Selective binding and sensing of guanidinium ions by lipophilic cyclodextrins

Ritu Kataky; Patricia M. Kelly; David Parker; Antonio F. Patti

Selective binding and sensing of guanidinium ions by lipophilic cyclodextrins

Ritu Kataky, Patricia M. Kelly, David Parker, Antonio F. Patti

School of Chemistry

Research output: Contribution to journal › Article › Research › peer-review

17 Citations (Scopus)

Abstract

Potentiometric sensors based on lipophilic alkylated cyclodextrins exhibit a good response to the guanidinium ion, with higher selectivity over sodium than previously reported ionophores; 2.6-didodecyl-β-cyclodextrin has also been shown to exhibit selective response to the guanidine derivatives metformin and phenformin in a simulated clinical electrolyte background.

Original language	English
Pages (from-to)	2381-2382
Number of pages	2
Journal	Journal of the Chemical Society, Perkin Transactions 2
Issue number	12
Publication status	Published - 1 Dec 1994

Cite this

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title = "Selective binding and sensing of guanidinium ions by lipophilic cyclodextrins",

abstract = "Potentiometric sensors based on lipophilic alkylated cyclodextrins exhibit a good response to the guanidinium ion, with higher selectivity over sodium than previously reported ionophores; 2.6-didodecyl-β-cyclodextrin has also been shown to exhibit selective response to the guanidine derivatives metformin and phenformin in a simulated clinical electrolyte background.",

author = "Ritu Kataky and Kelly, {Patricia M.} and David Parker and Patti, {Antonio F.}",

year = "1994",

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language = "English",

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journal = "Journal of the Chemical Society, Perkin Transactions 2",

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publisher = "The Royal Society of Chemistry",

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T1 - Selective binding and sensing of guanidinium ions by lipophilic cyclodextrins

AU - Kataky, Ritu

AU - Kelly, Patricia M.

AU - Parker, David

AU - Patti, Antonio F.

PY - 1994/12/1

Y1 - 1994/12/1

N2 - Potentiometric sensors based on lipophilic alkylated cyclodextrins exhibit a good response to the guanidinium ion, with higher selectivity over sodium than previously reported ionophores; 2.6-didodecyl-β-cyclodextrin has also been shown to exhibit selective response to the guanidine derivatives metformin and phenformin in a simulated clinical electrolyte background.

AB - Potentiometric sensors based on lipophilic alkylated cyclodextrins exhibit a good response to the guanidinium ion, with higher selectivity over sodium than previously reported ionophores; 2.6-didodecyl-β-cyclodextrin has also been shown to exhibit selective response to the guanidine derivatives metformin and phenformin in a simulated clinical electrolyte background.

UR - http://www.scopus.com/inward/record.url?scp=37049070889&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:37049070889

SN - 1472-779X

SP - 2381

EP - 2382

JO - Journal of the Chemical Society, Perkin Transactions 2

JF - Journal of the Chemical Society, Perkin Transactions 2

IS - 12

ER -

Selective binding and sensing of guanidinium ions by lipophilic cyclodextrins

Abstract

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