A rhodamine based chemodosimeter for the detection of Group 13 metal ions.
Sneha GhoshPartha RoyPublished in: Analytical methods : advancing methods and applications (2022)
A new rhodamine derivative, HL-CIN, derived from a reaction between N -(rhodamine-6G)lactam-ethylenediamine (L1) and trans -cinnamaldehyde, is reported here for the colorimetric and fluorogenic sensing of Group 13 trivalent cations, namely Al 3+ , Ga 3+ , In 3+ and Tl 3+ . The absorption intensity of the probe increases significantly at 530 nm whereas the fluorescence intensity enhances massively at 558 nm upon interaction with these metal ions. Other relevant metal ions could not impart any noticeable color change or fluorescence enhancement. The quantum yield or fluorescence life time of HL-CIN increases considerably in the presence of these Group 13 metal ions. Different spectral studies such as ESI-mass, FT-IR, 1 H and 13 C NMR spectra, establish that HL-CIN undergoes hydrolysis in the presence of the trivalent cations and a rhodamine species in its ring opened form ( i.e. N -(2-aminoethyl)-2-((6 Z )-3-(ethylamino)-6-(ethylimino)-2,7-dimethyl-6 H -xanthen-9-yl)benzamide, (L2)) along with cinnamaldehyde are produced. The rhodamine species in its ring opened form (L2) is responsible for the color change and strong increment in the absorbance and fluorescence of HL-CIN with Group 13 cations. Interaction between L1 and these metal ions could not produce the same outcome. It has been used in test paper strips and to detect these cations in real samples.
Keyphrases
- fluorescent probe
- quantum dots
- energy transfer
- living cells
- aqueous solution
- ionic liquid
- single molecule
- water soluble
- photodynamic therapy
- sensitive detection
- high intensity
- high resolution
- magnetic resonance
- nitric oxide
- mass spectrometry
- molecular dynamics
- multidrug resistant
- computed tomography
- density functional theory
- dual energy
- light emitting