Coordination diversity in tin compounds with bis(benzoxazole)phenol as a polydentate ligand: Synthesis and crystal structure studies
The reaction of 2,6-bis(benzoxazolyl)-4-tert-butylphenol (HL) with [nBuxSnCl4−x] (x = 0, 1) in 1:1 stoichiometry yielded the tin coordination complexes [(HL)SnnBuxCl4−x] [x = 0 (1); x = 1 (2)]. Deprotonation of HL was performed using reagents having groups with high basicity such as nBuLi or [Sn{N(SiMe3)2}2]. These basic reagents prompted the coordination of the ligand in its anionic form, yielding the complexes [(thf)2Li(L)SnCl4] (3) and [(L)Sn{N(SiMe3)2}] (4), respectively. The molecular structure of HL displayed an intramolecular hydrogen bond OH—N and a planar arrangement of the bis(benzoxazolyl)phenolic system. In the molecular structures of both complexes containing HL an intramolecular hydrogen bond of NH—O type was also present. The coordination of the ligand in either neutral or anionic form is described by a κO,κN chelate mode toward Sn. All complexes displayed bis(benzoxazolyl)phenolic moieties close to planar; the least planar system was observed in 4 that was also studied by DFT methods.
