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1.
A new macrocyclic receptor 1 having [1,8]-naphthyridine fluorophore is designed and synthesized for selective fluorescence sensing of Cd2+. Receptor 1 selectively responds to Cd2+ over other tested metal ions via a large enhancement of emission intensity due to the cation-induced CHEF (chelation enhanced fluorescence) effect. Receptor 1 although exhibits some affinity towards Zn2+, it selectively binds Cd2+ over Zn2+. Binding and selectivity were examined by 1H-NMR, fluorescence, UV-vis, mass and IR-spectroscopic techniques.  相似文献   

2.
Imbalance of zinc ion (Zn2+) in human body causes diseases like Alzheimer’s and Parkinson’s and therefore Zn2+ estimation in biological fluids has diagnostic values. Fluorescence “off-on” sensors have advantages of high sensitivity and in situ application over other sensors. A new fluorescent “off-on” Zn2+ sensor, N-benzoate-N′ salicylaldehyde ethynelediamine (L), has been synthesisied. In 1:1(v/v) CH3OH:PBS (PBS?=?phosphate buffer solution), L shows ca. 20 times enhancement in fluorescence intensity on interaction with Zn2+, due to snapping of photoinduced electron transfer (PET) process, which is selective over metal ions - Na+, K+, Ca2+, Ni2+, Cu2+, Cd2+, Hg2+ and Pb2+. These metal ions either individually or all together does not interfere the sensing ability of L towards Zn2+. A 1:1 interaction between L and Zn2+ ion with binding constant 104.25 has been established from spectroscopic data.  相似文献   

3.
In this study, we report the synthesis of new Schiff base E-1-(((1-benzylpiperidin-4-yl)imino)methyl)naphthalenee-2-ol (L) and evaluation of its fluorescence response toward Cu2+ ion. Preliminary, solvent effect, metal selectivity and metal ligand ratio were analyzed through UV-Visible study. Fluorescence response toward Cu2+ was carried to assess the fluorescent property of synthesized Schiff base. The probe exhibited a higher fluorescence enhancement in the presence of Cu2+ over other metal ions (Ni2+, Zn2+, Hg2+, Co2+, Cd2+, Al3+, Fe2+, and Pb2+). The binding stoichiometry between L and Cu2+ has been investigated using Job’s plot and Benesi-Hildebrand equation and it was found that ligand L can form 1:1 L-Cu2+ complex with binding constant (K a) of 4?×?104 LM?1.  相似文献   

4.
A new fluorescent chemosensor 2-(2-thiophene)imidazo [4,5,f]-1,10-phenanthroline (L) was prepared and characterized. By adding univalent or divalent metal ions such as Na+, K+, Mg2+, Ba2+, Mn2+, Fe2+, Co2+, Ni2+, Cu2+, Ag+, Zn2+, Cd2+ and Hg2+ ions into the solution of L in DMF under buffered conditions with the working pH ranging from 7.0 to 8.0, we found that L could be used to detect K+ ratiometricly and it could also be applied to sense Co2+ with the phenomenon of fluorescence quenching of L. While the response behavior of L was not discernibly affected by other examined metal ions.  相似文献   

5.
A novel conjugated molecule, L, based on 2,4,5-triphenylimidazole and 6-phenyl-2,2′-bipyridine (HCNN) was synthesized in two steps. The molecule can recognize Fe3+ in aqueous solution (THF/H2O, 1/1, v/v) by the appearance of new emission bands at 416 and 442 nm, which can be attributed to the emission of the newly formed L-Fe3+ complex. The binding constant of the complex was calculated to be (6.6±0.39)×103 M−1, and its formation was also confirmed by the appearance of isosbestic points at 312 and 381 nm in the UV-visible spectral titration experiment. While other transition and rare-earth metal ions, such as Mn2+, Fe2+, Co2+, Ni2+, Zn2+, Cd2+, Hg2+, Pb2+, Eu3+ and Nd3+, can only cause some decrease of L's fluorescence, alkali and alkaline earth metal ions, such as Li+, Na+, K+, Mg2+ and Ca2+, almost have no effect on L's fluorescence. The fluorescence of L can be recovered by the addition of EDTA to the L-Fe3+ system just due to EDTA's stronger chelating ability than that of L.  相似文献   

