z-logo
Premium
Synthesis and Reactivity of a Silylalkyl Double Tuck‐in Uranium Metallocene [(η 5 :η 1 ‐C 5 Me 4 SiMe 2 CH 2 ) 2 U] and its Conversion to Bis(tethered) Metallocenes
Author(s) -
Evans William J.,
Siladke Nathan A.,
Ziller Joseph W.
Publication year - 2010
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.200902428
Subject(s) - reactivity (psychology) , metallocene , uranium , double bond , metallacycle , isocyanide , chemistry , crystallography , materials science , x ray crystallography , stereochemistry , polymer chemistry , physics , organic chemistry , metallurgy , polymerization , alternative medicine , pathology , polymer , medicine , diffraction , optics
Tuck in! CH bond activation involving two methyl groups in [(C 5 Me 4 SiMe 3 ) 2 UMe 2 ] generates a double tuck‐in uranium metallocene that allows UC bond reactivity to be studied in a tethered environment as shown here with isocyanide to make a bis(tethered iminoacyl) complex (see scheme).

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom