TY - JOUR
T1 - Molecular design, characterization, and application of multi-information dyes for multi-dimensional optical chemical sensing. Molecular design concepts of the dyes and their fundamental spectral characteristics
AU - Hisamoto, Hideaki
AU - Tohma, Hajime
AU - Yamada, Toshiki
AU - Yamauchi, Ki Ichiro
AU - Siswanta, Dwi
AU - Yoshioka, Naoki
AU - Suzuki, Koji
N1 - Funding Information:
Partial support of this investigation by The Kawakami Memorial Foundation, Iketani Science and Technology Foundation, and the Ministry of Education is acknowledged.
PY - 1998/11/11
Y1 - 1998/11/11
N2 - The molecular design of multi-functional dyes, called 'multi-information dyes' (MIDs), and their application to several methods of optical chemical sensing were proposed. The concepts for the molecular design of the dyes were as follows: (1) the introduction of multiple (both positive and negative) charges on both ends of the large conjugated π-electron system of the dye molecule, so that the dye interacts with many chemical species or environments; (2) the introduction of different substitution (electron-donating or electron-accepting) groups in the conjugated π-electron system of the dye molecule, so that the dye has a different pK(a) and solvatochromic property; and (3) the introduction of an immobilization site in the dye molecule, so that the dye can be easily prepared as a sensing probe.Based on these concepts, sixteen kinds of dyes were synthesized, all being of the merocyanine type. The basic color-change characteristics of the MIDs were evaluated with a homogeneous system and a solvent extraction two-phase system. Some of these dyes (e.g., KD-M5) offered two-dimensional sensing information for sensing the water content in organic solvents, in which the absorbance maximum wavelength (λ(max)) shift and absorbance change were both utilized as the detecting signals.From these results, the MIDs developed in this study have several possibilities for analytical applications in optical chemical sensing such as pH sensing, ion sensing, neutral molecule sensing, and water content-sensing in organic solvents. Copyright (C) 1998 Elsevier Science B.V.
AB - The molecular design of multi-functional dyes, called 'multi-information dyes' (MIDs), and their application to several methods of optical chemical sensing were proposed. The concepts for the molecular design of the dyes were as follows: (1) the introduction of multiple (both positive and negative) charges on both ends of the large conjugated π-electron system of the dye molecule, so that the dye interacts with many chemical species or environments; (2) the introduction of different substitution (electron-donating or electron-accepting) groups in the conjugated π-electron system of the dye molecule, so that the dye has a different pK(a) and solvatochromic property; and (3) the introduction of an immobilization site in the dye molecule, so that the dye can be easily prepared as a sensing probe.Based on these concepts, sixteen kinds of dyes were synthesized, all being of the merocyanine type. The basic color-change characteristics of the MIDs were evaluated with a homogeneous system and a solvent extraction two-phase system. Some of these dyes (e.g., KD-M5) offered two-dimensional sensing information for sensing the water content in organic solvents, in which the absorbance maximum wavelength (λ(max)) shift and absorbance change were both utilized as the detecting signals.From these results, the MIDs developed in this study have several possibilities for analytical applications in optical chemical sensing such as pH sensing, ion sensing, neutral molecule sensing, and water content-sensing in organic solvents. Copyright (C) 1998 Elsevier Science B.V.
KW - Alcohol sensor
KW - Functional dye
KW - Ion sensor
KW - Optical sensor
KW - Optode
KW - Solvatochromism
KW - Water-content sensor
KW - pH sensor
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U2 - 10.1016/S0003-2670(98)00421-8
DO - 10.1016/S0003-2670(98)00421-8
M3 - Article
AN - SCOPUS:0032508955
SN - 0003-2670
VL - 373
SP - 271
EP - 289
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
IS - 2-3
ER -