Reactions of LiCHR2 and related lithium alkyls with alpha-H free nitriles and the crystal structures of eleven representative lithium 1,3-diazaallyls, 1-azaallyls and beta-diketiminates
Pb. Hitchcock et al., Reactions of LiCHR2 and related lithium alkyls with alpha-H free nitriles and the crystal structures of eleven representative lithium 1,3-diazaallyls, 1-azaallyls and beta-diketiminates, J CHEM S DA, (14), 2000, pp. 2301-2312
Citations number
46
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS
Reactions between bis(trimethylsilyl)methyllithium LiCHR2 and a nitrile R'C
N gave lithium 1-azaallyls, beta-diketiminates or 1,3-diazaallyls. The prod
ucts of related processes involving the lithium alkyl LiCH2R, LiCH(R)Ph or
[Li(tmen)](2)[1,2-{C(H)R}(2)C6H4] have also been obtained (R = SiMe3 and R'
= Bu-t, Ph or C6H4Me-4). Analytical and spectroscopic data served to ident
ify the following crystalline compounds: [Li{N(R)C(Bu-t)C(H)R}(D)](n) [D ab
sent and n = 2; D = tmen or dme and n = 1], [Li{N(R)C(Ph)C(H)R}(D)](n) [D =
tmen or pmdien and n = 1, or D = thf and n = 2], [Li{N(R)C(Ph)C(H)C(R ")NR
}(D)](n) [D absent, n = 2 and R " = Ph (4a), C6H4Me-4 (4b) or Bu-t; or D =
tmen, (thf)(2) (9b), NEt3 or thf and NCPh and n=1 and R " = Ph], [Li{N(R)C(
Ph)C(H)C(Ph)NR}(D)Li(CHR2)] [D = OEt2 or thf], [Li{N(R)C(Ar)NC(Ph)=C(H)R}(D
)](n) [D = tmen, n = 1 and Ar = Ph or C6H4Me-4; or D = thf, n = 2 and Ar =
Ph], [Li{N(Ph)C(R)NC(Ph)=C(H)R}(tmen)], [Li{N(R)C(Bu-t)CH2](2), [Li{N(R)C(P
h)=C(H)Ph}(tmen)], and [Li(tmen)](2)[1,2-{N(R)C(Bu-t)CH}(2)C6H4]. Each of t
he three classes of ligands has a diversity of ligating possibilities, func
tioning towards lithium variously in a terminal or bridging and mono- or bi
-dentate fashion, the role of a neutral donor D often being crucial. For an
isomeric pair, the lithium beta-diketiminate was thermodynamically preferr
ed over the 1,3-diazaallyl. From [Li{N(R)C(Bu-t)C(H)R}](2) and successively
CH2Br2 and LiBun, the further lithium 1-azaallyl compound [Li{N(R)C(Bu-t)C
(H)C(H)(R)Bu-n}](2) was obtained. From 4a and CH2Br2 or (BrCH2)(2) a bis(be
ta-diketiminyl)methane CH2[C{C(Ph)NR}C(Ph)N(H)R](2) or 9b or beta-diketimin
e HN(R)C(Ph)C(H)C(Ph)NR were obtained, while 4b with successively KOBut and
H2O gave the beta-diketimine HN(R)C(C6H4Me-4)C(H)C(C6H4Me-4)NR. Mechanisti
c pathways are proposed, which involve Me3Si migrations: from C to N or N t
o N; or, for the latter a 1,2-dyotropic Me3Si/H exchange. The crystal struc
tures of eleven of these compounds have been determined. Each of the new li
thium compounds may in principle behave as an N-, C-, (N,N')-, or (N,C)-cen
tred nucleophile. Reactions demonstrating the first two alternatives for th
e beta-diketiminate [Li{N(R)C(Ar)C(H)C(Ar)NR}](2) are (i) those with water
(Ar = C6H4Me-4) or (BrCH2)(2) (Ar = Ph) which gave the diketimine N(R)C(Ar)
C(H)C(Ar)N(H)R, whereas (ii) that with CH2Br2 (Ar = Ph) yielded CH2[C{C(Ph)
NR}C(Ph)N(H)R](2).