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Synthetic, spectral and structural study of mono bis(pyridine)dichloro bis(dimethyl sulfoxide-S) ruthenium(II) complex, [RuCl2(py)2(dmso-S)2] and its reactivity with nitrogen donor bases in polar and non-polar solvent

✍ Scribed by Manoj Trivedi; Yogesh K. Sharma; R. Nagarajan; Nigam P. Rath


Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
853 KB
Volume
975
Category
Article
ISSN
0022-2860

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✦ Synopsis


Reaction of the cis-[RuCl 2 (dmso) 4 ] with pyridine (py) at room temperature in MeOH/H 2 O afforded a neutral mononuclear complex cis,cis,cis-[RuCl 2 (py) 2 (dmso-S) 2 ] 1. The complex 1 reacted with nitrogen donor bases such as pyridine (py), pyrazine (pyz), 4,4 0 -bipyridine (bp) and 1,4-bis(4-pyridyl)ethane (bpeta) in different solvents to give substitution products. The nature of the substitution product was governed by the polarity of the solvents employed in the reaction. Resulting complexes have been characterized by elemental analyses, IR, NMR ( 1 H and 1 H-1 H COSY), ESI-MS, FAB-MS and electronic spectral studies. Molecular structures of the complexes 1 and 5 have been determined crystallographically. Complex 1 exhibits the strong intra-and inter-molecular CAHÁ Á ÁX (X = Cl, p) and face-to-face p-p stacking interactions but only intra-and inter-molecular CAHÁ Á ÁCl and p-p stacking interactions are present in 5 which play important roles to stabilize crystal packing. Furthermore, the CAHÁ Á ÁO interactions in 1 and CAHÁ Á ÁCl interactions in 5 lead to a single and double-helical motif.