Synthesis of azacrown sulfonamides via ring closing metathesis and their evaluation in lithium ion selective electrodes

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Abstract

New diazapolyoxa macrocyclic ditosylates with 17-28-membered rings were synthesized by the application of the RCM technique to suitable α,ω-dienes. These compounds were employed as neutral carriers in Li+-selective electrodes. The electrodes exhibited nearly Nernstian responses with relatively high selectivity for lithium over other inorganic cations. ©ARKAT-USA, Inc.

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APA

Ibrahim, Y. A., Behbehani, H., John, E., Shuaib, N. M., & Shoukry, A. F. (2008). Synthesis of azacrown sulfonamides via ring closing metathesis and their evaluation in lithium ion selective electrodes. Arkivoc, 2008(10), 5–16. https://doi.org/10.3998/ark.5550190.0009.a02

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