6.
The recognition ability of N-Furfurylsalicylaldimine (HL) toward various cations (Pb2+, Hg2+, Ba2+, Cd2+, Ag+, Zn2+, Cu2+, Ni2+, Co2+, K+, Sr2+, and Na+) has been studied by UV–Vis and fluorescence spectroscopy. The compound showed highly selective fluorescence signaling behaviour for Zn2+ ions in methanol-water medium based on CHEF process and is capable of distinguishing Zn2+ from Cd2+ ion. From single crystal X-ray analysis it is revealed that a Zn2+ ion binds two ligand molecules through imine nitrogen and phenolate oxygen atom.
Figure
N-Furfurylsalicylaldimine as a selective sensing of Zn2+ ion through CHEF process. The x-ray structure of the receptor-Zn(II) complex shows 2:1 stochiometry  相似文献   

7.
A coumarin-based fluorescent chemosensor 1 for Zn2+ was designed and synthesized. Compound 1 exhibits lower background fluorescence due to intramolecular photoinduced electron transfer. However, upon mixing with Zn2+ in 30% (v/v) aqueous ethanol, a “turn-on” fluorescence emission is observed. The fluorescence emission increases linearly with Zn2+ concentration in the range 0.5–10 μmol L−1 with a detection limit of 0.29 μmol L−1. No remarkable emission enhancement was, however, observed for other metal ions. The proposed chemosensor was applied to the determination of Zn2+ in water samples with satisfactory results.  相似文献   

8.
The fluorescence intensity of salicylaldehyde phenylhydrazone (L), in 1:1 (v/v) CH3OH:H2O was enhanced by ca. 100 times with a blue shift in emission maximum, on interaction with Pb2+ ion. No enhancement in fluorescent intensity of L was observed on interaction with metal ions - Na+, K+, Ca2+, Cu2+, Ni2+, Zn2+, Cd2+ and Hg2+. This signal transduction was found to occur via photoinduced electron transfer (PET) mechanism. A 1:1 complexation between Pb2+ and L with log β?=?7.86 has been proved from fluorescent and UV/Visible spectroscopic data. The detection limit of Pb2+ was calculated to be 6.3?×?10?7?M.  相似文献   

9.
The condensation product (L) of 4-methoxybenzaldehyde and ethylenediamine has been synthesised and characterised. L showed a 21 times enhancement in fluorescence intensity on interaction with Ce3+ in CH3OH at λmax?=?360 nm when excited with 270 nm photons. Metal ions K+, Na+, Al3+, Co2+, Hg2+, Cd2+, Ni2+, Zn2+, Mn2+, Mg2+ and Ca2+ do not interfere. The stoichiometry of binding and the binding constants were determined from spectroscopic data and found to be 1:1 and 104.8 M respectively. The detection limit was found to be 10–5.2 M. The protonation/de-protonation of water molecules coordinated to Ce3+ was found to show interesting behaviour on the fluorescence of L:Ce3+.  相似文献   

10.
A novel fluorescent rhodamine based chemosensor (E)-3′,6′-bis(diethylamino)-2-((2-(pyridin-2-ylmethoxy)benzylidene)amino)spiro[isoindoline-1,9′-xanthen]-3-one, RSP, had been successfully developed and well characterized by NMR, FT-IR and Mass spectroscopy. The chemosensor exhibits high selectivity for Hg2+ over other ions (Ag+, Pb2+, Cu2+, Ni2+, Fe3+, Co2+, Zn2+ and Cd2+) with fluorescence enhancement in ethanol solution. More over the detection limit of the sensor is in the 10?6 M level. The binding ratio of RSP-Hg2+ complex was determined to be 1:1 according to the Job plot. Test strips based on RSP were fabricated, which showed the application of the sensor for detection of mercuric ions in water by naked eyes.  相似文献   

