Issue 3, 1984

Metal secondary amides derived from the highly hindered 2,4,6-tri-t-butylaniline; X-ray crystal structure of trans-[Li(µ-NHAr)(OEt2)]2(Ar = C6H2But3-2,4,6)

Abstract

Treatment of 2,4,6-tri-t-butylaniline (NH2Ar) with LiBun in OEt2 yields the white crystalline trans-[Li(µ-NHAr)(Oet2)]2, (2), which in turn furnishes the orange Sn(NHAr)2(with SnCl2) or a mixture of NiI/NiIIamides {using [Nil2(PPh3)2]} which with CO affords colourless crystalline cis-[Ni(Co)2(NHAr)2];the lithium amide(2) has a centrosymmetric four- membered planar LiNLiN ring with the substituents at N arranged in a transoid fashion: Li–N = 2.041(6) and 1.987(5)Å, Li–O = 1.906(5)Å, and ∠NLiN = 102.2(2)°

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 148-149

Metal secondary amides derived from the highly hindered 2,4,6-tri-t-butylaniline; X-ray crystal structure of trans-[Li(µ-NHAr)(OEt2)]2(Ar = C6H2But3-2,4,6)

B. <img border="0" src="https://www.rsc.org/images/entities/char_0043_0323.gif" alt="[C with combining dot below]" xmlns="http://www.rsc.org/schema/rscart38" />etinkaya, P. B. Hitchcock, M. F. Lappert, M. C. Misra and A. J. Thorne, J. Chem. Soc., Chem. Commun., 1984, 148 DOI: 10.1039/C39840000148

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