A Cr(VI) selective probe based on a quinoline-amide calix[4]arene
A new quinoline-amide calix[4]arene 3-receptor for detection of hazardous anions and cations have been synthesized. The 3-receptor was examined for its sensing properties towards several different anions (Cr2O72−, SCN−, F−, Cl−, NO3−) and metal ions (Hg2+, Cd2+, Ag+) by UV–vis and fluorescence spect...
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Published in: | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy Vol. 189; pp. 44 - 50 |
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15-01-2018
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Abstract | A new quinoline-amide calix[4]arene 3-receptor for detection of hazardous anions and cations have been synthesized. The 3-receptor was examined for its sensing properties towards several different anions (Cr2O72−, SCN−, F−, Cl−, NO3−) and metal ions (Hg2+, Cd2+, Ag+) by UV–vis and fluorescence spectroscopies. It was detected that the 3-receptor has only sensing ability for Cr2O72− and Hg2+ ions, resulting in the association constants higher for Cr2O72− than to the Hg2+ ions. High selectivity towards Cr2O72− were also observed by fluorescence measurement among other ions (F−, Cl−, SCN−, Hg2+, Cd2+, Ag+) with a low limit of detection (7.36×10−6moldm−3). Proton NMR anion-binding investigations revealed a strong interaction of Cr2O72− anion with NH and CH groups of the receptor, showing that the combination with hydrogen-bonds donor groups strengthened the anion receptor association. Furthermore, remarkable association constants for dichromate anion obtained by all techniques strongly suggest the 3-receptor as a selective Cr(VI) sensor.
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•Simultaneous association with NH and CH groups reflect synergistic anion binding ability of 3.•Selectivity of sensor towards Cr2O72− validated in the presence of interfering ions.•Remarkable association constants for Cr2O72− suggest 3 as a selective Cr(VI) sensor.•Low detection limit on sensor 3 for Cr2O72− was obtained by fluorescence measurement.•Development of probes for hazardous metals and toxic species could be enlarged. |
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AbstractList | A new quinoline-amide calix[4]arene 3-receptor for detection of hazardous anions and cations have been synthesized. The 3-receptor was examined for its sensing properties towards several different anions (Cr2O72−, SCN−, F−, Cl−, NO3−) and metal ions (Hg2+, Cd2+, Ag+) by UV–vis and fluorescence spectroscopies. It was detected that the 3-receptor has only sensing ability for Cr2O72− and Hg2+ ions, resulting in the association constants higher for Cr2O72− than to the Hg2+ ions. High selectivity towards Cr2O72− were also observed by fluorescence measurement among other ions (F−, Cl−, SCN−, Hg2+, Cd2+, Ag+) with a low limit of detection (7.36×10−6moldm−3). Proton NMR anion-binding investigations revealed a strong interaction of Cr2O72− anion with NH and CH groups of the receptor, showing that the combination with hydrogen-bonds donor groups strengthened the anion receptor association. Furthermore, remarkable association constants for dichromate anion obtained by all techniques strongly suggest the 3-receptor as a selective Cr(VI) sensor.
