The ratio between the trans-trans and cis-trans isomers has been measured in the 2,2'-dithienyl ketyl and in its Li, Na, K and Cs complexes. The stability of the trans-trans conformation was found to increase with increasing size of the alkali counter-ion. This trend has been interpreted in terms of steric interaction between the cation and the atoms adjacent to the binding site. © 1974.

Influence of the size of the counter-ion on the conformational stability of the alkali metal complexes of 2,2'-dithienyl ketyl

Alberti A
1974

Abstract

The ratio between the trans-trans and cis-trans isomers has been measured in the 2,2'-dithienyl ketyl and in its Li, Na, K and Cs complexes. The stability of the trans-trans conformation was found to increase with increasing size of the alkali counter-ion. This trend has been interpreted in terms of steric interaction between the cation and the atoms adjacent to the binding site. © 1974.
1974
Istituto per la Sintesi Organica e la Fotoreattivita' - ISOF
Inglese
26
3
392
394
3
http://www.scopus.com/inward/record.url?eid=2-s2.0-49549159531&partnerID=q2rCbXpz
Sì, ma tipo non specificato
EPR spectroscopy; Alkali radical ion pairs; Size of the counter-ion
2
info:eu-repo/semantics/article
262
Pedulli, Gf; Alberti, A
01 Contributo su Rivista::01.01 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/314076
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