Bisphenol A derived chemosensors for various ionic species: Small progress, long way to go and ample opportunities

Search for new fluorophoric platforms is of great demand for the efficient identification as well as quantification of various metal ions and anions. In this regard, bisphenol A could be a promising fluorophore. Formylation on bisphenol A results ‘bisphenol A dialdehyde’ i.e. 5,5′-(propane-2,2-diyl)...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Nandi, Mahasweta [verfasserIn] Roy, Partha [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2023

Schlagwörter:	Chemosensor Fluorescence Bisphenol A Cation Anion

Übergeordnetes Werk:	Enthalten in: Inorganica chimica acta - New York, NY [u.a.] : Elsevier, 1967, 557
Übergeordnetes Werk:	volume:557

DOI / URN:	10.1016/j.ica.2023.121709

Katalog-ID:	ELV062171054

Internformat


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245	1	0	\|a Bisphenol A derived chemosensors for various ionic species: Small progress, long way to go and ample opportunities
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520			\|a Search for new fluorophoric platforms is of great demand for the efficient identification as well as quantification of various metal ions and anions. In this regard, bisphenol A could be a promising fluorophore. Formylation on bisphenol A results ‘bisphenol A dialdehyde’ i.e. 5,5′-(propane-2,2-diyl)bis(2-hydroxybenzaldehyde) which has two CHO groups for further reactions with suitable amine compounds. This gives an excellent opportunity to prepare a number of chemosensors. In this article, we have summarized and discussed chemosensors, which are derived from bisphenol A dialdehyde, for the detection of metal ions and simple inorganic anions. Binding of metal ions with the complementary donor atoms also plays significant role. This article will give all the required information on bisphenol A derived chemosensors published so far at fingertips and help to design future chemosensors for efficient detection of metal cations and anions.
650		4	\|a Chemosensor
650		4	\|a Fluorescence
650		4	\|a Bisphenol A
650		4	\|a Cation
650		4	\|a Anion
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912			\|a GBV_ILN_23
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912			\|a GBV_ILN_31
912			\|a GBV_ILN_32
912			\|a GBV_ILN_40
912			\|a GBV_ILN_60
912			\|a GBV_ILN_62
912			\|a GBV_ILN_65
912			\|a GBV_ILN_69
912			\|a GBV_ILN_70
912			\|a GBV_ILN_73
912			\|a GBV_ILN_74
912			\|a GBV_ILN_90
912			\|a GBV_ILN_95
912			\|a GBV_ILN_100
912			\|a GBV_ILN_101
912			\|a GBV_ILN_105
912			\|a GBV_ILN_110
912			\|a GBV_ILN_150
912			\|a GBV_ILN_151
912			\|a GBV_ILN_187
912			\|a GBV_ILN_213
912			\|a GBV_ILN_224
912			\|a GBV_ILN_230
912			\|a GBV_ILN_370
912			\|a GBV_ILN_602
912			\|a GBV_ILN_702
912			\|a GBV_ILN_2001
912			\|a GBV_ILN_2003
912			\|a GBV_ILN_2004
912			\|a GBV_ILN_2005
912			\|a GBV_ILN_2007
912			\|a GBV_ILN_2008
912			\|a GBV_ILN_2009
912			\|a GBV_ILN_2010
912			\|a GBV_ILN_2011
912			\|a GBV_ILN_2014
912			\|a GBV_ILN_2015
912			\|a GBV_ILN_2020
912			\|a GBV_ILN_2021
912			\|a GBV_ILN_2025
912			\|a GBV_ILN_2026
912			\|a GBV_ILN_2027
912			\|a GBV_ILN_2034
912			\|a GBV_ILN_2044
912			\|a GBV_ILN_2048
912			\|a GBV_ILN_2049
912			\|a GBV_ILN_2050
912			\|a GBV_ILN_2055
912			\|a GBV_ILN_2056
912			\|a GBV_ILN_2059
912			\|a GBV_ILN_2061
912			\|a GBV_ILN_2064
912			\|a GBV_ILN_2088
912			\|a GBV_ILN_2106
912			\|a GBV_ILN_2110
912			\|a GBV_ILN_2111
912			\|a GBV_ILN_2112
912			\|a GBV_ILN_2122
912			\|a GBV_ILN_2129
912			\|a GBV_ILN_2143
912			\|a GBV_ILN_2152
912			\|a GBV_ILN_2153
912			\|a GBV_ILN_2190
912			\|a GBV_ILN_2232
912			\|a GBV_ILN_2336
912			\|a GBV_ILN_2470
912			\|a GBV_ILN_2507
912			\|a GBV_ILN_4035
912			\|a GBV_ILN_4037
912			\|a GBV_ILN_4112
912			\|a GBV_ILN_4125
912			\|a GBV_ILN_4242
912			\|a GBV_ILN_4249
912			\|a GBV_ILN_4251
912			\|a GBV_ILN_4305
912			\|a GBV_ILN_4306
912			\|a GBV_ILN_4307
912			\|a GBV_ILN_4313
912			\|a GBV_ILN_4322
912			\|a GBV_ILN_4323
912			\|a GBV_ILN_4324
912			\|a GBV_ILN_4325
912			\|a GBV_ILN_4326
912			\|a GBV_ILN_4333
912			\|a GBV_ILN_4334
912			\|a GBV_ILN_4338
912			\|a GBV_ILN_4393
912			\|a GBV_ILN_4700
936	b	k	\|a 35.00 \|j Chemie: Allgemeines \|q VZ
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Indexfelder

