Repozytorium

Synthesis, characterization, single crystal X-ray structural studies and packing analyses of two novel copper(II) complexes: [Cu(2-Cl-5-FC7H3O2)2(β-picoline)2(H2O)2] and [Cu(en)2(H2O)2](2-Cl-5-FC7H3O2)2.

Autorzy

Raj Pal Sharma

Anju Saini

S. Singh

A. Singh

Paloth Venugopalan

Przemysław Starynowicz

Julia Jezierska

Rok wydania

2011

Czasopismo

Journal of Molecular Structure

Numer woluminu

988

Strony

9-16

DOI

10.1016/j.molstruc.2010.11.052

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

Two novel copper(II) complexes, [Cu(2-Cl-5-FC7H3O2)2(β-pic)2(H2O)2] 1 and [Cu(en)2(H2O)2] (2-Cl-5-F-C7H3O2)2 2 (where β-pic = β-picoline, en = ethylenediamine) were isolated by addition of β-picoline and ethylenediamine respectively to the hydrated copper(II) aryl carboxylate, Cu(2-Cl-5-F-C7H3O2)2 suspended in water–methanol (1:4) mixture. The newly isolated complexes have been characterized by elemental analyses, TGA, spectroscopic techniques (EPR, IR and UV/Vis), conductance, magnetic susceptibility studies and single crystal X-ray structure determination. Single crystal X-ray structure determinations revealed the presence of covalently bonded 2-Chloro-5-fluorobenzoate groups in the complex, viz: [Cu(2-Cl-5-FC7H3O2)2(β-picoline)2(H2O)2] 1 and ionic 2-Chloro-5-fluorobenzoate groups in [Cu(en)2(H2O)2] (2-Cl-5-FC7H3O2)2 in 2. In 1, two β-picoline, two unidentate carboxylate groups and two water molecules are coordinated to copper(II) ion. In 2, two ethylenediamine molecules (4 N) and two oxygen from water molecules are coordinated to copper(II) ion. Hexacoordination around copper(II) is achieved with distorted octahedral geometry in both the cases. The crystal network in complex 1 is stabilized by O–H⋯O, C–H⋯π, Cl⋯F, and Cl⋯H–C and in complex 2 cationic and anionic layers are held together by the N–H⋯O, O–H⋯O, C–H⋯F, C–H⋯O interactions.

Słowa kluczowe

copper(II), Coordination Chemistry, Ethylenediamine, β-Picoline, 2-Chloro-5-fluorobenzoate

Adres publiczny

https://doi.org/10.1016/j.molstruc.2010.11.052

Strona internetowa wydawcy

http://www.elsevier.com

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