Let’s imagine molecules as precision-engineered machines — and fluorinated metal complexes as the turbocharged engines driving tomorrow’s innovations. These remarkable compounds, with their robust thermal resistance, fine-tuned electronic behavior, and customizable architectures, are reshaping the future of catalysis, materials design, biomedical breakthroughs, and energy solutions. At Alfa Chemistry, we’re inspired by the science that pushes boundaries. That’s why we offer a handpicked collection of fluorinated metal complexes — crafted for researchers and innovators ready to take on the most advanced challenges in modern chemistry.
View Product ListFluorinated metal complexes are coordination compounds formed by combining fluoride ions (F-) or fluorinated organic ligands (e.g., β-diketone, trifluoromethyl pyridine, etc.) as a ligand with a central metal atom or ion via a coordination bond. The central features of these complexes are the high electronegativity (3.98) and small atomic size (covalent radius of about 64 pm) of fluorine, resulting in a significantly stronger coordination ability than other halogens. Fluorine's strong σ-donor ability and weak π-acceptor properties allow it to form bonds with metals with high bond energies, which endows the complexes with excellent thermal stability, chemical inertness, and unique electronic structures.
Typical compositions:
Center Metals
including transition metals (e.g., Cu, Fe, Co, Ni), rare earth metals (e.g., Y, Eu), and main group metals (e.g., Al, Mg).
Fluorinated Ligands
e.g. Hexafluoroacetylacetone (Hhfac), trifluoromethylbenzoic acid (TFA), fluorinated β-diketones, etc.
Auxiliary Ligands
Tetramethylethylenediamine (TMEDA), pyridine derivatives, etc., are used to regulate coordination number and space configuration.
Electronic Effects
Fluorinated ligands increase the Lewis acidity of metal centers, enhancing catalytic potential. They also induce spin-state changes in Co(II)/Fe(II) systems via non-covalent interactions (e.g., C-F···H bonding).
Spatial Modulation
Fluorinated MOFs can be tuned for porosity and selectivity, with pore sizes modifiable from 5.8 to 7.2 Å depending on fluorine content.
Dynamic Behavior
Weakly coordinating fluorinated anions (e.g., PF6-, BF6-) enable responsive structural transformations under external stimuli such as ammonia.
Explore our most in-demand fluorinated metal complexes, trusted by researchers and industry professionals across advanced materials, electronics, and catalysis. Our best-selling fluorinated metal complexes products are trusted by professionals for their unmatched performance and versatility. Click on the links below to explore products that fit your needs. If you don't see your product here, we can still custom synthesize it.
(OC-6-33)-[4,4'-Bis-trifluoromethyl]bis[(5-fluoro-2-(5-methyl-2-pyridinyl)phenyl]iridium(III) hexafluorophosphate
OFC2829292739
Copper(II) trifluoromethanesulfonate
OFC34946822
μ-[(1,2-η:3,4-η)-Copper(I) Trifluoromethanesulfonate Benzene Complex
OFC37234972
Neodymiumtrifluoroacetylacetonate
OFC37473679
Neodymium(III) hexafluoroacetylacetonate dihydrate
OFC47814186
Praseodymium(III) hexafluoroacetylacetonate
OFC47814200
fac-Ir(p-CF3ppy)3
OFC500295523
Bis(trifluoromethanesulfonate) Manganese
OFC55120768
Nickeltrifluoroacetylacetonate,dihydrate
OFC55534899