author_variant	m n mn p r pr
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hierarchy_sort_str	2023
bklnumber	35.00
publishDate	2023
allfields	10.1016/j.ica.2023.121709 doi (DE-627)ELV062171054 (ELSEVIER)S0020-1693(23)00334-1 DE-627 ger DE-627 rda eng 540 VZ 35.00 bkl Nandi, Mahasweta verfasserin aut Bisphenol A derived chemosensors for various ionic species: Small progress, long way to go and ample opportunities 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Search for new fluorophoric platforms is of great demand for the efficient identification as well as quantification of various metal ions and anions. In this regard, bisphenol A could be a promising fluorophore. Formylation on bisphenol A results ‘bisphenol A dialdehyde’ i.e. 5,5′-(propane-2,2-diyl)bis(2-hydroxybenzaldehyde) which has two CHO groups for further reactions with suitable amine compounds. This gives an excellent opportunity to prepare a number of chemosensors. In this article, we have summarized and discussed chemosensors, which are derived from bisphenol A dialdehyde, for the detection of metal ions and simple inorganic anions. Binding of metal ions with the complementary donor atoms also plays significant role. This article will give all the required information on bisphenol A derived chemosensors published so far at fingertips and help to design future chemosensors for efficient detection of metal cations and anions. Chemosensor Fluorescence Bisphenol A Cation Anion Roy, Partha verfasserin (orcid)0000-0001-5387-5626 aut Enthalten in Inorganica chimica acta New York, NY [u.a.] : Elsevier, 1967 557 Online-Ressource (DE-627)301510946 (DE-600)1484441-2 (DE-576)081952694 0020-1693 nnns volume:557 GBV_USEFLAG_U GBV_ELV SYSFLAG_U 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_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_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 Chemie: Allgemeines VZ AR 557
spelling	10.1016/j.ica.2023.121709 doi (DE-627)ELV062171054 (ELSEVIER)S0020-1693(23)00334-1 DE-627 ger DE-627 rda eng 540 VZ 35.00 bkl Nandi, Mahasweta verfasserin aut Bisphenol A derived chemosensors for various ionic species: Small progress, long way to go and ample opportunities 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Search for new fluorophoric platforms is of great demand for the efficient identification as well as quantification of various metal ions and anions. In this regard, bisphenol A could be a promising fluorophore. Formylation on bisphenol A results ‘bisphenol A dialdehyde’ i.e. 5,5′-(propane-2,2-diyl)bis(2-hydroxybenzaldehyde) which has two CHO groups for further reactions with suitable amine compounds. This gives an excellent opportunity to prepare a number of chemosensors. In this article, we have summarized and discussed chemosensors, which are derived from bisphenol A dialdehyde, for the detection of metal ions and simple inorganic anions. Binding of metal ions with the complementary donor atoms also plays significant role. This article will give all the required information on bisphenol A derived chemosensors published so far at fingertips and help to design future chemosensors for efficient detection of metal cations and anions. Chemosensor Fluorescence Bisphenol A Cation Anion Roy, Partha verfasserin (orcid)0000-0001-5387-5626 aut Enthalten in Inorganica chimica acta New York, NY [u.a.] : Elsevier, 1967 557 Online-Ressource (DE-627)301510946 (DE-600)1484441-2 (DE-576)081952694 0020-1693 nnns volume:557 GBV_USEFLAG_U GBV_ELV SYSFLAG_U 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_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_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 Chemie: Allgemeines VZ AR 557
allfields_unstemmed	10.1016/j.ica.2023.121709 doi (DE-627)ELV062171054 (ELSEVIER)S0020-1693(23)00334-1 DE-627 ger DE-627 rda eng 540 VZ 35.00 bkl Nandi, Mahasweta verfasserin aut Bisphenol A derived chemosensors for various ionic species: Small progress, long way to go and ample opportunities 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Search for new fluorophoric platforms is of great demand for the efficient identification as well as quantification of various metal ions and anions. In this regard, bisphenol A could be a promising fluorophore. Formylation on bisphenol A results ‘bisphenol A dialdehyde’ i.e. 5,5′-(propane-2,2-diyl)bis(2-hydroxybenzaldehyde) which has two CHO groups for further reactions with suitable amine compounds. This gives an excellent opportunity to prepare a number of chemosensors. In this article, we have summarized and discussed chemosensors, which are derived from bisphenol A dialdehyde, for the