SYNTHESES AND CHARACTERIZATION OF DIAMINE COMPLEXES OF NICKEL(II) TRIFLUOROACETATE - THERMOCHROMISM AND X-RAY SINGLE-CRYSTAL STRUCTURE ANALYSES OF [NI(PREN)(2)(CF3CO2)(2)] AND [NI(IPREN)(2)(CF3CO2)(2)] (PREN =N-PROPYLETHANE-1,2-DIAMINE AND IPREN= N-ISOPROPYLETHANE-1,2-DIAMINE)
D. Das et al., SYNTHESES AND CHARACTERIZATION OF DIAMINE COMPLEXES OF NICKEL(II) TRIFLUOROACETATE - THERMOCHROMISM AND X-RAY SINGLE-CRYSTAL STRUCTURE ANALYSES OF [NI(PREN)(2)(CF3CO2)(2)] AND [NI(IPREN)(2)(CF3CO2)(2)] (PREN =N-PROPYLETHANE-1,2-DIAMINE AND IPREN= N-ISOPROPYLETHANE-1,2-DIAMINE), Polyhedron, 17(15), 1998, pp. 2567-2574
The complexes, [NiL2(CF3CO2)(2)] [L = N-methylethane-1,2-diamine (meen
), N-ethylethane-1,2-diamine (eten), N-propylethane-1,2-diamine (pren)
and N-isopropylethane-1,2-diamine (ipren)] have been prepared and X-r
ay single crystal structures of [Ni(pren)(2)(CF3CO2)(2)] 3 and [Ni(pre
n)(2)(CF3CO2)(2)] 4 are determined. Both 3 and 4 have slightly distort
ed trans-octahedral geometry with N4O2-chromophore around nickel(II).
The crystals are stabilized by H-bonds and this interaction is higher
in 4 due to close proximity of methyl H-atoms of isopropyl group with
oxygen atoms of trifluoroacetate groups. The complexes 3 and 4 exhibit
blue to light-violet. irreversible discontinuous thermochromism. [Ni(
meen)(2)(CF3CO2)(2)] 1 also shows thermochromism, blue-violet to blue
bur reverts on keeping in humid atmosphere. On the other hand, [Ni(ete
n)(2)(CF3CO2)(2)] 2 undergoes decomposition without showing any phase
transition. However, thermochromism here is considered to be due to a
decreased in-plane ligand field strength resulting from the conformati
onal changes in diamine chelate rings. (C) 1998 Elsevier Science Ltd.
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