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1Author    D. M. Kaminaris, A. G. GalinosRequires cookie*
 Title    New Metal -Pentafluorothiophenol Compounds  
 Abstract    In the present paper the reactions of pentafluorothiophenol with nonaqueous solutions (absolute n-hexane) of anhydrous AICI3, FeBr3, RI1CI3 and CrCl3 are described. Analytical data, some physical and chemical properties and the IR spectra of the new compounds are reported and discussed. 
  Reference    Z. Naturforsch. 33b, 149—150 (1978); received November 17 1977 
  Published    1978 
  Keywords    Pentafluorothiophenol, Iron, Alluminium, Rhodium 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-0149.pdf 
 Identifier    ZNB-1978-33b-0149 
 Volume    33 
2Author    Ernst Guggolz, ManfredL. Ziegler, Willibald Kalcher, Johann Plank, Doris Riedel, WolfgangA. HerrmannRequires cookie*
 Title    Synthese und Molekülstruktur der dreikernigen Cluster-Verbindung (^-C5Me5)IrFea(CO)9 Synthesis and Molecular Structure of the Trinuclear Cluster Compound (^ 5 -C5Me5)IrFe2(CO)g  
 Abstract    Reaction of triirondodecacarbonyl (1) with the dinuclear chloroiridium complex [(?? 5 -C5Me5)Ir(//-Cl)Cl]2 (2) in benzene at 50 °C yields the novel mixed iron iridium cluster of composition (rj 5 -C&Mes)IrFe2(C0)9 (8) the molecular structure of which has been established by X-ray diffraction methods. The mononuclear half-sandwich complex (j7 5 -C5Me5)Ir(CO)2 (4) present in the reaction mixture was found to represent the immediate precursor of the cluster compound 8. 
  Reference    Z. Naturforsch. 36b, 1053—1059 (1981); eingegangen am 8. April 1981 
  Published    1981 
  Keywords    Iron, Iridium, Carbonyl Complexes, Pentamethylcyclopentadienyl 
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 TEI-XML for    default:Reihe_B/36/ZNB-1981-36b-1053.pdf 
 Identifier    ZNB-1981-36b-1053 
 Volume    36 
3Author    HerbertW. Roesky, Ulrich Seseke, Mathias Noltemeyer, GeorgeM. SheldrickRequires cookie*
 Title    Darstellungen und Strukturen viergliedriger Metall-Stickstoff-Ringe Preparations and Structures of Four-Membered Metal-Nitrogen Rings  
 Abstract    Ph 3 P=NSiMe 3 (1) reacts with InCl 3 , SnCl, and FeCl, to yield (Ph,P=N) 2 (InCl 2) 2 • 2 DMF (2a), (Ph 3 P=N) 2 Sn 2 Cl 4 • 2 CH 3 CN (3a) and (Ph 3 P=N) 2 (FeCl 2) 2 (4). The X-ray single crystal structures of 2a, 3a and 4 are reported. The compounds form four-membered rings consisting of alternating metal and nitrogen atoms. 2a and 4 are symmetrical, but 3a has both a Sn(II)Cl and a Sn(IV)Cl 3 group in the four-membered ring. 
  Reference    Z. Naturforsch. 43b, 1130—1136 (1988); eingegangen am 29. März 1988 
  Published    1988 
  Keywords    Indium, Tin, Iron, X-Ray 
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 TEI-XML for    default:Reihe_B/43/ZNB-1988-43b-1130.pdf 
 Identifier    ZNB-1988-43b-1130 
 Volume    43 
4Author    Requires cookie*
 Title    Reaktionen von Metallcarbonylen mit Diazirin1  
 Abstract    W o l f g a n g B e c k u n d W o l f g a n g D a n z e r Pentamethylendiazirine (N = N) has been found in metal carbonyl compounds as a monodentate two electron ligand (7t-CH3C5H 4Mn(CO)2 N = N , (OC)sW N = N) or as a 
  Reference    (Z. Naturforsch. 30b, 716—719 [1975]; eingegangen am 2. Juni 1975) 
  Published    1975 
  Keywords    Diazirine Carbonyl Complexes, Manganese, Iron, Molybdenum, Tungsten 
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 TEI-XML for    default:Reihe_B/30/ZNB-1975-30b-0716.pdf 
 Identifier    ZNB-1975-30b-0716 
 Volume    30 
5Author    Hk Müller-Buschbaum, M. HarderRequires cookie*
 Title    Zur Kenntnis von Ba2Fe2 Fe9 3 Aln034 About Ba2Fe2 2+ Fe9 3+ Alii034  
 Abstract    Single crystals of the compound Ba2FenAln034 were prepared by solid state reac-tion (1700 °C) of Ba0-Fe203-Al203 mixtures. The crystal structure was investigated by X-rav data (space group D6h-P63/mmc, lattice constants: a = 565.3, c = 2281.0 pm). Ba2FenAln034 is isotypic with Na20 • 11 AI2O3, the structure of)S-alumina. 