[Ir2(2-(2,4-difluorophenyl)pyridine)4Cl2]
OFC562824275
Palladium(II) hexafluoroacetylacetonate
OFC64916489
5,10,15,20-Tetrakis(pentafluorophenyl)-21H,23H-porphine Palladium(II)
OFC72076096
Iridium(1+), [4,4'-bis(1,1-dimethylethyl)-2,2'-bipyridine-κN1,κN1']bis[5-fluoro-2-(5-methyl-2-pyridinyl-κN)phenyl-κC]-, (OC-6-33)-, hexafluorophosphate(1-) (1:1)
OFC808142883
Iridium-(2,2'-bipyridine-κN1,κN1')bis[5-fluoro-2-(5-methyl-2-pyridinyl-κN)phenyl-κC]-(OC-6-33)-hexafluorophosphate
OFC855523545
(2,2'-Bipyridine)bis[2-(2,4-difluorophenyl)pyridine]iridium(III) Hexafluorophosphate
OFC864163804
Triphenylphosphinegold(I) Bis(trifluoromethanesulfonyl)imidate
OFC866395166
(Ir[dF(CF3)ppy]2(dtbpy))PF6
OFC870987636-1
Di-µ-chlorotetrakis[3,5-difluoro-2-[5-trifluoromethyl-2-pyridinyl-kN)phenyl-kC]diiridium(III)
OFC870987647
[1,3-Bis(2,6-di-i-propylphenyl)imidazol-2-ylidene][bis(trifluoromethanesulfonyl)imide]gold(I)
OFC951776242
Trifluoromethylsulfonatotricarbonyl(2,2'-bipyridine)rhenium(I)
OFC97170940
Catalog: OFC2829292739
CAS Number: 2829292-73-9
Molecular Formula: C36H24F14IrN4P
Molecular Weight: 1001.77
Catalog: OFC34946822
CAS Number: 34946-82-2
Molecular Formula: C2CuF6O6S2
Molecular Weight: 361.68
Catalog: OFC37234972
CAS Number: 37234-97-2
Molecular Formula: C8H6Cu2F6O6S2
Molecular Weight: 503.34
Catalog: OFC37473679
CAS Number: 37473-67-9
Molecular Formula: C15H15F9NdO6
Molecular Weight: 606.5
Catalog: OFC47814186
CAS Number: 47814-18-6
Molecular Formula: C15H3F18NdO62H2O
Molecular Weight: 801.42
Catalog: OFC47814200
CAS Number: 47814-20-0
Molecular Formula: C15H3F18O6P
Molecular Weight: 762.06
Catalog: OFC500295523
CAS Number: 500295-52-3
Molecular Formula: C36H21F9IrN3
Molecular Weight: 858.79
Catalog: OFC55120768
CAS Number: 55120-76-8
Molecular Formula: C2F6MnO6S2
Molecular Weight: 353.08
Catalog: OFC55534899
CAS Number: 55534-89-9
Molecular Formula: C10H14F6NiO6
Molecular Weight: 402.9
Catalog: OFC562824275
CAS Number: 562824-27-5
Molecular Formula: C44H24Cl2F8Ir2N4
Molecular Weight: 1216.03
Catalog: OFC64916489
CAS Number: 64916-48-9
Molecular Formula: C10H2F12O4Pd
Molecular Weight: 520.52
Catalog: OFC72076096
CAS Number: 72076-09-6
Molecular Formula: C44H8F20N4Pd
Molecular Weight: 1078.95
Catalog: OFC808142883
CAS Number: 808142-88-3
Molecular Formula: C42H42F8IrN4P
Molecular Weight: 977.99
Catalog: OFC855523545
CAS Number: 855523-54-5
Molecular Formula: C34H26F8IrN4P
Molecular Weight: 865.78
Catalog: OFC864163804
CAS Number: 864163-80-4
Molecular Formula: C32H20F10IrN4P
Molecular Weight: 873.71
Catalog: OFC866395166
CAS Number: 866395-16-6
Molecular Formula: C20H15AuF6NO4PS2
Molecular Weight: 739.4
Catalog: OFC870987636-1
CAS Number: 870987-63-6
Molecular Formula: C42H34F16IrN4P
Molecular Weight: 1121.91
Catalog: OFC870987647
CAS Number: 870987-64-7
Molecular Formula: C48H20Cl2F20Ir2N4
Molecular Weight: 1488.01
Catalog: OFC951776242
CAS Number: 951776-24-2
Molecular Formula: C29H36AuF6N3O4S2
Molecular Weight: 865.7
Catalog: OFC97170940
CAS Number: 97170-94-0
Molecular Formula: C14H8F3N2O6ReS
Molecular Weight: 575.49
Extensive Portfolio of Fluorinated Metal Complexes
We offer a diverse range of fluorinated coordination compounds, including rare earth, transition metal, and main group complexes—optimized for high-performance applications in catalysis, electronics, imaging, and beyond.
