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    Syntheses of [Ni<sub>2</sub>(dien)<sub>2</sub>(NCS) <sub>2</sub>(H<sub>2</sub>O)] and [Ni(aepn)(NCS) <sub>2</sub>]<sub>n</sub>((dien = bis(2-aminoethyl)amine and aepn = N-(2-aminoethyl)-1,3-propanediamine): single crystal structure analysis and thermal behaviour in the solid state

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    [Ni<sub>2</sub>(dien) <sub>2</sub>(NCS) <sub>4</sub>(H<sub>2</sub>O)] (1) and [Ni(aepn)(NCS) <sub>2</sub>]<sub>n</sub> (2) (where dien = bis(2-aminoethyl)amine and aepn = N-(2-aminoethyl)-1,3-propanediamine) have been synthesised from solution. Single crystal X-ray structure analyses of 1 and 2 reveal that the metal atoms in both the complexes display distorted octahedral geometry with the triamine coordinating facially in 1 and meridionally in 2. The dinuclear [Ni<sub>2</sub>(dien) <sub>2</sub>(NCS) <sub>4</sub>(H<sub>2</sub>O)] unit in 1 is bridged via a thiocyanate moiety while in 2 the nickel (II) octahedra form a polymeric chain. The species 1 on deaquation at &#8764; 165°C followed by cooling yields a conglomerated mass (1a). The species 2 melts at &#8764; 230°C which on cooling yields conglomerated mass (2a). Both 1a and 2a are amorphous; the former reverts to 1 in a humid atmosphere
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