Polymers can help to enhance radiation effects:
Alkyl Chloride-Functionalized Polymers Mediate Oxidation of
Thioethers Initiated by Ionizing Radiation
out today in ACS Applied Polymer Materials
#OpenAccess #HealthChemEDelft
Alkyl Chloride-Functionalized Polymers Mediate Oxidation of
Thioethers Initiated by Ionizing Radiation
out today in ACS Applied Polymer Materials
#OpenAccess #HealthChemEDelft
March 20, 2025 at 9:46 AM
Polymers can help to enhance radiation effects:
Alkyl Chloride-Functionalized Polymers Mediate Oxidation of
Thioethers Initiated by Ionizing Radiation
out today in ACS Applied Polymer Materials
#OpenAccess #HealthChemEDelft
Alkyl Chloride-Functionalized Polymers Mediate Oxidation of
Thioethers Initiated by Ionizing Radiation
out today in ACS Applied Polymer Materials
#OpenAccess #HealthChemEDelft
Congratulations to the team on our latest paper published in @jacs.acspublications.org @cardiffuni.bsky.social
pubs.acs.org/doi/10.1021/...
pubs.acs.org/doi/10.1021/...
Thiol-Free Sulfenylation Redefined: A Single-Atom Transfer Pathway to Symmetrical Di(hetero)arylthioethers via B(C6F5)3 Catalysis
Diarylated thioethers are privileged scaffolds found across pharmaceuticals, functional materials, and molecular electronics. Conventional approaches to these motifs, typically via C–H functionalizati...
pubs.acs.org
January 29, 2026 at 4:32 PM
Congratulations to the team on our latest paper published in @jacs.acspublications.org @cardiffuni.bsky.social
pubs.acs.org/doi/10.1021/...
pubs.acs.org/doi/10.1021/...
On the front cover of this week's #JACS: "Asymmetric Enantio-complementary Synthesis of Thioethers via Ene-Reductase-Catalyzed C–C Bond Formation"
Read it here 🔗 buff.ly/RIVQKo0
#ChemSky
Read it here 🔗 buff.ly/RIVQKo0
#ChemSky
June 4, 2025 at 12:00 PM
On the front cover of this week's #JACS: "Asymmetric Enantio-complementary Synthesis of Thioethers via Ene-Reductase-Catalyzed C–C Bond Formation"
Read it here 🔗 buff.ly/RIVQKo0
#ChemSky
Read it here 🔗 buff.ly/RIVQKo0
#ChemSky
since thioethers are in the news thought i'd mention i reference them in my sci fi WIP; the protagonist lands on an ocean planet but the local biology doesn't produce thioethers like dms in the same quantities and so the ocean smells more of bromoform — a background sweeter smell of earth's oceans
April 17, 2025 at 12:58 PM
since thioethers are in the news thought i'd mention i reference them in my sci fi WIP; the protagonist lands on an ocean planet but the local biology doesn't produce thioethers like dms in the same quantities and so the ocean smells more of bromoform — a background sweeter smell of earth's oceans
Good news, our collaboration with Dr Laura Winfrey, Dr Dominic Willcox and Prof Mike Ingleson has been published in Angewandte Chemie
@angewandtechemie.bsky.social Read it below.
doi.org/10.1002/anie... @domrwillcox.bsky.social #ChemSky
@angewandtechemie.bsky.social Read it below.
doi.org/10.1002/anie... @domrwillcox.bsky.social #ChemSky
Three Component Thio‐ and Carboboration of Alkynes: A Modular Route to Functionalised Bicyclic Boronates
Three-component thio- and carbo-boration reactions to form functionalised benzoxaborinines and benzazaborinines are reported. The nucleophile scope includes thioethers, thiols, and (hetero)arenes. Me...
doi.org
June 3, 2026 at 8:50 AM
Good news, our collaboration with Dr Laura Winfrey, Dr Dominic Willcox and Prof Mike Ingleson has been published in Angewandte Chemie
@angewandtechemie.bsky.social Read it below.
doi.org/10.1002/anie... @domrwillcox.bsky.social #ChemSky
@angewandtechemie.bsky.social Read it below.
doi.org/10.1002/anie... @domrwillcox.bsky.social #ChemSky
www.organic-chemistry.org/abstracts/li...
