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Monojit Mitra

Researcher at Jadavpur University

Publications -  13
Citations -  669

Monojit Mitra is an academic researcher from Jadavpur University. The author has contributed to research in topics: Supramolecular chemistry & Hydrogen bond. The author has an hindex of 9, co-authored 12 publications receiving 573 citations.

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Molecular architecture using novel types of non-covalent π-interactions involving aromatic neutrals, aromatic cations and π-anions

TL;DR: In this article, a solid-state complex utilizing non-covalent interactions between two aromatic cations is synthesized and characterized, and the X-ray study of the structure shows that the anion templated π+−π+ interactions are the major driving force in the crystal packing.
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A successive layer-by-layer assembly of supramolecular frameworks driven by a novel type of face-to-face π+–π+ interactions

TL;DR: The solid-state complex [PTPH3]-NO3)3·2(HNO3] (1) has been synthesized and characterized by X-ray studies, where PTPH-3 is the triply protonated form of 4′-(4-pyridyl)-2,2′:6′, 2′′-terpyridine (PTP).
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Experimental and Computational Study of Counterintuitive ClO4–···ClO4– Interactions and the Interplay between π+–π and Anion···π+ Interactions

TL;DR: In this paper, the authors used noncovalent interactions between the charged and neutral aromatic rings and with anions to design the solid-state assembly of triply protonated PTPH3 (PTP = 4′-(4-pyridyl)-3,2′:6′,3″-terpyridine) with H2O and three ClO4−, which is synthesized and characterized by single-crystal X-ray diffraction analysis.
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3-Picoline Mediated Self-Assembly of M(II)–Malonate Complexes (M = Ni/Co/Mn/Mg/Zn/Cu) Assisted by Various Weak Forces Involving Lone Pair−π, π–π, and Anion···π–Hole Interactions

TL;DR: Five M(II)-malonate complexes having a common formula have been synthesized and their crystal structures have been determined and the lone pair-π and π-π noncovalent interactions have been analyzed by means of DFT calculations, mainly focusing on the influence of the coordinating metal on the strength of the interactions and the interplay between hydrogen bonding and ρ-interactions.
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pH Dependent Formation of Unprecedented Water–Bromide Cluster in the Bromide Salts of PTP Assisted by Anion−π Interactions: Synthesis, Structure, and DFT Study

TL;DR: In this paper, two terpyridine derivatives [PTPH3](Br)3·3H2O (1) and [PORH3]-Br3)(Br)2·H 2O (2), (PTP = 4′-(4-pyridyl)-2,2′:6′,2″-terpyrine) were synthesized and characterized by single crystal X-ray diffraction analyses.