Synthesis and Characterization of New Photo-responsive, Ortho and Para Oriented Azomethine Polymers

Five new azomethine polymers having aliphatic-aromatic moieties were synthesized by polycondensation reaction of dialdehydes and diamines. The dialdehyde monomers differ only in the orientation of the aromatic ring (ortho or para) and were synthesized by condensation reaction between aromatic aldehy...

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Main Authors: Farah Qureshi, Muhammad Yar Khuhawar, Taj Muhammad Jahangir
Format: Article
Language:English
Published: Slovenian Chemical Society 2018-09-01
Series:Acta Chimica Slovenica
Subjects:
Online Access:https://journals.matheo.si/index.php/ACSi/article/view/4419
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spelling doaj-c29c8a887fec497ab1a98f14796972cd2020-11-24T21:35:08ZengSlovenian Chemical SocietyActa Chimica Slovenica1318-02071580-31552018-09-0165371872910.17344/acsi.2018.4419624Synthesis and Characterization of New Photo-responsive, Ortho and Para Oriented Azomethine PolymersFarah Qureshi0Muhammad Yar Khuhawar1Taj Muhammad Jahangir2Institute of Advanced Research Studies in Chemical Sciences, University of Sindh, Jamshoro.Institute of Advanced Research Studies in Chemical Sciences, University of Sindh, Jamshoro.Institute of Advanced Research Studies in Chemical Sciences, University of Sindh, Jamshoro.Five new azomethine polymers having aliphatic-aromatic moieties were synthesized by polycondensation reaction of dialdehydes and diamines. The dialdehyde monomers differ only in the orientation of the aromatic ring (ortho or para) and were synthesized by condensation reaction between aromatic aldehyde and 1,6-dibromohexane. The molecular mass of the monomers was recorded through E.I mass spectrum. The polymers structures were confirmed by elemental microanalysis, FT-IR, 1HNMR and UV-Vis Spectroscopy. The morphology of monomers and polymers was evaluated by scanning electron microscopy (SEM). All the polymers were soluble in DMSO (on heating) and somewhat in other solvents. Thermal stability of polymers was analyzed by thermogravimetry (TG) and differential thermal analysis (DTA), all the polymers showed good thermal stability higher than their corresponding monomers. The TG of polymers indicated maximum rate of weight loss (Tmax) within 412-708 °C. Fluorescence emission spectra of polymers were recorded and the results indicated that all the polymers were photo-responsive and indicated 1 to 4 emission bands with maximum within 349-606 nm. The limit of detection of polymers was within 0.625-1.25 µg/ml. The polymers were also examined for their antimicrobial activities against bacteria and fungi.https://journals.matheo.si/index.php/ACSi/article/view/4419Polymers synthesisthermal stabilityfluorescenceantimicrobial activitiesmorphology
collection DOAJ
language English
format Article
sources DOAJ
author Farah Qureshi
Muhammad Yar Khuhawar
Taj Muhammad Jahangir
spellingShingle Farah Qureshi
Muhammad Yar Khuhawar
Taj Muhammad Jahangir
Synthesis and Characterization of New Photo-responsive, Ortho and Para Oriented Azomethine Polymers
Acta Chimica Slovenica
Polymers synthesis
thermal stability
fluorescence
antimicrobial activities
morphology
author_facet Farah Qureshi
Muhammad Yar Khuhawar
Taj Muhammad Jahangir
author_sort Farah Qureshi
title Synthesis and Characterization of New Photo-responsive, Ortho and Para Oriented Azomethine Polymers
title_short Synthesis and Characterization of New Photo-responsive, Ortho and Para Oriented Azomethine Polymers
title_full Synthesis and Characterization of New Photo-responsive, Ortho and Para Oriented Azomethine Polymers
title_fullStr Synthesis and Characterization of New Photo-responsive, Ortho and Para Oriented Azomethine Polymers
title_full_unstemmed Synthesis and Characterization of New Photo-responsive, Ortho and Para Oriented Azomethine Polymers
title_sort synthesis and characterization of new photo-responsive, ortho and para oriented azomethine polymers
publisher Slovenian Chemical Society
series Acta Chimica Slovenica
issn 1318-0207
1580-3155
publishDate 2018-09-01
description Five new azomethine polymers having aliphatic-aromatic moieties were synthesized by polycondensation reaction of dialdehydes and diamines. The dialdehyde monomers differ only in the orientation of the aromatic ring (ortho or para) and were synthesized by condensation reaction between aromatic aldehyde and 1,6-dibromohexane. The molecular mass of the monomers was recorded through E.I mass spectrum. The polymers structures were confirmed by elemental microanalysis, FT-IR, 1HNMR and UV-Vis Spectroscopy. The morphology of monomers and polymers was evaluated by scanning electron microscopy (SEM). All the polymers were soluble in DMSO (on heating) and somewhat in other solvents. Thermal stability of polymers was analyzed by thermogravimetry (TG) and differential thermal analysis (DTA), all the polymers showed good thermal stability higher than their corresponding monomers. The TG of polymers indicated maximum rate of weight loss (Tmax) within 412-708 °C. Fluorescence emission spectra of polymers were recorded and the results indicated that all the polymers were photo-responsive and indicated 1 to 4 emission bands with maximum within 349-606 nm. The limit of detection of polymers was within 0.625-1.25 µg/ml. The polymers were also examined for their antimicrobial activities against bacteria and fungi.
topic Polymers synthesis
thermal stability
fluorescence
antimicrobial activities
morphology
url https://journals.matheo.si/index.php/ACSi/article/view/4419
work_keys_str_mv AT farahqureshi synthesisandcharacterizationofnewphotoresponsiveorthoandparaorientedazomethinepolymers
AT muhammadyarkhuhawar synthesisandcharacterizationofnewphotoresponsiveorthoandparaorientedazomethinepolymers
AT tajmuhammadjahangir synthesisandcharacterizationofnewphotoresponsiveorthoandparaorientedazomethinepolymers
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