TY - JOUR
T1 - Solid state and solution studies of lithium tris(n-butyl)magnesiates stabilised by Lewis donors
AU - Zaragoza-Calero, Silvia
AU - Francos, Javier
AU - Kennedy, Alan R.
AU - O'Hara, Charles T.
PY - 2015/3/9
Y1 - 2015/3/9
N2 - Several Lewis base adducts of the synthetically important lithium tris(n-butyl)magnesiate LiMg(nBu)3 have been prepared and structurally characterised. The complexes were prepared by a co-complexation approach i.e., by combining the monometallic nBuLi and nBu2Mg reagents in hydrocarbon solution before adding a molar equivalent of a donor molecule (a bidentate amine, tridentate amine or cyclic ether). The lithium magnesiates all adopt variants of the "Weiss motif" structure, i.e., contacted ion pair dimers with a linear arrangement and metals connected by butyl anions, where tetrahedral magnesium ions are in the central positions and the lithiums occupy the outer region, solvated by a neutral Lewis donor [(donor)Li([small mu ]-nBu)2Mg([small mu ]-nBu)2Mg([small mu ]-nBu)2Li(donor)]. When TMPDA, PMDETA or (R,R)-TMCDA [TMPDA = N,N,N[prime or minute]N[prime or minute]-tetramethylpropanediamine; PMDETA = N,N,N[prime or minute],N[prime or minute][prime or minute],N[prime or minute][prime or minute]-pentamethyldiethylenetriamine; and (R,R)-TMCDA = (R,R)-N,N,N[prime or minute],N[prime or minute]-tetramethylcyclohexane-1,2-diamine], are employed, dimeric tetranuclear lithium magnesiates are produced. Due to the tridentate nature of the ligand, the PMDETA-containing structure (2) has an unusual 'open'-motif. When TMEDA (TMEDA = N,N,N[prime or minute],N[prime or minute]-tetramethylethylenediamine) is employed, a n-butoxide-containing complex [(TMEDA)Li([small mu ]-nBu)([small mu ]-OnBu)Mg2(nBu)2([small mu ]-nBu)([small mu ]-OnBu)Li(donor)] has been serendipitously prepared and adopts a ladder conformation which is commonly observed in lithium amide chemistry. This complex has also been prepared using a rational methodology. When 1,4-dioxane is employed, the donor stitches together a polymeric array of tetranuclear dimeric units (6). The hydrocarbon solution structures of the compounds have been characterised by 1H, 7Li, 13C NMR spectroscopy; 2 has been studied by variable temperature and DOSY NMR.
AB - Several Lewis base adducts of the synthetically important lithium tris(n-butyl)magnesiate LiMg(nBu)3 have been prepared and structurally characterised. The complexes were prepared by a co-complexation approach i.e., by combining the monometallic nBuLi and nBu2Mg reagents in hydrocarbon solution before adding a molar equivalent of a donor molecule (a bidentate amine, tridentate amine or cyclic ether). The lithium magnesiates all adopt variants of the "Weiss motif" structure, i.e., contacted ion pair dimers with a linear arrangement and metals connected by butyl anions, where tetrahedral magnesium ions are in the central positions and the lithiums occupy the outer region, solvated by a neutral Lewis donor [(donor)Li([small mu ]-nBu)2Mg([small mu ]-nBu)2Mg([small mu ]-nBu)2Li(donor)]. When TMPDA, PMDETA or (R,R)-TMCDA [TMPDA = N,N,N[prime or minute]N[prime or minute]-tetramethylpropanediamine; PMDETA = N,N,N[prime or minute],N[prime or minute][prime or minute],N[prime or minute][prime or minute]-pentamethyldiethylenetriamine; and (R,R)-TMCDA = (R,R)-N,N,N[prime or minute],N[prime or minute]-tetramethylcyclohexane-1,2-diamine], are employed, dimeric tetranuclear lithium magnesiates are produced. Due to the tridentate nature of the ligand, the PMDETA-containing structure (2) has an unusual 'open'-motif. When TMEDA (TMEDA = N,N,N[prime or minute],N[prime or minute]-tetramethylethylenediamine) is employed, a n-butoxide-containing complex [(TMEDA)Li([small mu ]-nBu)([small mu ]-OnBu)Mg2(nBu)2([small mu ]-nBu)([small mu ]-OnBu)Li(donor)] has been serendipitously prepared and adopts a ladder conformation which is commonly observed in lithium amide chemistry. This complex has also been prepared using a rational methodology. When 1,4-dioxane is employed, the donor stitches together a polymeric array of tetranuclear dimeric units (6). The hydrocarbon solution structures of the compounds have been characterised by 1H, 7Li, 13C NMR spectroscopy; 2 has been studied by variable temperature and DOSY NMR.
KW - Lewis base aluminate
KW - lithium tetrahydroborate–tetramethylethylenediamine
KW - bidentate amine
KW - tridentate amine
KW - cyclic ether
KW - Weiss motif
UR - http://pubs.rsc.org/en/journals/journalissues/dt
U2 - 10.1039/C5DT00435G
DO - 10.1039/C5DT00435G
M3 - Article
SN - 1477-9226
VL - 44
SP - 7258
EP - 7267
JO - Dalton Transactions
JF - Dalton Transactions
IS - 16
ER -