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'Hexacyanoferrate III' in keywords
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1995 (1)
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1Author    D. BabelRequires cookie*
 Title    Die Kristallstruktur des Cyano-Elpasoliths [N(CH3)4]2CsFe(CN)6 The Crystal Structure of the Cyano Elpasolite [N(CH3)4]2CsFe(CN)6  
 Abstract    The crystal structure of the cubic compound [N(CH3)4]2CsFe(CN)6 was determined by X-ray methods: a = 2527.4(6) pm, space group Fd3c, Z = 32, Rg = 0.028 (260 independent single crystal reflections). The resulting distances within the practically undistorted Fe (CN) 6 3 ~ -octahedron are Fe-C = 193.4(6) and C-N = 115.7(7) pm. Compared to the ideal elpasolite structure of space group Fm3m, Z = 4, the octahedra are rotated by 7.4° through their 3 axis. This is discussed as caused by steric requirements of the tetramethyl-ammonium groups (N-C = 148.4(10) and 149.1(38) pm, resp.). Three quarters of them, of which also the hydrogen positions could bo located, are well oriented. The remaining quarter shows orientational disorder to approach similar contact distances as the other N(CH3)4+ ion exhibits between the methyl groups and the nitrogen ends of the anions. 
  Reference    Z. Naturforsch. 37b, 1534—1539 (1982); eingegangen am 11. August 1982 
  Published    1982 
  Keywords    Crystal Structure, Elpasolite, Hexacyanoferrate(III) 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-1534.pdf 
 Identifier    ZNB-1982-37b-1534 
 Volume    37 
2Author    M. Witzei, D. BabelRequires cookie*
 Title    Die Kristallstruktur des elpasolith-verwandten Cyanokomplexes [N(CH3)4]2NaFe(CN)6 * H20 The Crystal Structure of the Elpasolite-Related Cyano Complex [N(CH3)4]2NaFe(CN)6 * H20  
 Abstract    The compound [N(CH3)4]2NaFe(CN)6 • H20 crystallizes in the orthorhombic space group Pnma, Z = 4, a — 1863.9(2), b = 861.7(1), c — 1317.2(2) pm. The X-ray single crystal structure determination (2515 reflections, R — 0.04) revealed an elpasolite-related framework of slightly deformed Fe(CN)63_ octahedra, the mean distances in which are Fe —C = 194.0 and C—N = 113.9 pm. The strongly distorted octahedral N6 cavities formed by six Fe(CN)63_ units are occupied by monohydrated sodium ions, exhibiting a very short distance N a—O = 221.8(3) pm. By approach to one of the octahedral faces within their N6 environment the sodium ions obtain a distorted tetrahedral NaON3 coordination, N a—N = 2 x 238.0(3) and 241.3(3) pm. One of the compound's two tetramethylammonium ions, which are centered at mirror planes, is orientation-ally disordered. The reason for this is discussed. 
  Reference    Z. Naturforsch. 39b, 201 (1984); eingegangen am 21. Juli/19. Oktober 1983 
  Published    1984 
  Keywords    Crystal Structure, Elpasolite, Hexacyanoferrate(III), Monohydrated Sodium Ion 
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 TEI-XML for    default:Reihe_B/39/ZNB-1984-39b-0201.pdf 
 Identifier    ZNB-1984-39b-0201 
 Volume    39 
3Author    Svend Sievertsen, Lutz Galich, Heiner HomborgRequires cookie*
 Abstract    l e c t r o n i c R a m a n S p e c tr a o f a L o w -S p in F e r a P o r p h y r i n a n d R e e x a m in a tio n o f th e V ib r a t i o n a l S p e c tr a o f K 3[F e (C N)6] a n d [F e (C 5H 5)2]B F4 The resonance Raman spectra of (nBu4N)[Fe(CN)2TPP] (("BiitN): tetra(n-butyl)ammonium; TPP: m-tetraphenylporphyrin), K3 [Fe(CN)6] and [Fe(C5H5)2]BF4 have been investigated. A molec­ ular electronic Raman (ER) effect at 545 cm"1 is observed for (nBu4N)[Fe(CN)2TPP]. The transi­ tion occurs between lower 'TV' and upper 'Tg" level of the spin-orbit split ground state assuming pseudo-octahedral symmetry. In contrast to earlier studies no ER effect is detected for K3[Fe(CN)6] and [Fe(C5H5)2]BF4. For Raman shifts < 800 cm-1 only one strong Raman line is observed for [Fe(C5H5)2]BF4 at 311 cm-1, assigned to the iron ring stretch designated by u4 (aig in D5(j). Due to a phase transition of K3[Fe(CN)6], two additional strong vibrational lines at 329 and 352 cm-1 appear in the Raman spectrum taken at 10 K. Their intensities show A "term" behaviour of the resonance Raman effect with overtones and combinations for both lines. These are components of the vibronic combinations with the i/6, vi, and i/g modes (tiu in Oh) in the IR spectra, too. 
  Reference    Z. Naturforsch. 50a, 881—887 (1995); received May 26 1995 
  Published    1995 
  Keywords    Di(cyano)-m-tetraphenylporphinatoferrate(III), Hexacyanoferrate(III), Ferricenium, Electronic Raman Spectra, Vibrational Spectra 
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 TEI-XML for    default:Reihe_A/50/ZNA-1995-50a-0881.pdf 
 Identifier    ZNA-1995-50a-0881 
 Volume    50