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There is acatalytic low-temperature deFluorination

Photocatalytic cleavage of C-F bonds in perfluorohexane and the organization of isoxazolines and alkenes

Nagai, Y., Smith, R. L.Jr., Inomata, H. & Arai, K. Direct observation of polyvinylchloride degradation in water at temperatures up to 500°C and at pressures up to 700 MPa. J. Appl. Polym. Sci. 106 was published in 2007.

The discovery of oxygen -nucleophilic addition to,-unsaturated amides wascatalyzed by a redox neutral organic photoreductant. J. Am. Chem. Soc. 142, 20942–20947 (2020).

The C-F bond in perfluorohexane was cleavage with W, Si, P-, and I. J. Am. Mass. Spectrom. The film was made in 1998.

A photocatalytic cleavage of alkyl aryl ethers is accomplished by using carbazole catalysts and csium carbonate. J. Org. Chem. 86, 2545–2555 (2021).

Theeductive cleavage of C-X or N-S bonds wascatalyzed by a super organoreductant. It’s an organization. Lett. 25, 832–825 (2023)

Xiao, Z. F. et al. Iridium-catalyzed cyclization of isoxazolines and alkenes: divergent access to pyrrolidines, pyrroles, and carbazoles. There is an organization. Lett. 18, 5672–5675 (2016).

Super-reduction of an anion by visible-light TEMPOOH catalyzed by a surface-selective poly(tetrafluoroethylene)

Halder, S., Mandal, S., Kundu, A., Mandal, B. & Adhikari, D. Super-reducing behavior of benzo[b]phenothiazine anion under visible-light photoredox condition. J. Am. The drug is called Chem. Soc. 145, 22403–22412

The book is “K. et al.” Intermolecular oxyarylation of olefins with aryl halides and TEMPOH catalyzed by the phenolate anion under visible light. Chem. There was an article in the sci. 11 in 2020.

Kim, H., Kim, H., Lambert, T. H. & Lin, S. Reductive electrophotocatalysis: merging electricity and light to achieve extreme reduction potential. Someone is calling it J. Am. Chem. Soc. 142, 2087–2092 (2020).

The photophysical and redox potential of photosensitizers for organic photoredox transformations is discussed in this paper. Synlett 33, 1154–1179 (2022).

Sheldon, D. J., Parr, J. M. & Crimmin, M. R. Room temperature defluorination of poly(tetrafluoroethylene) by a magnesium reagent. J. Am. Is it Chem. Soc. 145, 10486–10490 (2023).

Costello, C. A. & McCarthy, T. J. Surface-selective introduction of specific functionalities onto poly(tetrafluoroethylene). Macromolecules 20 was published in 1987.

D C G., Mabury, S A., and Martin, J.W. examined the feasibility of lysis of fluoropolymers as a source of organic acids. Nature 386, 386, 389 (2001).

The end of life assessment of fluoropolymers is an area that has recently seen developments. Chem. Soc. Rev. 52, 4208–4247 (2023).

Characterization of the original extreme polymers was done by Puts, Crouse, P. and Ameduri. The Chem Rev. 119 was published in 2019.

Baumgartner, R., Stieger, G. K. & McNeill, K. Complete hydrodehalogenation of polyfluorinated and other polyhalogenated benzenes under mild catalytic conditions. Environ. Sci. Technol. There was a report on 47, 6545–6553

Singh, R. K., and others. Rapid removal of poly- and perfluorinated compounds from investigation-derived waste (IDW) in a pilot-scale plasma reactor. Environ. Sci. Technol. 53, 11375–11382 (2019).

Bentel, M. J. et al. Defluorination of per- and polyfluoroalkyl substances (PFASs) with hydrated electrons: structural dependence and implications to PFAS remediation and management. It is called the Environ. The journal of technical sciences, Sc. Technol. 53, 3718–3728 (2019).

Yang, N. et al. Solvent-free nonthermal destruction of PFAS chemicals and PFAS in sediment by piezoelectric ball milling. There is a belief that the house is Environ. It is an area of science and technology. Lett. 10, 198–203 (2023).

J. Gao and his research work on a project called “Collaborative Research between Universities and NGOs.” Photochemical degradation pathways and near-complete defluorination of chlorinated polyfluoroalkyl substances. Nat. Water 1, 381–390 (2023).

The article was written by Z. et al. Accelerated degradation of perfluorosulfonates and perfluorocarboxylates by UV/sulfite + iodide: reaction mechanisms and system efficiencies. Environ. The science of Technol. There is a count of 56, 3699–3709.

Source: Photocatalytic low-temperature defluorination of PFASs

The Environ. Facts and figures of human exposure to perfluoroalkyl substances (PFAS) in New Jersey soils

Gaballah, S. et al. It was found that developmental toxicity, developmental neurotoxicity and tissue dose in zebrafish were exposed to GenX and other PFAS. It’s called the Environ. Health facts and figures. 128, 047005 (2020).

They named it E. M. et al. A review of the pathways of human exposure to poly- and perfluoroalkyl substances are presented. J. Expo. That’s a journal of environmental science. Epidemiol 29 was published in 2019.

Washington, J. W. et al. There are chloroperfluoropolycarboxylates in New Jersey soils. Science 368, 1103–1107 (2020).

Medicinal chemists are trying to make drug molecules that contain C–F bonds but can biodegrade safely once they leave the body. In some circumstances, PFAS have replaced other harmful chemicals — for example, outdated, ozone-destroying chlorofluorocarbon (CFC) refrigerants. Non-fluorinated refrigerants are also available, including ammonia and carbon dioxide, but large-scale roll out will need regulatory input.

Such bonds lie at the heart of per- and polyfluoroalkyl substances (PFAS), a group of compounds, numbering in the millions, that are remarkably water-, heat- and greaseproof. The invention of Teflon in the 1930s made pans non-stick and keep the rain off our jackets. Varieties of cosmetics, fire-retardant foam, kitchen utensils, metal coatings, packaging, textiles and more all contain them.

Chemical Cleansing: A Light-Driven Catalyst for Nano-scale Chemical Production and Implications for the Future of Organic Chemistry

The world is starting to act to stop forever chemicals from entering the environment and to clean them up already there. But more action is needed — and faster.

Both methods combine a catalyst with some relatively simple chemistry that is driven by visible light. The catalyst absorbs light and then makes a reaction.

The Colorado State University chemist, along with colleagues, use absorbed energy to decrease the C–F bond to carbon–hydrogen. In temperatures as low as 40 C, the chemist and his colleagues break the bond and the overall molecule down into smaller parts, using this energy. The papers mark a major step forward.

Next steps include use of these ideas in real-world settings, for example to develop catalysts that work in waste water or that can be used to clean up contaminated soils. A method can be adapted to be powered by sunlight.

The international agreement that regulates persistent organic pollutants is looking to update it’s list of banned substances.

The European proposal doesn’t extend to banning PFAS in applications like medicine or transport, for the simple reason that these chemicals are too useful and adequate alternatives aren’t yet found. The shelf life of the pharmaceuticals are dependent on the C–F bonds being stable.