11.
The photophysical and complexing properties of Rhod-5N (commercially available) in MOPS buffer are reported. This fluorescent molecular sensor consists of a BAPTA chelating moiety bound to a rhodamine fluorophore. Its fluorescence quantum yield is low and a drastic enhancement of fluorescence intensity upon cation binding was observed. Special attention was paid to the complexation with Cd2+, a well known toxic metal ion. Possible interference with other metal ions (Na+, K+, Mg2+, Ca2+, Zn2+, Pb2+) was examined. Rhod-5N was found to be highly selective of Cd2+ over those interfering cations except Pb2+. The limit of detection is 3.1 μg l−1.  相似文献   

12.
Two highly photostable yellow–green emitting 1,8-naphthalimides 5 and 6, containing both N-linked hindered amine moiety and a secondary or tertiary cation receptor, were synthesized for the first time. Novel compounds were configured as “fluorophore–spacer–receptor” systems based on photoinduced electron transfer. Photophysical characteristics of the dyes were investigated in DMF and water/DMF (4:1, v/v) solution. The ability of the new compounds to detect cations was evaluated by the changes in their fluorescence intensity in the presence of metal ions (Cu2+, Pb2+, Zn2+, Ni2+, Co2+) and protons. The presence of metal ions and protons was found to disallow a photoinduced electron transfer leading to an enhancement in the dye fluorescence intensity. Compound 5, containing secondary amine receptor, displayed a good sensor activity towards metal ions and protons. However the sensor activity of dye 6, containing a tertiary amine receptor and a shorter hydrocarbon spacer, was substantially higher. The results obtained indicate the potential of the novel compounds as highly photostable and efficient “off–on” pH switchers and fluorescent detectors for metal ions with pronounced selectivity towards Cu2+ ions.  相似文献   

13.
In this study, the coumarin-derived schiff bases (HL1 and HL2) have been designed and synthesized. Upon the addition of Zn2+, both of them show significant fluorescence enhancement owing to inhibits PET and ESIPT process respectively. However, the receptor HL2 response toward Cd2+, Mg2+, Ba2+, Ca2+ besides Zn2+ and exhibits fluorescence enhancement but not enough to detection of the concentration levels of Zn2+.  相似文献   

14.
An efficient “off–on” type fluorescent chemosensor, (E)-N′-(4-(diethylamino)-2-hydroxybenzylidene)-2-hydroxybenzohydrazide (H 2 L), based on Schiff base for the determination of Al3+ has been designed, synthesized, and evaluated. Upon treated with Al3+, the fluorescence of H 2 L was enhanced 45-fold due to the chelation-enhanced fluorescence (CHEF) effect based on the formation of a 1:1 complex between the chemosensor and Al3+. Other metal ions, such as Na+, K+, Mg2+, Ca2+, Cu2+, Ga3+, Zn2+, Cr3+, Cd2+, Ag+, Fe3+, In3+, Mn2+, Pb2+, Co2+, and Ni2+ had little effect on the fluorescence. The results demonstrate that the chemosensor H 2 L has stronger affinity with Al3+ than other metal ions. The detection limit of H 2 L for sensing Al3+ is 3.60 × 10?6 M in EtOH–H2O (3:7, v/v) solution. And the recognizing behavior has been investigated both experimentally and computationally.  相似文献   

15.
A carbon nanotube-based fluorescent chemosensor MWNTs-glycine-N-8-quinolylamide (MWNTs-GNQ) has been designed and synthesized. Steady-state fluorescence emission studies showed that this material displays high selectivity and sensitivity for the Cu2+ ion over other cations such as Zn2+, Cd2+, Mg2+, Ca2+, and Ni2+.  相似文献   

