Functionalized alkynyl-chlorogermanes: hydrometallation, Ge-Cl bond activation, Ge-H bond formation and chlorine-tert-butyl exchange via a transient germyl cation.

Treatment of alkynyl-arylchlorogermanes ArylnGe(Cl)(C[triple bond, length as m-dash]C-(t)Bu)3-n (n = 1, 2) with HM(t)Bu2 (M = Al, Ga) yielded mixed Al or Ga alkenyl-alkynylchlorogermanes via hydrometallation reactions. Intramolecular interactions between the Lewis-basic Cl atoms and the Lewis-acidic Al or Ga atoms afforded MCGeCl heterocycles. The endocyclic M-Cl distances were significantly lengthened compared to the starting compounds and indicated Ge-Cl bond activation.

Germacyclobutenes: generation by 1,1-carbalumination or 1,1-carbagallation and their photophysical properties.

Aluminium- and gallium-functionalised alkenylalkynylgermanes, R(1) 2 Ge(C≡C-R(2) )[C{E(CMe3 )2 }=C(H)-R(2) ] (E=Al, Ga), exhibit a close contact between the coordinatively unsaturated Al or Ga atoms and the α-C atoms of the intact ethynyl groups. These interactions activate the Ge-C(alkynyl) bonds and favour the thermally induced insertion of these C atoms into the E-C(vinyl) bonds by means of 1,1-carbalumination or 1,1-carbagallation reactions. For the first time the latter method was shown to be a powerful alternative to known metallation processes.

Cooperative Ge-N Bond activation in aluminium-functionalised aminogermanes and spontaneous imine elimination via an intermediate germyl cation.

Hydrometallation of iPr2 N-Ge(CMe3 )(C≡C-CMe3 )2 with H-M(CMe3 )2 (M=Al, Ga) affords alkenyl-alkynylgermanes in which the Lewis-acidic metal atoms are not coordinated by the amino N atoms but by the α-C atoms of the ethynyl groups. These interactions result in a lengthening of the Ge-C bonds by approximately 10 pm and a comparably strong deviation of the Ge-CC angle from linearity (154.3(1)°).

CO2 and formate complexes of phosphine/borane frustrated Lewis pairs.

The reaction of a solution of B(C6F4H)3 and either iPr3P or tBu3P with CO2 afforded the species R3P(CO2)B(C6F4H)3 (R=iPr (1), tBu (2)). In a similar fashion the boranes, RB(C6F5)2 (R=hexyl, cyclohexyl (Cy), norbornyl), ClB(C6F5)2, or PhB(C6F5)2 were combined with tBu3P and CO2 to give the species tBu3P(CO2)BR(C6F5)2 (R=hexyl (3), Cy (4), norbornyl (5), Cl (6), Ph (7)). Similarly, the compounds [tBu3PH][RBH(C6F5)2] (R= hexyl (8), Cy (9), norbornyl (10)) were prepared by reaction of the precursor frustrated Lewis pair (FLP) with H2.