[Display omitted]
•Simultaneous association with NH and CH groups reflect synergistic anion binding ability of 3.•Selectivity of sensor towards Cr2O72− validated in the presence of interfering ions.•Remarkable association constants for Cr2O72− suggest 3 as a selective Cr(VI) sensor.•Low detection limit on sensor 3 for Cr2O72− was obtained by fluorescence measurement.•Development of probes for hazardous metals and toxic species could be enlarged. |
Author | Bagatin, Izilda A. Ferreira, Juliane F. |
Author_xml | – sequence: 1 givenname: Juliane F. surname: Ferreira fullname: Ferreira, Juliane F. – sequence: 2 givenname: Izilda A. orcidid: 0000-0002-3957-2730 surname: Bagatin fullname: Bagatin, Izilda A. email: ibagatin@unifesp.br |
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Cites_doi | 10.1039/c2nj20974h 10.3906/kim-1405-69 10.1021/jo048228i 10.1039/C1DT11546D 10.1007/s10847-004-6385-2 10.1007/s00216-011-5403-7 10.1016/j.tet.2007.06.120 10.1016/j.saa.2014.05.002 10.1039/b513355f 10.1002/1521-3773(20010202)40:3<486::AID-ANIE486>3.0.CO;2-P 10.1016/S0277-5387(96)00410-X 10.1021/ic980964f 10.1139/v11-021 10.1039/C2NJ20776A 10.1016/j.tet.2012.01.010 10.1016/j.tetlet.2014.12.015 10.1021/ja000012k 10.1007/s10847-008-9472-y 10.1016/j.tetlet.2007.02.026 10.1039/a807763k 10.1002/poc.3332 10.1016/j.molliq.2017.05.088 10.1016/j.aca.2006.08.006 10.1016/j.tet.2014.07.100 10.1016/j.tetlet.2014.10.149 10.1016/j.tetlet.2007.06.075 10.1007/s11743-015-1754-y 10.1016/j.saa.2015.04.025 10.1039/c3dt51292d 10.1016/j.jhazmat.2010.05.121 10.1016/j.tetlet.2007.08.045 10.1039/b005127f 10.1016/j.msec.2009.06.008 |
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References | Ertul, Bayrakci, Yilmaz (bb0130) 2010; 181 Zhang, Yu, Lu, Fu, Li, Ji (bb0065) 2012; 36 Akkus, Cebeci (bb0040) 2008; 62 Ozcan, Ersoz, Yilmaz (bb0045) 2009; 29 Miao, Zhan, Zou, Tian, Li (bb0100) 2012; 68 Ji, Dabestani, Brown (bb0115) 2000; 122 Basaran, Wang, Alamgir, Wang, Haque, Zhang, Powell, Leszczynski, Hossain (bb0025) 2015; 56 Othman, Lee, Huh, Abidi, Kim, Vicens (bb0080) 2007; 63 Darjee, Mishra, Bhatt, Vyas, Modi, Jain (bb0090) 2014; 55 Kumar, Rub, Akrama, ud Din, Kumar, Rub, Akram, ud Din, Kumar, Neo, Rub, Kumar, Rub (bb0020) 2014; 27 Evans, Rahman, Davis, Beer (bb0050) 2012; 402 Jiang, Wong, Lo, Ng (bb0060) 2012; 41 Zhan, Wen, Miao, Tian, Zhu, Li (bb0095) 2012; 36 Sayin, Dogan (bb0055) 2015; 39 Chawla, Sahu, Shrivastava (bb0110) 2007; 48 Bagatin, Toma (bb0070) 2000; 24 Aragoni, Arca, Bencini, Caltagirone, Garau, Isaia, Light, Lippolis, Lodeiro, Mameli, Montis, Mostallino, Pintus, Puccioni (bb0125) 2013; 42 Ghosh, Alam, Ganguly, Guchhait (bb0030) 2015; 149 Lee, Kim, Jung, Kim (bb0085) 2005; 70 Beer, Gale (bb0005) 2001; 40 Kingston, Asford, Beer, Drew (bb0010) 1999 Lee, Park, Cho, Kim (bb0120) 2007; 48 Chang, Su, Lee, Chung (bb0035) 2007; 48 Bagatin, Araki, Toma (bb0075) 2011; 89 Chen, Chen (bb0105) 2006; 30 Connors (bb0155) 1987 Xiang, Mei, Li, Tong (bb0140) 2007; 581 Sahin, Akceylan (bb0015) 2014; 70 Georgiev, Wolf, Roundhill (bb0135) 1997; 16 Bagatin, Cruz, Toma, Politi, Demets (bb0145) 2005; 52 Bagatin, Matt, Thönnessen, Jones (bb0150) 1999; 38 Miao (10.1016/j.saa.2017.07.056_bb0100) 2012; 68 Kumar (10.1016/j.saa.2017.07.056_rf0030) 2016; 19 Kumar (10.1016/j.saa.2017.07.056_rf0035) 2017; 240 Bagatin (10.1016/j.saa.2017.07.056_bb0075) 2011; 89 Ji (10.1016/j.saa.2017.07.056_bb0115) 2000; 122 Bagatin (10.1016/j.saa.2017.07.056_bb0145) 2005; 52 Bagatin (10.1016/j.saa.2017.07.056_bb0150) 1999; 38 Jiang (10.1016/j.saa.2017.07.056_bb0060) 2012; 41 Lee (10.1016/j.saa.2017.07.056_bb0085) 2005; 70 Kumar (10.1016/j.saa.2017.07.056_rf0020) 2014; 27 Zhan (10.1016/j.saa.2017.07.056_bb0095) 2012; 36 Kingston (10.1016/j.saa.2017.07.056_bb0010) 1999 Connors (10.1016/j.saa.2017.07.056_bb0155) 1987 Chawla (10.1016/j.saa.2017.07.056_bb0110) 2007; 48 Kumar (10.1016/j.saa.2017.07.056_rf0025) 2014; 132 Chang (10.1016/j.saa.2017.07.056_bb0035) 2007; 48 Georgiev (10.1016/j.saa.2017.07.056_bb0135) 1997; 16 Lee (10.1016/j.saa.2017.07.056_bb0120) 2007; 48 Ozcan (10.1016/j.saa.2017.07.056_bb0045) 2009; 29 Xiang (10.1016/j.saa.2017.07.056_bb0140) 2007; 581 Sahin (10.1016/j.saa.2017.07.056_bb0015) 2014; 70 Evans (10.1016/j.saa.2017.07.056_bb0050) 2012; 402 Darjee (10.1016/j.saa.2017.07.056_bb0090) 2014; 55 Basaran (10.1016/j.saa.2017.07.056_bb0025) 2015; 56 Akkus (10.1016/j.saa.2017.07.056_bb0040) 2008; 62 Beer (10.1016/j.saa.2017.07.056_bb0005) 2001; 40 Bagatin (10.1016/j.saa.2017.07.056_bb0070) 2000; 24 Chen (10.1016/j.saa.2017.07.056_bb0105) 2006; 30 Othman (10.1016/j.saa.2017.07.056_bb0080) 2007; 63 Zhang (10.1016/j.saa.2017.07.056_bb0065) 2012; 36 Ghosh (10.1016/j.saa.2017.07.056_bb0030) 2015; 149 Ertul (10.1016/j.saa.2017.07.056_bb0130) 2010; 181 Sayin (10.1016/j.saa.2017.07.056_bb0055) 2015; 39 Aragoni (10.1016/j.saa.2017.07.056_bb0125) 2013; 42 |
References_xml | – volume: 40 start-page: 486 year: 2001 end-page: 516 ident: bb0005 publication-title: Angew. Chem. Int. Ed. contributor: fullname: Gale – volume: 48 start-page: 2541 year: 2007 end-page: 2546 ident: bb0120 publication-title: Tetrahedron Lett. contributor: fullname: Kim – volume: 48 start-page: 7274 year: 2007 end-page: 7278 ident: bb0035 publication-title: Tetrahedron Lett. contributor: fullname: Chung – volume: 70 start-page: 1463 year: 2005 end-page: 1466 ident: bb0085 publication-title: J. Org. Chem. contributor: fullname: Kim – volume: 581 start-page: 132 year: 2007 end-page: 136 ident: bb0140 publication-title: Anal. Chim. Acta contributor: fullname: Tong – volume: 52 start-page: 189 year: 2005 end-page: 193 ident: bb0145 publication-title: J. Incl. Phenom. Macrocycl. Chem. contributor: fullname: Demets – volume: 27 start-page: 729 year: 2014 end-page: 734 ident: bb0020 publication-title: J. Phys. Org. Chem. contributor: fullname: Rub – volume: 39 start-page: 130 year: 2015 end-page: 138 ident: bb0055 publication-title: Turk. J. Chem. contributor: fullname: Dogan – volume: 24 start-page: 841 year: 2000 end-page: 844 ident: bb0070 publication-title: New J. Chem. contributor: fullname: Toma – start-page: 251 year: 1999 end-page: 257 ident: bb0010 publication-title: J. Chem. Soc. Dalton