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'Manganese' in keywords Facet   section ZfN Section B  [X]
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21Author    Anne Utzolino, Karsten BluhmRequires cookie*
 Title    Neue Einsichten zur Stabilisierung des Hulsit-Strukturtyps am Beispiel von Mnl,2MnIII( B 0 ,) 0 2 und Mn,lSrMnlll( B 0 ,) 0 , New Insights into the Stabilization of the Hulsite Structure During Crystal Structure Determination of M nII2M nIII(B 0 3)0-) and MnllSrM nIII(B 0 3) 0 2  
 Abstract    The compounds MnII2M nIII(B 0 3)02 (I) and MnnSrM nm(B0 3)0 2 (II) were prepared by using a B20 3 flux technique. Single crystals were investigated by X-ray diffraction. I showed ortho-rhombic symmetry, space group D2h -Pbam (No. 55), a = 926.0; b = 1241.5; c = 304.96pm ; Z = 4 and II monoclinic symmetry, space group C2h -P2/m (No. 10), a = 1107.5; b = 311.04; c = 542.93 pm, ß = 95,10(2)°; Z = 2. M n '^ M n '^ B O d O i is isotypic with the mineral Lud­ wigite while MnnSrM nm(B0 3)0 2 is isostructural with the mineral Hulsite. In the structure of M niI2M nlll(B 0 :,) 0 2 (I) all metal point positions showed octahedral oxygen coordination, one point position is occupied by M nu . The structure of M nll2Sr2M nlll2(B O 02O 4 (II) contains five octahedrally coordinated metal sites, three of them statistically occupied by Mn:+ or Mn '+ and Sr2+. The incorperation of S r + seems to be responsible for the Hulsite structure. Both structures contain isolated, trigonal planar B 0 3 units and oxygen atoms that are not coordinated to boron. 
  Reference    Z. Naturforsch. 51b, 1433—1438 (1996); eingegangen am 12. April 1996 
  Published    1996 
  Keywords    Manganese, Strontium Borate Oxide, Ludwigite, Hulsite 
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 TEI-XML for    default:Reihe_B/51/ZNB-1996-51b-1433.pdf 
 Identifier    ZNB-1996-51b-1433 
 Volume    51 
22Author    R. Rettich, Hk Müller-BuschbaumRequires cookie*
 Title    Isolierte MnCl6-Oktaeder im Oxohalogeno-Vanadat Ba5(Mg0,4Mn0,6)(V2O7)2MnCl6 Isolated MnCl6 Octahedra in the Oxohalogeno Vanadate Ba5(M g0 4Mn0 6)(V20 7)2MnCl6  
 Abstract    Single crystals o f Ba5(M g0 4Mn0 6)(V20 7)2MnCl6 have been prepared by solid state reactions of M g C 0 3, Mn20 3, V20<i and BaCl2 -2H20 below the melting point of BaCl2. The new vanadium oxide chloride crystallizesowith monoclinic symmetry, space group C2h-P2/c, a = 13.345(4), b = 5.711(2), c = 15.859(4) Ä, ß = 113.69(2)°, Z = 2. Special features of the crystal structure are isolated MnCl6 octahedra and layers created by divanadat groups and (M g,M n)06 octahedra. The ^ [(Mg,Mn)V20 7] nets of Ba5(Mg0 4Mn0 6)(V20 7)2MnCl6 are discussed with respect to other oxohalogeno vanadates containing divanadate groups. 
  Reference    Z. Naturforsch. 52b, 457—461 (1997); eingegangen am 15. Januar 1997 
  Published    1997 
  Keywords    Barium, Magnesium, Manganese, Chlorine, Vanadium Oxide 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0457.pdf 
 Identifier    ZNB-1997-52b-0457 
 Volume    52 
23Author    R. Rettich, Hk Müller-BuschbaumRequires cookie*
 Title    Ein [Ba(Ca,Mn)06]-Gerüst mit eingelagerten V-O-V-Gruppen in der Kristallstruktur von Ba(Ca0,6Mn0,4)V20 7 A [Ba(Ca,Mn)06] Framework with Incorporated V-O-V Groups in the Crystal Structure of Ba(CaQ 6Mn0 4)V20  
 Abstract    Single crystals of Ba(Ca<).6Mn0 4)V20 7 have been prepared by crystallization from melts. X-ray investigations revealed a new quaternary vanadium oxide of the type BaMV20 7. The M positions are occupied statistically by Ca2+ and Mn2+. The compound crystallizes wi|h orthorhombic symmetry, space group D^-Pnma, a = 15.429(2), b -5.7005(12), c = 7.364(2) A, Z = 4. The crystal structure can be interpreted as a [Ba(Ca,Mn)06] network with incorporated V-O-V groups. Considering the nearest O2-neighbours of the incorporated vanadium, the V-O-V groups are complemented to give V20 7 divanadate units. Ba(Ca« 6Mn0 4)V20 7 is isotypic to BaMV20 7 (M=Ca,Cd) but not to BaMnV20 7. 
