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dppm (Bis(diphenylphosphino)methane) | CAS 2071-20-7 | 98%
dppm (Bis(diphenylphosphino)methane) | CAS 2071-20-7 | 98%
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Technical Specifications
| CAS Number | 2071-20-7 |
| EC / EINECS Number | 218-194-2 |
| MDL Number | MFCD00003537 |
| SMILES | C1=CC=C(C=C1)P(CP(C2=CC=CC=C2)C3=CC=CC=C3)C4=CC=CC=C4 |
| InChI | InChI=1S/C25H22P2/c1-5-13-22(14-6-1)26(23-15-7-2-8-16-23)21-27(24-17-9-3-10-18-24)25-19-11-4-12-20-25/h1-20H,21H2 |
| InChIKey | XGCDBGRZEKYHNV-UHFFFAOYSA-N |
| PubChem CID | 74952 |
| Molecular Formula | C₂₅H₂₂P₂ |
| Molecular Weight | 384.4 g/mol |
| Melting Point | 118–122 °C |
| Solubility | Insoluble in water; soluble in common organic solvents |
| Purity | ≥98% |
| Physical Form | White to off-white crystalline powder |
| HS Code | 2931.49 |
| Shelf Life | Retest period: 36 months from date of manufacture |
| Storage Conditions | Store tightly sealed under inert gas (N2 or Ar) at room temperature, protected from light, air and moisture. Long-term storage at 2-8 °C recommended. |
Product Description & Scientific Applications
dppm (1,1-bis(diphenylphosphino)methane; methylenebis(diphenylphosphine)) is a classical diphosphine ligand in which a single methylene unit links the two phosphorus donor atoms. This short backbone gives dppm a small natural bite angle of about 73°, so chelation to a single metal forms a strained four-membered ring. Its defining behaviour, however, is bridging two metal centres and holding them in close proximity, making dppm a classic ligand for binuclear and cluster chemistry. The methylene group between the two phosphorus atoms is mildly acidic, especially in coordinated complexes, and can be deprotonated or further functionalised.
Bridging ligand for bimetallic and A-frame complexes
dppm is one of the defining short-bridge diphosphines for assembling binuclear complexes in which two metal centres are held face-to-face by one or more μ-dppm ligands. It is closely associated with A-frame complexes, where a pair of square-planar metal centres is spanned by two bridging dppm ligands and a single bridging atom or group such as carbonyl, hydride, chloride, or a related small bridging ligand. Such systems are documented for metals that favour square-planar geometry, including rhodium, iridium, nickel, palladium, platinum, and gold, and are used to study metal–metal cooperativity, bridging-ligand chemistry, and two-centre reactivity.
Cluster synthesis and di- and polynuclear coordination chemistry
As a short-bite ligand, dppm is used to prepare di- and polynuclear coordination compounds and metal clusters, including palladium, platinum, silver, and gold assemblies. The rigid single-carbon bridge enforces close metal–metal contact, supporting the study of bimetallic cooperativity and two-centre reactivity. It is also used as a supporting ligand in homogeneous catalysis where small bite angle or bimetallic proximity is relevant.
Coinage-metal assemblies and Au(I) luminescence
dppm is used to construct polynuclear coinage-metal assemblies, with Au(I) systems especially prominent in studies of aurophilic interactions and luminescence. Binuclear and polynuclear gold(I) complexes bridged by dppm can hold gold centres at close range, giving rise to Au···Au interactions and associated emission behaviour. These systems are studied for structure–emission relationships, aurophilic interactions, and supramolecular solid-state behaviour.
Reference small-bite-angle diphosphine
Because of its well-defined short backbone, dppm is often used as a small-bite-angle comparator when probing the influence of bite angle on the structure, stability, and reactivity of metal complexes. It can act either as a strained chelate at a single metal or as a bridge between two metals, allowing the same ligand to serve in both roles across comparative studies.
Handling note
As a tertiary arylphosphine, dppm is mildly air-sensitive and oxidises slowly to the corresponding phosphine oxide; for coordination and catalysis work, minimise air exposure and handle under inert atmosphere where ligand purity is critical.
Shipping Destinations
- EU & UK: Priority delivery, 2–5 business days.
- United States (DDP): 3–7 business days, duties and taxes prepaid.
- EFTA Countries (DDP): 3–7 business days, duties and taxes prepaid.
- Worldwide: 7–14 business days, selected locations.
The NorrChemica™ Standard
Identity Verified — Batch-verified via analytical QC; documentation available on request.
Direct EU Distribution — Dispatched from Finland for fast delivery to EU-based laboratories.
Professional Logistics — Tracked courier shipping via UPS / Matkahuolto / Posti.
Packaging & Storage
- Supplied in tightly sealed containers suitable for laboratory handling.
- Store under recommended conditions as specified on the product label and SDS.
- Retest period per lot-specific CoA / label under recommended conditions.
Technical Documentation
- Batch-specific Certificate of Analysis (CoA) included with every order.
- GHS-compliant Safety Data Sheet (SDS) provided with every shipment.
- Batch documentation available for institutional procurement.
| Payment: Wise (Bank Transfer) or Manual Invoice. |
| Disclaimer: Research Use Only (RUO) — not for human or veterinary use. Sold strictly for laboratory research and technical applications. By purchasing this item, the buyer confirms professional intent and compliance with applicable regulations. |
Safety Information
| GHS Pictograms |
|
| Signal Word | Warning |
| Hazard Class | GHS — Warning. Skin Irrit. 2; Eye Irrit. 2; STOT SE 3 (respiratory) per generic phosphine-ligand classification. |
| Transport Category | Not classified as dangerous goods for transport (ADR/IATA/IMDG) |
| H-Statements | H315 - H319 - H335 |
| P-Statements | P261 - P264 - P271 - P280 - P302+P352 - P305+P351+P338 - P332+P313 - P337+P313 - P362+P364 - P501 |
NorrChemica™ is a Finnish supplier of niche research reagents — focused on reliable EU distribution, transparent analytical documentation, and specialist technical support.
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