Trans. contributor: fullname: Drew – volume: 402 start-page: 1739 year: 2012 end-page: 1748 ident: bb0050 publication-title: Anal. Bioanal. Chem. contributor: fullname: Beer – volume: 36 start-page: 819 year: 2012 end-page: 822 ident: bb0065 publication-title: New J. Chem. contributor: fullname: Ji – volume: 55 start-page: 7094 year: 2014 end-page: 7098 ident: bb0090 publication-title: Tetrahedron Lett. contributor: fullname: Jain – volume: 68 start-page: 2409 year: 2012 end-page: 2413 ident: bb0100 publication-title: Tetrahedron contributor: fullname: Li – volume: 41 start-page: 1801 year: 2012 end-page: 1807 ident: bb0060 publication-title: Dalton Trans. contributor: fullname: Ng – volume: 38 start-page: 1585 year: 1999 end-page: 1591 ident: bb0150 publication-title: Inorg. Chem. contributor: fullname: Jones – volume: 16 start-page: 1581 year: 1997 end-page: 1584 ident: bb0135 publication-title: Polyhedron contributor: fullname: Roundhill – volume: 36 start-page: 656 year: 2012 end-page: 661 ident: bb0095 publication-title: New J. Chem. contributor: fullname: Li – volume: 29 start-page: 2378 year: 2009 end-page: 2383 ident: bb0045 publication-title: Mater. Sci. Eng. C contributor: fullname: Yilmaz – start-page: 141 year: 1987 end-page: 187 ident: bb0155 article-title: In Binding Constants — The Measurement of Molecular Complex Stability contributor: fullname: Connors – volume: 56 start-page: 657 year: 2015 end-page: 661 ident: bb0025 publication-title: Tetrahedron Lett. contributor: fullname: Hossain – volume: 48 start-page: 6054 year: 2007 end-page: 6058 ident: bb0110 publication-title: Tetrahedron Lett. contributor: fullname: Shrivastava – volume: 70 start-page: 6944 year: 2014 end-page: 6950 ident: bb0015 publication-title: Tetrahedron contributor: fullname: Akceylan – volume: 149 start-page: 869 year: 2015 end-page: 874 ident: bb0030 publication-title: Spectrochim. Acta A contributor: fullname: Guchhait – volume: 30 start-page: 143 year: 2006 end-page: 147 ident: bb0105 publication-title: New J. Chem. contributor: fullname: Chen – volume: 89 start-page: 562 year: 2011 end-page: 567 ident: bb0075 publication-title: Can. J. Chem. contributor: fullname: Toma – volume: 62 start-page: 303 year: 2008 end-page: 309 ident: bb0040 publication-title: J. Incl. Phenom. Macrocycl. Chem. contributor: fullname: Cebeci – volume: 181 start-page: 1059 year: 2010 end-page: 1065 ident: bb0130 publication-title: J. Hazard. Mater. contributor: fullname: Yilmaz – volume: 63 start-page: 10793 year: 2007 end-page: 10800 ident: bb0080 publication-title: Tetrahedron contributor: fullname: Vicens – volume: 42 start-page: 14516 year: 2013 end-page: 14530 ident: bb0125 publication-title: Dalton Trans. contributor: fullname: Puccioni – volume: 122 start-page: 9306 year: 2000 end-page: 9307 ident: bb0115 publication-title: J. Am. Chem. Soc. contributor: fullname: Brown – volume: 36 start-page: 819 year: 2012 ident: 10.1016/j.saa.2017.07.056_bb0065 publication-title: New J. Chem. doi: 10.1039/c2nj20974h contributor: fullname: Zhang – volume: 39 start-page: 130 