Organofluorine / Alfa Chemistry
Fluorinated Metal Complexes Products

Fluorinated Metal Complexes Products

Discover the Power of Fluorinated Metal Complexes

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.

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What Are Fluorinated Metal Complexes?

Fluorinated 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.

What Makes Their Structures Unique?

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.

Customers Often Look For

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

2829292-73-9

(OC-6-33)-[4,4'-Bis-trifluoromethyl]bis[(5-fluoro-2-(5-methyl-2-pyridinyl)phenyl]iridium(III) hexafluorophosphate

Catalog: OFC2829292739

CAS Number: 2829292-73-9

Molecular Formula: C36H24F14IrN4P

Molecular Weight: 1001.77

34946-82-2

Copper(II) trifluoromethanesulfonate

Catalog: OFC34946822

CAS Number: 34946-82-2

Molecular Formula: C2CuF6O6S2

Molecular Weight: 361.68

37234-97-2

μ-[(1,2-η:3,4-η)-Copper(I) Trifluoromethanesulfonate Benzene Complex

Catalog: OFC37234972

CAS Number: 37234-97-2

Molecular Formula: C8H6Cu2F6O6S2

Molecular Weight: 503.34

37473-67-9

Neodymiumtrifluoroacetylacetonate

Catalog: OFC37473679

CAS Number: 37473-67-9

Molecular Formula: C15H15F9NdO6

Molecular Weight: 606.5

47814-18-6

Neodymium(III) hexafluoroacetylacetonate dihydrate

Catalog: OFC47814186

CAS Number: 47814-18-6

Molecular Formula: C15H3F18NdO62H2O

Molecular Weight: 801.42

47814-20-0

Praseodymium(III) hexafluoroacetylacetonate

Catalog: OFC47814200

CAS Number: 47814-20-0

Molecular Formula: C15H3F18O6P

Molecular Weight: 762.06

500295-52-3

fac-Ir(p-CF3ppy)3

Catalog: OFC500295523

CAS Number: 500295-52-3

Molecular Formula: C36H21F9IrN3

Molecular Weight: 858.79

55120-76-8

Bis(trifluoromethanesulfonate) Manganese

Catalog: OFC55120768

CAS Number: 55120-76-8

Molecular Formula: C2F6MnO6S2

Molecular Weight: 353.08

55534-89-9

Nickeltrifluoroacetylacetonate,dihydrate

Catalog: OFC55534899

CAS Number: 55534-89-9

Molecular Formula: C10H14F6NiO6

Molecular Weight: 402.9

562824-27-5

[Ir2(2-(2,4-difluorophenyl)pyridine)4Cl2]

Catalog: OFC562824275

CAS Number: 562824-27-5

Molecular Formula: C44H24Cl2F8Ir2N4

Molecular Weight: 1216.03

64916-48-9

Palladium(II) hexafluoroacetylacetonate

Catalog: OFC64916489

CAS Number: 64916-48-9

Molecular Formula: C10H2F12O4Pd

Molecular Weight: 520.52

72076-09-6

5,10,15,20-Tetrakis(pentafluorophenyl)-21H,23H-porphine Palladium(II)

Catalog: OFC72076096

CAS Number: 72076-09-6

Molecular Formula: C44H8F20N4Pd

Molecular Weight: 1078.95

855523-54-5

Iridium-(2,2'-bipyridine-κN1,κN1')bis[5-fluoro-2-(5-methyl-2-pyridinyl-κN)phenyl-κC]-(OC-6-33)-hexafluorophosphate

Catalog: OFC855523545

CAS Number: 855523-54-5

Molecular Formula: C34H26F8IrN4P

Molecular Weight: 865.78

864163-80-4

(2,2'-Bipyridine)bis[2-(2,4-difluorophenyl)pyridine]iridium(III) Hexafluorophosphate

Catalog: OFC864163804

CAS Number: 864163-80-4

Molecular Formula: C32H20F10IrN4P

Molecular Weight: 873.71

866395-16-6

Triphenylphosphinegold(I) Bis(trifluoromethanesulfonyl)imidate

Catalog: OFC866395166

CAS Number: 866395-16-6

Molecular Formula: C20H15AuF6NO4PS2

Molecular Weight: 739.4

870987-63-6

(Ir[dF(CF3)ppy]2(dtbpy))PF6

Catalog: OFC870987636-1

CAS Number: 870987-63-6

Molecular Formula: C42H34F16IrN4P

Molecular Weight: 1121.91

870987-64-7

Di-µ-chlorotetrakis[3,5-difluoro-2-[5-trifluoromethyl-2-pyridinyl-kN)phenyl-kC]diiridium(III)

Catalog: OFC870987647

CAS Number: 870987-64-7

Molecular Formula: C48H20Cl2F20Ir2N4

Molecular Weight: 1488.01

951776-24-2

[1,3-Bis(2,6-di-i-propylphenyl)imidazol-2-ylidene][bis(trifluoromethanesulfonyl)imide]gold(I)

Catalog: OFC951776242

CAS Number: 951776-24-2

Molecular Formula: C29H36AuF6N3O4S2

Molecular Weight: 865.7

97170-94-0

Trifluoromethylsulfonatotricarbonyl(2,2'-bipyridine)rhenium(I)

Catalog: OFC97170940

CAS Number: 97170-94-0

Molecular Formula: C14H8F3N2O6ReS

Molecular Weight: 575.49

Why Choose Alfa Chemistry

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.

