Patent Application
20160252488
The invention discloses a novel ligand (Lx) of Formula-I with high selectivity to Cr (III) and a process for the preparation thereof. Particularly, the invention further discloses a method of determining Cr (III) in fluids, where the ligand should have solubility in aqueous medium with the aid of non-ionic surfactant.
Due to its high paramagnetic behavior it is challenging for chemists to develop fluorogenic receptors specific for Cr (III) detection with fluorescence on response, as it is well known to quench the luminescence of a fluorophore. Further, due to the high solvation enthalpy of Cr (III)-ion in aqueous medium, it is also difficult to find an appropriate receptor for Cr(III-ion that works in pure aqueous medium.
There are only few examples of receptors available in the literature, which binds exclusively to Cr (III) in an ensemble of several other competing metal ions. The Receptor 1 was reported by Li et. al, Chem. commun, 2008, 3387. It is a FRET based chemo sensor for detection of Cr(III) in ethanol/water (2/1, v/v) medium and it can be used as an imaging agent in HeLa cell.
Li et at also reported another Ferrocene Based Receptor 2 (Org. lett, 2008, 2557) for selective detection of Cr(III) in ethanol/water (1/1, v/v) with an association constant of 7.5×103 M−1. Receptors 3 (Anal. Methods, 2012, 3163; receptor is effective in acetonitrile/water (9/1, v/v)) and 4 (Anal. Methods, 2012, 2254; receptor is effective in methanol/water (9/1, v/v)) were developed by D. Das and his co-workers and both reagents showed high selectivity towards Cr(III) in predominantly organic medium. Receptor 5 is a BODIPY based Cr(III) sensors synthesised by D. Wang et al. (Tetrahedron Letters, 2010, 51, 2545). It can detect Cr(III) selectively in acetonitrite with binding stoichiometry of 2:2.
Further Hassan S S, et al. in Analytical Sciences (Impact Factor: 1.57). 07/2005; 21(6):673-8 discloses use of a rhodamine-B chromate ion-associate complex as an electroactive material in a poly(vinyl chloride) membrane plasticized with o-nitrophenytoctyl ether as a solvent mediator. It is to be noted that the oxidation state for Chromium in chromate is (VI). They reported a Potentiometric Rhodamine B based Membrane Sensor for selective determination of Chromium ions [Cr(VI) & Cr(III)] in waste water. Firstly it can't detect Cr(III) directly. To detect Cr(III) they have adopted an indirect methodology in which Cr(III) was first oxidised to Cr(VI) by adding H2O2, that can be sensed by the reported sensor. Another important thing, this types of sensors cannot be applied for bio imaging application to monitor intra cellular Cr(III) activity.
In the present invention L1 it can selectively detect only Cr(III) in pure aqueous medium. It does not have any interferences of Cr(VI) at all. It is a fluoromertic as well as colorimetric sensor for Cr(III) detection. It can be used for monitoring intra cellular imaging of Cr(III). Fluorescence detection methods are more sensitive and simpler compare to other analytical methods.
Highly sensitive and selective fluorescence chemosensor for Cr3+ based on rhodamine B and a 4,13-diaza-18-crown 6-ether conjugate” is disclosed by Duliang Liu, in RSC Adv., 26 Nov. 2013,4, 2563-2567, where detection of Cr3+ was possible only in predominantly non aqueous environment (3:2, MeOH—H2O (v/v).
There are only three previous reports that describe the use of reagents for the detection of Cr(III) in pure aqueous solution; (Mao, J et al. Org. Lett., 2007, 9, 4567-4570 and Mao, J et al. Anal. Bioanal. Chem., 2010, 396, 1197) one of them describes the interference by Fe3+. The most recent report reveals that a rhodamine derivative within a polymeric matrix could be utilized for specific detection of Cr (III) in pure aqueous medium and the hydrophobic micro-environment generated around the binding core of the receptor induces a favourable influence for the detection of Cr(III) (Macromol. Rapid Commun. 2014, 35, 323) However, the possibility of using these three molecular probes as an imaging reagent for studying the cellular uptake of Cr(III) is not explored and discussed.
