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Pure α‐Metallated Benzyllithium from a Single‐Crystal‐to‐Single‐Crystal Transition
Author(s) -
Tatic Tanja,
Hermann Stefanie,
John Michael,
Loquet Antoine,
Lange Adam,
Stalke Dietmar
Publication year - 2011
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201102068
Subject(s) - tetramer , crystal (programming language) , single crystal , crystallography , transition (genetics) , cannibalization , ligand (biochemistry) , toluene , chemistry , materials science , computer science , organic chemistry , business , biochemistry , enzyme , receptor , gene , programming language , industrial organization
Crystal cannibalization : In a solution‐mediated single‐crystal‐to‐single‐crystal transition the colorless starting material [{Me 2 N(CH 2 ) 2 OMe}⋅(LiCH 2 SiMe 3 )] 2 converts in toluene into yellow crystals of the benzyllithium tetramer [{Me 2 N(CH 2 ) 2 OMe}⋅(LiCH 2 C 6 H 5 )] 4 (see picture, microscope photograph of the transforming crystals). A straightforward convenient access to commercially interesting benzyllithium in ligand‐stabilized form is thus provided.

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