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    Analysis of 5-chloro-8-methoxy-2-(bromomethyl)quinoline by XPS

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    18(bromomethyl)quinoline(SSS).pdf (150.5Kb)
    Date
    2004
    Author
    Thomson, Jeff
    Stoker, Josh
    Bunker, Jared
    Agbonkonkon, Nosa
    Iyer, Gayathri
    Bronson, R. Todd
    Savage, Paul B.
    Linford, Matthew R.
    Husseini, Ghaleb
    Advisor(s)
    Unknown advisor
    Type
    Peer-Reviewed
    Article
    Published version
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    Abstract
    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.
    DSpace URI
    http://hdl.handle.net/11073/21336
    External URI
    https://doi.org/10.1116/11.20030403
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