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Syntheses, Spectroscopic, Structural, Fluorescent and Thermal Properties of Bis(saccharinato)copper(II) Complexes with two Bis(pyridylamine) Ligands
Author(s) -
Guney Emel,
Yilmaz Veysel T.,
Sengul Abdurrahman,
Büyükgüngör Orhan
Publication year - 2011
Publication title -
zeitschrift für anorganische und allgemeine chemie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.354
H-Index - 66
eISSN - 1521-3749
pISSN - 0044-2313
DOI - 10.1002/zaac.201000347
Subject(s) - chemistry , copper , crystallography , ligand (biochemistry) , hydrogen bond , intermolecular force , octahedron , molecule , square pyramidal molecular geometry , amine gas treating , ion , inorganic chemistry , crystal structure , organic chemistry , biochemistry , receptor
Two new copper(II) complexes of saccharinate (sac) with bis(2‐pyridylmethyl)amine (bpma) and N , N ′‐bis[1‐(pyridin‐2‐yl)ethylidene]ethane‐1,2‐diamine (bapen), [Cu(bpma)(sac) 2 ] · H 2 O ( 1 ) and [Cu(bapen)(sac) 2 ] ( 2 ), were synthesized and characterized by elemental analysis, TG‐DTA, X‐ray diffraction, and UV/Vis and IR spectroscopy, respectively. In 1 , the copper(II) ion is coordinated by two N‐bonded sac ligands, and three nitrogen atoms of bpma, in a distorted square‐pyramidal coordination arrangement, whereas the arrangement around the copper ion in 2 is a distorted octahedron with two N‐coordinated sac ligands and a tetradentate bapen ligand. In addition to hydrogen bonding involving the water molecule in 1 , the mononuclear species of 1 and 2 are further connected by weak intermolecular C–H ··· π and C–H ··· O interactions to form a three‐dimensional network. Both complexes are luminescent at room temperature and their emissions seem to be due to ligand‐based π–π* transitions.