The synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor

In this paper, a new “turn-on” aromatic polycarboxylic fluorescent probe L was designed and synthesized based on 4,4′-diaminobiphenyl-2,2′-dicarboxylic acid and salicylaldehyde. The probe L could not only be used as a fluorescent probe to detect Al3+ ions in various solvents, but also be used to det...
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Gespeichert in:

Autor*in:	Zhao, Yichen [verfasserIn] Cheng, Jiapeng [verfasserIn] Li, Jiaxin [verfasserIn] Wang, Lin [verfasserIn] Li, Wenjun [verfasserIn] Chang, Zhidong [verfasserIn] Sun, Changyan [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2021

Schlagwörter:	Fluorescent probe Al Fe Aromatic polycarboxylic ligand Chelation enhanced fluorescence

Übergeordnetes Werk:	Enthalten in: Journal of molecular structure - New York, NY [u.a.] : Elsevier, 1967, 1251
Übergeordnetes Werk:	volume:1251

DOI / URN:	10.1016/j.molstruc.2021.132042

Katalog-ID:	ELV007228538

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245	1	0	\|a The synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor
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520			\|a In this paper, a new “turn-on” aromatic polycarboxylic fluorescent probe L was designed and synthesized based on 4,4′-diaminobiphenyl-2,2′-dicarboxylic acid and salicylaldehyde. The probe L could not only be used as a fluorescent probe to detect Al3+ ions in various solvents, but also be used to detect Fe3+ ions by naked eyes. The detection limits were 5.34 × 10−8 and 1.38 × 10−6 M, respectively. Job′s plot, 1H NMR titration experiments and ESI mass spectrometry proved that the coordination ratio of L and Al3+ ions was 1:1, and Al3+ ions were coordinated with hydroxyl oxygen atoms on the carboxyl groups of probe L. The mechanism could be deduced as chelation enhanced fluorescence.
650		4	\|a Fluorescent probe
650		4	\|a Al
650		4	\|a Fe
650		4	\|a Aromatic polycarboxylic ligand
650		4	\|a Chelation enhanced fluorescence
700	1		\|a Cheng, Jiapeng \|e verfasserin \|4 aut
700	1		\|a Li, Jiaxin \|e verfasserin \|4 aut
700	1		\|a Wang, Lin \|e verfasserin \|4 aut
700	1		\|a Li, Wenjun \|e verfasserin \|4 aut
700	1		\|a Chang, Zhidong \|e verfasserin \|4 aut
700	1		\|a Sun, Changyan \|e verfasserin \|4 aut
773	0	8	\|i Enthalten in \|t Journal of molecular structure \|d New York, NY [u.a.] : Elsevier, 1967 \|g 1251 \|h Online-Ressource \|w (DE-627)302469745 \|w (DE-600)1491504-2 \|w (DE-576)255266626 \|x 0022-2860 \|7 nnns
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912			\|a GBV_ILN_2112
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allfields	10.1016/j.molstruc.2021.132042 doi (DE-627)ELV007228538 (ELSEVIER)S0022-2860(21)02162-1 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Zhao, Yichen verfasserin aut The synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this paper, a new “turn-on” aromatic polycarboxylic fluorescent probe L was designed and synthesized based on 4,4′-diaminobiphenyl-2,2′-dicarboxylic acid and salicylaldehyde. The probe L could not only be used as a fluorescent probe to detect Al3+ ions in various solvents, but also be used to detect Fe3+ ions by naked eyes. The detection limits were 5.34 × 10−8 and 1.38 × 10−6 M, respectively. Job′s plot, 1H NMR titration experiments and ESI mass spectrometry proved that the coordination ratio of L and Al3+ ions was 1:1, and Al3+ ions were coordinated with hydroxyl oxygen atoms on the carboxyl groups of probe L. The mechanism could be deduced as chelation enhanced fluorescence. Fluorescent probe Al Fe Aromatic polycarboxylic ligand Chelation enhanced fluorescence Cheng, Jiapeng verfasserin aut Li, Jiaxin verfasserin aut Wang, Lin verfasserin aut Li, Wenjun verfasserin aut Chang, Zhidong verfasserin aut Sun, Changyan verfasserin aut Enthalten in Journal of molecular structure New York, NY [u.a.] : Elsevier, 1967 1251 Online-Ressource (DE-627)302469745 (DE-600)1491504-2 (DE-576)255266626 0022-2860 nnns volume:1251 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1251
spelling	10.1016/j.molstruc.2021.132042 doi (DE-627)ELV007228538 (ELSEVIER)S0022-2860(21)02162-1 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Zhao, Yichen verfasserin aut The synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this paper, a new “turn-on” aromatic polycarboxylic fluorescent probe L was designed and synthesized based on 4,4′-diaminobiphenyl-2,2′-dicarboxylic acid and salicylaldehyde. The probe L could not only be used as a fluorescent probe to detect Al3+ ions in various solvents, but also be used to detect Fe3+ ions by naked eyes. The detection limits were 5.34 × 10−8 and 1.38 × 10−6 M, respectively. Job′s plot, 1H NMR titration experiments and ESI mass spectrometry proved that the coordination ratio of L and Al3+ ions was 1:1, and Al3+ ions were coordinated with hydroxyl oxygen atoms on the carboxyl groups of probe L. The mechanism could be deduced as chelation enhanced fluorescence. Fluorescent probe Al Fe Aromatic polycarboxylic ligand Chelation enhanced fluorescence Cheng, Jiapeng verfasserin aut Li, Jiaxin verfasserin aut Wang, Lin verfasserin aut Li, Wenjun verfasserin aut Chang, Zhidong verfasserin aut Sun, Changyan verfasserin aut Enthalten in Journal of molecular structure New York, NY [u.a.] : Elsevier, 1967 1251 Online-Ressource (DE-627)302469745 (DE-600)1491504-2 (DE-576)255266626 0022-2860 nnns volume:1251 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1251
