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Modern Fluoroorganic Chemistry: Synthesis, Reactivity, Applications
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“Their unique properties arise primarily from their strong carbon-fluorine (C-F) bonds, which are reinforced by the overlap between fluorine's 2s and 2p orbitals with the carbon orbitals [68].”
From Industrial Applications, Environmental Fate, Human Exposure, and Health Effects of PFAS (2025) · cites this paper as [68]
In the citing paper
“The chemical stability of a molecule greatly influences its persistence in the environment [24,25,26].”
From The EU’s Per- and Polyfluoroalkyl Substances (PFAS) Ban: A Case of Policy over Science (2023) · cites this paper as [24]
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Metadata
- Authors
- Kirsch, P.
- Corresponding author
- Kirsch, Peer
- ORCID
- Kirsch, Peer
- Venue
- Wiley eBooks
- Publisher
- Wiley
- Published
- 2013-03-05
- OpenAlex
- W4291208076
- Cited by
- 1,029
- References
- 0
- Citations by year
- 2026: 34 · 2025: 52 · 2024: 64 · 2023: 90 · 2022: 74 · 2021: 93 · 2020: 96 · 2019: 90 · 2018: 96 · 2017: 83 · 2016: 111 · 2015: 71 · 2014: 59 · 2013: 11
- FWCI
- 25.46
- Type
- book
- Language
- en
- Open access
- closed
- Locations
- Wiley eBooks (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Fluorine in Organic Chemistry
- Physical Sciences › Chemistry › Organic Chemistry › Organoboron and organosilicon chemistry
- Physical Sciences › Chemistry › Organic Chemistry › Organic and Inorganic Chemical Reactions
- Keywords
- fluorine chemistry, organofluorine synthesis
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