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Read e-book online Alkoxo and Aryloxo Derivatives of Metals PDF

By Don Bradley, R. C. Mehrotra, Ian Rothwell, A. Singh

ISBN-10: 0121241408

ISBN-13: 9780121241407

This article relies on steel Alkoxides (Academic Press, 1978), and has been up-to-date and extended to incorporate advancements during this transforming into box from the previous two decades. insurance comprises homometallic alkoxides; heterometallic alkoxides; x-ray crystal buildings of alkoxo steel compounds; steel oxo-alkoxides; steel aryloxides; and their commercial purposes in such parts as microelectronics, ceramics, non-linear optical fabrics, high-temperature superconductors, and really expert glasses. meant as a reference for these operating within the box, in addition to to be used as a supplementary textual content for complex inorganic chemistry classes.

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Extra resources for Alkoxo and Aryloxo Derivatives of Metals

Example text

7 By Exchange Reactions (J-7) Exchange reactions between two different metal chlorides and alkoxides have been employed for the synthesis of a wide variety of homo- and heteroleptic metal alkoxides. For example, Bradley and Hill426 observed that a mixture of excess titanium tetrachloride and silicon dichloride diethoxide at 0Ž C deposited a crystalline product which was characterized as titanium trichloride monoethoxide: TiCl4 C SiCl2 OEt ! 163). TiCl4 C SiCl OEt 3 ! TiCl3 OEt C SiCl2 OEt TiCl4 C Si OEt 4 !

P. 9Ž C). Using this modified technique, it is now possible to prepare mixed alkoxides also by taking the reactants in the desired stoichiometric ratios: M(OEt)x C nCH3 COOR ! 98 As stated earlier, the method has been extended for the preparation of alkoxides and mixed alkoxides of a large number of metals. However, Mehrotra and Srivastava327 made the interesting observation that boron alkoxides do not appear to undergo transesterification reactions at all, although they do undergo alcoholysis reactions.

274 and Mehrotra,305 however, made the interesting observation that zirconium methoxide, after prolonged refluxing with excess tert-butyl alcohol274 or tert-amyl alcohol305 in the presence of benzene, finally yielded monomethoxide tri-tert-alkoxide only: Zr(OMe)4 C 3Rt OH (excess) ! 88 where Rt D tert-butyl or tert-amyl. The final product was found to be a stable dimeric species [ Rt O 3 Zr OMe 2 Zr ORt 3], which did not undergo further alcoholysis for steric reasons. In the light of the above factors, the alcoholysis reactions of a few metal alkoxides may be briefly summarized.

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Alkoxo and Aryloxo Derivatives of Metals by Don Bradley, R. C. Mehrotra, Ian Rothwell, A. Singh


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