A COMPOUND WITH A TIN-CARBON DOUBLE-BOND, (2,4,6-TRIISOPROPYLPHENYL)(FLUORENYLIDENE)STANNANE - ASPECTS OF ITS REACTIVITY AND X-RAY STRUCTURE OF ITS DIMER
G. Anselme et al., A COMPOUND WITH A TIN-CARBON DOUBLE-BOND, (2,4,6-TRIISOPROPYLPHENYL)(FLUORENYLIDENE)STANNANE - ASPECTS OF ITS REACTIVITY AND X-RAY STRUCTURE OF ITS DIMER, Journal of organometallic chemistry, 458(1-2), 1993, pp. 49-56
(2,4,6-triisopropylphenyl)(fluorenylidene)stannane (1) reacts nearly q
uantitatively with compounds having active hydrogen atoms (alcohols, a
mines, mineral acids, phenylacetylene) and with lithium aluminium hydr
ide to give the corresponding stannanes. Methyl iodide also adds easil
y to the tin-carbon double bond. Compound 1 slowly dimerizes at room t
emperature in solution. The head-to-tail dimer 10 has been structurall
y characterized by X-ray analysis which reveals long intracyclic Sn-C
bonds (2.288(4) to 2.293(5) angstrom) and a planar four-membered ring.