How to Select and Use Platinum Catalysts: A Complete Guide to Homogeneous, Heterogeneous, and Electrocatalysis (with an Aladdin Catalog No. Cross-Reference Table)
How to Select and Use Platinum Catalysts: A Complete Guide to Homogeneous, Heterogeneous, and Electrocatalysis (with an Aladdin Catalog No. Cross-Reference Table)
What Is a Platinum Catalyst?
A platinum (Pt) catalyst refers to a catalytic material or catalytic system that uses platinum (Pt) as the active center to significantly lower the activation energy of a reaction, thereby increasing reaction rate and selectivity. It can be either:
- Homogeneous catalyst: Platinum is dissolved in the reaction system as molecules/complexes (e.g., platinum catalysts commonly used for hydrosilylation/silicon–hydrogen addition in the organosilicon industry). It is especially critical in “addition-cure” systems such as silicone rubber, adhesives, and electronic encapsulation.
- Heterogeneous catalyst: Platinum is present as metal nanoparticles or oxides supported on a carrier, and is widely used in hydrogenation, dehydrogenation, redox reactions, as well as electrocatalysis.
- Supported type: Pt/support (Pt/C, Pt/Al₂O₃, Pt/SiO₂, …)
- Unsupported powders/oxides: Pt black, Pt sponge, PtO₂ (Adams’ catalyst), etc. (PtO₂ is often a precatalyst)
Term | One-sentence explanation | Typical form | Where it is used |
Homogeneous Pt catalyst | Dissolves in the reaction medium; catalysis proceeds via a molecular-level Pt active center cycling through elementary steps | Pt complex solution | Hydrosilylation; addition curing of silicone rubber |
Heterogeneous Pt catalyst | Pt catalyzes on solid surface sites and can be filtered and recovered after reaction | Pt/C, Pt/Al₂O₃, Pt black, etc. | Hydrogenation, dehydrogenation, redox reactions |
Pt metal source/precursor | Not necessarily “directly catalytic,” but can be reduced/deposited or undergo ligand exchange to generate active Pt | H₂PtCl₆, K₂PtCl₄, PtCl₄, etc. | Preparing supported catalysts / in situ generation of active species |
You can think of “platinum catalysts” as a family: although they are all called “Pt catalysts,” differences in form (homogeneous/heterogeneous/electrocatalytic), oxidation state (Pt(0)/Pt(II)/Pt(IV)), and ligands/supports can lead to completely different performance and application scenarios.
What Makes Platinum Catalysts “Special”?
Platinum has remained a “top performer” in catalysis mainly for three reasons:
1. Strong interactions with key small molecules/bonds and reversible activation capability
- Pt can efficiently adsorb and activate substrates such as H₂, alkenes, and alkynes. In homogeneous systems, Pt centers can also form new bonds efficiently through typical organometallic steps such as oxidative addition–migratory insertion–reductive elimination. In hydrosilylation, for example, the classic Chalk–Harrod mechanism represents such an “organometallic catalytic cycle.”
2. High selectivity and mild conditions
- In the organosilicon industry, Pt-catalyzed hydrosilylation (addition of Si–H across C=C) is the core reaction for forming Si–C bonds and achieving crosslinking/curing. This reaction “hardly proceeds without a catalyst, but with an appropriate Pt catalyst it can be completed rapidly under mild conditions,” making it one of the industrial standard approaches.
3. A toolbox enabled by ligand/support engineering
- Even for the same hydrosilylation, Speier’s catalyst (a chloroplatinic-acid-based system) and Karstedt’s catalyst (a Pt(0) system with vinyl-siloxane ligands) each have advantages in solubility, activity, controllability, and side reactions. In practice, inhibitors can be used to create a time window such as “no reaction at room temperature, curing only upon heating.”
Are Platinum Catalysts Important?
Yes—platinum catalysts are “key enabling technologies” in multiple industries.
- In the organosilicon industry, Pt-catalyzed hydrosilylation is the core pathway for forming Si–C bonds and enabling addition curing, and is considered one of the highly relied-upon key processes in this industry.
- In hydrogen energy and fuel cells, Pt-based electrocatalysis remains one of the mainstream routes (also driving a wave of research on “reducing Pt usage and improving durability”).
- Without a catalyst: slow reactions, harsh conditions, more side reactions, and difficult scale-up
- With an appropriate Pt catalyst: fast completion under mild conditions, good selectivity, a designable process window (inhibition/heat-triggering), and stronger reproducibility
How to Understand Pt-Catalyzed Mechanisms
A. Homogeneous: Think of It as “a Metal Center Running a Cycle”
Using Pt-catalyzed hydrosilylation (Si–H addition) as an example, the classic Chalk–Harrod (and modified) models can be understood by the sequence “coordination → oxidative addition → migratory insertion → reductive elimination” (a simplified description intended to capture the logic of the catalytic cycle).
