An azaindole–hydrazine imine moiety as sensitive dual cation chemosensor depending on surface plasmon resonance and emission properties

•Novel azaindole-based colorimetric and fluorescent sensor with an attached hydrazine group.•Dual function of azaindole derivative L favoring reduction of silver ions and their stabilization as nanoparticles.•Naked eye detection of Ag+ ions through color change of solution from colorless to yellow.•...

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Veröffentlicht in:Sensors and actuators. B, Chemical Chemical, 2016-01, Vol.222, p.397-406
Hauptverfasser: Kaur, Kamaljot, Chaudhary, Savita, Singh, Sukhjinder, Mehta, Surinder K.
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creator Kaur, Kamaljot
Chaudhary, Savita
Singh, Sukhjinder
Mehta, Surinder K.
description •Novel azaindole-based colorimetric and fluorescent sensor with an attached hydrazine group.•Dual function of azaindole derivative L favoring reduction of silver ions and their stabilization as nanoparticles.•Naked eye detection of Ag+ ions through color change of solution from colorless to yellow.•Selective sensing of Fe2+ ions using quenched emission response.•Logic circuit operating with incorporation of AND and OR logic gate. A novel azaindole-based colorimetric and fluorescent sensor with an attached hydrazine group (L) was synthesized and characterized by FT-IR, NMR, and CHNS analyses. L exhibited high colorimetric selectivity and sensitivity toward Ag+ ions over other common cation solutions (Ag+, Na+, K+, Ba2+, Cd2+, Co2+, Cu2+,Cr3+, Fe2+, Mg2+, Mn2+, Ni2+, Sr2+, Zn2+, and Al3+) in ethanol:HEPES buffer (1:9, v/v) solution. Upon addition of Ag+ ions, the maximum absorption band of L displayed a red shift from 332 to 400nm. The efficient electron transfer ability of the molecular receptor L lead to the easy formation of silver nanoparticles (AgNPs) that manifested naked eye detection through color change of solution from colorless to yellow. The AgNPs thus obtained using organic compound L as stabilizer were characterized by light scattering, zeta potential and transmission electron microscopy (TEM). Meanwhile, the results of fluorescence titration experiments illustrated that the sensor functions as “turn-off” receptor upon selective binding with Fe2+. Comparative studies revealed that quenched emission originated from selective chelation of Fe2+ ions with the lone pair of the azaindole receptor's nitrogen atom and causes enhanced PET process Both B.-H. plot and emission spectra analysis reveals a 1:2 stoichiometric relationship between L and the added Fe2+ ions. The designed probe L permitted accurate detection of respectiveAg+ and Fe2+ down to 2.8nM and 2.17×10−7M with rapid response times. Finally, by using Ag+ and Fe2+ ions as chemical inputs and the absorbance and emission response as outputs, logic circuits are constructed at the nanoscale level.
doi_str_mv 10.1016/j.snb.2015.07.072
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A novel azaindole-based colorimetric and fluorescent sensor with an attached hydrazine group (L) was synthesized and characterized by FT-IR, NMR, and CHNS analyses. L exhibited high colorimetric selectivity and sensitivity toward Ag+ ions over other common cation solutions (Ag+, Na+, K+, Ba2+, Cd2+, Co2+, Cu2+,Cr3+, Fe2+, Mg2+, Mn2+, Ni2+, Sr2+, Zn2+, and Al3+) in ethanol:HEPES buffer (1:9, v/v) solution. Upon addition of Ag+ ions, the maximum absorption band of L displayed a red shift from 332 to 400nm. The efficient electron transfer ability of the molecular receptor L lead to the easy formation of silver nanoparticles (AgNPs) that manifested naked eye detection through color change of solution from colorless to yellow. The AgNPs thus obtained using organic compound L as stabilizer were characterized by light scattering, zeta potential and transmission electron microscopy (TEM). Meanwhile, the results of fluorescence titration experiments illustrated that the sensor functions as “turn-off” receptor upon selective binding with Fe2+. Comparative studies revealed that quenched emission originated from selective chelation of Fe2+ ions with the lone pair of the azaindole receptor's nitrogen atom and causes enhanced PET process Both B.-H. plot and emission spectra analysis reveals a 1:2 stoichiometric relationship between L and the added Fe2+ ions. The designed probe L permitted accurate detection of respectiveAg+ and Fe2+ down to 2.8nM and 2.17×10−7M with rapid response times. 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B, Chemical</title><description>•Novel azaindole-based colorimetric and fluorescent sensor with an attached hydrazine group.•Dual function of azaindole derivative L favoring reduction of silver ions and their stabilization as nanoparticles.•Naked eye detection of Ag+ ions through color change of solution from colorless to yellow.