Open Access. Powered by Scholars. Published by Universities.®
![Digital Commons Network](http://assets.bepress.com/20200205/img/dcn/DCsunburst.png)
Physical Sciences and Mathematics Commons™
Open Access. Powered by Scholars. Published by Universities.®
Articles 1 - 2 of 2
Full-Text Articles in Physical Sciences and Mathematics
Exploring The Chemistry Of Asymmetric Phosphines & Phosphinidene Sulfides, Taylor E. Pritchard
Exploring The Chemistry Of Asymmetric Phosphines & Phosphinidene Sulfides, Taylor E. Pritchard
Electronic Thesis and Dissertation Repository
The field of low-coordinate main group chemistry has seen huge development in the last 30 years, with novel compounds that demonstrate unique structures and reactivity. Isolation of these species has relied on thoughtfully designed substituents normally containing substructure steric bulk. The area of phosphinidene chalcogenide isolation and transfer remains poorly understood by comparison. In this context, the major focus of thesis was on the development of a room-temperature method for the transfer of RP=S moieties with and without sterically demanding substituents. The preparation and complete characterization of new asymmetric phosphines with m-terphenyl ligands was also reported. In Chapter 2, …
Exploring The Synthesis, Structure, And Reactivity Of Phosphorus-Chalcogen Heterocycles, Cameron Graham
Exploring The Synthesis, Structure, And Reactivity Of Phosphorus-Chalcogen Heterocycles, Cameron Graham
Electronic Thesis and Dissertation Repository
In recent years, the field of low-coordinate main group chemistry has seen significant research interest due to their unique structures and unprecedented reactivity. Conversely, the area of phosphinidene chalcogenides, a low-coordinate phosphorus and chalcogen species, have yet to be thoroughly explored. In this context, this dissertation describes the synthesis of a number of phosphorus-chalcogen heterocycles that can be degraded to provide stoichiometric access to low-coordinate phosphorus species. The ability for successful P-Ch transfer relies on using a bulky m-terphenyl group at phosphorus that provides enough steric bulk to kinetically stabilize the phosphorus centre, but also accommodating enough to allow …