- Oxidative addition of Si–H to Pt (Pt inserts into Si–H to form Pt–H / Pt–Si)
- Migratory insertion of the alkene (alkene inserts into the Pt–H bond)
- Reductive elimination to form a new Si–C bond, releasing the product and regenerating a Pt species that can continue catalysis
Key step | What happens | Observable implications / significance |
Oxidative addition | Pt “splits” Si–H to form Pt–H / Pt–Si | Generates reactive intermediates that can proceed further |
Migratory insertion | Alkene inserts into Pt–H (or related bond) | Determines regioselectivity and reaction rate |
Reductive elimination | Forms the Si–C bond; Pt returns to a catalytically competent state | Product formation; catalytic cycle closes |
Note: Common industrial “inhibitors” can be understood as follows: they temporarily occupy/passivate Pt active sites, preventing rapid crosslinking at low temperature. Heating typically changes the coordination equilibrium/dissociation rate between the inhibitor and Pt, or leads to inhibitor consumption, so that the system exhibits “controllably triggered accelerated curing.” Studies on inhibition mechanisms (e.g., β-alkynols) indicate that temperature and functional-group selectivity are key factors.
B. Heterogeneous/Electrocatalysis: Think of It as “Surface Sites Doing Adsorption–Reaction–Desorption”
For Pt/C, Pt black, Pt/Al₂O₃, etc., the key points are:
- Activity originates from surface sites (in general, larger specific surface area and better metal dispersion often lead to higher activity)
- Reactions usually proceed through: substrate adsorption → surface activation/transformation → product desorption
- In electrocatalysis (fuel cells/water electrolysis), the site structure and adsorption strength of surface intermediates determine overpotential, durability, and poisoning resistance. Pt/C is commonly used as a fuel-cell electrocatalyst material.
One-line flow diagram for heterogeneous mechanisms:
Substrate diffusion to the surface → adsorption (site occupation) → surface activation / bond formation or bond cleavage → product desorption → site regeneration
Platinum Catalysts and Related Products: How to Classify Products
Primary category | Secondary category | Representative form | Typical use | Advantages | Common limitations | Activation/pretreatment essentials | Recovery/handling recommendations | Key specifications |
Direct Pt catalysts | Homogeneous hydrosilylation / addition curing | Pt(0) complex solutions; modified Pt(0); in situ activation systems from Pt sources | Hydrosilylation, silicone gel addition curing, crosslinking | High activity; process window possible (with inhibitors) | Sensitive to inhibition/poisoning; overdosing may cause runaway | Usually no pretreatment; pay attention to addition order, thorough mixing, temperature control | Collect Pt-containing residues for centralized recovery; follow enterprise/lab disposal rules | Pt concentration/unit; solvent system; controllability (pot life); impurity control |
Direct Pt catalysts | Supported heterogeneous (general hydrogenation) | Pt/C, Pt/Al₂O₃, Pt/SiO₂, PtO₂, etc. | Hydrogenation/reduction; dehydrogenation/redox (system-dependent) | Easy separation; recyclable; suitable for scale-up | Mass-transfer limitations; batch variability; easily poisoned | Pre-reduction/drying as needed; standardized pretreatment improves reproducibility | Filter and recover solids; calcination/regeneration possible (depending on system and regulations) | Pt loading (wt%); moisture content; support type/pore structure; particle size/dispersion; whether pre-reduced |
Direct Pt catalysts | Specific selectivity / anti-poisoning type | S-modified Pt / Pt on S-doped supports / Pt–S related systems; modified-support Pt, etc. | Selective hydrogenation; special substrate systems | Better selectivity or tolerance | Highly application-specific; narrower operating window | Often requires specified activation steps (reduction/sulfidation conditions, etc.) | Handle solid waste/residues per SDS and regulations | Whether sulfidized; whether pre-reduced; support and promoters; moisture content |
Electrocatalyst materials | Electrocatalysis-grade Pt/C | Pt/C (fuel-cell grade/electrocatalysis grade) | PEM fuel cells; general electrode research | Benchmark material; comparable datasets | Degradation (agglomeration/support corrosion) | For electrode prep, focus on ink formulation (solvent/ionomer) and ultrasonic dispersion | Collect remaining electrodes/slurries for centralized recovery | Particle size/dispersion; grade (FC grade); support type; Pt loading (wt%) |
Electrocatalyst materials | Alloy/bimetallic electrocatalysts | PtRu/C, Pt₃Co/C, PtCo/C, etc. | CO tolerance; tuning intermediate adsorption; ORR enhancement, etc. | Improved activity/tolerance | High demands on composition/preparation consistency | Electrode prep depends more strongly on formulation and process window | Same as above | Alloy composition; particle-size distribution; support stability; grade |
Catalyst materials | Pt black / Pt sponge / nano-Pt | Pt black, sponge Pt, nanoparticles, colloids/dispersions | Heterogeneous catalysis, model studies, electrode fabrication, deposition/loading | High specific surface area (especially Pt black/nano-Pt) | Higher requirements for powder/colloid stability and safety | For nanosystems, consider dispersion medium and stabilizers; for powders, avoid dust and agglomeration | Collect residual powders/dispersions for Pt recovery | Particle size; dispersion medium; surfactant-free or not; purity (metals basis) |