  Reference    Z. Naturforsch. 33b, 146—148 (1978); eingegangen am 8. Dezember 1977 
  Published    1978 
  Keywords    Barium, Iron, Aluminium, X-ray, Crystal Structure 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-0146.pdf 
 Identifier    ZNB-1978-33b-0146 
 Volume    33 
6Author    Helmut Behrens, Anton JungbauerRequires cookie*
 Title    Über die Reaktionen von ein-und zweikernigen, kationischen ?/ 5 -Cyelopentadienyl-carbonyl-Komplexeii des Eisens, Rutheniums und Osmiums mit flüssigem Ammoniak [1] On the Reactions of Mono-and Dinuclear, Cationic ^-Cyclopentadienyl Carbonyl Complexes of Iron, Ruthenium and Osmium with Liquid Ammonia [1]  
 Abstract    The covalent carbamoyl compounds 7?5.c5H5Ru(CO)(L)(CONH2) (L = CO, MeCN, MeNC, PPh3, PEt3) and ^-CsHsOsfCOMCONI^) are formed by the reactions of the cationic complexes [7?5.C5H5Ru(CO)2(L)]+ (L = CO, MeCN, MeNC, PPh3, PEt3) and [^ 5 -C5H5Os(CO)3]+ with liquid NH3 below 10 °C. In contrast, the reaction of [^ 5 -C5H5Ru(CO)2(r? 2 -C2H4)]PF6 with liquid NH3 yields the quarternary ammonium salt 
  Reference    Z. Naturforsch. 34b, 1477—1486 (1979); eingegangen am 3. August 1979 
  Published    1979 
  Keywords    ^-Cyclopentadienyl Carbamoyl Carbonyl Complexes, Iron, Ruthenium, Osmium 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-1477.pdf 
 Identifier    ZNB-1979-34b-1477 
 Volume    34 
7Author    JaapN. Louwen, Jaap Hart, DerkJ. Stufkens, Ad OskamRequires cookie*
 Title    The Hei and HeH Photoelectron Spectra of [Fe*? 3 -C3H5(CO)3X] and [Fe^ 3 -C4H7 (CO)3X] (X = Cl, Br, I) and [CoC3H5(CO)3]  
 Abstract    By means of UV photoelectron spectroscopy (UPS) the electronic structures of [Fe^3.C3H5(CO)3X], [Fe^3-(2-CH3C3H4)(CO)3X] (X = Cl, Br, I) and [Co(C3H5)(CO)3] have been studied. Detailed assignments are possible and surprisingly low ionization energies (as low as 8.19 eV) are found for iodine lone pair type Orbitals. From the spectra a large difference in n backbonding is found between the cobalt and iron complexes. 
  Reference    Z. Naturforsch. 37b, 179—185 (1982); received September 29 1981 
  Published    1982 
  Keywords    Photoelectron Spectra, Iron, Cobalt, Allyl Complexes 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-0179.pdf 
 Identifier    ZNB-1982-37b-0179 
 Volume    37 
8Author    F.-DM. Artin, H.K M Üller-B, UschbaumRequires cookie*
 Title    Eine synthetische Spezies zum Mineral Howardevansit mit Eisen anstelle von Kupfer: NaFe3V 30 12  
 Abstract    Single crystals of NaFe3V30 12 have been prepared by solid state reaction below the melt­ ing point of the reaction mixture. This compound is isotypic to the mineral Howardevansite but shows lower triclinic symmetry, space group C }-P 1 , a = 6.757(2), b = 8.155(2), c = 9.816(3) Ä, a = 106.05(2), ß = 104.401(9), y = 102.09(2)°, Z = 2. The acentric space group is caused by the sodium positions, all other atoms comply with the space group PI of Howarde­ vansite. The different ions are coordinated by O2-forming V 0 4 tetrahedra, FeOfi octahedra, trigonal FeOs bipyramids and irregular NaOs and NaOy polyhedra, respectively. The crystal chemistry is discussed with respect to Howardevansite. 
