Yuming Zhao, Ph.D.
Affiliations: | 2002 | University of Alberta, Edmonton, Alberta, Canada |
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"Yuming Zhao"Mean distance: 8.71 | S | N | B | C | P |
Parents
Sign in to add mentor| Rik R. Tykwinski | grad student | 2002 | University of Alberta | |
| (Cross -conjugated enyne oligomers: Synthesis, properties, and nonlinear optical investigations.) | ||||
| James M. Tour | post-doc | 2002-2004 | Rice University | |
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Publications
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| Shahrokhi F, Estabragh RF, Zhao Y. (2020) Synthesis and comparative studies of K-region functionalized pyrene derivatives New Journal of Chemistry |
| Younes EA, Hussein NA, Shtaiwi M, et al. (2020) N-(cyano(naphthalen-1-yl)methyl)benzamides: synthesis, crystal structures, and colorimetric sensing for fluoride anion New Journal of Chemistry |
| Salami F, Zhao Y. (2020) Synthesis and characterization of bis(dithiafulvenyl)-substituted fluorenones and fluorenylidene-1,3-dithioles New Journal of Chemistry. 44: 9179-9189 |
| Abdollahi MF, Zhao Y. (2020) Recent advances in dithiafulvenyl-functionalized organic conjugated materials New Journal of Chemistry. 44: 4681-4693 |
| Tabasi ZA, Walsh JC, Bodwell GJ, et al. (2020) Crystal Engineering and Photophysical Properties of Phenyl-Pyrenoimidazole Systems Crystal Growth & Design. 20: 1681-1693 |
| Zreid MS, Tabasi ZA, Ma X, et al. (2020) Highly Twisted Aryl-Anthraquinodimethanes: Synthesis, Characterization, and Fluorescence Sensing of TNT European Journal of Organic Chemistry. 2020: 4031-4041 |
| Walsh JC, Hogan DT, Williams KM, et al. (2019) Synthesis of Oligo(1,8-pyrenylene)s: A Series of Functional Molecular Liquids. Chempluschem. 84: 754-765 |
| Shahrokhi F, Zhao Y. (2019) Self-Condensation of Pyrene-4,5-dione: An Approach To Generate Functional Organic Fluorophores. Organic Letters |
| Johnson MA, Tabasi Z, Zhao Y. (2019) Tuning alkynyl-extended 9,10-dihydroanthracene-based systems into aggregation-induced emission (AIE) luminophores New Journal of Chemistry. 43: 8325-8331 |
| Dong H, Zhao Y. (2019) Highly regioselective synthesis of 7-oxo-7H-[1,3,4]thiadiazolo[3,2-a]pyrimidine-5-carboxylate derivatives under mild conditions Tetrahedron Letters. 60: 1399-1403 |