year: 2015 ident: 10.1016/j.saa.2017.07.056_bb0055 publication-title: Turk. J. Chem. doi: 10.3906/kim-1405-69 contributor: fullname: Sayin – volume: 70 start-page: 1463 year: 2005 ident: 10.1016/j.saa.2017.07.056_bb0085 publication-title: J. Org. Chem. doi: 10.1021/jo048228i contributor: fullname: Lee – volume: 41 start-page: 1801 year: 2012 ident: 10.1016/j.saa.2017.07.056_bb0060 publication-title: Dalton Trans. doi: 10.1039/C1DT11546D contributor: fullname: Jiang – volume: 52 start-page: 189 year: 2005 ident: 10.1016/j.saa.2017.07.056_bb0145 publication-title: J. Incl. Phenom. Macrocycl. Chem. doi: 10.1007/s10847-004-6385-2 contributor: fullname: Bagatin – volume: 402 start-page: 1739 year: 2012 ident: 10.1016/j.saa.2017.07.056_bb0050 publication-title: Anal. Bioanal. Chem. doi: 10.1007/s00216-011-5403-7 contributor: fullname: Evans – volume: 63 start-page: 10793 year: 2007 ident: 10.1016/j.saa.2017.07.056_bb0080 publication-title: Tetrahedron doi: 10.1016/j.tet.2007.06.120 contributor: fullname: Othman – volume: 132 start-page: 288 year: 2014 ident: 10.1016/j.saa.2017.07.056_rf0025 publication-title: Spectrochim. Acta A doi: 10.1016/j.saa.2014.05.002 contributor: fullname: Kumar – volume: 30 start-page: 143 year: 2006 ident: 10.1016/j.saa.2017.07.056_bb0105 publication-title: New J. Chem. doi: 10.1039/b513355f contributor: fullname: Chen – volume: 40 start-page: 486 year: 2001 ident: 10.1016/j.saa.2017.07.056_bb0005 publication-title: Angew. Chem. Int. Ed. doi: 10.1002/1521-3773(20010202)40:3<486::AID-ANIE486>3.0.CO;2-P contributor: fullname: Beer – volume: 16 start-page: 1581 year: 1997 ident: 10.1016/j.saa.2017.07.056_bb0135 publication-title: Polyhedron doi: 10.1016/S0277-5387(96)00410-X contributor: fullname: Georgiev – volume: 38 start-page: 1585 year: 1999 ident: 10.1016/j.saa.2017.07.056_bb0150 publication-title: Inorg. Chem. doi: 10.1021/ic980964f contributor: fullname: Bagatin – volume: 89 start-page: 562 year: 2011 ident: 10.1016/j.saa.2017.07.056_bb0075 publication-title: Can. J. Chem. doi: 10.1139/v11-021 contributor: fullname: Bagatin – volume: 36 start-page: 656 year: 2012 ident: 10.1016/j.saa.2017.07.056_bb0095 publication-title: New J. Chem. doi: 10.1039/C2NJ20776A contributor: fullname: Zhan – volume: 68 start-page: 2409 year: 2012 ident: 10.1016/j.saa.2017.07.056_bb0100 publication-title: Tetrahedron doi: 10.1016/j.tet.2012.01.010 contributor: fullname: Miao – volume: 56 start-page: 657 year: 2015 ident: 10.1016/j.saa.2017.07.056_bb0025 publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2014.12.015 contributor: fullname: Basaran – volume: 122 start-page: 9306 year: 2000 ident: 10.1016/j.saa.2017.07.056_bb0115 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja000012k contributor: fullname: Ji – volume: 62 start-page: 303 year: 2008 ident: 10.1016/j.saa.2017.07.056_bb0040 publication-title: J. Incl. Phenom. Macrocycl. Chem. doi: 10.1007/s10847-008-9472-y contributor: fullname: Akkus – volume: 48 start-page: 2541 year: 2007 ident: 10.1016/j.saa.2017.07.056_bb0120 publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2007.02.026 