Coordination modes of two flexidentate salicylaldimine ligands derived from N-(3-aminopropyl)morpholine toward zinc and copper

Two flexidentate Schiff-base ligands condensed from salicylaldehyde or 5-chlorosalicylaldehyde with N-(3-aminopropyl)morpholine were prepared in situ and reacted with Zn(II) and Cu(II) salts. Upon complexation, the Schiff bases underwent deprotonation at hydroxyl to act as mono-anionic ligands. When...

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Main Authors: Hisham, N.A.I., Hadi, H.A., Ali, Hapipah Mohd, Khaledi, H.
Format: Article
Published: 2012
Subjects:
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author Hisham, N.A.I.
Hadi, H.A.
Ali, Hapipah Mohd
Khaledi, H.
author_facet Hisham, N.A.I.
Hadi, H.A.
Ali, Hapipah Mohd
Khaledi, H.
author_sort Hisham, N.A.I.
collection UM
description Two flexidentate Schiff-base ligands condensed from salicylaldehyde or 5-chlorosalicylaldehyde with N-(3-aminopropyl)morpholine were prepared in situ and reacted with Zn(II) and Cu(II) salts. Upon complexation, the Schiff bases underwent deprotonation at hydroxyl to act as mono-anionic ligands. When a ligand : metal ratio of 2 : 1 was applied, the deprotonated Schiff bases coordinated metal ions through phenolate and imine in a square-planar or tetrahedral geometry. In contrast, 5-chlorosalicylaldimine reacted with the metal ions in a 1 : 1 ratio to form complexes wherein morpholine nitrogen also participates in an N,N,O-tridentate coordination mode. The structures of the complexes were characterized by spectroscopic methods and single-crystal X-ray diffraction.
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spelling um.eprints-51412019-01-30T01:28:18Z http://eprints.um.edu.my/5141/ Coordination modes of two flexidentate salicylaldimine ligands derived from N-(3-aminopropyl)morpholine toward zinc and copper Hisham, N.A.I. Hadi, H.A. Ali, Hapipah Mohd Khaledi, H. QD Chemistry Two flexidentate Schiff-base ligands condensed from salicylaldehyde or 5-chlorosalicylaldehyde with N-(3-aminopropyl)morpholine were prepared in situ and reacted with Zn(II) and Cu(II) salts. Upon complexation, the Schiff bases underwent deprotonation at hydroxyl to act as mono-anionic ligands. When a ligand : metal ratio of 2 : 1 was applied, the deprotonated Schiff bases coordinated metal ions through phenolate and imine in a square-planar or tetrahedral geometry. In contrast, 5-chlorosalicylaldimine reacted with the metal ions in a 1 : 1 ratio to form complexes wherein morpholine nitrogen also participates in an N,N,O-tridentate coordination mode. The structures of the complexes were characterized by spectroscopic methods and single-crystal X-ray diffraction. 2012 Article PeerReviewed Hisham, N.A.I. and Hadi, H.A. and Ali, Hapipah Mohd and Khaledi, H. (2012) Coordination modes of two flexidentate salicylaldimine ligands derived from N-(3-aminopropyl)morpholine toward zinc and copper. Journal of Coordination Chemistry, 65 (17). pp. 2992-3006. ISSN 0095-8972, DOI https://doi.org/10.1080/00958972.2012.708412 <https://doi.org/10.1080/00958972.2012.708412>. http://www.tandfonline.com/doi/pdf/10.1080/00958972.2012.708412 10.1080/00958972.2012.708412
spellingShingle QD Chemistry
Hisham, N.A.I.
Hadi, H.A.
Ali, Hapipah Mohd
Khaledi, H.
Coordination modes of two flexidentate salicylaldimine ligands derived from N-(3-aminopropyl)morpholine toward zinc and copper
title Coordination modes of two flexidentate salicylaldimine ligands derived from N-(3-aminopropyl)morpholine toward zinc and copper
title_full Coordination modes of two flexidentate salicylaldimine ligands derived from N-(3-aminopropyl)morpholine toward zinc and copper
title_fullStr Coordination modes of two flexidentate salicylaldimine ligands derived from N-(3-aminopropyl)morpholine toward zinc and copper
title_full_unstemmed Coordination modes of two flexidentate salicylaldimine ligands derived from N-(3-aminopropyl)morpholine toward zinc and copper
title_short Coordination modes of two flexidentate salicylaldimine ligands derived from N-(3-aminopropyl)morpholine toward zinc and copper
title_sort coordination modes of two flexidentate salicylaldimine ligands derived from n 3 aminopropyl morpholine toward zinc and copper
topic QD Chemistry
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