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900965

Sigma-Aldrich

CzSi

Synonym(s):

9-(4-tert-Butylphenyl)-3,6-bis(triphenylsilyl)-9H-carbazole, 9-[4-(1,1-Dimethylethyl)phenyl]-3,6-bis(triphenylsilyl)-9H-carbazole

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About This Item

Empirical Formula (Hill Notation):
C58H49NSi2
CAS Number:
Molecular Weight:
816.19
MDL number:
UNSPSC Code:
12352103
NACRES:
NA.23
Pricing and availability is not currently available.

Assay

≥97%

form

solid

InChI

1S/C58H49NSi2/c1-58(2,3)44-34-36-45(37-35-44)59-56-40-38-52(60(46-22-10-4-11-23-46,47-24-12-5-13-25-47)48-26-14-6-15-27-48)42-54(56)55-43-53(39-41-57(55)59)61(49-28-16-7-17-29-49,50-30-18-8-19-31-50)51-32-20-9-21-33-51/h4-43H,1-3H3

InChI key

WIHKEPSYODOQJR-UHFFFAOYSA-N

Application

Carbazole-based host materials for blue electrophosphorescence.
CzSi is a host material with tetrahedral Si atoms that act as effective spacers and thereby block the π conjugation of the carbazole core. It is used as a hole transporting molecule (HTM) that is mainly used in the development of organic light-emitting diodes (OLEDs). CzSi can also be used in the formation of a blue electrophosphorescence.[1][2]

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Highly efficient blue-emitting iridium(III) carbene complexes and phosphorescent OLEDs.
Chiung-Fang Chang et al.
Angewandte Chemie (International ed. in English), 47(24), 4542-4545 (2008-05-08)
Leakage-free solution-processed organic light-emitting diode using a ternary host with single-diode emission area up to 6times 11.5 cm 2
Liao S, et al.
Royal Society of Chemistry Advances, 9(19), 10584-10598 (2019)
Highly efficient organic blue electrophosphorescent devices based on 3,6-bis(triphenylsilyl)carbazole as the host material.
Tsai MH, et al.
Advanced Materials, 18(9), 1216-1220 (2006)
Triphenylsilyl-and trityl-substituted carbazole-based host materials for blue electrophosphorescence
Tsai M, et al.
ACS Applied Materials & Interfaces, 1(3), 567-574 (2009)
Efficient blue organic light-emitting diodes employing thermally activated delayed fluorescence
Zhang et al.
Nature Photonics, 8(4), 326-332 (2014)

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