High Purity, Consistent Quality
Each product is manufactured under rigorous quality standards to ensure high chemical purity, excellent batch-to-batch consistency, and reliable performance in both research and industrial settings.
Custom Synthesis and Bulk Supply
Whether you're looking for gram-scale samples or kilogram-level bulk supply, we provide flexible production capabilities and tailor-made synthesis to meet specific project needs.
Technical Support from Fluorine Chemistry Experts
Our team of experienced chemists offers deep technical expertise in organofluorine coordination chemistry, helping you select the right compound and optimize its use in your application.
Global Logistics & Timely Delivery
With a worldwide logistics network and responsive service, we ensure fast, secure delivery to laboratories and production facilities across the globe.
Catalysis
Medical Imaging and Therapeutics
Energy Materials
Agrochemistry
Fluorinated metal complexes are widely used in the development of pesticides and insecticides to improve crop yields and pest control.
Prepared by the substitution reaction of a metal salt with a fluorinated ligand. For example, a β-diketone ligand reacts with a metal chloride under alkaline conditions to form a fluorinated β-diketonate, with subsequent introduction of an auxiliary ligand (e.g., TMEDA) to stabilize the structure.
are used for the synthesis of fluorinated metal-organic frameworks (F-MOFs). For example, Cu2+ reacts with fluorinated bipyridine ligands in DMF at 85°C for 96 h to form two- or three-dimensional MOFs.
Solvent-free synthesis by ball-milling. For example, in the synthesis of Cu3(BTC)3, the metal acetate reacts directly with the organic ligand by high-energy ball milling, and a trace addition of ethanol reduces structural defects.
Selective fluorination was achieved using novel fluorination reagents such as DMPU/HF complexes. For example, the gold-catalyzed monofluorination of alkynes leads to the highly regioselective synthesis of fluoroolefins.
The following case studies demonstrate how our products have led to significant technological breakthroughs and economic benefits in real-world applications.
Customer background: A German advanced materials research institute
Direction of application: Metal Organic Chemical Vapor Deposition (MOCVD)
Products used: Chromium(III) hexafluoroacetylacetonate(Cr(hfac)3) (Catalog OFC14592804)
Project Objective: Development of corrosion-resistant chromium oxide thin films for aerospace alloys
Case Overview:
The organization chose Cr(hfac)3 as the chromium source for the low-temperature MOCVD process, and thanks to its excellent volatility and controlled decomposition around 250 °C, the homogeneous deposition of the chromium oxide thin films was achieved. Uniform deposition of Cr3 The resulting Cr2O3 coatings on aluminum and titanium alloys show excellent adhesion and corrosion resistance, significantly better than conventional chromium precursors. The purity of the product was stable (>98%), which effectively supported batch-to-batch consistency and pilot scale-up.
Customer Background: A North American clean energy laboratory
Application Direction: Construction of Fluorinated Metal-Organic Frameworks (F-MOFs) for Gas Separation
Products Used: Bis ( hexafluoroacetylacetonato)nickel(II) (Ni(hfac)2) (Catalog OFC14949690)
Project Goal: Construction of hydrophobic MOF materials with high selectivity for Xe/Kr
Case Overview:
The researchers needed a Ni(II) source with a strong electron-attracting effect to introduce fluorine into the MOF structure to enhance gas recognition. A three-dimensional MOF structure (F-MOF-Ni) was successfully constructed using Ni(hfac)2 by DMF solvothermal reaction, and the highly selective adsorption of xenon gas was achieved by adjusting the pore size and surface fluorination properties (Xe/Kr separation ratio was enhanced to 9.2). The product's good solubility and insensitivity to moisture are key to achieving crystalline and high specific surface area structures.
