Beauty K Chabuka: h-index, Total Citations, and Citation Map
Beauty K Chabuka's h-index is 5 (4 i10-index, 116+ total citations across 18+ publications) according to Google Scholar as of May 2026. Beauty K Chabuka is affiliated with Florida State University.
Beauty K Chabuka is a researcher affiliated with Florida State University, specializing in Computational Chemistry| Physical Organic| Chemometrics. Their work has been cited 116 times. This profile visualizes their global influence, highlighting strong citation networks in United States.
Beauty K Chabuka's Citation Metrics
Bibliometric impact based on 18 indexed publications.
- H-Index
- 5
- i10-Index
- 4
- Total Citations
- 116
- Citing Countries
- 13
As of May 2026.
Beauty K Chabuka has an h-index of 5 and 116 total citations across 18 publications, with research cited by institutions in 13 countries.
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Top Cited Works
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Application of a hybrid fusion classification process for identification of microplastics based on Fourier transform infrared spectroscopy
202053
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Significant Contributions
Auto-detected research lines — a seminal paper and the follow-up work building on it. Review and edit before using in a petition. Each Free PDF opens in a new tab — EB-1A organises this into the structure USCIS applies to Criterion 5 of 8 CFR § 204.5(h)(3)(v); EB-1B re-frames it under § 204.5(i)(3) (outstanding researcher); NIW presents it under prong 2 of Matter of Dhanasar.
8 citing papers could not be classified (no author data) — excluded from the percentages above.
The researcher pioneered hole-catalyzed cycloaddition strategies, establishing a framework for controlling oxidant upconversion in radical-cationic Diels–Alder reactions and extending these principles to electron catalysis and Si–Si bond activation.
The researcher developed a hybrid fusion classification process using Fourier transform infrared spectroscopy to improve the identification of microplastics.
The researcher developed a novel strategy converting strain release into aromaticity loss to activate donor-acceptor cyclopropanes, enabling the generation of quinone methide traps for C-nucleophiles.
Citation trend (last 10 years)Click to expand
Citation Trend (Last 10 Years)
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