Abstract
The reaction of the tripod ligand hydrotris(
N
-(2-methylphenyl)-2-thioimidazol-1-yl)borate,
Tt
with zinc(II) chloride yielded the chloro complex [
Tt
Zn–Cl]
1
. The hydrolytic reactivity of its hydroxo complex [
Tt
Zn–(μ-OH)Zn
Tt
]Cl
2
towards
p
-nitrophenyl acetate was hampered due to the formation of the stable phenolate complex [
Tt
Zn–O–Ar–
p
-NO
2
]
3
as a product inhibition. The X-ray structure analysis of complex
3
was determined and showed that its Zn[S
3
O] coordination sphere includes three thione donors from the ligand
Tt
and one oxygen donor from the hydrolysed product
p
-nitrophenolate in an ideally tetrahedral arrangement around the zinc(II) centre.