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Ejabul Mondal

Researcher at National Taiwan University

Publications -  46
Citations -  1246

Ejabul Mondal is an academic researcher from National Taiwan University. The author has contributed to research in topics: Ammonium bromide & Catalysis. The author has an hindex of 20, co-authored 46 publications receiving 1182 citations. Previous affiliations of Ejabul Mondal include Indian Institute of Technology Guwahati & Bar-Ilan University.

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Incorporation of a CN group into mCP: a new bipolar host material for highly efficient blue and white electrophosphorescent devices

TL;DR: In this article, a novel bipolar host material mCPCN has been designed and synthesized by incorporating the electron-accepting CN group into the well-known benchmark host materialmCP, which significantly improves thermal/morphological stabilities and increases the electron affinity.
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Fluorene‐Based Asymmetric Bipolar Universal Hosts for White Organic Light Emitting Devices

TL;DR: In this paper, two new bipolar host molecules composed of holetransporting carbazole and electron-transporting cyano (CzFCN) or oxadiazole-substituted fluorenes are synthesized and characterized.
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A dicarbazole–triazine hybrid bipolar host material for highly efficient green phosphorescent OLEDs

TL;DR: In this article, a bipolar host material 9-(4,6-diphenyl-1,3,5-triazin-2-yl)-9′-phenyl-3,3′-bicarbazole (CzT) comprising a dicarazole donor linking to an electron deficient 1, 3, 5-triazine acceptor was synthesized and characterized, allowing the spatial separation of HOMO and LUMO on the donor and acceptor moieties, respectively, giving sufficient triplet energy (2.67 eV
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Carbazole-based coplanar molecule (CmInF) as a universal host for multi-color electrophosphorescent devices

TL;DR: In this paper, a carbazole-based coplanar molecule (CmInF) obtained through the intramolecular ring closure of aryl substitutions at the C3 and C6 positions exhibits a high triplet energy (ET = 2.77 eV), morphological stability (Tg = 195 °C) and hole mobility in the range of up to 5 × 10−3 cm2 V−1 s−1.
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An environmentally benign synthesis of aurones and flavones from 2′-acetoxychalcones using n-tetrabutylammonium tribromide

TL;DR: A wide variety of aurones (3a-f ) can be prepared exclusively from 2′-acetoxychalcones (1a-,f ) in high yields in two steps, by bromination using n-tetrabutylammonium tribromide (TBATB) in the presence of CaCO3 in CH2Cl2-MeOH (5:2) at 0-5°C followed by cyclization of the brominated products 2a-, f on treating with 0.2 M ethanolic KOH solution at 0−5