contributor: fullname: Lee – start-page: 251 year: 1999 ident: 10.1016/j.saa.2017.07.056_bb0010 publication-title: J. Chem. Soc. Dalton Trans. doi: 10.1039/a807763k contributor: fullname: Kingston – volume: 27 start-page: 729 year: 2014 ident: 10.1016/j.saa.2017.07.056_rf0020 publication-title: J. Phys. Org. Chem. doi: 10.1002/poc.3332 contributor: fullname: Kumar – volume: 240 start-page: 253 year: 2017 ident: 10.1016/j.saa.2017.07.056_rf0035 publication-title: J. Mol. Liq. doi: 10.1016/j.molliq.2017.05.088 contributor: fullname: Kumar – volume: 581 start-page: 132 year: 2007 ident: 10.1016/j.saa.2017.07.056_bb0140 publication-title: Anal. Chim. Acta doi: 10.1016/j.aca.2006.08.006 contributor: fullname: Xiang – volume: 70 start-page: 6944 year: 2014 ident: 10.1016/j.saa.2017.07.056_bb0015 publication-title: Tetrahedron doi: 10.1016/j.tet.2014.07.100 contributor: fullname: Sahin – volume: 55 start-page: 7094 year: 2014 ident: 10.1016/j.saa.2017.07.056_bb0090 publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2014.10.149 contributor: fullname: Darjee – volume: 48 start-page: 6054 year: 2007 ident: 10.1016/j.saa.2017.07.056_bb0110 publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2007.06.075 contributor: fullname: Chawla – volume: 19 start-page: 101 year: 2016 ident: 10.1016/j.saa.2017.07.056_rf0030 publication-title: J. Surfactant Deterg. doi: 10.1007/s11743-015-1754-y contributor: fullname: Kumar – volume: 149 start-page: 869 year: 2015 ident: 10.1016/j.saa.2017.07.056_bb0030 publication-title: Spectrochim. Acta A doi: 10.1016/j.saa.2015.04.025 contributor: fullname: Ghosh – volume: 42 start-page: 14516 year: 2013 ident: 10.1016/j.saa.2017.07.056_bb0125 publication-title: Dalton Trans. doi: 10.1039/c3dt51292d contributor: fullname: Aragoni – volume: 181 start-page: 1059 year: 2010 ident: 10.1016/j.saa.2017.07.056_bb0130 publication-title: J. Hazard. Mater. doi: 10.1016/j.jhazmat.2010.05.121 contributor: fullname: Ertul – volume: 48 start-page: 7274 year: 2007 ident: 10.1016/j.saa.2017.07.056_bb0035 publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2007.08.045 contributor: fullname: Chang – volume: 24 start-page: 841 year: 2000 ident: 10.1016/j.saa.2017.07.056_bb0070 publication-title: New J. Chem. doi: 10.1039/b005127f contributor: fullname: Bagatin – volume: 29 start-page: 2378 year: 2009 ident: 10.1016/j.saa.2017.07.056_bb0045 publication-title: Mater. Sci. Eng. C doi: 10.1016/j.msec.2009.06.008 contributor: fullname: Ozcan – start-page: 141 year: 1987 ident: 10.1016/j.saa.2017.07.056_bb0155 contributor: fullname: Connors |
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Snippet | A new quinoline-amide calix[4]arene 3-receptor for detection of hazardous anions and cations have been synthesized. The 3-receptor was examined for its sensing... |
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SubjectTerms | Dichromate Hazardous anions Hydrogen-bonds Mercury Quinoline Sensor |
Title | A Cr(VI) selective probe based on a quinoline-amide calix[4]arene |
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