459968
1,2,3,4-Tetraphenyl-1,3-cyclopentadiene
95%
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About This Item
Empirical Formula (Hill Notation):
C29H22
CAS Number:
Molecular Weight:
370.48
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
95%
form
solid
mp
180-182 °C (lit.)
functional group
phenyl
SMILES string
C1C(c2ccccc2)=C(c3ccccc3)C(c4ccccc4)=C1c5ccccc5
InChI
1S/C29H22/c1-5-13-22(14-6-1)26-21-27(23-15-7-2-8-16-23)29(25-19-11-4-12-20-25)28(26)24-17-9-3-10-18-24/h1-20H,21H2
InChI key
JCXLYAWYOTYWKM-UHFFFAOYSA-N
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General description
1,2,3,4-Tetraphenyl-1,3-cyclopentadiene is formed as one of the condensation products during the reactions of diphenylacetylene with methylchromium systems.
Application
1,2,3,4-Tetraphenyl-1,3-cyclopentadiene (TPCP) may be employed for the fabrication of triple-layer blue-emitting device.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Effect of electric field strength on the electroluminescence spectra of a blue-emitting device.
Cao H, et al.
Synthetic Metals, 96(3), 191-194 (1998)
Formation of 1, 3, 4, 5-tetraphenyl-2, 6, 7-trioxabicyclo [3.2. 1] oct-3-ene from the ozonolysis of 1, 2, 3, 4-tetraphenyl-1, 3-cyclopentadiene. First [3+ 4] addition of a carbonyl oxide moiety to an. alpha.,. beta.-unsaturated carbonyl group.
Mori M, et al.
Journal of the American Chemical Society, 109(14), 4407-4408 (1987)
Cyclization of diphenylacetylene on methylchromium s-complexes II. Cyclic and linear condensations.
Michman M and Zeiss HH.
Journal of Organometallic Chemistry, 25(1), 161-166 (1970)
Yang Yang et al.
Nature communications, 10(1), 3165-3165 (2019-07-20)
Vitrimers are one kind of covalently crosslinked polymers that can be reprocessed. Topology freezing transition temperature (Tv) is vitrimer's upper limit temperature for service and lower temperature for recycle. However, there has been no proper method to detect the intrinsic
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