Synthesis and binding pattern of Calix[4]Pyrrole compounds
نویسنده
چکیده
In this short review, focus has been on the improvisations in the synthetic procedures of the Calix[4] pyrrole type compounds, since their first discovery in the year 1886 and subsequent discussion on their binding pattern towards different chemical species. Calix[4] pyrrole, which is an analogue of hetero calixarenes, is the representative of a group of macrocycles. It has an ability to bind neutral and anionic species. The selectivity towards guest species emerges from the energetics and conformational features of this compound. Different structural modifications and fuctionalizations have been incorporated in the parent Calix[4] pyrrole moiety in order to achieve better selectivity.
منابع مشابه
Syntheses of calix[4]pyrroles by amberlyst-15 catalyzed cyclocondensations of pyrrole with selected ketones.
A facile and efficient protocol is reported for the synthesis of calix[4]pyrroles and N-confused calix[4]pyrroles in moderate to excellent yields by reaction of dialkyl or cycloalkyl ketones with pyrrole catalyzed by reusable Amberlyst(TM)-15 under eco-friendly conditions.
متن کاملCreated Using the Rsc Communication Template (ver. 2.1) - See Www.rsc.org/electronicfiles for Details
Calix[4]pyrroles such as meso-octamethylcalix[4]pyrrole 1 have been extensively studied as anion and ion-pair receptors over recent years. Subsequently ‘strapped’ calix[4]pyrroles, pioneered by Lee and Sessler, have been synthesised that contain a single linker between distal meso-positions. These compounds have increased 15 affinity for anions relative to the parent macrocycle. Recently there ...
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تاریخ انتشار 2015