Tetrathiafulvalene (TTF) Precursors
Tetrathiafulvalene (TTF) precursors are compounds that can be used to synthesize TTF-based molecular conductors. TTF is a well-known electron donor with high conductivity and stability. By using TTF precursors, researchers can tailor the properties of molecular conductors to meet specific application requirements. Applications of TTF-based molecular conductors include organic solar cells, OLEDs, and sensors. The unique properties of TTF, such as the ability to form stable radical cations, make it an attractive material for organic electronics.
Technical Resources
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Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiralChiral chloro-indeno pybox has served as a new ligand for the Yb(OTf)3-catalyzed asymmetric Friedel–Crafts alkylation reaction of indoles with nitroalkenes. The tunable nature of pybox ligands
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2Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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3Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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4Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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5Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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In-stockPurity: ≥95%
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In-stockPurity: ≥98%
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In-stockPurity: 95+%
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In-stockPurity: ≥98%
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