allfields_unstemmed	10.1016/j.molstruc.2021.132042 doi (DE-627)ELV007228538 (ELSEVIER)S0022-2860(21)02162-1 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Zhao, Yichen verfasserin aut The synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this paper, a new “turn-on” aromatic polycarboxylic fluorescent probe L was designed and synthesized based on 4,4′-diaminobiphenyl-2,2′-dicarboxylic acid and salicylaldehyde. The probe L could not only be used as a fluorescent probe to detect Al3+ ions in various solvents, but also be used to detect Fe3+ ions by naked eyes. The detection limits were 5.34 × 10−8 and 1.38 × 10−6 M, respectively. Job′s plot, 1H NMR titration experiments and ESI mass spectrometry proved that the coordination ratio of L and Al3+ ions was 1:1, and Al3+ ions were coordinated with hydroxyl oxygen atoms on the carboxyl groups of probe L. The mechanism could be deduced as chelation enhanced fluorescence. Fluorescent probe Al Fe Aromatic polycarboxylic ligand Chelation enhanced fluorescence Cheng, Jiapeng verfasserin aut Li, Jiaxin verfasserin aut Wang, Lin verfasserin aut Li, Wenjun verfasserin aut Chang, Zhidong verfasserin aut Sun, Changyan verfasserin aut Enthalten in Journal of molecular structure New York, NY [u.a.] : Elsevier, 1967 1251 Online-Ressource (DE-627)302469745 (DE-600)1491504-2 (DE-576)255266626 0022-2860 nnns volume:1251 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1251
allfieldsGer	10.1016/j.molstruc.2021.132042 doi (DE-627)ELV007228538 (ELSEVIER)S0022-2860(21)02162-1 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Zhao, Yichen verfasserin aut The synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this paper, a new “turn-on” aromatic polycarboxylic fluorescent probe L was designed and synthesized based on 4,4′-diaminobiphenyl-2,2′-dicarboxylic acid and salicylaldehyde. The probe L could not only be used as a fluorescent probe to detect Al3+ ions in various solvents, but also be used to detect Fe3+ ions by naked eyes. The detection limits were 5.34 × 10−8 and 1.38 × 10−6 M, respectively. Job′s plot, 1H NMR titration experiments and ESI mass spectrometry proved that the coordination ratio of L and Al3+ ions was 1:1, and Al3+ ions were coordinated with hydroxyl oxygen atoms on the carboxyl groups of probe L. The mechanism could be deduced as chelation enhanced fluorescence. Fluorescent probe Al Fe Aromatic polycarboxylic ligand Chelation enhanced fluorescence Cheng, Jiapeng verfasserin aut Li, Jiaxin verfasserin aut Wang, Lin verfasserin aut Li, Wenjun verfasserin aut Chang, Zhidong verfasserin aut Sun, Changyan verfasserin aut Enthalten in Journal of molecular structure New York, NY [u.a.] : Elsevier, 1967 1251 Online-Ressource (DE-627)302469745 (DE-600)1491504-2 (DE-576)255266626 0022-2860 nnns volume:1251 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1251
allfieldsSound	10.1016/j.molstruc.2021.132042 doi (DE-627)ELV007228538 (ELSEVIER)S0022-2860(21)02162-1 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Zhao, Yichen verfasserin aut The synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this paper, a new “turn-on” aromatic polycarboxylic fluorescent probe L was designed and synthesized based on 4,4′-diaminobiphenyl-2,2′-dicarboxylic acid and salicylaldehyde. The probe L could not only be used as a fluorescent probe to detect Al3+ ions in various solvents, but also be used to detect Fe3+ ions by naked eyes. The detection limits were 5.34 × 10−8 and 1.38 × 10−6 M, respectively. Job′s plot, 1H NMR titration experiments and ESI mass spectrometry proved that the coordination ratio of L and Al3+ ions was 1:1, and Al3+ ions were coordinated with hydroxyl oxygen atoms on the carboxyl groups of probe L. The mechanism could be deduced as chelation enhanced fluorescence. Fluorescent probe Al Fe Aromatic polycarboxylic ligand Chelation enhanced fluorescence Cheng, Jiapeng verfasserin aut Li, Jiaxin verfasserin aut Wang, Lin verfasserin aut Li, Wenjun verfasserin aut Chang, Zhidong verfasserin aut Sun, Changyan verfasserin aut Enthalten in Journal of molecular structure New York, NY [u.a.] : Elsevier, 1967 1251 Online-Ressource (DE-627)302469745 (DE-600)1491504-2 (DE-576)255266626 0022-2860 nnns volume:1251 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1251
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topic_facet	Fluorescent probe Al Fe Aromatic polycarboxylic ligand Chelation enhanced fluorescence
