Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/173782
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dc.contributor.authorHum, Gavin Gao Xiaoen_US
dc.date.accessioned2024-02-27T05:04:11Z-
dc.date.available2024-02-27T05:04:11Z-
dc.date.issued2024-
dc.identifier.citationHum, G. G. X. (2024). Cyclodiphosphazane frameworks as enhanced anion receptors and N-heterocyclic carbenes. Doctoral thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/173782en_US
dc.identifier.urihttps://hdl.handle.net/10356/173782-
dc.description.abstractFirst isolated in the late 1890s, cyclodiphosphazanes have been known to be thermal stable and robust four-membered heterocycles comprising of alternating phosphorus and nitrogen. Although these species have experienced slow progress over the years, recent developments in this field have led to an increase in methodologies related to their syntheses and functionalization. This has led to their applications as versatile building blocks in other fields of chemistry. In this work, P(V) oxidized and metal chelated NH-bridged bis-cyclodiphosphazane consisting of two cyclodiphosphazane units will be explored as enhanced phosphazane anion receptors. In addition, a new series of phosphazane hybrid N-heterocyclic carbenes (PHNHCs) with increased robustness was synthesized allowing for the study of their reactivity towards olefins.en_US
dc.language.isoenen_US
dc.publisherNanyang Technological Universityen_US
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).en_US
dc.subjectChemistryen_US
dc.titleCyclodiphosphazane frameworks as enhanced anion receptors and N-heterocyclic carbenesen_US
dc.typeThesis-Doctor of Philosophyen_US
dc.contributor.supervisorMihaiela Stuparuen_US
dc.contributor.schoolSchool of Chemistry, Chemical Engineering and Biotechnologyen_US
dc.description.degreeDoctor of Philosophyen_US
dc.identifier.doi10.32657/10356/173782-
dc.contributor.supervisoremailmstuparu@ntu.edu.sgen_US
item.grantfulltextembargo_20260227-
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