Molecular structure and magnetic properties of [Gd(LH4)(NO3)2(H2O)]NO3(H2O)2, [Sm(LH4)(NO3)2(H2O)]NO3 (H2O)1.5(CH3OH)0.5 and [Cu2(LH2)(H2O)2](NO3)2 complexes (LH4: Schiff base ligand derived from 4-methyl-2,6-diformylphenol and 1,3-diaminopropanol)

AbstractSynthesis and structural characterization of two heterodinuclear ZnII-LnIII complexes with the formula [ZnLn(HL)(µ-OAc)(NO3)2(H2O)x(MeOH)1-x]NO3 · n H2O · n MeOH [Ln = Pr (1), Nd (2)] and the crystal and molecular structure of [ZnNd(HL)(µ-OAc)(NO3)2(H2O)] [ZnNd(HL)(OAc)(NO3)2(H2O)](NO3)2 · n H2O · n MeOH (3) are reported. The asymmetrical compartmental ligand (E)-2-(1-(2-((2-hydroxy-3-methoxybenzylidene)amino)-ethyl)imidazolidin-2-yl)-6-methoxyphenol (H2L) is formed from N1,N3-bis(3-methoxysalicylidene)diethylenetriamine (H2valdien) through intramolecular aminal formation, resulting in a peripheral imidazoline ring. The structures of 1–3 were revealed by X-ray crystallography. The smaller ZnII ion occupies the inner N2O2 compartment of the ligand, whereas the larger and more oxophilic LnIII ions are found in the outer O2O2’ site. Graphic Abstract Synthesis and structural characterization of two heterodinuclear ZnII-LnIII complexes (Ln = Pr, Nd) bearing an asymmetrical compartmental ligand formed in situ from N1,N3-bis(3-methoxysalicylidene)diethylenetriamine (H2valdien) through intramolecular aminal formation are reported.

Download Full-text

Interactions of Trivalent Lanthanide Cations with a New Hexadentate Di-Schiff Base: New Lanthanide(III) Complexes from (NE,N′E)-2,2′-(ethane-1,2-diylbis(oxy))bis(N-(pyridin-2-ylmethylene)ethanamine)

Bioinorganic Chemistry and Applications ◽

10.1155/2010/613140 ◽

2010 ◽

Vol 2010 ◽

pp. 1-7 ◽

Cited By ~ 2

Author(s):

Mantha Tsiouri ◽

Konstantina Skorda ◽

Christos Papadimitriou ◽

Yang Li ◽

J. Derek Woollins ◽

...

Keyword(s):

Molecular Structure ◽

Schiff Base ◽

Schiff Base Ligand ◽

Direct Reaction ◽

The Novel ◽

Trivalent Lanthanide ◽

Lanthanide Cations ◽

Oxygen Atoms

The novel lanthanide(III) complexes[Ln(NO3)2L](NO3)⋅3MeOH (Ln = La1, Pr2) and[Ln(NO3)3L](NO3)⋅2MeOH (Ln = Gd3, Yb4), where L = (NE,N′E)-2,2′-(ethane-1,2-diylbis(oxy))bis(N-(pyridin-2-ylmethylene)ethanamine), have been obtained by direct reaction of the Schiff base ligand and the corresponding hydrated lanthanide(III) nitrates in methanol. All complexes were characterized spectroscopically and thermogravimetrically. Complex4was also characterized with crystallographic studies: orthorhombic P212121,a=10.6683(14),b=13.4752(15),c=19.3320(26) Å. In the molecular structure of4, Yb(III) is surrounded by all donor atoms of the Schiff base (four nitrogen and two oxygen atoms) and four oxygen atoms belonging to two bidentate chelating nitrato ligands.

Download Full-text

Anion coordination selective [Mn3] and [Mn4] assemblies: synthesis, structural diversity, magnetic properties and catechol oxidase activity

Dalton Transactions ◽

10.1039/c5dt01157d ◽

2015 ◽

Vol 44 (26) ◽

pp. 11741-11754 ◽

Cited By ~ 18

Author(s):

Moumita Pait ◽

Michael Shatruk ◽

Debashis Ray

Keyword(s):

Magnetic Properties ◽

Magnetic Property ◽

Schiff Base ◽

Schiff Base Ligand ◽

Structural Diversity ◽

Manganese Complexes ◽

Catechol Oxidase ◽

Oxidation Study ◽

Anion Coordination ◽

Catechol Oxidation

The present manuscript reports the detail synthesis, characterization, magnetic property and catechol oxidation study of a family of mixed valent (MnIIMnIII) and trivalent (MnIII) manganese complexes from a Schiff base ligand.

Download Full-text