Catalyst precursors/metal sources | Inorganic salts/acids/standard solutions | Chloroplatinic acid and salts, chloroplatinite salts, platinum nitrate solutions, Pt halides, etc. | Preparing Pt/support catalysts, in situ reduction to Pt nanoparticles, starting materials for coordination synthesis | Flexible; suitable for impregnation/deposition; easy quantification | Usually not “directly catalytic”; needs reduction/deposition | Key variables: reductant, pH, temperature, chloride ions and washing, loading procedure | Collect Pt-containing solutions for centralized recovery; handle per corrosive/sensitization risk | Purity (metals basis); concentration; counter-anion system (Cl⁻/NO₃⁻); water/solvent compatibility |
Catalyst precursors/metal sources | Organometallic precursors | Pt(acac)₂, Pt(hfac)₂, Pt(II)/Pt(IV) organometallics, etc. | Thin films/nanomaterial preparation; specific ligation and activation | Suitable for materials processing | More “materials precursors” than general catalysts | Optimize by process (thermal decomposition/reduction/deposition) | Dispose residues per organometallic waste rules | Purity; metal content; volatility/solubility; process window |
Analysis-dedicated catalysts | Pt catalysts for elemental analyzer combustion | Fixed-bed granules/packing | Combustion/oxidation in CHNS/O elemental analysis | Clear purpose; mature methodology | Different evaluation system from synthetic catalysis catalysts | Operate per instrument method and packing procedures | Replace/dispose consumables per regulations | Particle size; Pt content; compatible consumable specifications |
Related materials (boundary note) | Electrode/structural materials | Pt foil/wire/alloy wire, conductive pastes, etc. | Electrodes/connections, thermocouples/high-temperature parts, conductive coatings | Corrosion-resistant; stable | Not the same as “catalyst”; catalytic function depends on structure/surface | Usually no activation required (but surface state affects electrochemical behavior) | High recycling value as precious metal materials | Form factor/dimensions; purity; alloy composition; processing state |
Related materials (boundary note) | Analytical standards | Pt standard solutions/CRMs | Quantification in ICP/AA, etc. | Traceable; accurate | Not for catalysis | — | — | Concentration; acid matrix; certificate information |
Common R&D/Lab Uses and “Selection Methods” — Application Scenario → Recommended Form → Typical Product Category
Application scenario | Recommended Pt catalyst form | Typical product category | Can be dosed directly? | Most critical specs | Common risks/notes |
Organosilicon hydrosilylation / addition curing (silicone rubber, encapsulants, gels, etc.) | Homogeneous Pt catalysts (Pt(0) complexes or in situ activation from Pt sources) | Karstedt-type Pt(0) solutions; modified Pt(0) (e.g., NHC-stabilized); Speier-type systems (chloroplatinic acid in isopropanol, system/solution) | Usually yes (some systems generate active species in situ) | Pt concentration (mol/L or wt%); solvent/carrier (siloxanes/xylene, etc.); system controllability (pot life/inhibitor compatibility) | Susceptible to inhibition/poisoning (S/P/amines/alkynols, etc.); overdosing may cause runaway exotherm/side reactions; sensitive to mixing uniformity and temperature |
Hydrogenation/reduction in organic synthesis (common in labs) | Supported heterogeneous Pt | Pt/C; Pt/Al₂O₃; Pt/SiO₂; PtO₂ (Adams type) | Yes | Pt loading (wt%); moisture content (wet cake/dry powder); support type; dispersion/specific surface area; need for pre-reduction | Easily poisoned by S/P/strongly coordinating impurities; activity fluctuations due to moisture/pretreatment differences; pay attention to filtration, stirring/mass transfer, and hydrogen safety |
Selective hydrogenation / anti-poisoning needs (more process/scale-up oriented) | Supported heterogeneous Pt (modified/sulfidized if needed) | Sulfidized Pt/C; Pt on specific supports (carbon/alumina/silica, etc.) | Yes (may require activation) | Whether “pre-reduced/pre-sulfidized”; support and promoters; moisture and storage form | Selectivity depends on system and pretreatment; sulfidized catalysts have higher requirements for operation/disposal (per SDS) |
Oxidation / catalytic combustion (CO/VOCs environmental and process oxidation) | Supported heterogeneous Pt | Pt/Al₂O₃, Pt/SiO₂, Pt black, etc. (engineering often uses fixed-bed/coated forms) | Yes | Support heat resistance/pore structure; Pt dispersion; presence of promoters; formed shape (powder/pellet/coating) | Sintering deactivation at high temperature; sulfur/halogens easily poison; manage bed pressure drop and thermal management |
Dehydrogenation / reforming / petrochemical applications (macroscopically important) | Supported heterogeneous Pt (often with promoters/acidic supports) | Pt/Al₂O₃ types (industrial systems are often composite formulations) | Often usable as supplied (highly application-specific formulations) | Form factor and promoter system; heat resistance/anti-sintering; regeneration method | Highly system-specific; regeneration conditions are critical; impurities (S/Cl/water) greatly affect performance |
