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Synthesis, X-ray cr...
Synthesis, X-ray crystal structure, and electrochemistry of copper(II) complexes of a new tridentate unsymmetrical Schiff base ligand and its hydrolytically rearranged isomer
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- Meghdadi, S. (författare)
- Isfahan University of Technology
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- Mereiter, K. (författare)
- Technische Universität Wien,Vienna University of Technology
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- Langer, Vratislav, 1949 (författare)
- Chalmers tekniska högskola,Chalmers University of Technology
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- Amiri, Ahmad (författare)
- Isfahan University of Technology
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- Erami, R. S. (författare)
- Isfahan University of Technology
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- Massoud, Al-Shimaà A A, 1980 (författare)
- Chalmers tekniska högskola,Chalmers University of Technology
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- Amirnasr, Mehdi (författare)
- Isfahan University of Technology
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(creator_code:org_t)
- Elsevier BV, 2012
- 2012
- Engelska.
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Ingår i: Inorganica Chimica Acta. - : Elsevier BV. - 0020-1693. ; 385, s. 31-38
- Relaterad länk:
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http://dx.doi.org/10...
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https://doi.org/10.1...
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https://research.cha...
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Abstract
Ämnesord
Stäng
- A new unsymmetrical Schiff base ligand HL1, HBacabza, and its copper(II) complexes [Cu2L21(OAc)(2)] (1) and [Cu2L22(N-3)(2)]center dot 2H(2)O (2) with HBacabza = 3-(2- aminobenzylimino)-1-phenylbutan-1-one as HL1 and its hydrolytically rearranged isomer 3-(2-aminomethylphenyleneimino)-1-phenylbutan-1-one as HL2, have been synthesized and characterized by elemental analyses and spectroscopic methods. The rearrangement of HL1 to HL2 occurs in a hydrolysis-recondensation process in the reaction of HL1 with Cu(ClO4)(2)center dot 6H(2)O and NaN3. The crystal structures of the ligand and its complexes have been determined by single crystal X-ray diffraction. The deprotonated Bacabza coordinates to the metal center as a tridentate ligand. The acetate anion coordinates through one oxygen atom in complex 1 leading to a mono-atomic acetate oxygen-bridging dimeric copper(II) complex. Similarly, the azide anion coordinates through one nitrogen atom in complex 2 leading to a mono-atomic azide nitrogen-bridging dimeric copper(II) complex. The copper(II) ions adopt a distorted square pyramidal (4 + 1) coordination in these two complexes. The cyclic voltammetric studies of these complexes in N, N-dimethylformamide indicate that the reduction process corresponding to Cu-II/Cu-I is electrochemically irreversible in complex 1, presumably due to the structural changes during the course of redox reaction, and quasi-reversible in complex 2.
Ämnesord
- NATURVETENSKAP -- Kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences (hsv//eng)
Nyckelord
- hydrolysis
- 2-aminobenzylamine
- copper(II)
- complexes
- coordination polymer
- cu(II)
- magnetic-properties
- dinuclear copper(ii)
- cyclic voltammetry
- Unsymmetrical Schiff base
- catalyzed hydrolysis
- cobalt(iii) complexes
- nickel(ii) complexes
- azide
- 1st evidence
- crystal structure
- cu(ii) complexes
Publikations- och innehållstyp
- art (ämneskategori)
- ref (ämneskategori)
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