While the receptors disclosed herein have the capability to detect Cr (III) in pure aqueous medium and in physiological condition. All other above examples suffer from a major drawback that they have this capability of detecting Cr (III) only in mixed aqueous organic solvents medium.
Detection of Cr (III) in pure aqueous solution is a very basic and vital need in the art, so that Cr(III) may be monitored for its presence and activity in cellular structure. There is also a need to detect Cr (III) in physiological fluids.
Main objective of the present invention is to provide a novel ligand that could selectively detects Cr (III) in aqueous medium as well as in physiological pH (7.2).
Another objective of the invention is to develop a methodology for solubilizing the reagent in pure aqueous medium in presence of non-ionic surfactant like Titron X 100.
Accordingly, the present invention provides novel ligands of Formula I (Lx) for detection of Chromium in pure aqueous medium
wherein R1 and R2 are same or different and individually selected from the group consisting of H, linear or branched (C1-C6) alkyl, aryl or dansyl; R3 is same selected from group H, methyl; R4 is selected from H, (C1-C6) alkyl;
where, R1 may form saturated or unsaturated carbocyclic (C4-C6) ring with R3 and similarly R2 may form saturated or unsaturated carbocyclic (C4-C6) ring with R4; and ( . . . ) line is optionally represents single bond.
In one embodiment of the present invention the ligand of formula-I, encompasses the compounds selected from the group consisting of;
In an embodiment of the present invention a process of preparation of ligands of Formula I(Lx), wherein the said process comprising the steps of:
wherein R1 and R2 are same or different and individually selected from the group consisting of H, linear or branched (C1-C6) alkyl, aryl or dansyl; R3 is same selected from group H, methyl;
wherein, R1 may form saturated or unsaturated carbocyclic (C4-C6) ring with R3.
In another embodiment of the present invention the organic solvent is polar organic solvent selected from the group consisting of methanol, isopropanoL, n-propanol, ethanol, water, butanol and mixtures thereof.
Still In another embodiment of the present invention the alliphatic bromide (A-Br) is alkene bromide selected from the group consisting of allyl bromide, 3-bromoprop-1-ene or alkyl bromide selected from the group consisting of propyl bromide, 1-bromopropane.
Still In another embodiment of the present invention a process for selective detection of Cr (111) using ligands of Formula-I, in aqueous medium as well as in physiological Liquid of pH (7.2) comprising steps of:
Still In another embodiment of the present invention the water miscible solvent is selected from acetonitrile, Methanol, DMSO, Ethanol, THF, DMF and mixtures thereof.
Still In another embodiment of the present invention a kit for selective detection of Cr (III) using novel ligands of Formula-I, comprising
a) Ligand L1 stock solution (6.9×10−4 M) in acetonitrile;
b) 0.32 mM Triton X 100 in Tris buffer solution at pH 7.2;
c) Aqueous Cr(III) solution (3.28×10−3M);
d) Final ligand solution (1.59×10−5 M) in 0.32 mM Triton X 100 in Tris buffer having solution pH of 7.2.
The invention will now be described in detail in connection with certain preferred and optional embodiments, so that various aspects thereof may be more fully understood and appreciated.
For the purpose of this invention, the expression ‘Novel Ligand (Lx)’ or ‘novel reagent’ or ‘receptor’ ‘colorimetric’ as well as ‘fluorescent chemosensor’ are used interchangeably throughout the specification and the same may be appreciated as such by the person skilled in the art.
The present invention discloses a novel ligand for selective detection of Cr (III) in aqueous medium.
The novel ligand (Lx) of Formula I is as disclosed herein:
wherein R1 and R2 are same or different and individually selected from the group consisting of H, linear or branched (C1-C6) alkyl, aryl or dansyl; R3 is same selected from group H, methyl; R4 is selected from H, (C1-C6) alkyl;
where, R1 may form saturated or unsaturated carbocyclic (C4-C6) ring with R3 and similarly R2 may form saturated or unsaturated carbocyclic (C4-C6) ring with R4; and ( . . . ) line is optionally represents single bond.