•Selective sensing of Fe2+ ions using quenched emission response.•Logic circuit operating with incorporation of AND and OR logic gate. A novel azaindole-based colorimetric and fluorescent sensor with an attached hydrazine group (L) was synthesized and characterized by FT-IR, NMR, and CHNS analyses. L exhibited high colorimetric selectivity and sensitivity toward Ag+ ions over other common cation solutions (Ag+, Na+, K+, Ba2+, Cd2+, Co2+, Cu2+,Cr3+, Fe2+, Mg2+, Mn2+, Ni2+, Sr2+, Zn2+, and Al3+) in ethanol:HEPES buffer (1:9, v/v) solution. Upon addition of Ag+ ions, the maximum absorption band of L displayed a red shift from 332 to 400nm. The efficient electron transfer ability of the molecular receptor L lead to the easy formation of silver nanoparticles (AgNPs) that manifested naked eye detection through color change of solution from colorless to yellow. The AgNPs thus obtained using organic compound L as stabilizer were characterized by light scattering, zeta potential and transmission electron microscopy (TEM). Meanwhile, the results of fluorescence titration experiments illustrated that the sensor functions as “turn-off” receptor upon selective binding with Fe2+. Comparative studies revealed that quenched emission originated from selective chelation of Fe2+ ions with the lone pair of the azaindole receptor's nitrogen atom and causes enhanced PET process Both B.-H. plot and emission spectra analysis reveals a 1:2 stoichiometric relationship between L and the added Fe2+ ions. The designed probe L permitted accurate detection of respectiveAg+ and Fe2+ down to 2.8nM and 2.17×10−7M with rapid response times. 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B, Chemical</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaur, Kamaljot</au><au>Chaudhary, Savita</au><au>Singh, Sukhjinder</au><au>Mehta, Surinder K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An azaindole–hydrazine imine moiety as sensitive dual cation chemosensor depending on surface plasmon resonance and emission properties</atitle><jtitle>Sensors and actuators. B, Chemical</jtitle><date>2016-01-01</date><risdate>2016</risdate><volume>222</volume><spage>397</spage><epage>406</epage><pages>397-406</pages><issn>0925-4005</issn><eissn>1873-3077</eissn><abstract>•Novel azaindole-based colorimetric and fluorescent sensor with an attached hydrazine group.•Dual function of azaindole derivative L favoring reduction of silver ions and their stabilization as nanoparticles.•Naked eye detection of Ag+ ions through color change of solution from colorless to yellow.•Selective sensing of Fe2+ ions using quenched emission response.•Logic circuit operating with incorporation of AND and OR logic gate. A novel azaindole-based colorimetric and fluorescent sensor with an attached hydrazine group (L) was synthesized and characterized by FT-IR, NMR, and CHNS analyses. L exhibited high colorimetric selectivity and sensitivity toward Ag+ ions over other common cation solutions (Ag+, Na+, K+, Ba2+, Cd2+, Co2+, Cu2+,Cr3+, Fe2+, Mg2+, Mn2+, Ni2+, Sr2+, Zn2+, and Al3+) in ethanol:HEPES buffer (1:9, v/v) solution. Upon addition of Ag+ ions, the maximum absorption band of L displayed a red shift from 332 to 400nm. The efficient electron transfer ability of the molecular receptor L lead to the easy formation of silver nanoparticles (AgNPs) that manifested naked eye detection through color change of solution from colorless to yellow. The AgNPs thus obtained using organic compound L as stabilizer were characterized by light scattering, zeta potential and transmission electron microscopy (TEM). Meanwhile, the results of fluorescence titration experiments illustrated that the sensor functions as “turn-off” receptor upon selective binding with Fe2+. Comparative studies revealed that quenched emission originated from selective chelation of Fe2+ ions with the lone pair of the azaindole receptor's nitrogen atom and causes enhanced PET process Both B.-H. plot and emission spectra analysis reveals a 1:2 stoichiometric relationship between L and the added Fe2+ ions. The designed probe L permitted accurate detection of respectiveAg+ and Fe2+ down to 2.8nM and 2.17×10−7M with rapid response times. Finally, by using Ag+ and Fe2+ ions as chemical inputs and the absorbance and emission response as outputs, logic circuits are constructed at the nanoscale level.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.snb.2015.07.072</doi><tpages>10</tpages></addata></record>
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subjects Azaindole
Cations
Colorimetric
Colorimetry
Complexation
Emission
Fluorescence
Fluorometric
Imines
Nanoparticles
Quenching
Receptors
Reduction
Sensors
Transmission electron microscopy
title An azaindole–hydrazine imine moiety as sensitive dual cation chemosensor depending on surface plasmon resonance and emission properties
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