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1.
Chem Sci ; 14(11): 3018-3023, 2023 Mar 15.
Article in English | MEDLINE | ID: mdl-36937589

ABSTRACT

The reactivity of Cp*Ga (Cp* = C5Me5) towards phosphanylidenephosphoranes of the type ArTerP(PMe3) (ArTer = DipTer 2,6-(2,6-iPr2C6H3)2C6H3), TipTer 2,6-(2,4,6-iPr3C6H2)2C6H3 was investigated. While no thermal reaction was observed (in line with DFT results), irradiation at 405 nm at low temperatures resulted in the formation of phosphagallenes DipTerP = GaCp* (1a) and TipTerP = GaCp* (1b) accompanied by release of PMe3. When warming the reaction mixture to ambient temperatures without irradiation, the clean re-formation of ArTerP(PMe3) and Cp*Ga in a second-order reaction was observed. Upon removal of PMe3, 1a and 1b were isolated and fully characterized. Both derivatives were found to be labile and decomposed to the phosphafluorenes 2a and 2b, indicating generation of the transient phosphinidene ArTerP along with Cp*Ga. First reactivity studies show that CO2 and H2O cleanly reacted with 1a, affording DipTerPCO (3) and DipTerPH2 (4), respectively.

2.
Dalton Trans ; 47(13): 4433-4436, 2018 Mar 26.
Article in English | MEDLINE | ID: mdl-29492506

ABSTRACT

Since the heavy biradicals [E(µ-NTer)]2 (E = Sb, Bi) are only of fleeting existence in solution, they were generated in situ and trapped by [2 + 2] addition reactions utilizing alkynes such as tolan (Ph-C[triple bond, length as m-dash]C-Ph). The structure, biradical character and bonding of [E(µ-NTer)]2 biradicals as well as their addition products are discussed on the basis of computations and experimental data.

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