Abstract
SnO is a rare example of a stable p-type semiconductor material. Here, we describe the synthesis and characterisation of a family of Sn(ii) pyrrolide complexes for future application in the MOCVD and ALD of tin containing thin films. Reaction of the Sn(ii) amide complex, [{(Me3Si)2N}2Sn], with the N,N-bidentate pyrrole pro-ligand, L1H, forms the hetero- and homoleptic complexes [{L1}Sn{N(SiMe3)2}] (1) and [{L1}2Sn] (2), respectively, bearing the 2-dimethylaminomethyl-pyrrolide ligand (L1). Reaction of [{(Me3Si)2N)}2Sn] with the pyrrole-aldimine pro-ligands, L2H-L7H, results in the exclusive formation of the homoleptic bis-pyrrolide complexes [{L2-7}2Sn] (3-8). All complexes have been characterised by elemental analysis and NMR spectroscopy, and the molecular structures of complexes 1-5 and 8 are determined by single crystal X-ray diffraction. TG analysis and isothermal TG analysis have been used to evaluate the potential utility of these systems as MOCVD and ALD precursors.
Highlights
Transparent semiconducting oxide (TSO) thin films have attracted considerable interest due to their omnipresence in modern technology, finding wide-spread application in solar cells, light emitting diodes, flat panel displays, optical communicators, gas sensors and thin film transistors.[1]
In all cases, isolated products were characterised by solution state NMR (1H, 13C and 119Sn) spectroscopy and elemental analysis
Reactions did result in the formation of bis( pyrrolide) compounds 2–8
Summary
Transparent semiconducting oxide (TSO) thin films have attracted considerable interest due to their omnipresence in modern technology, finding wide-spread application in solar cells, light emitting diodes, flat panel displays, optical communicators, gas sensors and thin film transistors.[1]. The asymmetric unit cell contains a single monomeric complex with a three coordinate, pseudo-trigonal-pyramidal geometry about the Sn(II) centre, with the {L1}− ligand coordinated in a κ2 fashion via the pyrrolide nitrogen and the pendant {NMe2} group, as well as the nitrogen of the {HMDS} ligand, in a terminal bonding mode (Fig. 2).
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