In another preferred embodiment, the invention provides the library of compounds of Formula-I.
The novel ligand (Lx) of Formula-I encompasses the compounds selected from the group consisting of;
The invention provides a process of preparation of novel ligands of Formula I (Lx) comprising steps of:
According to the process, the organic solvent is polar organic solvent selected from the group consisting of methanol, isopropanot, n-propanol, ethanol, water, butanol and mixtures thereof.
The atlliphatic bromide (A-Br) is preferably alkene or alkyl bromide such as, allyl bromide, propyl bromide, 1-bromopropane, 3-bromoprop-1-ene.
The said process is time saving due to fewer steps and industrially feasible. The invention provides a process of preparation of novel ligands (L1) and (L2) comprising steps of:
According to the process, the Intermediate compound L was synthesized following a literature procedure, (A. Org. Lett. 2008, 10, 3013-3016). Methodologies that were adopted for synthesis of the receptor L1 and the model compound L2 are presented in the scheme 2. Desired compound L1 and L2 were isolated in pure form after necessary workup and were thoroughly characterized by various analytical/spectroscopic techniques.
The invention discloses a process for solubilisation of ligand L1 in an aqueous medium employing non ionic surfactant, preferably Polyethylene glycol tert-octylphenyl ether (Triton X 100).
With reference to
In another preferred embodiment, the alkali, alkaline earth metals and transition metals are selected from, but not limited to Li, Na, K, Cs, Mg, Ca, Ba, Sr, Zn, Co, Cu, Ni, Fe, Pb, Hg and such like.
In another embodiment, the invention discloses the process of selective detection of Cr (III) by a process of fluorimetry comprising:
According to the process the water miscible solvent is selected from acetonitrile, Methanol, DMSO, Ethanol, THF, DMF and mixtures thereof.
According to the process a stock solution of the receptor/ligand L1 was prepared in acetonitrile medium with concentration ranges from 6.0 to 8.0×10−4 M, preferably (6.9×10−4 M); and the final concentration of metal salts is in the range of 1.0 to 2.0×10−4 M, preferably 1.62×10−4 M.
The UV-vis spectrum for the ligand L1 may be carried out from for the range 250-800 nm and a λmax of 562 nm is observed. The luminescence studies were carried out using an excitation wavelength of 530 nm and emission spectrum was monitored from 540 to 800 nm, with slit width of 2/2 nm; while a spectrum with λmax of 583 nm is observed.
The invention provides a kit for selective detection of Cr (III) is disclosed. a kit for selective detection of Cr (III) comprises:
a) Ligand L1 stock solution in acetonitrile.
b) 0.32 mM Triton X 100 in Tris buffer solution at pH 7.2.
c) Aqueous Cr (III) solution (3.28×10−3M).
d) Final ligand solution (1.59×105 M) in (0.4) mM Triton X 100 in Tris buffer having solution pH of 7.2.
It describes the method of detection of Cr(III) in an aqueous medium
Further the invention provides a method of separation Cr (III) selectively from a sample comprising other metals, or other ingredients employing the ligand of Formula I described herein. It is possible to extract Cr (III) from aqueous solution when the concentration of Cr (III) either equal to or higher than 8.0×10−4M. For extraction studies, dichloromethane (CH2Cl2) was used as the water immiscible organic solvent for extraction of Cr (III) from aqueous layer in the form of L1.Cr3+.
