Abstract
We have synthesized aniline based amides (3a-h) via palladium catalyzed Suzuki cross coupling of N-(2,5-dibromophenyl) acetamide with different arylboronic acids in moderate to good yields. A variety of functional groups were well tolerated in reaction conditions. For exploring the possible applications as optoelectronic devices, the nonlinear optical (NLO) properties of all synthesized derivatives (3a-h) were investigated with the help of density functional theory (DFT) methods. The frontier molecular orbitals analysis and reactivity descriptors were investigated for exploring the reactivities.
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Israr, H., Rasool, N., Rizwan, K., Hashmi, M. A., Mahmood, T., Rashid, U., … Akhtar, M. N. (2019). Synthesis and reactivities of triphenyl acetamide analogs for potential nonlinear optical material uses. Symmetry, 11(5). https://doi.org/10.3390/sym11050622
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