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 |
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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. 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.</description><identifier>ISSN: 0925-4005</identifier><identifier>EISSN: 1873-3077</identifier><identifier>DOI: 10.1016/j.snb.2015.07.072</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Azaindole ; Cations ; Colorimetric ; Colorimetry ; Complexation ; Emission ; Fluorescence ; Fluorometric ; Imines ; Nanoparticles ; Quenching ; Receptors ; Reduction ; Sensors ; Transmission electron microscopy</subject><ispartof>Sensors and actuators. B, Chemical, 2016-01, Vol.222, p.397-406</ispartof><rights>2015 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c330t-7b23b569aaa0f808ec9d06ee478e8d5da64496399bea051f82b544a85583c223</citedby><cites>FETCH-LOGICAL-c330t-7b23b569aaa0f808ec9d06ee478e8d5da64496399bea051f82b544a85583c223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.snb.2015.07.072$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids></links><search><creatorcontrib>Kaur, Kamaljot</creatorcontrib><creatorcontrib>Chaudhary, Savita</creatorcontrib><creatorcontrib>Singh, Sukhjinder</creatorcontrib><creatorcontrib>Mehta, Surinder K.</creatorcontrib><title>An azaindole–hydrazine imine moiety as sensitive dual cation chemosensor depending on surface plasmon resonance and emission properties</title><title>Sensors and actuators. 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. 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.</description><subject>Azaindole</subject><subject>Cations</subject><subject>Colorimetric</subject><subject>Colorimetry</subject><subject>Complexation</subject><subject>Emission</subject><subject>Fluorescence</subject><subject>Fluorometric</subject><subject>Imines</subject><subject>Nanoparticles</subject><subject>Quenching</subject><subject>Receptors</subject><subject>Reduction</subject><subject>Sensors</subject><subject>Transmission electron microscopy</subject><issn>0925-4005</issn><issn>1873-3077</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9UD1v3DAMFYoUyCXtD-imsYsvlGXZMjoFQT8CBOiSXaAlutHBllzJF-Ayde3cf9hfEhnXuQBBgh-P5HuMfRCwFyDam8M-h2Ffg1B76IrVb9hO6E5WErrugu2gr1XVAKhLdpXzAQAa2cKO_b4NHF_QBxcn-vvrz9PJJXzxgbifNz9HT-uJY-aZQvarfybujjhxi6uPgdsnmuPWiok7Wig4H37w0sjHNKIlvkyY55InyjFgKBUMjtPsc97wS4oLpdVTfsfejjhlev8vXrPHL58f775VD9-_3t_dPlRWSlirbqjloNoeEWHUoMn2DlqiptOknXLYNk3fyr4fCEGJUdeDahrUSmlp61pes4_nteXyzyPl1ZRXLE0TBorHbESnW9G2qtlGxXnUpphzotEsyc-YTkaA2VQ3B1NUN5vqBrpiG-bTGUOFwrOnZLL1VGg7n8iuxkX_H_Qr16iPDg</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Kaur, Kamaljot</creator><creator>Chaudhary, Savita</creator><creator>Singh, Sukhjinder</creator><creator>Mehta, Surinder K.</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>FR3</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20160101</creationdate><title>An azaindole–hydrazine imine moiety as sensitive dual cation chemosensor depending on surface plasmon resonance and emission properties</title><author>Kaur, Kamaljot ; Chaudhary, Savita ; Singh, Sukhjinder ; Mehta, Surinder K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c330t-7b23b569aaa0f808ec9d06ee478e8d5da64496399bea051f82b544a85583c223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Azaindole</topic><topic>Cations</topic><topic>Colorimetric</topic><topic>Colorimetry</topic><topic>Complexation</topic><topic>Emission</topic><topic>Fluorescence</topic><topic>Fluorometric</topic><topic>Imines</topic><topic>Nanoparticles</topic><topic>Quenching</topic><topic>Receptors</topic><topic>Reduction</topic><topic>Sensors</topic><topic>Transmission electron microscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaur, Kamaljot</creatorcontrib><creatorcontrib>Chaudhary, Savita</creatorcontrib><creatorcontrib>Singh, Sukhjinder</creatorcontrib><creatorcontrib>Mehta, Surinder K.</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Sensors and actuators. 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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