| 2 | Author
| | Requires cookie* | | Title
| Reaktionen koordinierter Liganden, V1  | | | Abstract
| Reaktionen an funktionellen Gruppen von Azido-, Amino-und Hydrazidophosphinkomplexen des Typs cis-Mo(CO)4L2 Reactions of Coordinated Ligands, V 1 Reactions a t Functional Groups of Azido-, Amino-, and Hydrazidophosphine Complexes of the Type a\s-Mo(CO)4L 2 O t h m a r S t e l z e r *, H a n s -B e r n h a r d E i k m e i e r u n d G e r d J o h a n n s e n Azidophosphine The azidophosphine complexes cis-Mo(CO)4 (R2PN3)2 (R = Me, Ph) may be ob tained by nucleophilic displacement reactions of chlorine by azide ion in complexes cis-Mo(CO)4 (R2PCl)2-The thermal decomposition and Staudinger reactions were studied. Silylation of NH-or NH2-functional groups in aminophosphine and hydrazinophosphine complexes with MesSiCl, Me2SiCl2 or Me2SiCl-SiClMe2 leads to a series of monodentate or bidentate silylaminophosphine complexes, e.g. (CO)4Mo(R2PNHSiMe3)2, (CO)4Mo-(R2PNH)2SiMe2, (CO)4Mo(R2PNH)2(SiMe2)2, (CO)4Mo[R2PN(SiMe3)(SiMe3)NPR2] or (CO)4Mo[R2P-N(SiMe3)SiMe2-SiMe2-N(SiMe3)PR2]. The structures of these complexes are discussed on the basis of their IR and NMR spectra. | | |
Reference
| (Z. Naturforsch. 32b, 1449—1454 [1977]; eingegangen am 6. Juli 1977) | | |
Published
| 1977 | | |
Keywords
| Complexes, Staudinger Reaction, Silylation, Aminophosphine Complexes | | |
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| default:Reihe_B/32/ZNB-1977-32b-1449.pdf | | | Identifier
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| 32 | |
3 | Author
| PeterG. Jones, Anke Meyer, Reinhard Schmutzler, FrauM. Prof, Becke | Requires cookie* | | Title
| Uber die Darstellung neuer spirocyclischer N,N'-Dimethylsulfamid-substituierter Phosphorverbindungen und N,N'-DimethyIsulfamid-verbrückter Diphosphorverbindungen The Preparation of New Spirocyclic N,N'-Dimethylsulphamide-Substituted Phosphorus Compounds, and of Some N,N'-Dimethylsulphamide-Bridged Diphosphorus Compounds  | | | Abstract
| The reactions of 4-chloro-l,3,5,7-tetramethyl-2,2,6,6-tetraoxa-2,6-dithia-l,3,5,7-tetraaza-4x:'-phosphaspiro[3.3]heptane (1) with trimethylsilyl compounds and sodium azide led to a series of spirocyclic N,N'-dimethylsulphamide-substituted phosphoranes (2—5). The nature of the penta-aza-spirophosphorane (4) was confirmed by an X-ray crystal structure determination (C2/c, a = 991.8(4), b = 1185.6(6), c = 1224.9(5) pm ,ß= 108.64(3)°, Z = 4, R = 0.041 for 1065 unique observed reflections); a crystallographic twofold axis passes through phosphorus and the nitrogen atom of the NMe2 group. The geometry at phosphorus is to a good approximation trigonal bipyramidal. The azido-spirophosphorane (5) undergoes Staudinger-type reactions with phosphorus(III) com pounds (PPh3, dppm) to form the mixed-valence phosphorus compounds 6—8 . The reaction of N,N'-dimethylsulphamide or N,N'-dimethyl-N,N'-bis(trimethylsilyl)-sulphamide with dichloro-phosphines RPC12 (R = Me, Ph) in a molar ratio 1:2 leads to the formation of the acyclic N,N'-dimethylsulphamide-bridged diphosphorus compounds 9 and 10, respectively. The spectro scopic properties (and, for 4, the X-ray crystal structure) of the products are compared with those of analogous urea-bridged phosphorus compounds. | | |
Reference
| Z. Naturforsch. 45b, 175 (1990); eingegangen am 26. Juni/7. September 1989 | | |
Published
| 1990 | | |
Keywords
| Spirophosphoranes, NN'-Dimethylsulphamide, X-Ray, Staudinger Reactions, Diphosphorus Compounds | | |
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| 45 | |
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