Four- and eight-membered cyclic phosphazene derivatives of zirconium, titanium and vanadium. Crystal structures of the complexes [ZrCl3(Me3SiNPPh2NSiMe3)]·MeCN and [{TiCl2(OPPh2N)}2]·4MeCN

1991 | journal article. A publication with affiliation to the University of Göttingen.

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​Four- and eight-membered cyclic phosphazene derivatives of zirconium, titanium and vanadium. Crystal structures of the complexes [ZrCl3(Me3SiNPPh2NSiMe3)]·MeCN and [{TiCl2(OPPh2N)}2]·4MeCN​
Witt, M.; Stalke, D. ; Henkel, T.; Roesky, H. W.   & Sheldrick, G. M. ​ (1991) 
Dalton Transactions, pp. 663​.​ DOI: https://doi.org/10.1039/DT9910000663 

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Authors
Witt, Michael; Stalke, Dietmar ; Henkel, Thomas; Roesky, Herbert W. ; Sheldrick, George M. 
Abstract
The reaction of ZrCl4 with (Me3Si)2NPPh2NSiMe31 yields the four-membered heterocycle [[graphic omitted]SiMe3)]. An improved synthesis of the aminoiminophosphorane 1 is described. The compound TiCl4 reacts with Me3SiOPPh2NSiMe3 unexpectedly with elimination of all Me3p. groups to yield the eight-membered heterocycle [{TiCl2(OPPh2N)}2]. A vanadium-containing dimetallacyclophosphazene [{VCl2(NPPh2N)}2] has been synthesised from [VCl3(NSiMe3)] and CiPPh2NSiMe3. The X-ray structures of [[graphic omitted]SiMe3)]·MeCN and [{TiCl2(OPPh2N)}2]·4MeCN have been determined. While the cyclic Zr–N distances in the former have to be considered as single bonds, the short Ti–N of the latter (almost planar) suggest double-bond character.
Issue Date
1991
Journal
Dalton Transactions 
Organization
Fakultät für Chemie 
File Format
application/pdf
Language
English

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