Metal alkoxides as versatile precursors for group 4 phosphonates: Synthesis and X-ray structure of a novel organosoluble zirconium phosphonate

2000 | journal article. A publication with affiliation to the University of Göttingen.

Jump to: Cite & Linked | Documents & Media | Details | Version history

Cite this publication

​Metal alkoxides as versatile precursors for group 4 phosphonates: Synthesis and X-ray structure of a novel organosoluble zirconium phosphonate​
Chakraborty, D.; Chandrasekhar, V.; Bhattacharjee, M.; Krätzner, R. ; Roesky, H. W. ; Noltemeyer, M. & Schmidt, H.-G.​ (2000) 
Inorganic Chemistry39(1) pp. 23​-26​.​ DOI: https://doi.org/10.1021/ic9907361 

Documents & Media

License

GRO License GRO License

Details

Authors
Chakraborty, Debashis; Chandrasekhar, Vadapalli; Bhattacharjee, Manesh; Krätzner, Ralph ; Roesky, Herbert W. ; Noltemeyer, Mathias; Schmidt, Hans-Georg
Abstract
Reactions of Ph2P(O)(OH) and t-BuP(O)(OSiMe3)(OH) with Ti(O-i-Pr)(4) in equimolar ratios gave titanium phosphonates of the type [(O-i-Pr)(3)Ti(mu-O)(2)(PRR2)-R-1](2) (1, R-1 = R-2 = Ph; 2, R-1 = t-Bu, R-2 = OSiMe3) as colorless crystalline solids in moderate yields. Reactions of Ph2P(O)(OH) and the isopropoxides of zirconium and hafnium resulted in products of the composition [(O-i-Pr)(3)M(mu-O-i-Pr)(2)(mu-OPOPh2)M(O-i-Pr)(2)]Ph2P(O)(OH) (M = Zr (3), Hf (4)) in high yields. The compounds were characterized by H-1, (31)p, and Si-29 NMR, infrared (IR), and mass spectroscopic (MS) techniques. The molecular structures of 2 and 3 were confirmed by X-ray crystallography.
Issue Date
2000
Journal
Inorganic Chemistry 
ISSN
0020-1669
Language
English

Reference

Citations


Social Media