Nahla Omer^1,2 and Hongyao Xu^1,3*

¹College of Material Science and Engineering and State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University, Shanghai, China
²Sudan University of Science and Technology (SUST), Sudan
³Research Center for Analysis and Measurement, Donghua University, Shanghai, China

*Corresponding Author: Hongyao Xu, College of Material Science and Engineering and State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University, Shanghai, China.

Received: June 17, 2021; Published: September 07, 2021

Abstract

SQuinoline forms the key skeletal component of a number for important natural products and active compounds. Despite a tremendous amount of research pertaining to the derivatization of quinoline, very few general synthetic routes are described in the literature starting from quinoline or tetra hydroquinone, and it is very simple synesthetic road we designed from the quinoline our monomer 6-Bromoquinaldine. The monomer structure of resulting was confirmed by UV, FTIR, NMR, and TGA, hence it used in our work as block in a main monomer in the polymers designed and applied in our work in chemical sensor and solar cell this study open new path for our future work and other works.

Keywords: 6-bromoquinoline; Amino Quinoline; Synthesis; Characterization

References

1. , et al. “Regioselective routes are described for convenient preparation of novel piperazine/morpholine substituted quinoline derivatives at C-3, C-6 and C-8 starting with 3, 6, 8-tribromoquinoline (6) by nucleophilic substitution via conventional heating or microwave”. Journal of Molecular (2020).
2. S Sandl., et al. “Cobalt-catalyzed hydrogenations via olefin cobaltate and hydride intermediates”. ACS Publications8 (2019): 7596-7606.
3. N Campbell. “Bicyclic Compounds Containing a Pyridine Ring: Quinoline and its Derivatives”. Rodd's Chemistry of Carbon Compounds (1964).
4. Y Hu., et al. “1, 3, 4-Thiadiazole: synthesis, reactions, and applications in medicinal, agricultural, and materials chemistry”. Chemical Reviews10 (2014): 5572-5610.
5. S Guang., et al. “A modified fluorescein derivative with improved water-solubility for turn-on fluorescent determination of Hg²+ in aqueous and living cells”. Talanta 170 (2017): 89-96.
6. Omer N., et al. “Highly selective chemo- sensor for repetitive detection of Fe+3 in pure water and bio image”. Analyst 144 (2019): 3414-3421.

Citation

Citation: Nahla Omer and Hongyao Xu. “Synthesis and Characterization of Monomer to Design a System of Optical Materials". Acta Scientific Pharmaceutical Sciences 6.10 (2022): 47-49.

Copyright

Copyright: © 2022 Nahla Omer and Hongyao Xu. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.