  Reference    (Z. Naturforsch. 50b, 51—55 [1995]; eingegangen am 5. August 1994) 
  Published    1995 
  Keywords    Sodium, Iron, Vanadium, Oxide, Crystal Structure 
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 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0051.pdf 
 Identifier    ZNB-1995-50b-0051 
 Volume    50 
9Author    Wolfgang Pohl, Ingo-Peter Lorenz, Heinrich Nöth, Martin SchmidtRequires cookie*
 Title    Offene und geschlossene Triferriophosphonium-Salze und Triferriophosphane O pen and Closed Triferriophosphonium Salts and Triferriophosphines  
 Abstract    The reaction of P(SiM e3)3 with an excess of C pFe(CO)2X (X = Cl, Br) through the action o f water gives the triferriophosphonium salt [{CpFe(CO)2}3PH]2FeX4 together with ferrocene as by-product. The cation of the salt can be deprotonated by D B U to afford the unstable triferriophosphine {CpFe(CO)2}3P. Its subsequent realkylation with RX (R = Me, CH2Ph; X = I, Br) leads to alkyltriferriophosphonium salts [{CpFe(CO)2}3PR]X. Photolysis of [{CpFe(CO)2}3PH]2FeX 4 induces the elimination of one CO group, and the CO-bridged and partly closed complex [{//-CO(CpFeCO)2}{CpFe(CO)2}PH]2FeX 4 is formed, the cation of which can also be deprotonated to give the corresponding m onobridged phosphine (w-CO(CpFeCO)2}{CpFe(CO)2}P. Both PH-phosphonium salts undergo a hydrogen-chlorine exchange reaction to give the P -C l analogues [{CpFe(CO)2}3PCl]2FeX4 and [{//-CO (CpFeCO)2}{CpFe(CO)2}PCl]2FeX 4. The IR and NM R spectra of all species as well as the X-ray structure analyses of the open and closed P -H functional com plexes are reported and discussed. 
  Reference    Z. Naturforsch. 50b, 1485—1493 (1995); eingegangen am 30. März 1995 
  Published    1995 
  Keywords    Iron, Tristrimethylsilylphosphine, Hydrogen Chlorine Exchange, X-Ray, Decarbonylation 
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 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-1485.pdf 
 Identifier    ZNB-1995-50b-1485 
 Volume    50 
10Author    O. Sedello, Hk Müller-BuschbaumRequires cookie*
 Title    Ein Oxometallat mit eindimensional flächenverknüpften Oktaederketten Synthesis and Crystal Structure of (C u,Fe)363M o3O i2. An Oxom etallate Showing One-Dimensional Chains of Face Sharing Octahedra  
 Abstract    Single crystals of (C u ,F e)3-63M o30 12 have been prepared by crystallisation from melts. X-ray investigations lead to orthorhombic symmetry, space group D : 2-P 2 12121, a = 5.0952(8), b = 10.637(2), c = 17.881(3) A , Z = 4. (C u ,F e)363M o3O i2 is isotypic to Cu385M o30 12 or (C u,Z n)3 75M o30 12. M olybdenum shows tetrahedral coordination by oxygen. Cu+ and Fe2+ are probably distributed statistically over four different point positions. Interesting features of the crystal structure are one-dim ensional chains of face shared (C u ,F e)0 6 octahedra. S y n t h e s e u n d K r i s t a l l s t r u k t u r v o n (C u , F e) 3 ,63 M o 3 0 12. 