Customer Background: A Japanese optoelectronic device manufacturing company
Application Direction: Preparation of Solution-processable ITO Precursors for OLED Displays
Product Used: Indium trifluoroacetylacetonate (In(tfac)3) (Catalog OFC15453879)
Project Objective: To realize the low-temperature preparation of highly transparent and conductive films on flexible substrates
Case Overview:
The R&D team used In(tfac)3 as the source of indium, which has good solubility in non-polar solvents and mild decomposition characteristics, to spin-coat on flexible PET substrates and anneal them at ~300 °C, obtaining a flat and smooth ITO precursor. Spin-coating and annealing at ~300 °C on a flexible PET substrate resulted in a flat and continuous In2O3 film, which was then Sn-doped to obtain an ITO structure. The final device film has a transmittance of more than 90%, low resistivity and good process compatibility. The products used have high purity and stability, effectively supporting the consistency of display device performance and mass production.
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What are the most commonly used metals in fluorinated metal complexes?
Transition metals such as palladium, platinum, ruthenium, iridium, copper, and lanthanides are commonly used. The choice of metal depends on the intended function, such as catalysis, luminescence, or electronic modulation.
How do fluorinated ligands affect the reactivity of metal complexes in catalysis?
Fluorinated ligands can alter the electron density of a metal center, making it more electrophilic or stabilizing a high-valent intermediate. This often improves reaction selectivity, reduces catalyst degradation, and opens up new reaction pathways, especially in oxidation or fluorination chemistry.
Are fluorinated metal complexes soluble in standard organic solvents?
Many fluorinated complexes show preferential solubility in fluorinated solvents (e.g., perfluorohexane, FC-77), but some are still soluble in conventional solvents such as dichloromethane or toluene. The solubility depends on the degree of fluorination of the ligand and the metal coordination environment.
Can fluorinated metal complexes be used in C-F bond activation or fluorination reactions?
Yes, of course. A number of complexes, especially those based on post-transition metals such as palladium or nickel, have been successfully applied in selective C-F bond activation or catalytic fluorination of organic substrates, providing a valuable tool for fluorine introduction strategies.
Are Alfa Chemistry's fluorinated metal complexes suitable for ALD or CVD applications?
Yes, some fluorinated complexes, especially volatile, thermally stable complexes such as fluorinated β-diketone salts of lanthanides or transition metals, are tailored for vapor deposition techniques. Specification parameters such as vapor pressure and decomposition curves are available upon request.
How do I select the right fluorinated metal complex for my catalytic system?
The choice depends on a number of factors, including metal type, ligand electronic/spatial site resistance, reaction solvent compatibility, and desired substrate conversion, and Alfa Chemistry's technical team can provide guidance and literature references to help you find the best candidate.
Are your lanthanide fluoride complexes suitable for luminescence studies?
Absolutely. Lanthanide trifluoroacetylacetonate compounds, such as Nd(tfac)3 and Eu(tfac)3, are commonly used as emission centers in photonic materials. They have strong ligand fields and low vibrational energy loss of fluorinated ligands, which improves emission efficiency and lifetime.
Can your fluorinated metal complexes be used to synthesize MOFs?
Yes, fluorinated ligands (e.g., hfac- and tfac-) can be used as structure-directing agents in metal-organic skeletons (MOFs) for pore size tuning, hydrophobic surface functionality, and even fluorophilic guest selectivity.
What is the typical purity of your fluorinated metal complexes? How is it verified?
The purity of most fluorinated metal complexes exceeds 98%, which has been confirmed by techniques such as nuclear magnetic resonance (NMR), elemental analysis, thermogravimetric analysis (TGA), and inductively coupled plasma emission spectroscopy (ICP-OES). Product-specific COAs are available upon request.