New organotin(IV) ascorbates: synthesis, spectral characterization, biological and potentiometric studies

被引:17
|
作者
Nath, M [1 ]
Jairath, R
Eng, G
Song, XQ
Kumar, A
机构
[1] Indian Inst Technol, Dept Chem, Roorkee 247667, Uttar Pradesh, India
[2] Univ Dist Columbia, Dept Chem & Phys, Washington, DC 20008 USA
[3] LLRM Med Coll, Dept Pharmacol, Meerut 250004, Uttar Pradesh, India
关键词
L-ascorbic acid; organotin(IV); potentiometric; anti-inflammatory agent; cardiovascular; Mossbauer;
D O I
10.1016/j.saa.2004.03.018
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
New organotin(TV) ascorbates of the general formulae R3Sn(HAsc) (where R = Me, n-Pr, n-Bu and Ph) and R2Sn(Asc) (where R = n-Bu and Ph) have been synthesized by the reaction of RnSnCl4-n (where n = 2 or 3) with inonosodiUln-L-ascorbate. The bonding and coordination behaviour in these complexes are discussed on the basis of UV-Vis, IR, Far-IR, H-1 and C-13 NMR, and Sn-119 Mossbauer spectroscopic studies. L-Ascorbic acid acts as a monoanionic bidentate ligand in R3Sn(HAsc) coordinating through O(1) and O(3). The Mossbauer studies together with IR and NMR studies suggest that for these polymeric derivatives, the polyhedron is trigonal bipyramidal around tin with three organic groups in the equatorial positions. In R2Sn(AsC), L-ascorbic acid acts as dianionic tetradentate ligand and a polymeric structure with octahedral geometry around tin with trans organic groups has been tentatively proposed. The complexes have been assayed for their anti-inflammatory and cardiovascular activity. Ph2Sn(Asc) has been found to show the highest activity among the studied complexes. It is suggested on the basis of potentiometric studies of Me2Sn(IV) and Me3Sn(IV) systems with L-ascorbic acid that under physiological conditions (PH = 7.0) Me2Sn(HAsc)(OH) (similar to60%), Me2Sn(OH)(2) (similar to40%) and Me3Sn(HAsc) (similar to60%), Me3Sn(OH) (similar to40%), respectively, are existing, which may be responsible for their biological activities. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:77 / 86
页数:10
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