๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Biocidal organotin compounds: Part 1. Preparation and characterization of triorganotin(IV) 4-pyridyl- and 2-pyrimidyl- thioacetates and the crystal structure of triphenyltin(2-pyrimidylthioacetate)

โœ Scribed by A. Chakrabarti; Sk. Kamruddin; T. K. Chattopadhyaya; A. Roy; B. N. Chakraborty; K. C. Molloy; E. R. T. Tiekink


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
584 KB
Volume
9
Category
Article
ISSN
0268-2605

No coin nor oath required. For personal study only.

โœฆ Synopsis


The preparation and spectroscopic characterization of [R3Sn(O2CCH,SC5H,N-4)], R = Ph, benzyl (Bz), cyclohexyl (c-Hex) and n-Bu, and of [R,Sn(02CCH2SC,H,N2-2,6)J, R =Me, Ph and n-Bu, are reported. The 2-pyrimidyl compounds feature trigonal bipyramidal tin centres with trans-R,SnO, geometries as was confirmed by X-ray crystallography for [Ph3Sn(02CCH2SC4H3N2-2,6].fi By contrast the 4pyridyl compounds have trigonal bipyramidal geometries in the solid state (arising from intermolecular Sn-.

.N interaction) and tetrahedral geometries in solution. The biocidal activity of these compounds against the fungi Helminthosporium muydis (ITCC 2675) and H. oryzue (ITCC 2537), both of which damage crops such as maize and rice, shows promise. Encouraging is the observation that the compounds show no adverse phytotoxicity at concentrations to M.


๐Ÿ“œ SIMILAR VOLUMES


Biocidal Organotin Compounds. Part 2. Sy
โœ S. K. Kamruddin; T. K. Chattopadhyaya; A. Roy; E. R. T. Tierkink ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 651 KB

The preparation and spectroscopic ('H NMR, UV and IR) characterization of three R,Sn(O,CCH,N(H)C(O)NH,) [R=Ph, c-Hex (cyclohexyl) or n-Bu] compounds are reported. A different mode of coordination is indicated for the hydantoate ligand in the R=Ph compound compared with the R=c-Hex and R=n-Bu compoun

Synthesis, characterization and crystal