Passa al contenuto
Merck
Tutte le immagini(1)

Documenti fondamentali

Visualizza tutta la documentazione

792144

Sigma-Aldrich

6,12-Bis(2,4,6-trimethylphenyl)indeno[1,2-b]fluorene

97% (HPLC)

Sinonimo/i:

6,12-Dimesitylindeno[1,2-b]fluorene

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(1)

About This Item

Formula empirica (notazione di Hill):
C38H32
Numero CAS:
1374154-86-5
Peso molecolare:
488.66
Codice UNSPSC:
12352103
ID PubChem:
329768315

Saggio

97% (HPLC)

Stato

powder

Energia dell’orbitale

HOMO -5.78 eV 
LUMO -3.56 eV 

Stringa SMILE

CC(C=C1C)=CC(C)=C1C2=C3C(C=CC=C3)=C(C2=C4)C=C5C4=C(C=CC=C6)C6=C5C7=C(C)C=C(C)C=C7C

InChI

1S/C38H32/c1-21-15-23(3)35(24(4)16-21)37-29-13-9-7-11-27(29)31-20-34-32(19-33(31)37)28-12-8-10-14-30(28)38(34)36-25(5)17-22(2)18-26(36)6/h7-20H,1-6H3
RVYZMPWWAUBURT-UHFFFAOYSA-N

Descrizione generale

6,12-Bis(2,4,6-trimethylphenyl)indeno[1,2-b]fluorene is a conjugated polycyclic hydrocarbon which has indeno[1,2-b]fluorene as the skeleton. It has a 6−5−6−5−6 fused ring system with small band gap absorption and biradicaloid properties. It can be potentially used in organic electronics based applications.[1][2][3]

Applicazioni

6,12-Bis(2,4,6-trimethylphenyl)indeno[1,2-b]fluorene can be potentially used in the fabrication of ambipolar semiconductors, organic light emitting diodes (OLEDs), organic field effect transistors (OFETs), and organic photovoltaic (OPV) devices.[3][4][5]
n-type electron-accepting organic semiconductor for Organic Field Effect Transistor (OFET) applications

Codice della classe di stoccaggio

13 - Non Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documenti section.

Se ti serve aiuto, non esitare a contattarci Servizio Clienti

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

Indeno [1, 2-b] fluorenes: Fully Conjugated Antiaromatic Analogues of Acenes.
Chase DT, et al.
Angewandte Chemie (International Edition in English), 123(5), 1159-1162 (2011)
Isomeric indacenedibenzothiophenes: synthesis, photoelectric properties and ambipolar semiconductivity.
Ren L, et al.
Journal of Material Chemistry C, 4(23), 5202-5206 (2016)
Toward tetraradicaloid: The effect of fusion mode on radical character and chemical reactivity.
Hu P, et al.
Journal of the American Chemical Society, 138(3), 1065-1077 (2016)
Daniel T Chase et al.
Journal of the American Chemical Society, 134(25), 10349-10352 (2012-06-16)
Herein we report the synthesis and characterization of a series of 6,12-diarylindeno[1,2-b]fluorenes (IFs). Functionalization with electron donor and acceptor groups influences the ability of the IF scaffold to undergo two-electron oxidation and reduction to yield the corresponding 18- and 22-π-electron
Electron-accepting 6, 12-diethynylindeno [1, 2-b] fluorenes: synthesis, crystal structures, and photophysical properties.
Chase DT, et al.
Angewandte Chemie (International Edition in English), 50(47), 11103-11106 (2011)

Articoli

Soluble Pentacene Precursors

Fabrication procedure of organic field effect transistor device using a soluble pentacene precursor.

Domande

Recensioni

Nessuna valutazione

Filtri attivi

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.