  Reference    (Z. Naturforsch. 51b, 90—9 [1996]; eingegangen am 20. Juni 1995) 
  Published    1996 
  Keywords    Copper, Iron, M olybdenum, Oxide, Crystal Structure 
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 TEI-XML for    default:Reihe_B/51/ZNB-1996-51b-0090.pdf 
 Identifier    ZNB-1996-51b-0090 
 Volume    51 
11Author    B. W. Edel, HkM. Üller-B, UschbaumRequires cookie*
 Title    Über die Kristallstrukturen der Tellurate Pb3Fe2Te20 12 und Pb2CoTe06  
 Abstract    Pb3Fe2Te20 |2 (I) and Pb2C oT e06 (II) have been prepared by crystallization from melts. Single crystal X-ray investigations led to monoclinic (I) and tetragonal (II) symmetry, space groups Cs-Cc and D{J-I4/mmm. Lattice constants I: a = 9.866(3), b = 15.332(4), c = 7.172(2) A, ß = 111.34(3)°, Z = 4. II: a = 5.661(5), c = 8.004(7) A, Z = 2. (I) represents a new crystal structure, characterized by a network of octahedra occupied by Fe + and Te6+ in a disordered manner. The centres of negative charge of the lone pairs of Pb2+ in I are estimated by Coulomb term calculations. II belongs to the elpasolithe type. 
  Reference    (Z. Naturforsch. 52b, 35—39 [1997]; eingegangen am 2. September 1996) 
  Published    1997 
  Keywords    Lead, Iron, Cobalt, Tellurium Oxide, Crystal Structure 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0035.pdf 
 Identifier    ZNB-1997-52b-0035 
 Volume    52 
12Author    Jutta Knaudta, Stefan Försterb, Ulrich Bartsch3, Anton Riekerb, Ernst-G JägeraRequires cookie*
 Title    Catalytic Oxidation of a Trialkyl-Substituted Phenol and Aniline with Biomimetic Schiff Base Complexes  
 Abstract    The catalytic oxidation of 2,4.6-tri-f6rr-butylphenol and 2,4,6-tri-te/-r-butylaniline with mo­ lecular oxygen and rerf-butylhydroperoxide was investigated using biomimetic Mn-, Fe-and Co-complexes as catalysts. The catalytic activity and product distribution were determined and compared with those observed in the reactions of the well-known Co(salen) complex. 
  Reference    (Z. Naturforsch. 55b, 86—93 [2000]; received Septem ber 22 1999) 
  Published    2000 
  Keywords    Biomimetic Catalysts, Oxidation, Macrocycles, Manganese, Iron, Cobalt 
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 TEI-XML for    default:Reihe_B/55/ZNB-2000-55b-0086.pdf 
 Identifier    ZNB-2000-55b-0086 
 Volume    55 
13Author    JohannesA. Schmitt, Hans-Ulrich Meisch, W. Olfgang ReinleRequires cookie*
 Title    Schwermetalle in höheren Pilzen, II * Mangan und Eisen Heavy Metals in Higher Fungi, II Manganese and Iron  
 Abstract    In several series of 262 samples, Higher Fungi, especially from the Tremellales and Gastero-mycetes, were analyzed by atomic absorption spectroscopy on their content of the trace metals manganese and iron. Both elements were found to be present in higher concentrations in some species of the Trem ellales and P hallales. In the case of wood-destroying fungi, the Fe-and Mn-contents of the substrates were compared to those of the corresponding fungi. Only the species with the highest level of these metals reached the same contents as their substrates or a poor enrichment. Among the remaining species of the Higher Fungi, only in the case of the epigean P hallales, a possible biochemical role of manganese has been discussed. 
  Reference    (Z. Naturforsch. 32c, 712 [1977]; eingegangen am 20. Juni 1977) 
  Published    1977 
  Keywords    Manganese, Iron, Higher Fungi, Tremellales, Gasterales 
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 TEI-XML for    default:Reihe_C/32/ZNC-1977-32c-0712.pdf 
 Identifier    ZNC-1977-32c-0712 
 Volume    32 
14Author    P. Scherer, Ch SauerRequires cookie*
 Title    State of Iron in the Archaebacterium Methanosarcina barkeri Grown on Different Carbon Sources as Studied by Mössbauer Spectroscopy  
 Abstract    Cells of the archaebacterium Methanosarcina barkeri were grown strictly anaerobic in defined media. 57Fe-Mössbauer Spectroscopy o f methanol grown cells oxidized in the presence o f air demonstrated only the state o f Fe3+ whereas active cells under reducing conditions offered spectra of two additional iron sites in the Fe2+ state. Furthermore the 57Fe hyperfine interaction data at different temperatures gave evidence that cells cultivated with methanol or acetate as substrate contained ferredoxin like compounds. 
