110231-30-6
Chemical Structure
Diphenyl-1-pyrenylphosphine
Synonym(s): DPPP
- CAS No.: 110231-30-6
- Formula:C28H19P
- Molecular Weight:386.42
IUPAC Name: diphenyl(pyren-1-yl)phosphane
InChIKey: DSYGKYCYNVHCNQ-UHFFFAOYSA-N
SMILES: P(C1=CC=CC=C1)(C2=CC=CC=C2)C3=C(C4=C56)C=CC6=CC=CC5=CC=C4C=C3
Biological Activity: Diphenyl-1-pyrenylphosphine (DPPP) is a functional organic molecule with both fluorescent properties and metal coordination ability, which is commonly used in materials and coordination chemistry research. Upon exposure to ultraviolet light, Diphenyl-1-pyrenylphosphine undergoes photoinduced phosphorus atom oxidation to form O-DPPP, triggering a transition from aggregation-induced emission (AIE) to aggregation-caused quenching (ACQ). Diphenyl-1-pyrenylphosphine reacts stoichiometrically with lipid hydroperoxides to produce fluorescent diphenyl-1-pyrenylphosphine oxide. Diphenyl-1-pyrenylphosphine can insert into cell membranes to monitor lipid peroxidation processes in living cells[1][2][3].
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Diphenyl-1-pyrenylphosphine | 98.56% | Diphenyl-1-pyrenylphosphine (DPPP) is a functional organic molecule with both fluorescent properties and metal coordination ability, which is commonly used in materials and coordination chemistry research. Upon exposure to ultraviolet light, Diphenyl-1-pyrenylphosphine undergoes photoinduced phosphorus atom oxidation to form O-DPPP, triggering a transition from aggregation-induced emission (AIE) to aggregation-caused quenching (ACQ). Diphenyl-1-pyrenylphosphine reacts stoichiometrically with lipid hydroperoxides to produce fluorescent diphenyl-1-pyrenylphosphine oxide. Diphenyl-1-pyrenylphosphine can insert into cell membranes to monitor lipid peroxidation processes in living cells. | ||||||||||||||||||||
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- [1]. Xing C, et al. Diphenyl-1-pyrenylphosphine: photo-triggered AIE/ACQ transition with remarkable third-order nonlinear optical signal change. Chem Commun (Camb). 2020;56(30):4220-4223. [Content Brief]
- [2]. Okimotoa Y, et al. A novel fluorescent probe diphenyl-1-pyrenylphosphine to follow lipid peroxidation in cell membranes. FEBS Lett. 2000;474(2-3):137-140. [Content Brief]
- [3]. Takahashi M, et al. Estimation of lipid peroxidation of live cells using a fluorescent probe, diphenyl-1-pyrenylphosphine. Free Radic Biol Med. 2001;31(2):164-174. [Content Brief]
Keywords