Rhodamine B, Ethylenediamine, 3-bromoprop-1-ene, 1-bromopropane, all metal perchlorate salts (e.g LiClO4, NaClO4, KClO4, CsClO4, Mg(ClO4)2, Ca(ClO4)2, Ba(ClO4)2, Sr(ClO4)2, Cu(ClO4)2, Zn(ClO4)2, Co(ClO4)2, Ni(ClO4)2, Cr(ClO4)3, Fe(ClO4)2, Cd(ClO4)2, Hg(ClO4)2, and Pb(ClO4)2) and lanthanide ions as nitrate salts were obtained from Sigma-Aldrich and were used as received. Et3N, Triton X-100, Tris Buffer, NaCl was procured from S.D. fine chemicals, India and was used as received. Solvents such as acetonitrile, chloroform were also purchased from S.D. Fine Chemicals, India and were used without further purification unless mentioned otherwise. Silica gel 100-200 mesh was used for column chromatography. Analytical thin layer chromatography was performed using silica Gel GF 254. HPLC grade water (Merck, India) was used for experiments and all spectral studies. Aminoethylene rhodamine B (L) was synthesized following a standard procedure (Org. Lett. 2008, 10, 3013-3016)
5.0 mM Tris-HCl aq. buffer solution was used for maintaining solution pH, unless mentioned otherwise. ESI-MS measurements were performed using a Micromass QTof-Micro instrument. FT-IR spectra were recorded as KBr pellets using a Perkin Elmer Spectra GX 2000 spectrometer. 1H and 13C NMR spectra were recorded on Bruker 500 MHz FT NMR (model: Avance-DPX 500). Electronic spectra were recorded with a Varian Cary 500 Scan UV-Vis-NIR Spectrophotometer, Isothermal Titration Calorimetry studies were performed in Microcal iTC200, while emission spectra were recorded using either Edinburgh Instrument Xe-900 Spectrofluorometer or PTI. For all spectroscopic studies in aqueous buffer medium as well as for studies with plant/algal cells, L1 self-assembled inside the miceller structure of TX100 was used, unless mentioned otherwise.
To check the selectivity of Receptor L1 towards various metal ions like Li+, Na+, K+, Cs+, Mg2+, Ca2+, Ba2+, Sr2+, Zn2+, Co3+, Cu2+, Ni2+, Fe2+, Pb2+, Hg2+ change in electronic as well as emission spectra were examined in 0.32 mM Triton X 100 in tris (5 mM, 25 mM NaCl) buffer medium at PH 7.2.
Absorption and emission spectra of receptor L1 in 0.32 mM Triton X 100 in Tris buffer (5 mM, 25 mM NaCl) pH 7.2 medium shows no absorption band at 562 nm and very weak emission band at 583 nm on excitation at 562 nm. This solution of L1 appears colourless and all these clearly suggest that L1 in this solution is present exclusively in spirolactam form. This is also confirmed from the 13C NMR studies, which shows a characteristic signal at 64.85 ppm for the tertiary C-atom. However only in presence of Cr3+, a strong absorption band at 562 nm and intense emission band at 583 nm (for λext=530 nm) are observed. These changes are also associated with simultaneous visually detectable change in solution colour from colourless to pink red. For other metal ions, no such changes are observed.
For calculating the binding affinity of ligand L1 (1.59×10−5 M) towards Cr3+ in aqueous solution, systematic absorption and emission spectral titration is performed in 0.32 mM Triton X 100 in tris buffer (5 mM, 25 mM NaCl) medium at PH 7.2. The association constant (Kabs) of 2.4×103 M−1 for the L-1.Cr3+ formation is evaluated from the absorption titration and B—H plot data (
To understand the role of Triton X 100 surfactant in the sensing of Cr3+, the emission intensity of receptor L1 (1.59×10−5 M) in presence of aqueous Cr3+ (5 mole eqv.) solution was plotted against different concentration of Triton X 100. The figure shows that sensing efficiency of the reagent described above is maximum when [Triton X]=0.4 mM. This is also a good agreement with the data obtained from photo physical study shown in table below. Thus the surfactant concentration is adjusted to achieve maximum sensing efficiency of receptor L1.
UV-Vis and Fluorescence studies:
A solution of the perchlorate salts of the respective ion (Li+, Na+, K+, Cs+, Ca2+, Mg2+, Ba2+, Sr2+, Fe2+, Ni2+, Co2+, Cu2+, Mn2+, Cd2+, Pb2+, Ba2+, Zn2+, Sr2+, Hg2+ and Cr3+) and nitrate salts of lanthanides ions (Tb3+, Ho3+, Ce3+, Sm3+, Rb+, Pr3+, Eu3+, Gd3+, Nd3+, Dy3+, Tm3+, Er3+, Yb3+) in pure aqueous medium were used for all studies. The effective final concentrations of all metal salts were maintained at 1.62×10−4 M.