  Reference    Z. Naturforsch. 37c, 877 (1982); received April 27/May 261982 
  Published    1982 
  Keywords    Archaebacterium, Methanosarcina, Methanol, Iron, Mössbauer, Ferredoxin 
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 TEI-XML for    default:Reihe_C/37/ZNC-1982-37c-0877.pdf 
 Identifier    ZNC-1982-37c-0877 
 Volume    37 
15Author    D. Ietrich, W. Ern Er, K. Lau, S-P Eter, K. Uhlm AnnRequires cookie*
 Title    Hairs o f Soybean (Glycine max)  
 Abstract    Root hairs of soybeans (Glycine max), target cells for infection by Rhizobium japonicum accumulate iron more than 10-fold, cobalt more than 8-fold and calcium more than 7-fold compared to the other parts of the root system. In root hairs of wheat (Triticum aestivum) a much smaller accumulation of these elements was found. The symbiont of Glycine max, Rhizobium japonicum, is known to have a high requirement for iron, cobalt and calcium. 
  Reference    Z. Naturforsch. 40c, 912 (1985); received May 30/July 31 1985 
  Published    1985 
  Keywords    Calcium, Cobalt, Glycine max, Iron, Root-Hair 
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 TEI-XML for    default:Reihe_C/40/ZNC-1985-40c-0912_n.pdf 
 Identifier    ZNC-1985-40c-0912_n 
 Volume    40 
16Author    Werner Buchholz, Hans-Uwe SchusterRequires cookie*
 Title    Die Verbindungen MgFe6Ge6 und LiCo6Ge6 The Compounds MgFeßGee and LiCoöGee  
 Abstract    The hexagonally crystallizing compounds MgFeeGeß and LiCoeGeß were prepared and structurally characterized by single crystal investigations. The lattice constants are a = 506.7 pm, c — 804.5 pm, c/a—1.58s for MgFe6Ge6 and a = 504.8 pm, c = 772.9 pm, c/a = 1.53i for LiCoßGee. The structures (space group P6/mmm) are closely related to the structure of LiFeeGe6 and the B35-type structure of FeGe. 
  Reference    Z. Naturforsch. 33b, 877—880 (1978); eingegangen am 26. Mai 1978 
  Published    1978 
  Keywords    Ternary Germanium Compounds, Magnesium, Iron, Lithium, Cobalt, Crystal Structure 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-0877.pdf 
 Identifier    ZNB-1978-33b-0877 
 Volume    33 
17Author    WolfgangA. Herrmann, Johann Plank, Ivan Bernal, Michael CreswickRequires cookie*
 Title    Übergangsmetall-Methylen-Komplexe, X [1] Methylen-und Alkyl-Eisen-Komplexe aus Diazoalkanen. Molekülstruktur von //-Carbonyl-//-feri-butoxycarbonyl-methylen- bis [carbonyl(^ 5 -cyclopentadienyl)eisen] (Fe-Fe) Transition Metal Methylene Complexes, X [1J Methylene and Alkyl Iron Complexes from Diazoalkanes. Molecular Structure of //-Carbonyl-^-Jerf-butoxycarbonyl-methylene- bis[carbonyl(if-cyclopentadienyl)iron] (Fe-Fe)  
 Abstract    The novel doubly bridged /i-methylene iron complexes /M-[C(H)C02R]-^-C0[(??5.C5H5)Fe(C0)]2 (R = C2H5: 3a; R — ^Hg: 3b) have been syn-thesized by low-temperature photolysis of the corresponding alkyldiazoacetates 2 a and 2 b, resp., in the presence of [(r? 5 -CsH5)Fe(CO)2]2 (1) and characterized by means of their analytical data and IR, X H NMR and mass spectroscopy. The geometry of 3 b has been established by single crystal X-ray diffraction techniques. cr-Alkyl iron complexes of the type (^ 5 -C5H5)Fe(C0)2[CHRR'] are accessible from the corresponding diazoalkanes N2 = CRR'. 