detection of metal ions and simple inorganic anions. Binding of metal ions with the complementary donor atoms also plays significant role. This article will give all the required information on bisphenol A derived chemosensors published so far at fingertips and help to design future chemosensors for efficient detection of metal cations and anions. Chemosensor Fluorescence Bisphenol A Cation Anion Roy, Partha verfasserin (orcid)0000-0001-5387-5626 aut Enthalten in Inorganica chimica acta New York, NY [u.a.] : Elsevier, 1967 557 Online-Ressource (DE-627)301510946 (DE-600)1484441-2 (DE-576)081952694 0020-1693 nnns volume:557 GBV_USEFLAG_U GBV_ELV SYSFLAG_U 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_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_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 Chemie: Allgemeines VZ AR 557
allfieldsGer	10.1016/j.ica.2023.121709 doi (DE-627)ELV062171054 (ELSEVIER)S0020-1693(23)00334-1 DE-627 ger DE-627 rda eng 540 VZ 35.00 bkl Nandi, Mahasweta verfasserin aut Bisphenol A derived chemosensors for various ionic species: Small progress, long way to go and ample opportunities 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Search for new fluorophoric platforms is of great demand for the efficient identification as well as quantification of various metal ions and anions. In this regard, bisphenol A could be a promising fluorophore. Formylation on bisphenol A results ‘bisphenol A dialdehyde’ i.e. 5,5′-(propane-2,2-diyl)bis(2-hydroxybenzaldehyde) which has two CHO groups for further reactions with suitable amine compounds. This gives an excellent opportunity to prepare a number of chemosensors. In this article, we have summarized and discussed chemosensors, which are derived from bisphenol A dialdehyde, for the detection of metal ions and simple inorganic anions. Binding of metal ions with the complementary donor atoms also plays significant role. This article will give all the required information on bisphenol A derived chemosensors published so far at fingertips and help to design future chemosensors for efficient detection of metal cations and anions. Chemosensor Fluorescence Bisphenol A Cation Anion Roy, Partha verfasserin (orcid)0000-0001-5387-5626 aut Enthalten in Inorganica chimica acta New York, NY [u.a.] : Elsevier, 1967 557 Online-Ressource (DE-627)301510946 (DE-600)1484441-2 (DE-576)081952694 0020-1693 nnns volume:557 GBV_USEFLAG_U GBV_ELV SYSFLAG_U 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_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_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 Chemie: Allgemeines VZ AR 557
allfieldsSound	10.1016/j.ica.2023.121709 doi (DE-627)ELV062171054 (ELSEVIER)S0020-1693(23)00334-1 DE-627 ger DE-627 rda eng 540 VZ 35.00 bkl Nandi, Mahasweta verfasserin aut Bisphenol A derived chemosensors for various ionic species: Small progress, long way to go and ample opportunities 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Search for new fluorophoric platforms is of great demand for the efficient identification as well as quantification of various metal ions and anions. In this regard, bisphenol A could be a promising fluorophore. Formylation on bisphenol A results ‘bisphenol A dialdehyde’ i.e. 5,5′-(propane-2,2-diyl)bis(2-hydroxybenzaldehyde) which has two CHO groups for further reactions with suitable amine compounds. This gives an excellent opportunity to prepare a number of chemosensors. In this article, we have summarized and discussed chemosensors, which are derived from bisphenol A dialdehyde, for the detection of metal ions and simple inorganic anions. Binding of metal ions with the complementary donor atoms also plays significant role. This article will give all the required information on bisphenol A derived chemosensors published so far at fingertips and help to design future chemosensors for efficient detection of metal cations and anions. Chemosensor Fluorescence Bisphenol A Cation Anion Roy, Partha verfasserin (orcid)0000-0001-5387-5626 aut Enthalten in Inorganica chimica acta New York, NY [u.a.] : Elsevier, 1967 557 Online-Ressource (DE-627)301510946 (DE-600)1484441-2 (DE-576)081952694 0020-1693 nnns volume:557 GBV_USEFLAG_U GBV_ELV SYSFLAG_U 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_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_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 Chemie: Allgemeines VZ AR 557
language	English
source	Enthalten in Inorganica chimica acta 557 volume:557
sourceStr	Enthalten in Inorganica chimica acta 557 volume:557
format_phy_str_mv	Article
bklname	Chemie: Allgemeines
institution	findex.gbv.de
