Publications associées à Tert-Butyllithium

Rotational disorder in lithium borohydride

LiBH4 has been discussed as a promising hydrogen storage material and as a solid-state electrolyte in lithiumion batteries. It contains 18.5 wt% hydrogen and undergoes a structural phase transition at 381K which is associated with a large increase in rotat ...

E D P Sciences2015

Molecular wiring of LiMnPO4 (olivine) by ruthenium(II)-bipyridine complexes

Michael Graetzel, Shaik Mohammed Zakeeruddin, Ladislav Kavan

LiMnPO4 (olivine) was surface-modified by two different complexes: Ru-bis(4,4'-diethoxycarbonyl-2,2'-bipyridine)(4,4'-dicarboxylate-2,2'-bipyridine) and Ru-bis(4-carboxylic acid-4'-carboxylate-2,2'-bipyridine)(4,4'-dinonyl-2,2'bipyridine). These complexes ...

Elsevier2009

The abnormal behavior of an atropisomer: 3,3'-dibromo-1,1'-difluoro-2,2'-binaphthyl reacting with alkyllithium compounds

Giuseppe Mangano

1-Fluoro-2-(triethylsilyl)naphthalene and other 1-fluoronaphthalene derivs. bearing a metalation-resistant substituent at the 2-position proved to be totally inert toward base attack. 3-Bromo-1-fluoronaphthalene, readily prepd. from a 2-bromo isomer by dep ...

2005

Meta- rather than ortho-directed metalations: Buttressing effects prejudicing the proton abstraction from (2,6-dihalophenyl)silanes

Christophe Heiss, Fabrice Cottet

(2,6-Dichlorophenyl)trimethyl- and -triethylsilane exhibit untypical reactivity patterns toward strong bases. When treated at -100 DegC with lithium 2,2,6,6-tetramethylpiperidide, they give rise to two, with sec- or tert-butyllithium even three, different ...

2005

The metalation of 1- and 2-(trifluoromethyl)naphthalenes: Noteworthy site selectivities

Fabrice Cottet

This article provides insight into the various factors by which electroneg. substituents affect the kinetic acidity of arenes and, more specifically, naphthalenes. Both 1- and 2-(trifluoromethyl)naphthalenes were consecutively treated with an organometalli ...

Georg Thieme Verlag2005

Buttressing effects responsible for the meta-deprotonation of trialkylsilyl-substituted haloarenes by organometallic reagents : an unprecedented phenomenon

Christophe Heiss

(2,6-Dichlorophenyl)trimethyl- and triethylsilane exhibit untypical reactivity patterns toward strong bases: when treated at -100 °C with lithium 2,2,6,6-tetramethylpiperidide two, with sec- or tert-butyllithium even three organometallic intermediates are ...

EPFL2005