16.
The acyclic tridentate blue luminescent ligand (λex=300 nm, λem=415 nm) quinoline-2-carboxaldehyde 2-pyridylhydrazone, HL, 1, was recognized as a new fluorescent chemosensor for Pd2+. In alkaline methanol complete fluorescent quenching was observed in the presence of 2 equivalents of Pd2+ that was further reflected in the solid phase fluorescence microscopic study.Ligand formed 1:1 complexes with Ni2+, Cu2+, Zn2+, Pd2+ and 1:2 complexes with Co2+, Fe2+ as obtained from Job's plot of continuous variation. The binding constants of different metal complexes (Fe2+, Co2+, Ni2+, Cu2+, Zn2+ and Pd2+) were estimated by fluorescence titrations. The ligand can selectively extract significant amount of Pd2+ from the aqueous mixture of metal ions, and the extraction efficiency was increased from 80% to 95% with increase in the molar ratio of HL, 1, to Pd2+ from 1 to 3. No significant interference was observed up to 2-fold excess addition of Cu2+ and Zn2+ and 100-fold excess addition of Co2+, Fe2+ and Ni2+over the Pd2+ ion concentration (1.0×10−3 M).  相似文献   

17.
The condensation product of phenylalanine and salicylaldehyde (L) was synthesised and characterised which was found to be selective fluorescent “off-on” sensor for Zn2+ ion with the detection limit 10?5 M. The sensor is free of interferences from metal ions - Na+, K+, Al3+, Mn2+, Co2+, Ni2+, Cu2+, Pb2+, Cd2+ and Hg2+. The Fluorescence and the UV/visible spectral data reveals a 1:1 interaction between the sensor and Zn2+ ion with binding constant 108. The DFT and TDDFT calculations confirm the structures of the sensor and the sensor-Zn2+ complex.  相似文献   

18.
A simple “off-on fluorescence type” chemosensor 1 3-((2-(dimethylamino)ethyl)amino)-N-(quinolin-8-yl)propanamide has been synthesized for Zn2+. The receptor 1 comprises the quinoline moiety as fluorophore and the N,N-dimethylethane-1,2-diamine as a binding site. 1 showed a remarkable fluorescence enhancement in the presence of Zn2+ in aqueous solution. Importantly, the chemosensor 1 could be used to detect and quantify Zn2+ in water samples. In particular, this chemosensor could clearly distinguish Zn2+ from Cd2+. The binding properties of 1 with Zn2+ ions were investigated by UV-vis, fluorescence, electrospray ionization mass spectroscopy and 1H NMR titration.  相似文献   

19.
Fluoroionophores consisting of coumarin-153 linked to mono- and diaza-crown ethers are able to complex transition metal cations (Ni2+, Zn2+, Cd2+) and Pb2+, with concomitant large changes in photophysical properties. The stability constants in acetonitrile are higher than 3×106 M –1 except for Ni2+.  相似文献   

20.
Condensation product (L) of salicylaldehyde and semicarbazide behaves as a fluorescent sensor for Cd2+ ion, in 1:1 DMSO:H2O, over Mn2+, Fe2+, Ni2+, Co2+, Cu2+, Pb2+ and Hg2+ ions. The emission peak of L at λmax = 520 nm, on excitation with 420 nm wavelength photons, showed an enhancement in intensity of ca 60-fold when interacted with Cd2+ ion. The intensity was however found to remain unaltered when interacted with metal ions—Mn2+, Fe2+, Ni2+, Co2+, Cu2+, Pb2+ and Hg2+. The intensity increases by approximately 20 fold on interaction with Zn2+ ion. The increase in the fluorescent peak can be explained on the basis of photo induced electron transfer (PET) mechanism. A 1:1 complexation between Cd2+ and L with log β = 4.25 has been proved.  相似文献   

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