A stock solution of the receptor L1 (6.9×10−4 M) was prepared in acetonitrile medium and 57 μL of this stock solution was added to 2.5 ml of 0.4 mM TX100 in Tris-HCL aqueous buffer medium having solution pH 7.2 to make the effective ligand concentration of 1.59×10−5 M. The solution was used for all the photophysical studies. Cr3+ stock solution (4.75×10−3 M) was prepared in pure aqueous medium and was used for all studies. Emission titrations were also performed as a function of [TX100](0.1 mM, 0.23 mM, 0.32 mM, 0.4 mM, 0.6 mM) in Tris-HCl buffer medium of pH 7.2 by monitoring the increase in emission intensity (using λExt=530 nm, λMon=583 nm and slit width 2/2 nm) on binding of L1 to Cr3+ for optimizing the maximum enhancement of the emission intensity. The relative fluorescence quantum yields (t) were estimated using equation 1 for different concentration of TX100 (0.1 mM, 0.23 mM, 0.32 mM, 0.4 mM, 0.6 mM) in Tris-HCl buffer medium (having solution pH of 7.2) and by using the Rhodamine B (φf=0.3 in aqueous medium at RT) as a reference.
φf=φf′(Isample/Istd)(Astd/Asample)(η2sample/η2std) Eq. 1
where, φf′ was the absolute quantum yield for the rhodamine B and was used as reference; Isample and Istd are the integrated emission intensities; Asample and Astd are the absorbances at the excitation wavelength, and ηsample and ηstd are the respective refractive indices.
The geometry of the compounds of Formula-I with chromium ion was examined by using known theories. The optimized geometry shows that the Cr3+ ion is coordinated with two nitrogen atoms, one oxygen atom, two olefinic n-bonds and a water molecule.
According to the invention,
Formation of Cr3+.L1 was also confirmed from the result “Formation of Cr3+.L1 was also confirmed from the result of FAB MS study. Signal at m/z value of 616.87 (Calc 616.75) for Cr3+.L1”. Affinity of L1 towards Cr(III) and the associated binding constant for the formation of Cr3+.L1 in aq. buffer medium (pH=7.2) was evaluated from the data obtained from B—H plots of the systematic absorption (KaAbs=3.2±0.2). 103 M−1) as well as emission (KaEms=(3.3±0.2)·103 M−1) spectral titrations.
To envisage the adverse role of high solvation enthalpy of Cr(III) in aqueous medium, similar Uv-vis and emission titrations were carried out in acetonitrile medium using ([Cr(III)]=(0-1.93×10−4)M; and [L1]=(1.59×10−5 M) in CH3CN) and the evaluated formation constant for Cr3+.L1 in acetonitrile was (KaAbs=(1.1±0.03)·106 M−1, KaEms=(1.0±0.02)·106 M−1 using λExt: 530 nm and λMon: 583 nm for emission titration). The binding affinity of L1 towards Cr3+ was evaluated as KaITC=(1.6±0.02)·106 M−1 in acetonitrile medium at 25° C. using ITC experiments. Comparison of the binding constants evaluated in pure aq. buffer medium and in acetonitrile clearly revealed the energy barrier imposed due to the unfavourable solvation of Cr3+ in aqueous medium and thus adversely affecting the affinity of L1 towards Cr3+. Thermodynamic parameters were obtained from ITC studies (ΔG (−(8.48±0.02) kcal mol−1), ΔH ((−20.8±0.4) kcal mol−1) and ΔS (−41.4±0.05) cal mol−1) (all symbols are used according to standard terminology). The higher −ΔH value revealed that binding was exclusively driven by enthalpy change; while small but negative entropy of binding supported the formation of the adduct Cr3+.L1.