Electrocatalysis (fuel cells/electrode research/electrolysis) | Electrocatalysis-grade Pt nano/alloys + conductive supports | Pt/C (electrocatalysis grade); PtRu/C; Pt₃Co/C; Pt black (fuel-cell grade); Pt-graphene/composites | Yes (for electrode/catalyst-layer fabrication) | Particle size/dispersion; ECSA/surface-area indicators (if available); support stability; alloy composition; grade (fuel-cell grade) | Sensitive to impurities (especially CO/S); degradation from support corrosion/particle agglomeration; match solvent/ionomer system |
Elemental analysis / combustion analysis (common “Pt catalyst” request) | Fixed-bed granular Pt catalytic packing | Pt catalysts for elemental analysis (various Pt contents and particle sizes) | Yes | Particle size and bed packing; Pt content; instrument/consumable compatibility | Different from organic-synthesis catalysts; instrument method/consumable specifications are more important |
Preparing supported Pt / nano-Pt (catalyst preparation routes) | Pt precursors/metal sources (solutions or salts) | Chloroplatinic acid and salts; chloroplatinite salts; platinum nitrate solutions; Pt halides, etc. | Usually no (needs reduction/deposition/activation) | Purity (metals basis); concentration (standard solutions preferred); anion type (Cl⁻/NO₃⁻, etc.); water/solvent system | “No reaction after addition” often due to being only a precursor; reduction conditions and residual chloride affect performance; handle corrosive/sensitization risks per SDS |
Thin films/coatings/material deposition (research preparation) | Organometallic precursors/complexes | Pt(acac)₂, Pt(hfac)₂, specific Pt(II)/Pt(IV) organometallics, etc. | Usually no (primarily for preparation) | Volatility/solubility; purity; metal content; process window (temperature/atmosphere) | More like “materials precursors” than general catalysts; processing conditions determine film/particle morphology |
Safety and Experimental Notes
Hazards vary widely among different Pt compounds/catalysts; always refer to the SDS. Only the most critical reminders are listed here:
- Chloroplatinic acid (hexachloroplatinic acid) is classified in some SDSs as corrosive, acutely toxic, and skin/respiratory sensitizing. Use appropriate PPE, avoid inhalation of dust/aerosols, and operate under ventilation.
- High-surface-area metal powders such as platinum black may show higher reactivity under certain conditions. Strictly follow the supplier’s SDS requirements for storage, transfer, and disposal. Avoid generating inhalable dust during filtration/drying; in hydrogenation systems, keep hydrogen isolated from ignition sources/heat and manage pyrophoricity/flammability risks (per the specific SDS).
- "Platinum is expensive": in experimental planning, it is recommended to incorporate “Pt recovery/centralized handling of Pt-containing residues” into the SOP.
Q&A
Q1: Does higher Pt content always mean better catalytic performance?
Not necessarily.
- Homogeneous: activity depends on the “Pt species available for the catalytic cycle.” Too high a loading may increase side reactions or cause an uncontrollably fast reaction.
- Heterogeneous: performance depends on surface area and dispersion. A 10 wt% Pt/C is not necessarily faster than a 5 wt% Pt/C; if particles are larger and dispersion is poorer, there may be fewer effective active sites.
Q2: Why do different brands/batches vary so much even if they are all called Pt/C?
- Because Pt/C has many key variables: support type, pore structure, Pt particle size, dispersion, reduction degree, moisture content, and residual additives can all affect activity and selectivity. Recommendations: lock the supply specification + lock the pretreatment procedure + run small-scale benchmarking.
Q3: Are chloroplatinic acid (Speier system) and Karstedt’s catalyst the same thing?
No.
- The chloroplatinic-acid system is more like a “Pt source + solvent/ligand environment” and often needs to form active species in situ.
- Karstedt-type catalysts are commonly used Pt(0) complex systems and, in practice, are more like “ready-to-use catalyst product forms.”
Q4: Why does my silicone addition-cure system sometimes “not cure at all”?
- A common cause is inhibition/poisoning: sulfur, phosphorus, amines, certain alkyne inhibitors, and even impurities in some additives may passivate Pt. A practical troubleshooting approach is “one-by-one raw-material exclusion”: first validate the base formulation + catalyst, then add additives one at a time.
Q5: Why do bubbles, yellowing, or side reactions occur after adding a Pt catalyst?
Possible causes:
- Excessive temperature or high local concentration leading to side reactions
- Activatable impurities in the formulation (e.g., certain unsaturated species, peroxides, sulfur-containing components)
Countermeasures: reduce dosage, optimize mixing order, use inhibitors/stepwise heating, improve raw-material purity.
Q6: How to choose between Pt black, Pt sponge, and nano-Pt dispersions?
- Pt black/nano-Pt: high specific surface area; suitable for electrocatalysis or model studies, but “more reactive” and requires more standardized handling.
- Pt sponge: coarser structure; often used in certain heterogeneous catalysis/high-temperature applications or as a material.
- Nano dispersions: good dispersion and easy for coatings/electrodes; pay attention to solvent systems, stabilizers, and long-term stability.
Q7: Are Pt foil/Pt wire considered “Pt catalyst-related”?
- Strictly speaking, they are mainly materials for electrodes/thermocouples rather than “catalyst products.”
