scispace - formally typeset
S

Sneha Bajpe

Researcher at Katholieke Universiteit Leuven

Publications -  24
Citations -  1003

Sneha Bajpe is an academic researcher from Katholieke Universiteit Leuven. The author has contributed to research in topics: Metal-organic framework & Polyoxometalate. The author has an hindex of 14, co-authored 24 publications receiving 878 citations. Previous affiliations of Sneha Bajpe include Catholic University of Leuven & Symbiosis International University.

Papers
More filters
Journal ArticleDOI

Convenient synthesis of Cu3(BTC)2 encapsulated Keggin heteropolyacid nanomaterial for application in catalysis

TL;DR: Nanomaterial of Cu(3)(BTC)(2) (BTC = benzene tricarboxylic acid) incorporating Keggin heteropolyacid conveniently prepared at room temperature and recovered by freeze drying outperforms ultrastable Y zeolite in acid catalysed esterification reaction.
Journal ArticleDOI

Direct Observation of Molecular‐Level Template Action Leading to Self‐Assembly of a Porous Framework

TL;DR: This is a unique instance in which a templating mechanism that relies on specific molecular-level matching and leads to explicit nanoscale building units can be observed in situ during formation of the synthetic nanoporous material.
Journal ArticleDOI

Copper benzene tricarboxylate metal-organic framework with wide permanent mesopores stabilized by Keggin polyoxometallate ions.

TL;DR: This work shows the rational development of an hierarchical variant of the microporous cubic Cu(3)(BTC)(2) (BTC = 1,3,5-benzenetricarboxylate) HKUST-1 MOF having strictly repetitive 5 nm wide mesopores separated by uniformmicroporous walls in a single crystal structure.
Journal ArticleDOI

Stability improvement of Cu3(BTC)2 metal-organic frameworks under steaming conditions by encapsulation of a Keggin polyoxometalate.

TL;DR: Cu(3)(BTC)(2) with an incorporated Keggin polyoxometalate was demonstrated to be stable under steaming conditions up to 483 K, while the isostructural HKUST-1 degrades and transforms into [Cu(2)OH(BTC)(H( 2)O)](n)·2nH(1)O from 343 K onwards.
Journal ArticleDOI

Extreme Flexibility in a Zeolitic Imidazolate Framework: Porous to Dense Phase Transition in Desolvated ZIF‐4

TL;DR: The mechanism of the phase transition involves a cooperative rotation of imidazolate linkers resulting in isotropic framework contraction and pore space minimization and the energy of the new structure relative to those of the room temperature phase and ZIF-zni is established.