dc.contributor.advisor | Gottardo, Christine | |
dc.contributor.author | Boissy, Christine | |
dc.date | 2017 | |
dc.date.accessioned | 2018-02-22T18:21:31Z | |
dc.date.available | 2018-02-22T18:21:31Z | |
dc.date.issued | 2017 | |
dc.identifier.uri | https://knowledgecommons.lakeheadu.ca/handle/2453/4101 | |
dc.description.abstract | A variety of room temperature ionic liquids have been synthesized and applied to various
reactions. Four of these ionic liquids were prepared in a chiral manner: [1-butyl-3-
methylimidazolium][L-lactate], [1-butyl-3-methylimidazolium][D-lactate], [1-butyl-3-
methylimidazolium][(1S)(+)-10-camphorsulfonate], and [1-butyl-3-methylimidazolium][(1R)(-)-10-
camphorsulfonate]. These chiral ionic liquids were used as solvents in asymmetric spiroacetal
cyclizations and Truce-Smiles rearrangements to induce chirality to the reactions.
Additionally, four other ionic liquids were synthesized for use in electrochemical
experiments: [1-butyl-3-methylimidazolium][BF4], [1-butyl-3-methylimidazolium][PF6], [1-butyl-3-
methylimidazolium][SCN] and [1-butyl-3-methylimidazolium][Tau]. These ionic liquids were used
as an additive during electrochemical nickel deposition and dissolution to improve the effect of
the Watts solution. | en_US |
dc.language.iso | en_US | en_US |
dc.subject | Synthetic applications of RTILs | en_US |
dc.subject | Asymmetric synthesis | en_US |
dc.subject | Asymmetric spiroacetal cyclization | en_US |
dc.subject | Truce-smiles rearrangement | en_US |
dc.subject | Electrodeposition/dissolution of nickel in RTIL | en_US |
dc.title | Synthesis and applications of room temperature ionic liquids | en_US |
dc.type | Thesis | |
etd.degree.name | Master of Science | en_US |
etd.degree.level | Master | en_US |
etd.degree.discipline | Chemistry | en_US |
etd.degree.grantor | Lakehead University | en_US |