- However, if your scenario is electrode fabrication, catalytic electrode supports, or corrosion-resistant conductors, they can be regarded as “catalysis-related materials.”
Q8: Do I have to use Pt for electrocatalysis? What is the logic of PtRu and PtCo?
Pt is still a benchmark material in many systems. Alloying (e.g., PtRu, Pt₃Co) is often used to:
- Change intermediate adsorption strength and improve activity
- Improve poisoning resistance, durability, or specific reaction performance—while also bringing considerations of cost, stability, and preparation consistency.
Q9: Can I use a “Pt salt” directly as a catalyst?
- Sometimes yes, but more often it is a precursor: it must be reduced/ligated/deposited in the system before it shows the expected catalytic performance. If “controllability and reproducibility” are required, it is generally recommended to choose a “direct catalyst form” (homogeneous solutions or mature supported catalysts).
Q10: Is a “purer” Pt catalyst always better?
- For “trace-sensitive” research (electrocatalysis, ultra-low loading, precision organosilicon curing), higher purity is usually more stable. For general hydrogenation scale-up, specification consistency and repeatable pretreatment are often the key—purity is not the only variable.
Representative Aladdin Platinum Catalysts and Pt Source Products
The table below summarizes representative Aladdin platinum catalysts and Pt source products, covering two major groups—from ready-to-use catalyst forms to metal sources/precursors used for catalyst preparation, deposition, or coordination synthesis—to help readers quickly locate suitable options by application scenario.
It is recommended to first review the categories to clarify the intended use (e.g., homogeneous Pt(0) solutions for hydrosilylation, heterogeneous supported Pt catalysts/metal powders, electrocatalyst materials, Pt salts and solution-type Pt sources), then screen by key specifications (such as Pt content/loading (wt%), concentration (mol/L), particle size/dispersion, grade and purity (metals basis), and the solvent/carrier system), and finally use the Aladdin catalog number and CAS number for lookup and cross-referencing.
Please note that the same system may correspond to different CAS numbers depending on its form (e.g., solution, hydrate, or hexahydrate). For solution-type products, it is recommended to consider both the active component and the solvent/carrier information to ensure accurate dosing, compatibility, and reproducibility. For more specifications, please refer to the consolidated product list at the end of the article or search the Aladdin website by CAS number or product name.
Category | Aladdin Cat. No. | Product name | CAS No. | Specification or purity | Key features or applications |
Heterogeneous: supported/doped Pt (ready to use) | Platinum on silica | – | extent of labeling: 1 wt% loading, dry | Pt supported on SiO₂ (1 wt%); easy filtration and recovery; suitable for heterogeneous screening/pre-scale evaluation | |
Heterogeneous: supported/doped Pt (ready to use) | G489426 | Pt-doped graphene powder | 7782-42-5 | Pt content: 40–50 wt% | Conductive composite material; preferred for electrocatalysis research; high Pt content for benchmarking and materials development |
Heterogeneous: metallic Pt (Pt black/powder) (ready to use) | Platinum black | 7440-06-4 | ≥99.9% metals basis, fuel-cell grade | Preferred for electrocatalysis/fuel-cell work; low impurities and batch consistency are critical | |
Heterogeneous: metallic Pt (Pt black/powder) (ready to use) | Platinum black | 7440-06-4 | ≥99.99% trace metals basis, ≤100 nm | Nano Pt black; high activity; suitable for rapid screening/electrocatalysis research | |
Heterogeneous: metallic Pt (Pt black/powder) (ready to use) | Platinum black | 7440-06-4 | ≥99.9% metals basis, low bulk density | Low bulk density for easier dispersion/coating; more friendly for heterogeneous catalysis and electrocatalyst ink preparation | |
Heterogeneous: metallic Pt (powder) (ready to use) | Platinum | 7440-06-4 | Nano powder, <50 nm particle size (TEM) | Nano Pt powder; suitable for catalysis/conductive fillers/materials research | |
Heterogeneous: shaped catalyst (specific use) | Platinum catalyst | — | For elemental analysis, Pt 5%, Φ: 2–3 mm | Promotes combustion/oxidation for elemental analysis; shaped pellets for easy packing; CAS not provided | |