Selective C(sp3)-S Bond Cleavage of Thioethers to Build Up Unsymmetrical Disulfides
Selective C(sp3)-S Bond Cleavage of Thioethers to Build Up Unsymmetrical Disulfides
July 3, 2026 at 3:57 AM
www.organic-chemistry.org/abstracts/li...
Selective C(sp3)-S Bond Cleavage of Thioethers to Build Up Unsymmetrical Disulfides
Selective C(sp3)-S Bond Cleavage of Thioethers to Build Up Unsymmetrical Disulfides
Now published in ChemistryEurope: doi.org/10.1002/ceur...
Synthesis of Cyclic Sulfilimines and Sulfoximines via Copper‐Mediated C(sp2)–H Sulfanylation of Benzylamines with a Catalytic Transient Directing Group
Copper-mediated transient C─H sulfanylation of benzylamines with sulfenamides enables rapid access to thioethers, cyclic sulfilimines, and sulfoximines. Mechanistic investigations using 1H NMR and el....
doi.org
August 13, 2025 at 10:26 AM
Now published in ChemistryEurope: doi.org/10.1002/ceur...
www.organic-chemistry.org/abstracts/li...
Manganese porphyrins are effective molecular electrocatalysts for selective oxidation of thioethers to sulfoxides
Manganese porphyrins are effective molecular electrocatalysts for selective oxidation of thioethers to sulfoxides
June 6, 2025 at 10:55 AM
www.organic-chemistry.org/abstracts/li...
Manganese porphyrins are effective molecular electrocatalysts for selective oxidation of thioethers to sulfoxides
Manganese porphyrins are effective molecular electrocatalysts for selective oxidation of thioethers to sulfoxides
Carbazole-Functionalized MOFs for Efficient Selective Photocatalytic Oxidation of Thioethers to Sulfoxides http://pubs.rsc.org/en/Content/ArticleLanding/2025/CC/D5CC01247C
May 2, 2025 at 6:12 AM
Carbazole-Functionalized MOFs for Efficient Selective Photocatalytic Oxidation of Thioethers to Sulfoxides http://pubs.rsc.org/en/Content/ArticleLanding/2025/CC/D5CC01247C
We propose the elimination of thioethers as a general strategy to enhance the photostability of self-labeling protein tags. Happy that we could support this mechanism with a MS analysis. The M175L mutation of HaloTag yields up to 4-fold more photons. 🎇 (4/4)
www.pnas.org/doi/abs/10.1...
www.pnas.org/doi/abs/10.1...
Thioether editing generally increases the photostability of rhodamine dyes on self-labeling tags | PNAS
Self-labeling protein tags are widely used in advanced bioimaging where dyes with
high-photon budgets outperform their fluorescent protein counterp...
www.pnas.org
July 29, 2025 at 7:24 AM
We propose the elimination of thioethers as a general strategy to enhance the photostability of self-labeling protein tags. Happy that we could support this mechanism with a MS analysis. The M175L mutation of HaloTag yields up to 4-fold more photons. 🎇 (4/4)
www.pnas.org/doi/abs/10.1...
www.pnas.org/doi/abs/10.1...
Pleased to share our pre-print on using ene reductases to synthesise chiral thioethers: doi.org/10.26434/che...
Asymmetric Enantio-Complementary Synthesis of Thioethers via Ene-Reductase Catalysed C-C bond formation
Enzymes are attractive catalysts due to their high chemo-, regio-, and enantio-selectivity. In recent years the application of enzymes in organic synthesis has expanded dramatically, especially for th...
doi.org
December 20, 2024 at 7:53 PM
Pleased to share our pre-print on using ene reductases to synthesise chiral thioethers: doi.org/10.26434/che...
