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'Molybdenum Complexes' in keywords Facet   section ZfN Section B  [X]
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1Author    O. Laf Walter, G. Ottfried Hüttner, R. Ainer KernRequires cookie*
 Title    D a r s  
 Abstract    t e llu n g u n d C h a r a k t e r is ie r u n g v o n N (C H 2P P h 2)3, N (C H 2P P h 2)3M o (C O)3 u n d [ H N (C H 2P P h 2)3M o (C Ö) 3 ] B F 4 Preparation and Characterisation o f N (C H 2PPh-,)3, N (C H 2P P h i)3M o(C O)3 and [H N (CH 2PPh2)3M o(C O)3]BF4 The synthesis of N(CH2PPh2)3 (1) and its spectroscopic properties are reported. Reaction of N(CH2PPh2)3 with (CH3CN)3M o(CO)3 leads to N(CH 2PPh2)3M o(CO)3 (2). The cationic complex [HN(CH2PPh2)3Mo(CO)3]+ (3) is obtained by protonating the N atom of 2 with aqueous HBF4. The spectroscopic and structural properties of 2 and the cation 3 are compared. The results indicate an interaction of the ligand N atom and the Mo atom through space over more than 350 pm. It is shown from IR data that 2 
  Reference    Z. Naturforsch. 51b, 922—928 (1996); eingegangen am 18. Januar 1996 
  Published    1996 
  Keywords    Tripod Ligands, Phosphorus Ligands, Molybdenum Complexes, Crystal Structure 
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 TEI-XML for    default:Reihe_B/51/ZNB-1996-51b-0922.pdf 
 Identifier    ZNB-1996-51b-0922 
 Volume    51 
2Author    Cornelia Borgmann, Christian Limberg, Läszlö Zsolnai, Katja HeinzeRequires cookie*
 Title    Syntheses, Structures, and Spectroscopic Properties of Alkoxide, Hydroxide, and Siloxide Complexes with (r73-Allyl)Mo Moieties  
 Abstract    Salts with binuclear anions of the general formula [(?73-C3H4R)(CO)2Mo(^-OR')2(/i-OR")-Mo(CO)2(f?3-C3H4R) r (R = h , R',R" = Me, 2 ; R = CH3, R' = CH(CH3)2, R" = OH, 3; R = CH3, R' = OH, R" = OSiMe3, 4) have been synthesised via reaction of [(r/3-C3H4R)-Mo(CO)2(CH3CN)2(thf)]+BF4_ , 1, with NaOMe, NaO'Pr, and KOSiMe3. All products were characterised spectroscopically and investigated by single crystal X-ray analysis. In the case of 3 low temperature 2D-NMR spectra revealed that the solid state structure is maintained in solution and that the compound shows a trigonal twist-rearrangement at room temperature. 
  Reference    Z. Naturforsch. 54b, 473—481 (1999); received October 28 1998 
  Published    1999 
  Keywords    Molybdenum Complexes, Allyl, Alkoxides, Hydroxides, NMR Data 
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 TEI-XML for    default:Reihe_B/54/ZNB-1999-54b-0473.pdf 
 Identifier    ZNB-1999-54b-0473 
 Volume    54 
3Author    Hans-Jürgen Plinta, Ion Neda, Reinhard SchmutzlerRequires cookie*
 Title    .3-Dimethyl-l,3-diaza-2-R-5,6-benzo-2 A3-phosphorinan-4-one (R = F, Me2N, 2-Methylpiperidino, MeC(: 0 ) N H -) als Liganden in Übergangsmetallkomplexen; Synthese und Struktur von Dichloro-Platin(II)-und Tetracarbonyl-Metall(O)- Koordinationsverbindungen (Metall = Cr, Mo und W) 1.3-Dimethyl-l,3-diaza-2-R-5,6-benzo-2/l3-phosphorinan-4-ones (R = F, Me2N, 2-Methylpiperidino, MeC(: 0 ) N H -) as Ligands in Transition-Metal Complexes; Synthesis and Structure o f Dichloro-Platinum(II)-and Tetracarbonyl-Metal(O) Coordination Compounds (Metal = Cr, Mo and W)  
 Abstract    -2-fluoro-5,6-benzo-l,3,2-phosphorinane-4-one (1) reacted with (COD)PtCl2 (COD = 1,5-cyclooctadiene) or K2PtCl4 to give the c/s-dichloro-platinum(II) complex (2). The reactions of 1 with the tetracarbonyl norbornadiene derivatives of Cr, Mo and W furnished the complexes 3 -6 . In the case of the chromium and tungsten complexes the trans-isomers 3 and 6 were formed, due to a c/s-?ra«s-isomerization. Room temperature and low temperature 3IP NMR spectra of a mixture of 5 and 6 show no significant temperature dependence of the cis-trans equilibrium. The reaction of 1 with the pentacarbonyl tetrahydro-furan derivative of W led to the product 7. The spirophosphoranes 8 and 9 were obtained in low yields. The analogous reactions of 10, 15 and 20 with (COD)PtCl2 and the tetracarbonyl norbornadiene derivatives of Cr and Mo furnished the coordination compounds 1 1 -1 4 , 16-18, 21 and 23. In the case of all chromium complexes only the /rarcs-isomers 11,16 and 21 were formed, whereas in the case of molybdenum m-fraH.s'-isomer mixtures 12 and 13, as well as 17 and 18 were obtained. An attempt to obtain the cis-isomer of the molybdenum complex 22 failed. In the case of platinum the expected m-complexes 14 and 23 were formed, while the attempted synthesis of 19 was unsuccessful. All these results are interpreted in terms of both steric and electronic factors. The ligands 1, 10, 15 and 20 coordinate via phosphorus. The va­ lidity of the concept of hard and soft acids and bases (HSAB) was confirmed. The characteri­ zation of 2 -7 , 1 1-14, 16-18, 21 and 23 rests, especially, on their 'H, 13C and 3IP NMR spec­ tra, and their mass and infrared spectra. 31p -3,p coupling constants 2/(PP) for the cis-coordi­ nated complexes 4, 5 and 14 involving two equivalent phosphorus ligands are also reported. 
  Reference    (Z. Naturforsch. 49b, 100—110 [1994]; eingegangen am 17. Mai 1993) 
  Published    1994 
  Keywords    Platinum Complexes, Chromium Complexes, Molybdenum Complexes, Tungsten Complexes, NMR Spectra 1, 3-Dimethyl-l, 3-diaza 
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 TEI-XML for    default:Reihe_B/49/ZNB-1994-49b-0100.pdf 
 Identifier    ZNB-1994-49b-0100 
 Volume    49