Hydrosilylation Pt(0) (silicone rubber curing) | Platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane | 68478-92-2 | Pt: ~2% in xylene | Classic Pt system for hydrosilylation; dosage can be accurately calculated based on Pt content | |
Hydrosilylation Pt(0) (silicone rubber curing) | Platinum(0)-2,4,6,8-tetramethyl-2,4,6,8-tetravinylcyclotetrasiloxane complex solution | 68585-32-0 | 0.104 M in methylvinylcyclosiloxanes | Solution-type Pt(0) for hydrosilylation; convenient formulation and suitable for process screening | |
Hydrosilylation Pt(0) (more stability-oriented ligands) | [1,3-Dicyclohexyl-imidazol-2-yl][1,3-divinyl-1,1,3,3-tetramethyldisiloxane]platinum(0) | 400758-55-6 | ≥99.95% metals basis | NHC-ligated system; often better for storage stability/controllability (relative) | |
Hydrosilylation Pt(0) (more stability-oriented ligands) | B196251 | [1,3-Bis(2,6-diisopropylphenyl)imidazol-2-yl][1,3-divinyl-1,1,3,3-tetramethyldisiloxane]platinum(0) | 873311-51-4 | ≥99.95% | NHC-ligated system; one option for improved stability; suitable where a wider formulation window is needed (relative) |
Hydrosilylation Pt(0) (more stability-oriented ligands) | [1,3-Di(2,6-diisopropylphenyl)-2-dihydroimidazolyl][1,3-divinyl-1,1,3,3-tetramethyldisiloxane]platinum(0) | 849830-54-2 | ≥99.95% metals basis | NHC-ligated system; for addition curing/hydrosilylation studies or process screening (relatively more storage-tolerant) | |
Pt sources: chloroplatinic acid/chloroplatinates (prep/deposition) | Chloroplatinic acid hydrate | 16941-12-1 | PrimorTrace™, ≥99.995% metals basis | Ultra-high purity with trace-metal control; preferred for mechanistic/high-sensitivity systems | |
Pt sources: chloroplatinic acid/chloroplatinates (prep/deposition) | Chloroplatinic acid, hydrate | 26023-84-7 | ≥99.95% metals basis | Classic Pt source for impregnation/supported catalyst preparation; broadly applicable | |
Pt sources: chloroplatinic acid/chloroplatinates (prep/deposition) | Chloroplatinic acid hexahydrate | 18497-13-7 | BioReagent | Common in bio/coupling-related research; also usable as a Pt source | |
Pt sources: chloroplatinic acid/chloroplatinates (prep/deposition) | Ammonium chloroplatinate | 16919-58-7 | Pt ≥43.4% | Common Pt source; convenient for solution preparation/impregnation | |
Pt sources: chloroplatinic acid/chloroplatinates (prep/deposition) | Ammonium chloroplatinite | 13820-41-2 | Pt 52.0% | Pt(II) salt source; for complex synthesis or supported catalyst preparation | |
Pt sources: chloroplatinic acid/chloroplatinates (prep/deposition) | Potassium chloroplatinate | 16921-30-5 | ≥99.9% metals basis | Common Pt source; for solution preparation/impregnation | |
Pt sources: chloroplatinic acid/chloroplatinates (prep/deposition) | Potassium chloroplatinite | 10025-99-7 | ≥99.9% metals basis, Pt ≥46% | Pt(II) salt source; suitable for coordination chemistry and catalyst-precursor preparation | |
Pt sources: chloroplatinic acid/chloroplatinates (prep/deposition) | Sodium tetrachloroplatinate(II) hydrate | 207683-21-4 | Pt 44.5% | Pt(II) chloro-complex salt; commonly used Pt source/precursor | |
Pt sources: chloroplatinic acid/chloroplatinates (prep/deposition) | Sodium hexachloroplatinate(IV) hexahydrate | 19583-77-8 | Pt 34.0% | Pt(IV) chloro-complex salt; common for impregnation/deposition | |
Pt sources: chloroplatinic acid/chloroplatinates (prep/deposition) | Sodium hexachloroplatinate | 16923-58-3 | ≥98% | General Pt source; commonly used for solution prep/impregnation | |
Pt sources: simple Pt chlorides (prep/synthesis) | Platinum(IV) chloride | 13454-96-1 | Pt ≥57% | Pt salt precursor; can be used to synthesize various Pt complexes/catalyst precursors | |
Pt sources: simple Pt chlorides (prep/synthesis) | Platinum(II) chloride | 10025-65-7 | Pt basis ≥73% | Common Pt(II) salt; for coordination chemistry/catalyst-precursor synthesis | |
Pt sources: simple chloro complexes (prep/synthesis) | cis-Diamminetetrachloroplatinum(IV) | 16893-05-3 | ≥99.9% metals basis | Pt(IV) chloro complex; precursor, mechanistic and synthetic starting material | |
Pt sources: simple chloro complexes (prep/synthesis) | Potassium trichloroammineplatinate(II) | 13820-91-2 | ≥99.9% metals basis | Pt(II) complex salt; for further ligand substitution/synthesis | |
Pt sources: simple chloro complexes (prep/synthesis) | Potassium trichloro(ethylene)platinate(II) monohydrate | 12012-50-9 | ≥98% | Pt(II) complex salt; precursor for synthesis/research | |
Pt sources: simple chloro complexes (prep/synthesis) | Potassium trichloro(ethylene)platinate(II) hydrate | 123334-22-5 | ≥95% | Pt(II) complex salt; precursor for synthesis/research | |
