350042-00-1 Usage
Molecular structure
2,5-Bis(2,2'-bipyridin-6-yl)-1,1-dimethyl-3,4-diphenylsilole consists of two 2,2'-bipyridine groups attached to a 1,1-dimethyl-3,4-diphenylsilole core.
Optoelectronic properties
The compound has unique light-emitting properties, making it a potential candidate for use in optoelectronic devices.
High photoluminescence
2,5-Bis(2,2'-bipyridin-6-yl)-1,1-dimethyl-3,4-diphenylsilole has been studied for its high photoluminescence, which contributes to its potential use in electronic devices.
Stability
The compound has been noted for its stability, which is important for its potential use in long-lasting electronic devices.
Potential applications
2,5-Bis(2,2'-bipyridin-6-yl)-1,1-dimethyl-3,4-diphenylsilole has been studied for its potential use in OLEDs (organic light-emitting diodes) and other electronic devices.
Ongoing research
Research on the compound is ongoing, and it may have future implications in the development of advanced electronic materials.
Check Digit Verification of cas no
The CAS Registry Mumber 350042-00-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,0,0,4 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 350042-00:
(8*3)+(7*5)+(6*0)+(5*0)+(4*4)+(3*2)+(2*0)+(1*0)=81
81 % 10 = 1
So 350042-00-1 is a valid CAS Registry Number.
350042-00-1Relevant articles and documents
Synthesis of 2,5-substituted siloles and optical study of interactions with mercury(II), copper(II), and nickel(II) cations
Carroll, James B.,Braddock-Wilking, Janet
, p. 1905 - 1912 (2013/05/09)
Several 2,5-diaryl-1,1-dimethyl-3,4-diphenylsiloles (with aryl = p-cyanophenyl (1), m,p-bis(methylthio)phenyl (2), p-N,N-dimethylaminophenyl (3), 2,2′-bipyridin-6-yl (4)) were synthesized and characterized by UV-vis, fluorescence, and NMR spectroscopy, along with crystal structure determinations for 1 and 2. Compounds 1-4 in methylene chloride were combined with 1-10 equiv of M(ClO4)2 (M = Ni, Cu, Hg) in methanol, and the resulting solutions were monitored by UV-vis and fluorescence spectroscopy. Compound 1 showed slight effects for each metal, 2 exhibited fluorescence quenching selectively for Hg(II), 3 showed significant changes for all cations, and 4 generally demonstrated fluorescence quenching for all cations. A discussion of the causes behind these changes is also presented.
