A quinolinium-derived turn-off fluorescent anion sensor

Adam N. Swinburne; Martin J. Paterson; Andrew Beeby; Jonathan W. Steed

doi:10.1039/b919821k

A quinolinium-derived turn-off fluorescent anion sensor

Adam N. Swinburne
, Martin J. Paterson
, Andrew Beeby
, Jonathan W. Steed

School of Engineering & Physical Sciences

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

41 Citations (Scopus)

Abstract

A quinolinium-derived anion sensor has been synthesised which shows a turn-off fluorescence response in the presence of anions, with selectivity for acetate. The compound exhibits complex anion binding comprising of a host dimer, 2:1 and 1:1 host:guest species. Fluorescent quenching is due to both dynamic and static processes with charge transfer being the dominant mechanism. © The Royal Society of Chemistry.

Original language	English
Pages (from-to)	1010-1016
Number of pages	7
Journal	Organic and Biomolecular Chemistry
Volume	8
Issue number	5
DOIs	https://doi.org/10.1039/b919821k
Publication status	Published - 2010

Access to Document

10.1039/b919821k

Cite this

@article{5bb3c23dee3d42fc82da698763a6a3bf,

title = "A quinolinium-derived turn-off fluorescent anion sensor",

abstract = "A quinolinium-derived anion sensor has been synthesised which shows a turn-off fluorescence response in the presence of anions, with selectivity for acetate. The compound exhibits complex anion binding comprising of a host dimer, 2:1 and 1:1 host:guest species. Fluorescent quenching is due to both dynamic and static processes with charge transfer being the dominant mechanism. {\textcopyright} The Royal Society of Chemistry.",

author = "Swinburne, \{Adam N.\} and Paterson, \{Martin J.\} and Andrew Beeby and Steed, \{Jonathan W.\}",

year = "2010",

doi = "10.1039/b919821k",

language = "English",

volume = "8",

pages = "1010--1016",

journal = "Organic and Biomolecular Chemistry",

issn = "1477-0520",

publisher = "Royal Society of Chemistry",

number = "5",

}

TY - JOUR

T1 - A quinolinium-derived turn-off fluorescent anion sensor

AU - Swinburne, Adam N.

AU - Paterson, Martin J.

AU - Beeby, Andrew

AU - Steed, Jonathan W.

PY - 2010

Y1 - 2010

N2 - A quinolinium-derived anion sensor has been synthesised which shows a turn-off fluorescence response in the presence of anions, with selectivity for acetate. The compound exhibits complex anion binding comprising of a host dimer, 2:1 and 1:1 host:guest species. Fluorescent quenching is due to both dynamic and static processes with charge transfer being the dominant mechanism. © The Royal Society of Chemistry.

AB - A quinolinium-derived anion sensor has been synthesised which shows a turn-off fluorescence response in the presence of anions, with selectivity for acetate. The compound exhibits complex anion binding comprising of a host dimer, 2:1 and 1:1 host:guest species. Fluorescent quenching is due to both dynamic and static processes with charge transfer being the dominant mechanism. © The Royal Society of Chemistry.

UR - https://www.scopus.com/pages/publications/77149175976

U2 - 10.1039/b919821k

DO - 10.1039/b919821k

M3 - Article

C2 - 20165790

SN - 1477-0520

VL - 8

SP - 1010

EP - 1016

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

IS - 5

ER -

A quinolinium-derived turn-off fluorescent anion sensor

Abstract

Access to Document

Other files and links

Fingerprint

Cite this