FTIR spectra recorded for L1 and Cr3+.L1, also revealed a distinct shift from 1617 cm−1 to 1587 cm−1 (ΔV=30 cm−1) for C═C stretching frequency. Blue shift in absorption of vinyl group in the FTIR spectrum on coordination to metal ion is reported earlier. This also supports the involvement of olefins in coordination to Cr(III)-centre and possible mode of binding of L1 to Cr(III) is shown in Scheme 1C. No such shifts were observed either in 1H NMR or in FTIR spectra of L1 in presence of certain other metal ions and these metal ions were chosen based on their ability to bind to the model reagent L2.
The following examples are given by way of illustration of the working of the invention in actual practice and therefore should not be construed to limit the scope of the present invention.
Amino ethyl rhodamine B is prepared according to literature (J.-H. Soh, K. M. K. Swamy, S. K. Kim, S. Kim, S.-H. Lee, J. Yoon, Tetrahedron Lett., 2007, 48, 5966).
Rhodamine B (1.0 g, 2.26 mmol) is dissolved in 30 mL of ethanol. It is then heated to 70° C. with constant starring. Then ethylene diamine (3 mL) is added to the reaction medium. It is then allowed to reflux at 75° C. for 12 hour. The solvent is removed under vacuum and is dissolved in diluted HCL. Then to this resulting solution, NaOH solution was added in a drop-wise manner until precipitation is complete. The resulting solution mixture is then filtered, washed with water and is further dried to achieve the desired compound, amino ethyl rhodamine derivative as light red colour solid.
Amino ethyl rhodamine B (400 mg, 0.826 mmol) was dissolved in 20 mL dry chloroform. To this Et3N (3 mL) was added and the resulting solution is kept under N2 atmosphere for 20 minutes. Then Allyl bromide (530 μL, 5.9 mmol) was added into starring solution. It was kept under reflux condition at temp 65° C. with constant stirring for 12 h until all the starting materials are consumed. Then 10 mL of water was added to it. The organic Layer is collected and dried over anhydrous Na2SO4 before concentration. It was finally purified by column chromatography using silica gel as stationary phase and 10% ethyl acetate in hexane as eluent or mobile phase to isolate L1 in pure form with 50% yield. 1H NMR (500 MHz, CDCl3, SiMe4, J (Hz), δ ppm): 7.80 (d, J=4.6), 7.35-7.30 (m), 6.99 (d, J=4.4), 6.35 6.27 (m), 6.16 (d, J=8.8), 5.56 (td, J=16.5, 6.5), 4.96-4.88 (m), 3.24 (dd, J=13.7, 6.8), 3.18-3.09 (m), 2.85 (d, J=6.2), 2.21-2.13 (m), 1.07 (t, J=6.8). 13C NMR (500 MHz, CDCl3, SiMe4, δ ppm): 167.70, 153.38, 148.70, 135.13, 132.22, 131.54, 128.98, 127.97, 123.78, 122.63, 117.53, 108.03, 105.58, 97.73, 64.85, 56.60, 50.46, 44.37, 37.75, 29.69, 12.60. ESI-MS (+ve mode, m/z): 565.93 (M+H+), Calc. for C36H44N4O2 is 564.76.