  Reference    Z. Naturforsch. 52b, 785—789 (1997); eingegangen am 14. April 1997 
  Published    1997 
  Keywords    Barium, Calcium, Manganese, Vanadium Oxide, Crystal Structure 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0785.pdf 
 Identifier    ZNB-1997-52b-0785 
 Volume    52 
24Author    R. Rettich, Hk Müller-BuschbaumRequires cookie*
 Title    Zur Kristallchemie der Silber-Mangan-Oxovanadate Ag2BaMnV20 8 und (AgCa2)Mn2(V 04)3 On the Crystal Chemistry of the Silver Manganese Oxovanadates Ag?BaMnV?Oo and (AgCa2)Mn2(V 0 4)3  
  Reference    Z. Naturforsch. 53b, 291—295 (1998); eingegangen am 12. Januar 1998 
  Published    1998 
  Keywords    Barium, Calcium, Manganese, Vanadium Oxide, Crystal Structure 
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 TEI-XML for    default:Reihe_B/53/ZNB-1998-53b-0291.pdf 
 Identifier    ZNB-1998-53b-0291 
 Volume    53 
25Author    R. Rettich, Hk Müller-BuschbaumRequires cookie*
 Title    Darstellung und Strukturbeschreibung von NaCa3 Mn(V2O7)(V3 O10) Preparation and Structure o f NaCa3M n(V2O 7)(V3O 10)  
 Abstract    Single crystals of NaCa3Mn(V2O7)(V3O 10) have been prepared by crystallization from flux in argon atmosphere. X-Ray single crystal methods led to triclinic symmetry, space group C '-P l, 
  Reference    Z. Naturforsch. 53b, 507—511 (1998); eingegangen am 22. Januar 1998 
  Published    1998 
  Keywords    Sodium, Calcium, Manganese, Vanadium Oxide, Crystal Structure 
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 TEI-XML for    default:Reihe_B/53/ZNB-1998-53b-0507.pdf 
 Identifier    ZNB-1998-53b-0507 
 Volume    53 
26Author    M. Staack, Hk Müller-BuschbaumRequires cookie*
 Title    Ba4M n2Ag20(As04)4? ein Barium-Mangan-Oxid-Arsenat mit nichtlinearen O-Ag-O-Hanteln. Ba4Mn2Ag2 0 (As0 4 )4, a Barium Manganese Oxide-Arsenate Showing Nonlinear O-Ag-O Dumbbells  
 Abstract    Single crystals of Ba4Mn2 Ag20 (A s04)4 have been prepared by solid state reactions using me­ tallic silver as reactant. X-ray techniques led to monoclinic symmetry, space group D2h-P2,/m, 
  Reference    Z. Naturforsch. 53b, 512—516 (1998); eingegangen am 29. Januar 1998 
  Published    1998 
  Keywords    Barium, Manganese, Silver, Oxide-Arsenate, Crystal Structure 
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 TEI-XML for    default:Reihe_B/53/ZNB-1998-53b-0512.pdf 
 Identifier    ZNB-1998-53b-0512 
 Volume    53 
27Author    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 
28Author    Jan-K Arel Buijink, M. Athias, Noltemeyer Und, FrankT. EdelmannRequires cookie*
 Title    Metall-N,N  
 Abstract    -bis(trimethylsilyl)benzamidinate: Synthese und Kristallstruktur von Bis[N,N-bis(trimethylsilyl)benzamidinato)chroni(II), [P hC (N SiM e3)2l2Cr Metal-N,N'-bis(trimethylsilyl)benzamidinates: Synthesis and Crystal Structure of Bis[N,N'-bis(trimethylsilyl)benzamidinato]chromium(II), [PhC(NSiM e3)2]2Cr The preparation o f N,N'-bis(trimethylsilyl)benzamidinates o f chromium, manganese, zinc and bismuth is described. The chromium(II) derivative [PhC(NSiM e3)2]2Cr (2) has been char­ acterized by an X-ray structure determination. Treatment o f CpTiCl3 with one equivalent o f N a[PhC (N SiM e3),] • 0.5 Et^O yields the mixed Cp/benzamidinate complex [PhC(NSiM e3)2]CpTiCl2 (9). 
  Reference    Z. Naturforsch. 46b, 1328—1332 (1991); eingegangen am 26. April 1991 
  Published    1991 
  Keywords    N, N'-Bis(trim ethylsilyl)benzam idinates, Chromium, Manganese, Zinc, Bismuth 
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 TEI-XML for    default:Reihe_B/46/ZNB-1991-46b-1328.pdf 
 Identifier    ZNB-1991-46b-1328 
 Volume    46 
29Author    AnjaL. Oose, W. Illiam, S. SheldrickRequires cookie*
 Title    Quaternary Selenidogermanates(IV) A3[AgGe4Se10]*2H2O and A2[MnGe4Se10]*3H2O (A = Rb, Cs) with Open Framework Structures  
 Abstract    Hydrothermal reaction of Ge and Se with Ag(CH3COO) in the presence of alkali metal carbonates affords the open framework selenidogermanates(IV) A^fAgGejSeiol ^H^O (A = Rb, Cs), 1 and 2, which contain corner linked adamantane-like Ge4Seio cages and AgSe4 tetrahedra. The analogous reaction with Mn(CHiCOO)2 yields the isostructural tetragonal compounds A2[MnGe4Seio]-3 H2 0 (A = Rb, Cs), 3 and 4. The cations are sited at a general position in the channels of the silver bridged anionic framework of 1 and 2 and exhibit a disordered pattern of occupation (s.o.f. = 0.75) with one of the two crystallographically independent water oxygen atoms 0 (2) (s.o.f. = 0.25). In contrast, the Rb+ cations in 3 are disordered over all three cation/oxygen sites, and the cation/water occupation pattern is fully reversed for the larger Cs+ cations in 4 in comparison to 1 and 2. 
  Reference    Z. Naturforsch. 52b, 687—692 (1997); received March 13 1997 
  Published    1997 
  Keywords    Selenidogermanates(IV), Silver, Manganese, Hydrothermal Synthesis, Framework Structure 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0687.pdf 
 Identifier    ZNB-1997-52b-0687 
 Volume    52