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797294

Sigma-Aldrich

1,1,2,3,4,5-Hexaphenyl-1H-silole

Sinonimo/i:

1,1,2,3,4,5-Hexaphenylsilacyclopenta-2,4-diene, 1,1,2,3,4,5-Hexaphenylsilacyclopentadiene, 1,1,2,3,4,5-Hexaphenylsilole, HPS, Hexaphenylsilacyclopenta-2,4-diene, Hexaphenylsilacyclopentadiene

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About This Item

Formula empirica (notazione di Hill):
C40H30Si
Numero CAS:
752-28-3
Peso molecolare:
538.75
Numero MDL:
MFCD27976827
Codice UNSPSC:
12352103
ID PubChem:
329768582
NACRES:
NA.23

Saggio

98%

Forma fisica

solid

Punto di fusione

188-193 °C

Stringa SMILE

C1(C2=CC=CC=C2)=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=C(C5=CC=CC=C5)[Si]1(C6=CC=CC=C6)C7=CC=CC=C7

InChI

1S/C40H30Si/c1-7-19-31(20-8-1)37-38(32-21-9-2-10-22-32)40(34-25-13-4-14-26-34)41(35-27-15-5-16-28-35,36-29-17-6-18-30-36)39(37)33-23-11-3-12-24-33/h1-30H
QAKMXYFDVPDIPT-UHFFFAOYSA-N

Descrizione generale

HPS is an aggregation-induced emission (AIE) material for use in the OLED emitting layer. Photolysis and thermolysis of 1,4,5,6,7,7-hexaphenyl-7-silabicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic anhydride (XIb) may lead to the formation of hexaphenylsilacyclopentadiene.

Applicazioni

Hexaphenylsilacyclopentadiene may undergo π4s+π2s cycloaddition with ethyl acrylate to form bicyclosilaheptene. The same study reports similar cycloaddition reactions with various dienophiles. The reaction of hexaphenylsilacyclopentadiene with perbenzoic acid yields a mixture of tetraphenylfuran and cis-dibenzoylstilbene.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Photochemical and thermal transformations of 7-silabicyclo[2.2.1]Heptadiene and 7-silabicyclo[2.2.1]heptene systems
Balasubramanian R and George MV
Journal of Organometallic Chemistry null
Synthesis, Light Emission, Nanoaggregation, and Restricted Intramolecular Rotation of 1,1-Substituted 2,3,4,5-Tetraphenylsiloles
Junwu Chen, Charles C. W. Law, Jacky W. Y. Lam, et al
Chemistry of Materials, 15(7), 1535-1546 (2003)
Symmetry allowed ?4s+?2s additions silacyclopentadienes
Balasubramanian R and George MV
Tetrahedron, 2395-2404 null
Photochemical and thermal transformations of 7-silabicyclo[2.2.1]Heptadiene and 7-silabicyclo[2.2.1]heptene systems
Balasubramanian R and George MV
Journal of Organometallic Chemistry, 131-139 null
Peracid oxidation and photooxygenation reactions of silacyclopentadienes,
Mahajan MP, et al.
Tetrahedron null
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