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Tetraethylammonium dicyanido(5,10,15,20-tetraphenylporphyrinato)ferrate(III) dichloromethane monosolvate
The title compound, (C(8)H(20)N)[Fe(C(44)H(28)N(4))(CN)(2)]·CH(2)Cl(2) or (Et(4)N)[Fe(TPP)(CN)(2)], was recrystallized from dichloromethane–diethyl ether. The compound crystallizes with the two unique halves of the Fe(III) porphyrinato complex, one tetraethylammonium cation and one interstitial...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793695/ https://www.ncbi.nlm.nih.gov/pubmed/24109282 http://dx.doi.org/10.1107/S1600536813019119 |
Sumario: | The title compound, (C(8)H(20)N)[Fe(C(44)H(28)N(4))(CN)(2)]·CH(2)Cl(2) or (Et(4)N)[Fe(TPP)(CN)(2)], was recrystallized from dichloromethane–diethyl ether. The compound crystallizes with the two unique halves of the Fe(III) porphyrinato complex, one tetraethylammonium cation and one interstitial dichloromethane molecule within the asymmetric unit. Both anionic Fe(III) complexes exhibit inversion symmetry. Both the cation and the solvent molecules show positional disorder. The cation is disordered over two sets of sites with an occupancy ratio of 0.710 (3):0.290 (3); the solvent molecule is disordered over three positions with a 0.584 (6):0.208 (3):0.202 (5) ratio. The crystal packing features columns of [Fe(TPP)(CN)(2)](−) anions that propagate along [001]. The columns further pack into layers that are parallel to (011) and also include the Et(4)N(+) cations. The interstitial CH(2)Cl(2) molecules appear in the interlayer space. This complex may serve as a useful precursor for the assembly of multinuclear and extended CN-bridged complexes for the design of single-molecule and single-chain magnets, respectively. |
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