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Issue 15, 2018
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Facile reactions of gold(I) complexes with tri(tert-butyl)azadiboriridine

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Direct structural evidence for group 11 metal-mediated B–B bond activation was obtained from reactions of tri(tert-butyl)azadiboriridine (1) with AuCl(L) complexes. The AuCl(SMe2) reaction afforded [η2-B,B-B(tBu)N(tBu)B(tBu)]AuCl (2) by ligand displacement. More donating phosphines as co-ligands led to B–B bond cleavage accompanied by either halide or L migration to form boron–gold complexes 3 (L = PPh3) and 4 (L = PMe3). A similar product 5, which is isostructural to 4, was obtained by the addition of dimethylaminopyridine (DMAP) to 2–4. Complexes 2–5 constitute rare examples of metal complexes bearing two Lewis acidic centres. The effect of the boryl ligand was demonstrated in the formation of a gold(I) complex 6 bearing a 5-membered heterocycle from 3 and tert-butylisonitrile. Plausible reaction mechanisms that led to these complexes and their bonding situation were explored computationally at the DFT level.

Graphical abstract: Facile reactions of gold(i) complexes with tri(tert-butyl)azadiboriridine

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The article was received on 21 Feb 2018, accepted on 06 Mar 2018 and first published on 08 Mar 2018

Article type: Paper
DOI: 10.1039/C8DT00697K
Citation: Dalton Trans., 2018,47, 5181-5188
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    Facile reactions of gold(I) complexes with tri(tert-butyl)azadiboriridine

    R. Shang, S. Saito, J. O. C. Jimenez-Halla and Y. Yamamoto, Dalton Trans., 2018, 47, 5181
    DOI: 10.1039/C8DT00697K

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