were performed under a nitrogen atmosphere using
standard Schlenk techniques. Solvents were dried using a column solvent
purification system.75 (link) Me3SiCl
(95%), GeCl4 (>98%), KOtBu (>98%),
ClCOMes
(99%), ClCO(oTol) (98%), C6H4-1-4–(COCl)2 (>99%), C6H4-1-3–(COCl)2 (>99%), Br(CH2)4Br (99%), MeI (>99%) and [18]-crown-6 (99%), toluene (≥99%),
toluene-d8 (99 atom % D), THF-d8 (99.5 atom % D), CDCl3 (99.8 atom % D), butyl acrylate
(≥99%), styrene (≥99%), and methyl methacrylate (99%)
were used without any further purification. Tetrakis(trimethylsilyl)germane,76 (link) tetraacylgermane
prepared according to published procedures.54 (link)1H, 13C, and 29Si NMR spectra
were recorded on either a Varian INOVA 300 spectrometer in C6D6, THF-d8, or CDCl3 solutions and referenced versus TMS using the internal 2H-lock signal of the solvent. HRMS spectra were run on a Kratos Profile
mass spectrometer. Infrared spectra were obtained on a Bruker Alpha-P
Diamond ATR Spectrometer from the solid sample. Melting points were
determined using a Stuart SMP50 apparatus and are uncorrected. Elemental
analyses were carried out on a Hanau Vario Elementar EL apparatus.
UV absorption spectra were recorded on a PerkinElmer Lambda 5 spectrometer.