Synthesis of novel squaraine derivatives- Development and validation of analytical applications

Postgraduate Thesis uoadl:1320086 324 Read counter

Unit:
Κατεύθυνση Χημική Ανάλυση-Έλεγχος Ποιότητας
Library of the School of Science
Deposit date:
2015-10-30
Year:
2015
Author:
Σκλαβούνος Αλέξανδρος
Supervisors info:
Α. Κ. Καλοκαιρινός Καθηγητής (Επιβλέπων), Μ. Α. Κουππάρης Καθηγητής, Γ. Χ. Βουγιουκαλάκης Λέκτορας
Original Title:
Σύνθεση νέων σκουαραϊνικών παραγώγων – Ανάπτυξη και επικύρωση αναλυτικών εφαρμογών
Languages:
Greek
Translated title:
Synthesis of novel squaraine derivatives- Development and validation of analytical applications
Summary:
In the present work, novel organic compounds were synthesized especially
designed for analytical applications. Among those compounds synthesized
wasasquaraine dye based on indole, whichshowed remarkable bleaching in the
presence of small, water soluble thiols. Additionally, in presence of mercury
ions, this squaraine, tended to form colored precipitates.
A spectrophotometric method was developed and validated for the determination
of thiols in aqueous solutions. This method was based on the decrease in the
absorbance of the squaraine caused by the thiols, at a wavelength of λ = 538 nm.
According to the optimization experiments, the optimum solvent for the method
was the mixture acetonitrile :water 30 : 70 v/v. The optimalsquaraine
concentration was 7.010–6 Μ in 0.01 M phosphate buffer, pH = 6.8. The method
validated thelinearity of the calibration curves, limit of detection (eg.
L-cysteine LoD = 8.710–7 Μ), selectivity, precision, ruggedness and
uncertainty.
Meanwhile, a paper–based technique was developed, with the squaraineon
cellulose membranes, to detect the presence of Hg2+ions in aqueous solutions.
This method allows forstraightforward “naked-eye” monitoring of the Hg2+ at
concentrations higher than 50 ng mL–1 Hg2+.
Keywords:
Squaraines, Thiols, Mercury, Photometry, Paper based techniques
Index:
Yes
Number of index pages:
IV - XIII
Contains images:
Yes
Number of references:
59
Number of pages:
XIII, 104
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