Inorganic precursors: oxides | Platinum oxide | 1314-15-4 | Pt, 80–86% | Platinum oxide; can be used directly for some reactions or reduced to active Pt | |
Inorganic precursors: oxides | Platinum(IV) oxide monohydrate | 12137-21-2 | Pt ≥75% | Pt(IV) oxide monohydrate; often used as a reducible precursor | |
Inorganic precursors: oxides | Platinum oxide hydrate | 52785-06-5 | ≥99.95% metals basis | High-purity Pt oxide hydrate; more suitable for mechanistic/material preparations | |
Inorganic precursors: iodides | Platinum(IV) iodide | 7790-46-7 | Pt content: 27% | Pt halide precursor; for coordination chemistry/catalyst-precursor synthesis | |
Inorganic precursors: iodides | Platinum(II) iodide | 7790-39-8 | ≥98% | Pt(II) halide; catalyst precursor/complex synthesis | |
Inorganic precursors: bromides | Platinum(II) bromide | 13455-12-4 | ≥98% | Pt(II) halide; coordination chemistry/catalyst precursor | |
Inorganic precursors: bromides | Platinum(IV) bromide | 68938-92-1 | — | Pt(IV) halide; precursor/synthetic starting material | |
Inorganic precursors: sulfides | Platinum(IV) sulfide | 12038-21-0 | ≥99.9% metals basis | For sulfide systems/electrocatalysis benchmarking; relevant to specific environments | |
Inorganic precursors: nitrate/sulfite solutions | Platinum nitrate solution | 18496-40-7 | Pt, 18.02% | Solution-type Pt source; convenient for quantitative impregnation/preparation | |
Inorganic precursors: nitrate/sulfite solutions | Platinum sulfite solution | 61420-92-6 | 15.3% Pt | Solution-type Pt source; suitable for aqueous/impregnation routes | |
Inorganic precursors: nitrate complexes | Tetraammineplatinum(II) nitrate | 20634-12-2 | ≥99.995% metals basis | High-purity inorganic Pt precursor; suitable for synthesis/deposition/mechanistic studies | |
Inorganic precursors: hexa-halo platinates | Sodium hexabromoplatinate(IV) hexahydrate | 39277-13-9 | Pt 23.5% | Pt(IV) hexa-halo complex; for complex synthesis/precursors | |
Inorganic precursors: hexa-halo platinates | Potassium hexabromoplatinate(IV) | 16920-93-7 | ≥99% | Pt(IV) hexa-halo salt; precursor/synthetic starting material | |
Inorganic precursors: hexa-halo platinates | Potassium hexaiodoplatinate(IV) | 16905-14-9 | ≥99.7% metals basis | Pt(IV) hexa-halo salt; precursor/synthetic starting material | |
Inorganic precursors: hexahydroxyplatinate (salts/acids) | Sodium hexahydroxyplatinate(IV) | 12325-31-4 | 51.2–62.5% Pt basis (gravimetric) | Water-soluble/alkaline Pt(IV) source; friendly for aqueous preparation/deposition | |
Inorganic precursors: hexahydroxyplatinate (salts/acids) | Potassium hexahydroxyplatinate(IV) | 12285-90-4 | ≥99.95% metals basis | High-purity hexahydroxyplatinate; more convenient in aqueous systems | |
Inorganic precursors: hexahydroxyplatinate (salts/acids) | Hexahydroxyplatinic acid(IV) | 51850-20-5 | ≥99% metals basis | Acid form; more flexible for formulation/system selection | |
Inorganic precursors: other solution-type Pt sources | Dihydrogen dinitrosyl sulfate platinum(II) solution, Pt 4–6% (cont. Pt) | 12033-81-7 | — | Solution-type Pt source; convenient dosing and content control | |
Solutions/colloids: dispersed Pt | Pt/tetra-n-octylammonium chloride colloid | 7440-06-4 | purified 70–85% Pt | Colloidal dispersed Pt; easy to introduce into organic phases/material systems; suitable for composite catalyst materials | |
Solutions/colloids: dispersed Pt | Platinum (TAA) solution | 127733-97-5 | ≥99.95% metals basis | Solution-type Pt; convenient for metering and homogeneous introduction | |
Homogeneous: COD / labile-ligand Pt(II) | (1,5-Cyclooctadiene)platinum(II) dichloride | 12080-32-9 | ≥99.95% metals basis | Common Pt(II) precursor; ligands readily exchanged; suitable for homogeneous catalysis/complex synthesis | |
Homogeneous: COD / labile-ligand Pt(II) | (1,5-Cyclooctadiene)platinum(II) dibromide | 12145-48-1 | ≥98% | Similar to COD dichloride; halide difference for route selection/comparison | |
Homogeneous: COD / labile-ligand Pt(II) | (1,5-Cyclooctadiene)platinum(II) dimethyl | 12266-92-1 | ≥97% | Pt(II) organometallic precursor; for synthesis/mechanistic studies | |
Homogeneous: labile-ligand Pt(II) | Dichloro(norbornadiene)platinum(II) | 12152-26-0 | ≥97% | NBD-type complex; suitable for further ligand exchange/homogeneous catalysis research | |
