Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2013
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dc.contributor.authorShubham-
dc.date.accessioned2022-12-22T17:54:00Z-
dc.date.available2022-12-22T17:54:00Z-
dc.date.issued2022-04-
dc.identifier.urihttp://hdl.handle.net/123456789/2013-
dc.description.abstractC-C bond cleaving reactions are very slow due the inertness of the bonds. However nature utilises metalloenzymes like ARD to cleave aliphatic c-c bonds effectively in presence of dioxygen. The ARD active site has N 3 O (3His,1Glu) coordination environment with two water molecules. This work is inspired by the activity and active site of ARD. In this context some mononuclear nickel(II) and cobalt(II) synthetic complexes were synthesised with N3O coordination from ligand. The substrate binding to this model complexes were studied and characterised by spectroscopic techniques.en_US
dc.language.isoen_USen_US
dc.publisherIISER Mohalien_US
dc.subjectSynthesisen_US
dc.subjectcharacterizationen_US
dc.subjectreactivity studiesen_US
dc.subjectbio-inspireden_US
dc.subjectacireductone dioxygenaseen_US
dc.titleSynthesis, characterization and reactivity studies of bio-inspired nickel based acireductone dioxygenase model complexesen_US
dc.typeThesisen_US
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