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Issue 42, 2014
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Reactivity of boryllithium with AlMe3, AlEt3, and GaMe3, including the synthesis of a lanthanum heterogallate complex

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Abstract

Treatment of boryllithium (THF)2Li[B(NDippCH)2] (Dipp = 2,6-diisopropylphenyl) with various amounts of AlMe3 or GaMe3 leads to the formation of inter group 13 compounds. Equimolar reactions result in ate complexes of the type (THF)nLi(Me3M)[B(NDippCH)2] (M = Al, Ga) with discrete (n = 2, 3) or eight-membered ring structures (n = 1). We reported previously that use of excessive amounts of group 13 metal methyl compounds can result in four-coordinate THF-adducts (THF)(Me2M)[B(NDippCH)2] or unsolvated complexes {(Me2M)[B(NDippCH)2]}x (M = Al, x = 2; M = Ga, x = 1) via separation of LiMMe4. Polymeric [(THF)Li(Et3Al){B(NDippCH)2}]n is formed when boryllithium is reacted with an equimolar amount of AlEt3. The discrete THF-adduct (THF)Et2Al[B(NDippCH)2] can be isolated when using a boryllithium/AlEt3 ratio of 1 : 5. The reaction of THF-adduct (THF)Me2Ga[B(NDippCH)2] with La(AlMe4)3 affords the heterogallate complex La[(Me3Ga){B(NDippCH)2}]3, according to a donor-assisted tetramethylaluminate/alkylgallate exchange. The obtained complexes feature rare examples of crystallographically characterized non-cluster compounds with unsupported B–Al and B–Ga contacts.

Graphical abstract: Reactivity of boryllithium with AlMe3, AlEt3, and GaMe3, including the synthesis of a lanthanum heterogallate complex

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Supplementary files

Article information


Submitted
16 Jul 2014
Accepted
28 Aug 2014
First published
28 Aug 2014

Dalton Trans., 2014,43, 15760-15770
Article type
Paper

Reactivity of boryllithium with AlMe3, AlEt3, and GaMe3, including the synthesis of a lanthanum heterogallate complex

N. Dettenrieder, C. Schädle, C. Maichle-Mössmer and R. Anwander, Dalton Trans., 2014, 43, 15760
DOI: 10.1039/C4DT02155J

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