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authorswithroles_txt_mv	Zhao, Yichen @@aut@@ Cheng, Jiapeng @@aut@@ Li, Jiaxin @@aut@@ Wang, Lin @@aut@@ Li, Wenjun @@aut@@ Chang, Zhidong @@aut@@ Sun, Changyan @@aut@@
publishDateDaySort_date	2021-01-01T00:00:00Z
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author	Zhao, Yichen
spellingShingle	Zhao, Yichen ddc 540 bkl 35.00 misc Fluorescent probe misc Al misc Fe misc Aromatic polycarboxylic ligand misc Chelation enhanced fluorescence The synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor
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topic_title	540 DE-600 35.00 bkl The synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor Fluorescent probe Al Fe Aromatic polycarboxylic ligand Chelation enhanced fluorescence
topic	ddc 540 bkl 35.00 misc Fluorescent probe misc Al misc Fe misc Aromatic polycarboxylic ligand misc Chelation enhanced fluorescence
topic_unstemmed	ddc 540 bkl 35.00 misc Fluorescent probe misc Al misc Fe misc Aromatic polycarboxylic ligand misc Chelation enhanced fluorescence
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title	The synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor
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title_full	The synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor
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author_browse	Zhao, Yichen Cheng, Jiapeng Li, Jiaxin Wang, Lin Li, Wenjun Chang, Zhidong Sun, Changyan
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title_sort	the synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor
title_auth	The synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor
abstract	In this paper, a new “turn-on” aromatic polycarboxylic fluorescent probe L was designed and synthesized based on 4,4′-diaminobiphenyl-2,2′-dicarboxylic acid and salicylaldehyde. The probe L could not only be used as a fluorescent probe to detect Al3+ ions in various solvents, but also be used to detect Fe3+ ions by naked eyes. The detection limits were 5.34 × 10−8 and 1.38 × 10−6 M, respectively. Job′s plot, 1H NMR titration experiments and ESI mass spectrometry proved that the coordination ratio of L and Al3+ ions was 1:1, and Al3+ ions were coordinated with hydroxyl oxygen atoms on the carboxyl groups of probe L. The mechanism could be deduced as chelation enhanced fluorescence.
abstractGer	In this paper, a new “turn-on” aromatic polycarboxylic fluorescent probe L was designed and synthesized based on 4,4′-diaminobiphenyl-2,2′-dicarboxylic acid and salicylaldehyde. The probe L could not only be used as a fluorescent probe to detect Al3+ ions in various solvents, but also be used to detect Fe3+ ions by naked eyes. The detection limits were 5.34 × 10−8 and 1.38 × 10−6 M, respectively. Job′s plot, 1H NMR titration experiments and ESI mass spectrometry proved that the coordination ratio of L and Al3+ ions was 1:1, and Al3+ ions were coordinated with hydroxyl oxygen atoms on the carboxyl groups of probe L. The mechanism could be deduced as chelation enhanced fluorescence.
abstract_unstemmed	In this paper, a new “turn-on” aromatic polycarboxylic fluorescent probe L was designed and synthesized based on 4,4′-diaminobiphenyl-2,2′-dicarboxylic acid and salicylaldehyde. The probe L could not only be used as a fluorescent probe to detect Al3+ ions in various solvents, but also be used to detect Fe3+ ions by naked eyes. The detection limits were 5.34 × 10−8 and 1.38 × 10−6 M, respectively. Job′s plot, 1H NMR titration experiments and ESI mass spectrometry proved that the coordination ratio of L and Al3+ ions was 1:1, and Al3+ ions were coordinated with hydroxyl oxygen atoms on the carboxyl groups of probe L. The mechanism could be deduced as chelation enhanced fluorescence.
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title_short	The synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor
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author2	Cheng, Jiapeng Li, Jiaxin Wang, Lin Li, Wenjun Chang, Zhidong Sun, Changyan
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doi_str	10.1016/j.molstruc.2021.132042
up_date	2024-07-07T00:02:29.342Z
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The probe L could not only be used as a fluorescent probe to detect Al3+ ions in various solvents, but also be used to detect Fe3+ ions by naked eyes. The detection limits were 5.34 × 10−8 and 1.38 × 10−6 M, respectively. Job′s plot, 1H NMR titration experiments and ESI mass spectrometry proved that the coordination ratio of L and Al3+ ions was 1:1, and Al3+ ions were coordinated with hydroxyl oxygen atoms on the carboxyl groups of probe L. 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The synthesis of a new aromatic polycarboxylic acid and its property as fluorescence-colorimetric chemosensor

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