Analysis of 5-chloro-8-methoxy-2-(bromomethyl)quinoline by XPS
Macrocyclic ethers are used extensively for their ability to form strong and selective interactions with charged species. It has been shown that the incorporation of heterocyclic groups into macrocylclic ethers increase rigidity and interaction with certain ions. Alkylation of these azacrowns with b...
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2004
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| Online Access: | http://hdl.handle.net/11073/21336 |
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| _version_ | 1864513433457655808 |
|---|---|
| author | Thomson, Jeff |
| author2 | Stoker, Josh Bunker, Jared Agbonkonkon, Nosa Iyer, Gayathri Bronson, R. Todd Savage, Paul B. Linford, Matthew R. Husseini, Ghaleb |
| author2_role | author author author author author author author author |
| author_facet | Thomson, Jeff Stoker, Josh Bunker, Jared Agbonkonkon, Nosa Iyer, Gayathri Bronson, R. Todd Savage, Paul B. Linford, Matthew R. Husseini, Ghaleb |
| author_role | author |
| dc.creator.none.fl_str_mv | Thomson, Jeff Stoker, Josh Bunker, Jared Agbonkonkon, Nosa Iyer, Gayathri Bronson, R. Todd Savage, Paul B. Linford, Matthew R. Husseini, Ghaleb |
| dc.date.none.fl_str_mv | 2004 2021-03-04T06:53:40Z 2021-03-04T06:53:40Z |
| dc.format.none.fl_str_mv | application/pdf |
| dc.identifier.none.fl_str_mv | Thomson, J., Stoker, J., Bunker, J., Agbonkonkon, N., Iyer, G., Todd Bronson, R., Savage, P. B., Linford, M. R., & Husseini, G. A. (2002). Analysis of 5-chloro-8-methoxy-2-(bromomethyl)quinoline by XPS. Surface Science Spectra, 9(1), 241-249. https://doi.org/10.1116/11.20030403 1055-5269 http://hdl.handle.net/11073/21336 10.1116/11.20030403 |
| dc.language.none.fl_str_mv | en_US |
| dc.publisher.none.fl_str_mv | American Vacuum Society |
| dc.relation.none.fl_str_mv | https://doi.org/10.1116/11.20030403 |
| dc.subject.none.fl_str_mv | X-ray photoelectron spectroscopy Pyridinoazacrown ethers 5-chloro-8-methoxy-2- (bromoethyl)quinoline |
| dc.title.none.fl_str_mv | Analysis of 5-chloro-8-methoxy-2-(bromomethyl)quinoline by XPS |
| dc.type.none.fl_str_mv | Peer-Reviewed Published version info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/article |
| description | Macrocyclic ethers are used extensively for their ability to form strong and selective interactions with charged species. It has been shown that the incorporation of heterocyclic groups into macrocylclic ethers increase rigidity and interaction with certain ions. Alkylation of these azacrowns with benzylic halides can attach fluorionophoric substituents onto the ring. One of the molecules used for this alkylation is 5-chloro-8-methoxy-2-(bromomethyl)quinoline. Azacrowns with this alkyl ligand have displayed interesting ion complexation properties. |
| format | article |
| id | aus_74f1cf901b5392c3e7d68b2204b8260e |
| identifier_str_mv | Thomson, J., Stoker, J., Bunker, J., Agbonkonkon, N., Iyer, G., Todd Bronson, R., Savage, P. B., Linford, M. R., & Husseini, G. A. (2002). Analysis of 5-chloro-8-methoxy-2-(bromomethyl)quinoline by XPS. Surface Science Spectra, 9(1), 241-249. https://doi.org/10.1116/11.20030403 1055-5269 10.1116/11.20030403 |
| language_invalid_str_mv | en_US |
| network_acronym_str | aus |
| network_name_str | aus |
| oai_identifier_str | oai:repository.aus.edu:11073/21336 |
| publishDate | 2004 |
| publisher.none.fl_str_mv | American Vacuum Society |
| repository.mail.fl_str_mv | |
| repository.name.fl_str_mv | |
| repository_id_str | |
| spelling | Analysis of 5-chloro-8-methoxy-2-(bromomethyl)quinoline by XPSThomson, JeffStoker, JoshBunker, JaredAgbonkonkon, NosaIyer, GayathriBronson, R. ToddSavage, Paul B.Linford, Matthew R.Husseini, GhalebX-ray photoelectron spectroscopyPyridinoazacrown ethers5-chloro-8-methoxy-2- (bromoethyl)quinolineMacrocyclic ethers are used extensively for their ability to form strong and selective interactions with charged species. It has been shown that the incorporation of heterocyclic groups into macrocylclic ethers increase rigidity and interaction with certain ions. Alkylation of these azacrowns with benzylic halides can attach fluorionophoric substituents onto the ring. One of the molecules used for this alkylation is 5-chloro-8-methoxy-2-(bromomethyl)quinoline. Azacrowns with this alkyl ligand have displayed interesting ion complexation properties.American Vacuum Society2021-03-04T06:53:40Z2021-03-04T06:53:40Z2004Peer-ReviewedPublished versioninfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfThomson, J., Stoker, J., Bunker, J., Agbonkonkon, N., Iyer, G., Todd Bronson, R., Savage, P. B., Linford, M. R., & Husseini, G. A. (2002). Analysis of 5-chloro-8-methoxy-2-(bromomethyl)quinoline by XPS. Surface Science Spectra, 9(1), 241-249. https://doi.org/10.1116/11.200304031055-5269http://hdl.handle.net/11073/2133610.1116/11.20030403en_UShttps://doi.org/10.1116/11.20030403oai:repository.aus.edu:11073/213362024-08-22T12:05:09Z |
| spellingShingle | Analysis of 5-chloro-8-methoxy-2-(bromomethyl)quinoline by XPS Thomson, Jeff X-ray photoelectron spectroscopy Pyridinoazacrown ethers 5-chloro-8-methoxy-2- (bromoethyl)quinoline |
| status_str | publishedVersion |
| title | Analysis of 5-chloro-8-methoxy-2-(bromomethyl)quinoline by XPS |
| title_full | Analysis of 5-chloro-8-methoxy-2-(bromomethyl)quinoline by XPS |
| title_fullStr | Analysis of 5-chloro-8-methoxy-2-(bromomethyl)quinoline by XPS |
| title_full_unstemmed | Analysis of 5-chloro-8-methoxy-2-(bromomethyl)quinoline by XPS |
| title_short | Analysis of 5-chloro-8-methoxy-2-(bromomethyl)quinoline by XPS |
| title_sort | Analysis of 5-chloro-8-methoxy-2-(bromomethyl)quinoline by XPS |
| topic | X-ray photoelectron spectroscopy Pyridinoazacrown ethers 5-chloro-8-methoxy-2- (bromoethyl)quinoline |
| url | http://hdl.handle.net/11073/21336 |