity of these [CuII(η1-O2•−)(Ar3-TMPA)]+ complexes was found to be sluggish attributed to steric hindrance. This study aims to produce more reactive derivatives of these complexes, by reducing their steric bulk, whilst also addressing some deficiencies in the existing Ar3-TMPA work. Master of Science 2022-01-21T01:04:45Z 2022-01-21T01:04:45Z 2022 Thesis-Master by Research Laxmi, S. (2022). Synthesis and reactivity of bioinspired superoxocopper(II) complexes. Master's thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/154960 https://hdl.handle.net/10356/154960 10.32657/10356/154960 en This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0). application/pdf Nanyang Technological University |
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Science::Chemistry Laxmi, Shoba Synthesis and reactivity of bioinspired superoxocopper(II) complexes |
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End-on superoxocopper(II) are evidenced to be active oxidants in a number of copper-containing oxygenase enzymes which are responsible for catalysing the stereoselective oxidation of moderate strength C─H bonds at ambient temperatures. Presently, there are over twenty synthetic biomimetic end-on superoxocopper(II) complexes which have played an invaluable role in understanding the factors that govern dioxygen activation and substrate reaction mechanisms. However, most of them are only stable at cryogenic temperatures and exhibit limited reactivity with exogenous substrates. The England group recently reported three end-on superoxocopper(II) complexes, [CuII(η1-O2•−)(Ar3-TMPA)]+ (Ar = tpb, dpb and dtbpb), that are fully stable against dimerization at all temperatures. However, the reactivity of these [CuII(η1-O2•−)(Ar3-TMPA)]+ complexes was found to be sluggish attributed to steric hindrance. This study aims to produce more reactive derivatives of these complexes, by reducing their steric bulk, whilst also addressing some deficiencies in the existing Ar3-TMPA work. |
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Mihaiela Stuparu |
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Mihaiela Stuparu Laxmi, Shoba |
format |
Thesis-Master by Research |
author |
Laxmi, Shoba |
author_sort |
Laxmi, Shoba |
title |
Synthesis and reactivity of bioinspired superoxocopper(II) complexes |
title_short |
Synthesis and reactivity of bioinspired superoxocopper(II) complexes |
title_full |
Synthesis and reactivity of bioinspired superoxocopper(II) complexes |
title_fullStr |
Synthesis and reactivity of bioinspired superoxocopper(II) complexes |
title_full_unstemmed |
Synthesis and reactivity of bioinspired superoxocopper(II) complexes |
title_sort |
synthesis and reactivity of bioinspired superoxocopper(ii) complexes |
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Nanyang Technological University |
publishDate |
2022 |
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https://hdl.handle.net/10356/154960 |
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1759854419635077120 |