Fluorophenylantimony carboxylates. 1. Synthesis and spectroscopic (UV, IR,H-1 and F-19 NMR) studies of some new monofluoro- and pentafluorophenylantimony(III and V) derivatives of 2-methoxybenzoic acid
Sk. Shukla et al., Fluorophenylantimony carboxylates. 1. Synthesis and spectroscopic (UV, IR,H-1 and F-19 NMR) studies of some new monofluoro- and pentafluorophenylantimony(III and V) derivatives of 2-methoxybenzoic acid, SYN REAC IN, 30(5), 2000, pp. 909-919
Citations number
19
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
SYNTHESIS AND REACTIVITY IN INORGANIC AND METAL-ORGANIC CHEMISTRY
A series of new mono- and pentafluorophenylantimony(III and V) arylcarboxyl
ates of the type ArnSb(OOCC6H4OCH3-2)(3-n) and Ar3Sb(OOCC6H4OCH3-2)(2) (Ar
= p-FC6H4-, m-FC6H4- and C6F5-, n =1 or 2) have been synthesized by the rea
ction of fluorophenylantimony (III or V) chlorides and the sodium salt of 2
-methoxybenzoic acid in the presence of 15-crown-5 as phase transfer cataly
st. A representative compound, namely trimethylantimony(V) bis(2-methoxyben
zoate) has also been synthesized for the sake of spectral comparisons. The
van't Hoff factor 'i' and molar conductance data of the compounds revealed
them to be monomeric and non-conducting in nature. The compounds were chara
cterised by the usual physicochemical techniques e.g., elemental analyses,
UV, IR and NMR (H-1, C-13 and F-19). Compound (III-VIII) are tentatively as
signed as a trigonal bipyramidal structure in which the 2-methoxybenzoate a
cted as monodentate ligand.