161583-75-1

Basic information

• Product Name: DIETHYL 2,2':6',2''-TERPYRIDINE-4'-PHOSPHONATE
• Synonyms: DIETHYL 2,2':6',2''-TERPYRIDINE-4'-PHOSPHONATE;Diethyl [2,2':6',2''-terpyridin]-4'-ylphosphonate;Diethyl-4-phosphonte-2,2':6',2''-terpyridine
• CAS NO: 161583-75-1
• Molecular Formula: C19H20N3O3P
• Molecular Weight: 369.35
• Mol File: 161583-75-1.mol
• Article Data: 3

Chemical Properties

• Melting Point: 147.0 to 151.0 °C
• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: DIETHYL 2,2':6',2''-TERPYRIDINE-4'-PHOSPHONATE(CAS DataBase Reference)
• NIST Chemistry Reference: DIETHYL 2,2':6',2''-TERPYRIDINE-4'-PHOSPHONATE(161583-75-1)
• EPA Substance Registry System: DIETHYL 2,2':6',2''-TERPYRIDINE-4'-PHOSPHONATE(161583-75-1)

Safety Data

• Hazardous Substances Data: 161583-75-1(Hazardous Substances Data)

Usage

Uses

Used in Coordination Chemistry:
DIETHYL 2,2':6',2''-TERPYRIDINE-4'-PHOSPHONATE is used as a ligand for forming coordination complexes with metal ions. Its ability to bind with metals allows for the development of new materials with tailored properties and potential applications in areas such as sensing, imaging, and catalysis.
Used in Material Science:
In the field of material science, DIETHYL 2,2':6',2''-TERPYRIDINE-4'-PHOSPHONATE is used as a building block for the construction of supramolecular structures and functional materials. Its unique structure and functional groups contribute to the design of novel materials with specific characteristics, which can be utilized in various high-tech applications.
Used in Catalysis:
DIETHYL 2,2':6',2''-TERPYRIDINE-4'-PHOSPHONATE is employed as a catalyst or catalyst precursor in chemical reactions. Its role in catalysis can enhance the efficiency and selectivity of reactions, making it a valuable component in the development of new catalytic processes and systems.
Overall, DIETHYL 2,2':6',2''-TERPYRIDINE-4'-PHOSPHONATE is a promising chemical compound with a wide range of potential applications across different industries, thanks to its distinctive structure and functional capabilities.

Upstream product

• 762-04-9 Diethyl phosphonate 
• 134653-69-3 4'-{[(Trifluoromethyl)sulfonyl]oxy}-2,2':6',2''-terpyridine 
• 762-04-9 phosphonic acid diethyl ester 
• 149817-62-9 4'-bromo-2,2':6',2''-terpyridine 
• 128143-88-4 2,2':6',2''-Terpyridin-4'(1'H)-one 

Relevant articles and documents

Phosphonate-functionalized heteroleptic ruthenium(II) bis(2,2′: 6′,2″-terpyridine) complexes

The heteroleptic complexes [Ru(1)(4)][PF6]2, [Ru(2)(4)][PF6]2, [Ru(Phtpy)(4)][PF6] 2, and [Ru(pytpy)(4)][PF6]2 (Phtpy = 4′-phenyl-2,2′:6′,2″-terpyridine, pytpy = 4′-(4-pyridyl)-2,2′:6′,2″-terpyridine, 1 and 2 = 4-methyl ester substituted derivatives of Phtpy and pytpy, 4 = ethyl 2,2′:6′,2″-terpyridine-4′-phosphonate) have been prepared. The single crystal structure of ligand 1 (1 = methyl 4-carboxy-4′-phenyl-2,2′:6′,2″-terpyridine) is reported. The introduction of the 4-methyl ester group causes a small red shift in the MLCT band of the ruthenium(II) complexes and a small shift to a more positive potential for the Ru2+/Ru3+ couple. The new complexes should serve as a useful starting point for development of ruthenium(II) dyes suited for sensitization of p-type semiconductors.

Preparation of Phosphonated Polypyridyl Ligands to anchor Transition-metal Complexes on Oxide Surfaces: Application for the Conversion of Light to Electricity with Nanocrystalline TiO2 Films

To anchor transition-metal compounds onto metal oxide surfaces 2,2':6',2''-terpyridine-4'-phosphonic acid (4'-PO3H2-terpy) is synthesized; strong surface adhesion as well as efficient charge-transfer sensitization of nanocrystalline TiO2 films has been observed with a ruthenium complex involving this ligand.