Isolation of Carbene-Stabilized Arsenic Monophosphide [AsP] and its Radical Cation [AsP]+. and Dication [AsP]2.
Adinarayana DoddiDirk BockfeldMarc-Kevin ZaretzkeThomas BannenbergMatthias TammPublished in: Chemistry (Weinheim an der Bergstrasse, Germany) (2019)
Arsenic monophosphide (AsP) species supported by two different N-heterocyclic carbenes were prepared by reaction of (IDipp)PSiMe3 (1) (IDipp=1,3-bis(2,6-diisopropylphenyl)imidazolin-2-ylidene) with (IMes)AsCl3 (2) (IMes=1,3-bis(2,4,6-trimethylphenyl)imidazolin-2-ylidene) to afford the dichloride [(IMes)As(Cl)P(IDipp)]Cl (3), which upon reduction with KC8 furnished heteroleptic [(IMes)AsP(IDipp)] (4). The corresponding mono- and dications [(IMes)AsP(IDipp)][PF6 ], [5]PF6 , and [(IMes)AsP(IDipp)][GaCl4 ]2, [6][GaCl4 ]2 , respectively, were prepared by one-electron oxidation of 4 with ferrocenium hexafluorophosphate, [Fc]PF6, or by chloride abstraction from 3 with two equivalents of GaCl3 , respectively. Compounds 4-6 represent rare examples of heterodiatiomic interpnictogen compounds, and X-ray crystal structure determinations together with density functional theory (DFT) calculations reveal a consecutive shortening of the As-P bond lengths and increasing bond order, in agreement with the presence of an arsenic-phosphorus single bond in 4 and a double bond in 62+ . The EPR signal of the cationic radical [5]+. indicates a symmetric spin distribution on the AsP moiety through strong hyperfine coupling with the 75 As and 31 P nuclei.