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Dinuclear and Trinuclear Complexes of Copper(I) and Silver(I) Supported by a Highly Fluorinated Pyrazolate [3,5‐(CF 3 ) 2 Pz] – and N ‐Heterocycles
Author(s) -
Dias H. V. Rasika,
Diyabalanage Himashinie,
Jayaratleen B.,
Shaw Daniel,
Hettiarachchi Champika V.,
Parasar Devaborniny
Publication year - 2019
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201900719
Subject(s) - chemistry , denticity , lone pair , crystallography , copper , stacking , ligand (biochemistry) , metal , phenanthroline , bipyridine , stereochemistry , molecule , crystal structure , organic chemistry , biochemistry , receptor
The chemistry of trinuclear silver(I) and copper(I) pyrazolates with aromatic, bidentate N ‐heterocycles, 2,2′‐bipyridine, 6,6′‐dimethyl‐2,2′‐bipyridine, 1,10‐phenanthroline, 2,9‐dimethyl‐1,10‐phenanthroline, and 1,8‐naphthyridine are presented. These N ‐donor ligands react readily with {[3,5‐(CF 3 ) 2 Pz]Ag} 3 and {[3,5‐(CF 3 ) 2 Pz]Cu} 3 providing mixed‐ligand complexes with all nitrogen coordination spheres at metal in high yield. The fluorinated pyrazolate acts as a bridging ligand in these complexes. The bipyridine and phenanthroline systems with donor lone pairs at an acute angle serve as bidentate chelators for copper and silver providing dinuclear complexes. They feature planar, boat or chair shaped Ag 2 N 4 or Cu 2 N 4 cores and four‐coordinate, tetrahedral metal sites. The 1,8‐naphthyridine that has donor nitrogen lone pairs at a parallel orientation affords trinuclear copper and silver complexes with two‐ and three‐coordinate metal centers. It uses only one of its lone pairs effectively in these adducts for metal ion coordination. In addition, 1,8‐naphthyridine moieties of these copper and silver complexes show intermolecular π–π stacking. Results presented here show the effects of donor nitrogen lone‐pair orientations of the bidentate N ‐heterocycles on the structures of the products resulting from their chemistry with {[3,5‐(CF 3 ) 2 Pz]Ag} 3 and {[3,5‐(CF 3 ) 2 Pz]Cu} 3 .