Amino ethyl rhodamine B (200 mg, 0.41 mmol) was dissolved in 15 mL dry chloroform. To this Et3N (500 μL) was added and the resulting solution was stirred for 20 minutes under N2 atmosphere. Then 1-bromopropane (120 μL, 1.35 mmol) was added and the resulting reaction mixture was refluxed at temp for 24 h until all the starting materials were consumed (Checked by TLC at different time interval). After this reaction mixture was allowed to attain the room temperature, 10 mL of water was added. The organic layer, after drying over anhydrous Na2SO4, was collected and followed by the removal of chloroform under vacuum to yield the crude product. Column chromatography was performed using silica gel as stationary phase and 10% ethyl acetate in hexane as mobile phase for isolating L2 in pure form with 40% yield. 1H NMR (500 MHz, CDCl3, SiMe4, J (Hz), δ ppm): δ 7.81 (dd, 1H, J=5.9, 2.6, H18), 7.37 (dd, 2H, J=5.6, 3.0, H16, H17), 7.05-7.00 (m, 1H, H15), 6.35 (s, 1H, H12), 6.33 (s, 1H, H2), 6.31 (d, 2H, J=2.5, H5, H9), 6.19 (dd, 2H, J=8.9, 2.6, H4, H10), 3.26 (q, 8H, J=7.0, H29, H31, H33, H35), 3.09 (d, 2H, J=5.8, H21), 2.15 (s, 6H, H22, H23, H26), 1.18 (d, 4H, J=6.7, H24, H27), 1.09 (t, 12H, J=7.0, H30, H32, H36, H34), 0.68 (t, 6H, J=6.8, H25, H28). 13C NMR (125 MHz, CDCl3, SiMe4, δ ppm): 167.75, 153.77, 148.72, 148.25, 132.25, 129.18, 127.78, 123.93, 122.59, 108.48, 105.63, 97.94, 64.95, 56.78, 50.96, 44.34, 37.79, 37.47, 20.27, 12.54, 11.82. IR (KBr): vmax/cm−1=1680. ESI-MS (+ve mode, m/z): 569.29 (M+H+), Calc. for C36H44N4O2 is 568.79. Elemental Analysis: Calculated (C76.02, H8.51, N9.85); Experimentally obtained (C76.20, H8.50, N9.88).
Method of Preparation of Ligand (L1) and Solubilization of L1 in Water Using Triton X 100:
Final Ligand (L1) Concentration=1.59×10−5 M
Concentration of Cr3+ in Aqueous Solution=10−4 M
1. Make 10 mL of 7.092×104 M stock solution of ligand L1 in pure HPLC grade acetonitrile (Dissolve 4 mg of ligand L1 in 10 mL HPLC grade acetonitrile).
2. Make a solution of 0.32 mM Triton X 100 in Tris-HCl Buffer (5 mM, 25 mM NaCl, pH 7.2) i.e medium. It is better to make 50 mL Tris-HCL Buffer solution (5 mM tris Buffer, 25 mM NaCl) and adjust the PH to 7.2. Then add 9.34 μL (10 mg) of Triton X 100 to 50 mL of Tris-HCl Buffer (pH 7.2) solution and stir the solution gently for 10 minutes just to homogenies (avoid vigorous shaking).
3. Take exactly 56 μL of ligand stocks solution and add to 2.5 mL of solvent solution (i.e. 0.32 mM Triton X 100 in Tris-HCL buffer solution of pH 7.2) to make 1.59×10−5 M of ligand (L1) solution for studies.
Molecular weight of the Ligand=564
Molecular weight of the Triton X 100=625
Molecular weight of the Tris buffer=121.14
3.28×10−3 M Cr(III) solution in water is prepared and then it is gradually added to a solution of the ligand L1, where effective ligand concentration is 1.59×10−5 M in a Tris buffer with solution pH of 7.2 having 0.32 mM Triton X 100. Uv-vis and luminescence spectra are recorded in absence and presence of [Cr(III)]. In emission spectra a 200 fold increase in spectral intensity at 583 nm (λext=530 nm and slit 2/2) is observed, while a simultaneous change in solution colour is observed from colourless to pink red (please refer to
To cheeked the applicability of the methods in real sample analysis, probe L1 was applied to detect Cr3+ in tap water. No Cr3+ was obtained in tap water samples. Water samples were collected and pH was adjusted to 7.2 using Tris buffer(10 mM, 25 mM NaCl), spiked with known (10 μM and 20 μM) concentration of Cr3+ and emission spectra was recorded. The result was summarised in Table 1.
1. With this ligand (L1), Cr(III) can be detected from pure aqueous solutions at physiological pH.
2. The ligand can also be used as a colorimetric as well as fluorescent chemosensor for the detection of Cr(III) in aqueous solutions.
3. The use of Triton X 100 to create micro-micellar environment that makes the ligand soluble in water or tri buffer medium having pH 7.2 cell membrane permeable in addition to maximizing the sensing efficiency.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2991/DEL/2013 | Oct 2013 | IN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IN2014/000646 | 10/8/2014 | WO | 00 |