Discover how Elias Picazo's team developed a groundbreaking iron-catalyzed reaction to synthesize
#thioethers
directly from alkyl halides and disulfides💥💡#crosscoupling
#ironcatalysis
Learn more👉 www.thieme-connect.com/products/ejo...
#thioethers
directly from alkyl halides and disulfides💥💡#crosscoupling
#ironcatalysis
Learn more👉 www.thieme-connect.com/products/ejo...
December 31, 2024 at 5:33 AM
Discover how Elias Picazo's team developed a groundbreaking iron-catalyzed reaction to synthesize
#thioethers
directly from alkyl halides and disulfides💥💡#crosscoupling
#ironcatalysis
Learn more👉 www.thieme-connect.com/products/ejo...
#thioethers
directly from alkyl halides and disulfides💥💡#crosscoupling
#ironcatalysis
Learn more👉 www.thieme-connect.com/products/ejo...
Klein-Hessling et al.: Synthesis, spectroscopic and crystallographic characterization of various cymantrenyl thioethers [Mn{C5HxBry(SMe)z}(PPh3)(CO)2] ##CrystalStructure##Cymantrene##Thioether... ##IUCrhttps://journals.iucr.org/paper?S205322962400603X
Synthesis, spectroscopic and crystallographic characterization of various cymantrenyl thioethers [Mn{C5HxBry(SMe)z}(PPh3)(CO)2]
Several manganese complexes of the type [MnCp(PPh3)(CO)2] containing a cyclopentadienyl (Cp) ligand with one to five SMe substituents were prepared and studied by X-ray crystallography. In these structures, a few S⋯S and/or S⋯Br interactions occur, and these are sometimes of significant importance for the arrangement of the molecules in the crystal.
journals.iucr.org
July 6, 2024 at 12:00 AM
Klein-Hessling et al.: Synthesis, spectroscopic and crystallographic characterization of various cymantrenyl thioethers [Mn{C5HxBry(SMe)z}(PPh3)(CO)2] ##CrystalStructure##Cymantrene##Thioether... ##IUCrhttps://journals.iucr.org/paper?S205322962400603X
www.organic-chemistry.org/abstracts/li...
A convenient visible-light-promoted oxidation of thioethers to sulfoxides is developed utilizing eosin Y as the photocatalyst and molecular oxygen from air as the oxidant.
A convenient visible-light-promoted oxidation of thioethers to sulfoxides is developed utilizing eosin Y as the photocatalyst and molecular oxygen from air as the oxidant.
September 4, 2026 at 8:44 AM
www.organic-chemistry.org/abstracts/li...
A convenient visible-light-promoted oxidation of thioethers to sulfoxides is developed utilizing eosin Y as the photocatalyst and molecular oxygen from air as the oxidant.
A convenient visible-light-promoted oxidation of thioethers to sulfoxides is developed utilizing eosin Y as the photocatalyst and molecular oxygen from air as the oxidant.
Micellar Ru(II)–bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
June 25, 2026 at 12:10 AM
Micellar Ru(II)–bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
June 18, 2026 at 8:10 AM
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
June 18, 2026 at 7:10 AM
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
June 18, 2026 at 5:10 AM
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
June 17, 2026 at 12:10 PM
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
June 17, 2026 at 10:10 AM
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
June 17, 2026 at 7:10 AM
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
June 17, 2026 at 12:10 AM
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
June 16, 2026 at 11:10 PM
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
June 16, 2026 at 10:10 PM
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C
June 16, 2026 at 7:10 PM
Micellar Ru(II)-bipyridine photocatalysts for selective oxidation of thioethers to sulfoxides in water http://pubs.rsc.org/en/Content/ArticleLanding/2026/CC/D6CC01994C