Rhodamine hydrazone derivatives bearing thiophene group as fluorescent chemosensors for Hg2+

Sunhi Park; Wantae Kim; K. M.K. Swamy; Hye Yeon Lee; Ji Young Jung; Gyoungmi Kim; Youngmee Kim; Sung Jin Kim; Juyoung Yoon

doi:10.1016/j.dyepig.2013.05.015

Rhodamine hydrazone derivatives bearing thiophene group as fluorescent chemosensors for Hg²⁺

Sunhi Park, Wantae Kim, K. M.K. Swamy, Hye Yeon Lee, Ji Young Jung, Gyoungmi Kim, Youngmee Kim, Sung Jin Kim, Juyoung Yoon

Chemistry & Nanoscience

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

76 Scopus citations

Abstract

Rhodamine derivatives bearing the thiophene (1) and bisthiophene (2) groups are synthesized and their binding selectivity toward various metal ions was studied. The X-ray crystal structure of 1 was also reported. Probes 1 and 2 showed highly selective "Off-On" fluorescence changes with Hg ²⁺ among various metal ions. These selective changes were attributed to the spirolactam ring opening processes and subsequent hydrolysis. Probes 1 and 2 were sucessfully applied to the cell-imaging of Hg²⁺ using HeLa cells.

Original language	English
Pages (from-to)	323-328
Number of pages	6
Journal	Dyes and Pigments
Volume	99
Issue number	2
DOIs	https://doi.org/10.1016/j.dyepig.2013.05.015
State	Published - 2013

Bibliographical note

Funding Information:
This CRI work was supported by the National Research Foundation of Korea(NRF) grant funded by the Korea government(MEST) (No. 2012R1A3A2048814 ). Mass spectral data were obtained from the Korea Basic Science Institute (Daegu) on a Jeol JMS 700 high resolution mass spectrometer.

Keywords

Colorimetric sensor
Fluorescent chemodosimeter
Fluorescent chemosensor
Mercury ion sensor
Rhodamine

Access to Document

10.1016/j.dyepig.2013.05.015

Cite this

@article{f07b52956e93419dadf6059fae3c0f13,

title = "Rhodamine hydrazone derivatives bearing thiophene group as fluorescent chemosensors for Hg2+",

abstract = "Rhodamine derivatives bearing the thiophene (1) and bisthiophene (2) groups are synthesized and their binding selectivity toward various metal ions was studied. The X-ray crystal structure of 1 was also reported. Probes 1 and 2 showed highly selective {"}Off-On{"} fluorescence changes with Hg 2+ among various metal ions. These selective changes were attributed to the spirolactam ring opening processes and subsequent hydrolysis. Probes 1 and 2 were sucessfully applied to the cell-imaging of Hg2+ using HeLa cells.",

keywords = "Colorimetric sensor, Fluorescent chemodosimeter, Fluorescent chemosensor, Mercury ion sensor, Rhodamine",

author = "Sunhi Park and Wantae Kim and Swamy, {K. M.K.} and Lee, {Hye Yeon} and Jung, {Ji Young} and Gyoungmi Kim and Youngmee Kim and Kim, {Sung Jin} and Juyoung Yoon",

note = "Funding Information: This CRI work was supported by the National Research Foundation of Korea(NRF) grant funded by the Korea government(MEST) (No. 2012R1A3A2048814 ). Mass spectral data were obtained from the Korea Basic Science Institute (Daegu) on a Jeol JMS 700 high resolution mass spectrometer. ",

year = "2013",

doi = "10.1016/j.dyepig.2013.05.015",

language = "English",

volume = "99",

pages = "323--328",

journal = "Dyes and Pigments",

issn = "0143-7208",

publisher = "Elsevier BV",

number = "2",

}

TY - JOUR

T1 - Rhodamine hydrazone derivatives bearing thiophene group as fluorescent chemosensors for Hg2+

AU - Park, Sunhi

AU - Kim, Wantae

AU - Swamy, K. M.K.

AU - Lee, Hye Yeon

AU - Jung, Ji Young

AU - Kim, Gyoungmi

AU - Kim, Youngmee

AU - Kim, Sung Jin

AU - Yoon, Juyoung

N1 - Funding Information: This CRI work was supported by the National Research Foundation of Korea(NRF) grant funded by the Korea government(MEST) (No. 2012R1A3A2048814 ). Mass spectral data were obtained from the Korea Basic Science Institute (Daegu) on a Jeol JMS 700 high resolution mass spectrometer.

PY - 2013

Y1 - 2013

N2 - Rhodamine derivatives bearing the thiophene (1) and bisthiophene (2) groups are synthesized and their binding selectivity toward various metal ions was studied. The X-ray crystal structure of 1 was also reported. Probes 1 and 2 showed highly selective "Off-On" fluorescence changes with Hg 2+ among various metal ions. These selective changes were attributed to the spirolactam ring opening processes and subsequent hydrolysis. Probes 1 and 2 were sucessfully applied to the cell-imaging of Hg2+ using HeLa cells.

AB - Rhodamine derivatives bearing the thiophene (1) and bisthiophene (2) groups are synthesized and their binding selectivity toward various metal ions was studied. The X-ray crystal structure of 1 was also reported. Probes 1 and 2 showed highly selective "Off-On" fluorescence changes with Hg 2+ among various metal ions. These selective changes were attributed to the spirolactam ring opening processes and subsequent hydrolysis. Probes 1 and 2 were sucessfully applied to the cell-imaging of Hg2+ using HeLa cells.

KW - Colorimetric sensor

KW - Fluorescent chemodosimeter

KW - Fluorescent chemosensor

KW - Mercury ion sensor

KW - Rhodamine

UR - http://www.scopus.com/inward/record.url?scp=84879487940&partnerID=8YFLogxK

U2 - 10.1016/j.dyepig.2013.05.015

DO - 10.1016/j.dyepig.2013.05.015

M3 - Article

AN - SCOPUS:84879487940

SN - 0143-7208

VL - 99

SP - 323

EP - 328

JO - Dyes and Pigments

JF - Dyes and Pigments

IS - 2

ER -