Homogeneous: labile-ligand Pt(II) | Dichloro(dicyclopentadienyl)platinum(II) | 12083-92-0 | ≥97% | Ligand-exchangeable Pt(II) precursor; for synthesis and catalysis research | |
Homogeneous: dba-type Pt(0) precursor | Tris(dibenzylideneacetone)platinum(0) | 11072-92-7 | ≥98% | Active Pt(0) precursor; commonly used for homogeneous screening/ligand-system development | |
Homogeneous: dba-type Pt(0) precursor | Tris(dibenzylideneacetone)dipltinum(0) | 63782-74-1 | ≥98% | Pt(0) precursor; used to generate active Pt(0) species for catalyst screening | |
Homogeneous: Cp/organometallic Pt precursor | (Trimethyl)ethylcyclopentadienylplatinum(IV) | 229621-40-3 | ≥99.999% | Organometallic Pt precursor; for synthesis/deposition/mechanistic studies | |
Homogeneous: Cp/organometallic Pt precursor | (Trimethyl)pentamethylcyclopentadienylplatinum(IV) | 97262-98-1 | ≥99% | Organometallic Pt precursor; for complex synthesis and catalysis research | |
Homogeneous: dedicated catalyst | Hydrido(dimethylphosphinate-kP)[bis(hydrido(dimethylphosphinate-kP))]platinum(II) [Ghaffar–Parkins catalyst] | 173416-05-2 | ≥95% | Classic research catalyst; for specific reactions/mechanistic benchmarking | |
Homogeneous: β-diketone Pt(II) | Platinum(II) acetylacetonate | 15170-57-7 | PrimorTrace™, ≥99.99% metals basis | Good solubility; commonly used in homogeneous catalysis/material deposition/precursors (high purity) | |
Homogeneous: β-diketone Pt(II) | Platinum(II) hexafluoroacetylacetonate | 65353-51-7 | ≥99.9% metals basis | Stronger electron-withdrawing ligand system; common in deposition/precursor and comparison studies | |
Homogeneous: carbonyl Pt(II) | cis-Dichlorodicarbonylplatinum(II) | 25478-60-8 | ≥99.9% metals basis | Carbonyl complex; for mechanistic studies/coordination-chemistry feedstock | |
Homogeneous: oxalate Pt complex salts | Potassium bis(oxalato)platinate(II) dihydrate | 14244-64-5 | ≥99.9% metals basis | Water-soluble Pt complex salt; for complex synthesis/deposition research | |
Homogeneous: oxalate Pt complex salts | Potassium oxalatoplatinate(II) dihydrate | 38685-12-0 | ≥99% | Same category as above; for comparison/route selection | |
Homogeneous: phosphine-ligated Pt (common) | Bis(tri-tert-butylphosphine)platinum(0) | 60648-70-6 | ≥95% | Pt(0) phosphine system; for homogeneous catalysis/ligand-effect research | |
Homogeneous: phosphine-ligated Pt (common) | Tetrakis(triphenylphosphine)platinum | 14221-02-4 | Pt 15.2% | Classic phosphine-ligated Pt; homogeneous catalysis/synthetic precursor | |
Homogeneous: phosphine-ligated Pt (common) | cis-Dichlorobis(triphenylphosphine)platinum | 15604-36-1 | Pt ≥24.2% | Classic starting material; convenient for ligand exchange/homogeneous benchmarking | |
Homogeneous: phosphine-ligated Pt (common) | trans-Dichlorobis(triphenylphosphine)platinum(II) | 14056-88-3 | ≥98% | trans isomer for comparison; ligand/configuration effect studies | |
Homogeneous: phosphine-ligated Pt (common) | Dichlorobis(tributylphosphine)platinum | 15076-72-9 | ≥98% | Alkyl-phosphine system; used to compare solubility/steric effects | |
Homogeneous: phosphine-ligated Pt (common) | cis-Dichlorobis(triethylphosphine)platinum(II) | 15692-07-6 | ≥98% | Small alkyl-phosphine system; electronic/steric comparisons | |
Homogeneous: phosphine-ligated Pt (common) | 1,4-Bis(diphenylphosphino)butane dichloroplatinum | 65097-96-3 | ≥95% | Chelating bisphosphine system; facilitates specific coordination environments | |
Homogeneous: aromatic nitrile-ligated Pt(II) | Bis(benzonitrile)dichloroplatinum(II) | 14873-63-3 | Pt ≥41.0% | Nitrile ligands readily exchanged; common for homogeneous precursors/ligand exchange | |
Homogeneous: nitrile-ligated Pt(II) | cis-Bis(acetonitrile)dichloroplatinum(II) | 13869-38-0 | ≥98% | Reactive precursor; acetonitrile is labile for introducing target ligands | |
Homogeneous: DMSO-ligated Pt(II) | cis-Dichlorobis(dimethyl sulfoxide)platinum(II) | 22840-91-1 | ≥97% | DMSO complex; common in synthesis/mechanistic/solubility studies | |
Homogeneous: pyridine-ligated Pt(II) | cis-Dichlorobis(pyridine)platinum(II) | 15227-42-6 | ≥99% | Classic pyridine complex; homogeneous research/precursor | |
Homogeneous: pyridine-ligated Pt(II) | cis-Dichlorobis(pyridyl)platinum(II) | 14872-21-0 | ≥99% | Pyridine-type comparison; ligand electronic-effect studies | |
Homogeneous: thioether-ligated Pt(II) | cis-Dichlorobis(diethyl sulfide)platinum(II) | 15442-57-6 | ≥98% | Thioether ligand system; coordination stability/reactivity comparisons |
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