Lead analogues of N-heterocyclic carbenes (NHPbs) are the least understood members of this increasingly important class of compounds. Here we report the design, preparation, isolation, structure, volatility, and decomposition pathways of a novel aliphatic NHPb: rac-N 2,N 3-di-tert-butylbutane-2,3-diamido lead(II) (1Pb). The large steric bulk of the tert-butylamido moieties and rac-butane backbone successfully hinder redox decomposition pathways observed for diamidoethylene and -ethane backbone analogues, pushing the onset of thermal decomposition from below 0 °C to above 150 °C. With an exceptionally high vapor pressure of 1 Torr at 94 ± 2 °C and excellent thermal stability among Pb(II) complexes, 1Pb is a promising precursor for the chemical vapor deposition (CVD) and atomic layer deposition (ALD) of functional lead-containing materials.

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Persistent URL dx.doi.org/10.1021/acs.inorgchem.8b00719
Journal Inorganic Chemistry
Citation
Bačić, G. (Goran), Zanders, D. (David), Mallick, B. (Bert), Devi, A. (Anjana), & Barry, S.T. (2018). Designing Stability into Thermally Reactive Plumbylenes. Inorganic Chemistry, 57(14), 8218–8226. doi:10.1021/acs.inorgchem.8b00719