Collection: Diketone Ligands [Catalysis]

Diketone Ligands [Catalysis] — contains 1,3-diketone and trifluoromethyl-diketone derivatives that function as bidentate ligands forming metal complexes through oxygen-oxygen chelate coordination. This group also includes halogen-substituted aromatic diketones that broaden the electronic variation of the ligands.

Diketone Ligands [Catalysis] are used in the synthesis of beta-diketonate metal complexes for catalysis applications as well as precursors for inorganic materials. Organometallic chemists utilize variations of aryl substituents and trifluoromethyl groups on these ligands to control the solubility, volatility, and electronic properties of the resulting metal complexes.

Example products in this collection: TCI T3283 15191-68-1 4,4,4-Trifluoro-1-(4-methoxyphenyl)-1,3-butanedione, TCI C1277 1694-29-7 3-Chloroacetylacetone, TCI T2997 720-94-5 4,4,4-Trifluoro-1-(p-tolyl)-1,3-butanedione, TCI C3139 18931-60-7 1-(4-Chlorophenyl)-4,4,4-trifluoro-1,3-butanedione, TCI T1583 893-33-4 4,4,4-Trifluoro-1-(2-naphthyl)-1,3-butanedione, TCI C4041 6302-55-2 1-(4-Chlorophenyl)butane-1,3-dione, TCI B4754 4023-81-8 1-(4-Bromophenyl)-1,3-butanedione, TCI D0039 520-45-6 Dehydroacetic Acid.

Pay attention to the type of substituent on the aromatic ring (halogen, methoxy, methyl) and the presence or absence of a trifluoromethyl group, as these affect the coordination strength and physical properties of the resulting metal complexes. All products are genuine products of Tokyo Chemical Industry (TCI) Japan, with purity, packaging, and storage conditions listed on each item's page.

Other categories at the same level under Catalysis & Inorganic Chemistry, often used together in one laboratory workflow:

Back to Catalysis & Inorganic Chemistry. For large-volume procurement, special packaging, or specific grades, contact the AMI Scientific team — official distributor of TCI Japan in Indonesia — to check availability and lead time directly from Japan.

30 products