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Atul C. Chaskar

Researcher at University of Mumbai

Publications -  125
Citations -  2116

Atul C. Chaskar is an academic researcher from University of Mumbai. The author has contributed to research in topics: Catalysis & One-pot synthesis. The author has an hindex of 21, co-authored 112 publications receiving 1838 citations. Previous affiliations of Atul C. Chaskar include National Taiwan University & Institute of Chemical Technology.

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Bipolar Host Materials: A Chemical Approach for Highly Efficient Electrophosphorescent Devices

TL;DR: This review highlights recently developed bipolar host materials with the focus on molecular design strategies and the structure-property-performance relationships of various classes ofipolar host materials, which are classified into several categories according to the structural features of their constituents (HT/ET blocks and spacers).
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A diarylborane-substituted carbazole as a universal bipolar host material for highly efficient electrophosphorescence devices

TL;DR: In this paper, the synthesis and physical properties of a novel bipolar host material containing the dimesityl borane/carbazole hybrid, CMesB, were reported and the results indicate that the bipolar host with high triplet energy has high potential in manufacturing RGBW OLEDs for display or lighting applications.
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Carbazole–benzimidazole hybrid bipolar host materials for highly efficient green and blue phosphorescent OLEDs

TL;DR: In this article, a series of bipolar hosts (CbzCBI, mCPCBI, CbzNBI, and mCPNBI) containing hole-transporting carbazole and electron-transported benzimidazole moieties were synthesized.
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Indolo[3,2-b]carbazole/benzimidazole hybrid bipolar host materials for highly efficient red, yellow, and green phosphorescent organic light emitting diodes

TL;DR: By incorporating electronaccepting benzimidazole and electron-donating indolo[3,2-b]carbazole into one molecule, two novel donor-acceptor bipolar host materials, TICCBI and TICNBI, have been synthesized.
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I2 catalyzed tandem protocol for synthesis of quinoxalines via sp3, sp2 and sp C–H functionalization

TL;DR: This metal-free, mechanistically distinct and functional group tolerant tandem approach could be a powerful complement to traditional approaches for the synthesis of quinoxalines.