The synthesis and characterization of several m-terphenyl stabilized germylyne transition metal complexes and related metallogermylenes are reported. The reaction of Na[M(η 5 -C 5 H 5 )(CO) 3 ] (M = Cr, or W) with Ge(Cl)C 6 H 3 -2,6-Trip 2 (Trip = −C 6 H 2 -2,4,6-i-Pr 3 ) below room temperature affords the metallogermylenes (η 5 -C 5 H 5 )(CO) 3 M-G̈e-C 6 H 3 -2,6-Trip 2 (M = Cr, 1; W, 5 ). However, for the analogous reaction with Na[Mo(η 5 -C 5 H 5 )(CO) 3 ], the metallogermylene was not isolated. Instead, the germylyne complex (η 5 -C 5 H 5 )(CO) 2 Mo⋮Ge−C 6 H 3 -2,6-Trip 2 ( 3 ) was obtained directly with elimination of carbon monoxide. The corresponding chromium and tungsten compounds (η 5 -C 5 H 5 )(CO) 2 M⋮Ge−C 6 H 3 -2,6-Trip 2 (M = Cr, 2; W, 6 ) could be obtained by refluxing 1 or 5 in toluene or by photolysis. The related germylyne (η 5 -C 5 H 5 )(CO) 2 W⋮Ge−C 6 H 3 -2,6-Mes 2 ( 7 ), as well as the recently reported molybdenum analogue (η 5 -C 5 H 5 )(CO) 2 Mo⋮Ge−C 6 H 3 -2,6-Mes 2 ( 4 ), which was the first example of a triply bonded germanium species, are also described. All compounds were characterized by 1 H and 13 C NMR, UV−vis, and IR spectroscopy, and by C, H analysis. The X-ray crystal structures of 1 − 3, 5, and 7 have also been determined. The M⋮Ge (M = Cr, Mo, W) triple bonds in the germylynes are typically ca. 0.4 Å shorter than the M−Ge single bonds in the metallogermylenes. In addition, angles at germanium in the germylynes are nearly linear (range 170.9(3)−175.99(6)°) whereas in the metallogermylenes the corresponding angles are 114.7(6) and 117.8(2)°, consistent with the presence of a lone pair at germanium. The synthesis of the series of compounds 1 − 7 has enabled, for the first time, a comparison of single and triple bond lengths between closely related species involving the same coordination number and substituents at the heavier group 14 element.
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