2022
DOI: 10.1016/j.arabjc.2022.104176
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A novel colorimetric and “turn-on” fluorescent sensor for selective detection of Cu2+

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Cited by 10 publications
(2 citation statements)
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“…The sensor was applied to detect changes in Cu­(II) in HeLa cells incubated in growth medium supplemented with 50 μM CuCl 2 . From this starting point, many similar hydrazide Cu­(II) probes that employ rhodamine ring-opening strategies have been developed and applied to detect exogenous addition of Cu­(II) in various cell types such as rhodamine B variants with dimethylaminovinylbenzene ( 252 ), ethyl hydroxide (RO1; 253 ), 2-methylpiperidine ( 254 ), Furan-2-carbaldehyde ( 255 ), 3-chloropyridazine ( 256 ), or benzyl-methyl-triazole (RHT; 257 ) substitutions, or a bis-spirocyclic configuration ( 258 ); rhodamine 6G variants with methanethioamide ( 259 ), ethyl hydroxide ( 260 ), tert -butylpyrrolyl methanimine ( 261 ), or trifluoroacetaldehyde substitutions ( 262 ); and fluorescein variants with pyridinylmethanimine (FHP; 263 ) and nitrobenzo-oxadiazole substitutions (NF; 264 ) . Other hydrazide variants have employed rhodamines with extended π-conjugation for a red-shifted emission such those with a vinylbenzonitrile (CSCN-Cu; 265 ), a naphthylamine (BF-Cu; 266 ), a carbazole (MeCzR-Cu; 267 ), a biscarbazole (BCX-Cu; 268 ), a benzimidazole with a six-membered spirocyclic hydrazide (BiF-Cu; 269 ), a quinazolinone (RQNA; 270 ), a benzene (FLACu; 271 ), a diethyl-tetrahydroquinoxaline/julolidine (JRQN; 272 ), and a quinoline (QFH; 273 ) …”
Section: Fluorescent Sensors For Coppermentioning
confidence: 99%
“…The sensor was applied to detect changes in Cu­(II) in HeLa cells incubated in growth medium supplemented with 50 μM CuCl 2 . From this starting point, many similar hydrazide Cu­(II) probes that employ rhodamine ring-opening strategies have been developed and applied to detect exogenous addition of Cu­(II) in various cell types such as rhodamine B variants with dimethylaminovinylbenzene ( 252 ), ethyl hydroxide (RO1; 253 ), 2-methylpiperidine ( 254 ), Furan-2-carbaldehyde ( 255 ), 3-chloropyridazine ( 256 ), or benzyl-methyl-triazole (RHT; 257 ) substitutions, or a bis-spirocyclic configuration ( 258 ); rhodamine 6G variants with methanethioamide ( 259 ), ethyl hydroxide ( 260 ), tert -butylpyrrolyl methanimine ( 261 ), or trifluoroacetaldehyde substitutions ( 262 ); and fluorescein variants with pyridinylmethanimine (FHP; 263 ) and nitrobenzo-oxadiazole substitutions (NF; 264 ) . Other hydrazide variants have employed rhodamines with extended π-conjugation for a red-shifted emission such those with a vinylbenzonitrile (CSCN-Cu; 265 ), a naphthylamine (BF-Cu; 266 ), a carbazole (MeCzR-Cu; 267 ), a biscarbazole (BCX-Cu; 268 ), a benzimidazole with a six-membered spirocyclic hydrazide (BiF-Cu; 269 ), a quinazolinone (RQNA; 270 ), a benzene (FLACu; 271 ), a diethyl-tetrahydroquinoxaline/julolidine (JRQN; 272 ), and a quinoline (QFH; 273 ) …”
Section: Fluorescent Sensors For Coppermentioning
confidence: 99%
“…Nowadays there has been a growing interest in developing fluorescent compounds for sensory biological or environmental applications because they are easy to be synthesized, highly sensitive and inexpensive [ 17 , 18 , 19 , 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 ]. Moreover, the ongoing development of confocal microscopy and optical imaging technologies facilitate the utilization of theses fluorescent probes for biological imaging [ 28 , 29 ].…”
Section: Introductionmentioning
confidence: 99%