Where Are Fluorinated Metal Complexes Used?

Catalysis

Medical Imaging and Therapeutics

Energy Materials

Agrochemistry

Catalysis

  • Homogeneous catalysis: Rhodium-based fluorinated complexes (e.g., [Rh(COD)(hfacac)]) for olefin hydroformylation, fluorinated ligands to enhance catalyst thermal stability.
  • Asymmetric catalysis: Chiral fluorinated copper complexes (e.g., Cu-BINOL derivatives) achieve >99% ee in asymmetric fluorination of α-keto esters.

Medical Imaging and Therapeutics

  • 19F MRI/PET Dual-Modal Probes: Highly fluorinated transition metal complexes (e.g., Gd-F15) with both paramagnetic relaxation enhancement (PARACEST) and 19F signals for tumor-targeting imaging.
  • Anti-cancer drugs: Fluorinated β-diketone-supported Cu(II)/Zn(II) complexes induce apoptosis in cancer cells via the mitochondrial pathway with an IC50 as low as 2.3 μM (e.g., [Cu(hfac)2]).

Energy Materials

  • Electrolyte for lithium-ion batteries: Boron fluoride (e.g., [BF3-DMPU]) is used as an additive to inhibit decomposition of the electrolyte and enhance cycle life (capacity retention >90% after 1000 cycles).
  • Photovoltaic materials: Fluorinated porphyrin metal complexes (e.g., Zn-F-Por) with broad absorption bands (400-700 nm) and low recombination energies are used in dye-sensitized solar cells (efficiency >10%).

Agrochemistry

Fluorinated metal complexes are widely used in the development of pesticides and insecticides to improve crop yields and pest control.

How Are Fluorinated Metal Complexes Synthesized?

Ligand Substitution Method

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.

Solvothermal/Hydrothermal Methods

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.

Mechanochemical Synthesis

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.

Fluorination Reagent-Assisted Synthesis

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.

Curious About Our Success Stories?

The following case studies demonstrate how our products have led to significant technological breakthroughs and economic benefits in real-world applications.

cas 14592-80-4

Case 1: Chromium(III) hexafluoroacetylacetonate for protective coatings in MOCVD

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.

cas 14949-69-0

Case 2: Bis(hexafluoroacetylacetonato)nickel(II) facilitates the construction of MOFs for gas adsorption

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.

cas 15453-87-9

Case 3: Application of Indium Trifluoroacetylacetonate in the Preparation of Flexible Transparent Conductive Films

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.

* You can reach out to us for additional product information or technical support.

What Our Customers Say

Prof. James R. Chen, Catalysis Research Group

"We’ve used their fluorinated palladium complexes in oxidative coupling reactions, and the results were consistently outstanding. The electron-withdrawing fluorine ligands enhance catalytic efficiency, making them ideal for fine-tuning selectivity."

Liang Wu, R&D Manager, Pharmaceutical Intermediates Division

"The coordination geometry and redox stability of these complexes have provided us with novel avenues for drug delivery system design. Their documentation and COA transparency greatly assist in regulatory submissions."

Dr. Anika Feldman, Head of Materials Science, Optoelectronics R&D Facility

"We tried several indium source materials in the development of our OLED panels, and indium trifluoroacetylacetonate stood out for its excellent solubility and controlled pyrolysis properties at low temperatures. The prepared In2O3 film exhibited more than 90% light transmittance and ideal resistivity performance on a flexible substrate."

Sophie Laurent, Postdoc, Bioinorganic Chemistry Group

"The unique fluorine-substituted metal centers facilitated metal-mediated biomolecule labeling in our protein tagging experiments. Their paramagnetic properties also aided in MR imaging contrast studies."

Emily Navarro, Senior Electrochemistry Researcher, Energy Research Laboratory

"We used cobalt(II) bis(trifluoromethylsulfonyl) imide as a redox-mediated additive in the construction of a 4.5 V high-voltage system, and found that its electrochemical in carbonate solvent system It is found that its electrochemical stability in a carbonate solvent system is much better than that of other Co(II) complexes, which greatly improves the cycle life."

Natalie Grant, Process Engineer

"These fluorinated complexes serve as superb precursors in CVD and ALD thin-film processes. Their volatility and decomposition profiles are well-suited for industrial-scale applications."

Dr. Rohit Meno, Postdoctoral Researcher, Photonic Functional Materials Research Institute

"In the process of synthesizing NIR luminescent coordination materials, we chose neodymium trifluoroacetylacetonate as the rare earth source material. Thanks to its fluorinated ligand structure, it effectively reduces non-radiative transition losses and improves near-infrared luminescence intensity and resolution. This product is very suitable for the precise synthesis of complex optical functional materials."

Carlos Mendes, Technical Director

"We’re exploring fluorinated metal complexes as enzyme mimics in catalytic pathways. Alfa Chemistry’s offerings have enabled us to screen multiple configurations with consistent batch quality and competitive pricing."

What Our Customers Ask

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.