topic_facet	Chemosensor Fluorescence Bisphenol A Cation Anion
dewey-raw	540
isfreeaccess_bool	false
container_title	Inorganica chimica acta
authorswithroles_txt_mv	Nandi, Mahasweta @@aut@@ Roy, Partha @@aut@@
publishDateDaySort_date	2023-01-01T00:00:00Z
hierarchy_top_id	301510946
dewey-sort	3540
id	ELV062171054
language_de	englisch
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author	Nandi, Mahasweta
spellingShingle	Nandi, Mahasweta ddc 540 bkl 35.00 misc Chemosensor misc Fluorescence misc Bisphenol A misc Cation misc Anion Bisphenol A derived chemosensors for various ionic species: Small progress, long way to go and ample opportunities
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topic_title	540 VZ 35.00 bkl Bisphenol A derived chemosensors for various ionic species: Small progress, long way to go and ample opportunities Chemosensor Fluorescence Bisphenol A Cation Anion
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title	Bisphenol A derived chemosensors for various ionic species: Small progress, long way to go and ample opportunities
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title_full	Bisphenol A derived chemosensors for various ionic species: Small progress, long way to go and ample opportunities
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title_sort	bisphenol a derived chemosensors for various ionic species: small progress, long way to go and ample opportunities
title_auth	Bisphenol A derived chemosensors for various ionic species: Small progress, long way to go and ample opportunities
abstract	Search for new fluorophoric platforms is of great demand for the efficient identification as well as quantification of various metal ions and anions. In this regard, bisphenol A could be a promising fluorophore. Formylation on bisphenol A results ‘bisphenol A dialdehyde’ i.e. 5,5′-(propane-2,2-diyl)bis(2-hydroxybenzaldehyde) which has two CHO groups for further reactions with suitable amine compounds. This gives an excellent opportunity to prepare a number of chemosensors. In this article, we have summarized and discussed chemosensors, which are derived from bisphenol A dialdehyde, for the detection of metal ions and simple inorganic anions. Binding of metal ions with the complementary donor atoms also plays significant role. This article will give all the required information on bisphenol A derived chemosensors published so far at fingertips and help to design future chemosensors for efficient detection of metal cations and anions.
abstractGer	Search for new fluorophoric platforms is of great demand for the efficient identification as well as quantification of various metal ions and anions. In this regard, bisphenol A could be a promising fluorophore. Formylation on bisphenol A results ‘bisphenol A dialdehyde’ i.e. 5,5′-(propane-2,2-diyl)bis(2-hydroxybenzaldehyde) which has two CHO groups for further reactions with suitable amine compounds. This gives an excellent opportunity to prepare a number of chemosensors. In this article, we have summarized and discussed chemosensors, which are derived from bisphenol A dialdehyde, for the detection of metal ions and simple inorganic anions. Binding of metal ions with the complementary donor atoms also plays significant role. This article will give all the required information on bisphenol A derived chemosensors published so far at fingertips and help to design future chemosensors for efficient detection of metal cations and anions.
abstract_unstemmed	Search for new fluorophoric platforms is of great demand for the efficient identification as well as quantification of various metal ions and anions. In this regard, bisphenol A could be a promising fluorophore. Formylation on bisphenol A results ‘bisphenol A dialdehyde’ i.e. 5,5′-(propane-2,2-diyl)bis(2-hydroxybenzaldehyde) which has two CHO groups for further reactions with suitable amine compounds. This gives an excellent opportunity to prepare a number of chemosensors. In this article, we have summarized and discussed chemosensors, which are derived from bisphenol A dialdehyde, for the detection of metal ions and simple inorganic anions. Binding of metal ions with the complementary donor atoms also plays significant role. This article will give all the required information on bisphenol A derived chemosensors published so far at fingertips and help to design future chemosensors for efficient detection of metal cations and anions.
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title_short	Bisphenol A derived chemosensors for various ionic species: Small progress, long way to go and ample opportunities
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