  Reference    Z. Naturforsch. 35b, 680—688 (1980); eingegangen am 3. Dezember 1979 
  Published    1980 
  Keywords    ^-Alkoxycarbonylmethylene, cr-Alkyl, Bridging Ligands, Carbonyl Complexes, Iron 
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 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0680.pdf 
 Identifier    ZNB-1980-35b-0680 
 Volume    35 
18Author    H. Kunkely, A. VoglerRequires cookie*
 Title    Photoredox Decomposition of [Cobalamin-^-NC-Fen(CN)5]3* Induced by Metal-to-Metal Charge Transfer Excitation  
 Abstract    In the presence of oxygen aqueous solutions of the binuclear complex [cobalamin-^-NC-Fe(C N)5]3' undergo a redox photolysis (0 ~ 2 x 10'3 at Airr = 405 nm) which yields aquocoba-lamin and [Fe(C N)6]3\ It is suggested that this photoreaction is induced by direct metal-to-metal charge transfer (M M CT) excitation. On the contrary, [cobalamin-fx-NC-Ru(CN)5]3' is photo-inert because a reactive MMCT state is not accessible. 
  Reference    Z. Naturforsch. 51b, 245 (1996); received July 7 1995 
  Published    1996 
  Keywords    Vitamin B I2, Photolysis, Electron Transfer, Cyano Complexes, Iron 
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 TEI-XML for    default:Reihe_B/51/ZNB-1996-51b-0245.pdf 
 Identifier    ZNB-1996-51b-0245 
 Volume    51 
19Author    Rüdiger Hofm, H. Artm, Ut FollmannRequires cookie*
 Title    Bleom ycin-Iron C om plex and Oxygen Activate Algal R ibonucleotide Reductase  
 Abstract    Ribonucleotide reductase of green algae (Scenedesmus obliquus) is a radical-containing enzyme which rapidly loses activity under anaerobic conditions. Reactivation in the presence of air is enhanced by 10 |j.m iron(II)-bleomycin chelate. The reaction lends new biochemical potential to the antibiotic and should be valuable in mechanistic studies of ribonucleotide reduction. 
  Reference    Z. Naturforsch. 40c, 919—921 (1985); received August 22 1985 
  Published    1985 
  Keywords    Bleomycin, Deoxyribonucleotide Synthesis, Iron, Oxygen Dependence, Ribonucleotide Reduction, Scenedesmus obliquus 
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 TEI-XML for    default:Reihe_C/40/ZNC-1985-40c-0919_n.pdf 
 Identifier    ZNC-1985-40c-0919_n 
 Volume    40 
20Author    Matthias Moll, Peter Würstl, Helmut Behrens, Peter MerbachRequires cookie*
 Title    Über neue zweikernige Metallcarbonylkomplexe mit Cyclohexadienyl-cycloheptatrien-und Cyclohexadienyl-isonitril-Brücken On New Dinuclear Metal Carbonyl Complexes with Cyclohexadienyl Cycloheptatriene and Cyclohexadienyl Isonitrile Bridges  
 Abstract    The reactions of the electrophilic [C6H7Fe(CO)3] + -and [C6H7Fe(CO)2CNEt]+-cations with theextremely nucleophilic [C7H7Fe(CO)3] _ -anion lead to the formation of the dinuclear cyclohexadienyl cycloheptatriene bridged complexes (OC)3FeC6H7-C7H7Fe(CO)3 and EtNC(OC)2FeCeH7-C7H7Fe(CO)3. In a similar reaction the tricarbonyl cation [CeH7Fe(CO)3] + with [Cr(CO)5CN] _ yields the dinuclear cyclohexadienyl isonitrile bridged compound (OC)3FeC6H7-NCCr(CO)5. The mass, IR and NMR data of the new complexes are reported. 
  Reference    Z. Naturforsch. 33b, 1304—1308 (1978); eingegangen am 19. Juli 1978 
  Published    1978 
  Keywords    Cyclohexadienyl Cycloheptatriene Iron Carbonyl Complexes, Iron Isonitrile Carbonyl Complexes, Dinuclear Cyclohexadienyl Isonitrile Carbonyl Complex, Iron, Chromium 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-1304.pdf 
 Identifier    ZNB-1978-33b-1304 
 Volume    33