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2,2'-Diiodo-9,9'-spirobifluorene is a chemical compound characterized by a spirobifluorene backbone with two iodine atoms attached at the 2 and 2' positions. It is known for its high thermal stability, good film-forming properties, and efficient charge transport capabilities. 2,2'-Diiodo-9,9'-spirobifluorene's structure also confers a high photoluminescence quantum yield, which makes it a valuable material for various electronic and optoelectronic applications.

790674-48-5

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790674-48-5 Usage

Uses

Used in Organic Light-Emitting Diodes (OLEDs):
2,2'-Diiodo-9,9'-spirobifluorene is used as a key component in the synthesis of organic light-emitting diodes due to its efficient charge transport and high photoluminescence quantum yield. These properties contribute to the improved performance and efficiency of OLEDs, making them suitable for use in display technologies and lighting applications.
Used in Organic Photovoltaic (OPV) Devices:
In the field of organic photovoltaics, 2,2'-Diiodo-9,9'-spirobifluorene serves as a crucial material for the development of OPV devices. Its high thermal stability and good film-forming properties are advantageous for creating stable and efficient solar cells that can convert sunlight into electricity.
Used in Electronic Applications:
Beyond its role in optoelectronic devices, 2,2'-Diiodo-9,9'-spirobifluorene is also utilized in other electronic applications due to its thermal stability and film-forming capabilities. These attributes make it a reliable material for use in various electronic components and systems that require high performance and durability.
Used in Optoelectronic Devices:
The efficient charge transport and high photoluminescence quantum yield of 2,2'-Diiodo-9,9'-spirobifluorene make it a promising candidate for use in a range of optoelectronic devices. These devices, which combine electronic and optical functionalities, can benefit from the compound's properties to achieve enhanced performance and efficiency in applications such as sensors, communication systems, and imaging technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 790674-48-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,0,6,7 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 790674-48:
(8*7)+(7*9)+(6*0)+(5*6)+(4*7)+(3*4)+(2*4)+(1*8)=205
205 % 10 = 5
So 790674-48-5 is a valid CAS Registry Number.

790674-48-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-Diiodo-9,9'-spirobi[fluorene]

1.2 Other means of identification

Product number -
Other names (rac)-2,2'-diiodo-9,9'-spirobifluorene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:790674-48-5 SDS

790674-48-5Relevant articles and documents

Synthesis of enantiomerically pure dissymmetric 2,2′-disubstituted 9,9′-spirobifluorenes

Thiemann, Frank,Piehler, Torsten,Haase, Detlev,Saak, Wolfgang,Luetzen, Arne

, p. 1991 - 2001 (2007/10/03)

Racemic dissymmetric 2,2′-dihydroxy-9,9′-spirobifluorene was prepared and resolved by clathrate formation with (R,R)-(+)-2,3-dimethoxy-N,N, N′,N′-tetracyclohexylsuccindiamide, giving rise to both enantiomers in very good yields. The absolute stereochemistry of the resolved material could be assigned by an X-ray structure analysis of single crystals of the clathrate. Enantiomerically pure diols could be transformed into the corresponding ditriflates, which were then used as starting materials in different cross-coupling procedures to provide a number of new enantiomerically pure spiro compounds bearing versatile functional groups suitable for further elaboration, as demonstrated by some examples. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.

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