Abstract:
Calixpyrroles are widely used as a neutral receptor for anion recognition, extraction and
transportation. They are also frequently used as a ligand for metal complexation in
organometallic chemistry. Depending on specific application and nature of guest molecules,
calixpyrrole was modified either at meso or β-pyrrole position. However modification is
always cumbersome and causes poor yield of the product. An easily available common mesosubstituted
calixpyrrole would be of great importance to achieve various customized
structures for specific interactions with different guest molecules. Substitution of alkyl chains
with a terminal double bond at the meso position of calixpyrrole would be a common precursor
for various modifications, where post functionalization of the terminal double bonds will aid
in synthesizing different calixlpyrrole with tunable cavities for specific interactions with
different guest molecules.
Chapter 1: Introduction
General accounts of calixpyrrole is narrated in first chapter. The synthetic strategy and the
modification of calixpyrrole for particular applications are described. In addition, the
overview of anion binding and metal complexation study are described.
Chapter 2: Perfluoroalkyl calix[4]pyrrole for extraction of fluoride ion from
aqueous media
Symmetrical alkenylcalix[4]pyrrole functions as common precursor for the synthesis of
various calixpyrrole with good yield. Incorporation of perfluoroalkyl groups [CF3(CF2)n-1,
abbreviated as Rfn] at the terminal double bond creates hydrophobic environment inside the
calix[4]pyrrole cavity owing to the highly hydrophobic nature of perfluoroalkyl chains.
Hofmeister biased anions like fluoride remain highly solvated in aqueous solutions, having a
very high hydration energy. Once the hydrated F
- interacts via hydrogen bonds in the calix
cavity, the hydration shell is broken by the hydrophobic environment of perfluoroalkyl chains
(Rfn). Then, the interaction between calix-NH and F
- depends only on charge density of the
anion without the hydration shell and overcomes the Hofmeister biasness and separates the
perfluoroalkylcalixpyrrole-fluoride ion complex as droplets from aqueous media. Chapter 3: Dipyrromethane and calixpyrrole embedded perfluoro copolymer for
rapid removal of perfluoro pollutants from water
The perfluoro pollutants like perfluorooctanoic acid (CF3(CF2)6COOH; PFOA) and perfluoro
octane sulfonate (PFOS) are generated from degradation of fluoropolymers and a diverse
collection of consumer goods ranging from pizza boxes to stain-resistant carpets to teflon
pans. Due to extensive use of perfluoro products, every year huge amount of perfluoro
chemicals are disposed to the environment. We have reported dipyrromethane embedded perfluoro copolymer which reduced more than
80% PFOA in a short time span of h from the industrial disposal site relevant concentration
with very high adsorption kinetics of 9.18×104 g mg-1 min-1.
Chapter 4: Metal alkenylcalixpyrrole towards ring closing metathesis
The peripheral olefin functionality of calixpyrrole could be activated by coordinating with
metals. The olefin moieties from alternate meso-posiiton of calixpyrrole undergoes ring
closing oolefin metathesis by [Ru(COD)Cl2]n. Ring closing olefin metathesis between olefin
moieties from alternate meso-positions by ruthenium complex is possible if calix[4]pyrrole adopts puckered conformation. Puckering of calix[4]pyrrole is feasible if metal is
incorporated inside the calix[4]pyrrole cavity. The ring closing olefin metathesis from
alternate meso-position is unable if metal is inhibited to incorporate inside the calixpyrrole
core.
Chapter 5: Summary and future perspective
Meso-substituted olefin and hydroxyl functionalized calixpyrroles were functionalized for
desire applications. Perfluoroalkyl calixpyrrole has been used to extract fluoride ion from
aqueous media. Dipyrro and perfluorocalixpyrrole embedded polymer has been employed to
remove perfluorooctanoic acid, an emerging perfluoro pollutant from water. The synthesized
calixpyrrole could be an effective ionophore in ion selective electrode (ISE). Additionally,
metal coordinated alkenylcalixpyrrole has been used to construct new C-C bond via cross
olefin metathesis.