๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Substituent effects on the fluxional rearrangements and isomerization of indenyl silanes and stannanes

โœ Scribed by M.N. Andrews; P.E. Rakita; G.A. Taylor


Publisher
Elsevier Science
Year
1973
Tongue
French
Weight
156 KB
Volume
14
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

โœฆ Synopsis


Recent studies have shown that the monohqto indenyl compounds (I) of a number of main group and transition series metals exhibit dynanic intramolecular (fluxional) rearrangements.' In the case of the indenylsilanes (Ia) a kinetically slower hydrogen migration occurs, giving rise to non-fluxional positional isomers. 2 Fran the relatively low activation energies for the migrations and the demonstrated intramolecularity of the reactions, it has been proposed that the rearrangements proceed through transition states and/or intermediates which involve little if any charge separation during the migration process. 3 The transition state for rearrange-


๐Ÿ“œ SIMILAR VOLUMES


The Effects of Substituents on the Degen
โœ Lloyd M. Jackman; Errol Fernandes; Markus Heubes; Helmut Quast ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 726 KB

The activation parameters [โˆ†G (200 K), โˆ†H , and โˆ†S ] for compounds, together with those for related compounds previously reported in the literature, show that conjugating the degenerate Cope rearrangements of barbaralane (1a) and several semibullvalenes (3a, 7a, 8a), and for those of a subsituents (

Substituent and solvent effects on elect
โœ Shunsuke Kobayashi; Hiroshi Yokoyama; Hirotake Kamei ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 496 KB

The electronic absorption spectra of push-pull-substituted cis-azobenzenes were measured using a newly devised spectroscopic method. The solvent effect on the absorption spectra of cis-4-anilino-4'nitroazobenzene is interpreted in terms of a structural change involving the N-N-C angle. The results s

Influence of the size of upper and lower
โœ George Ferguson; Anna Notti; Sebastiano Pappalardo; Melchiorre F. Parisi; Anthon ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 271 KB

A comparative study on a series of penta-O-alkylated p-H-calix[5]arenes lb-e and p-tertbutylcalix[5]arenes lg-m shows that the former are inherently mobile and adopt in solution non-cone conformations. The 1,2-alternate conformation for penta-O-benzyl ether lc was proven by single-crystal X-ray anal