753491-32-6 Usage
General Description
3,8-Di(thien-2-yl)-1,10-phenanthroline is a chemical compound that consists of two thien-2-yl groups and a phenanthroline moiety. It is commonly used as a ligand in coordination chemistry and has been investigated for various applications such as in the development of metal-organic frameworks and as a fluorophore in chemical sensing. 3,8-Di(thien-2-yl)-1,10-phenanthroline has also been studied for its potential use in organic light-emitting diodes (OLEDs) and other optoelectronic devices due to its unique electronic and photophysical properties. Additionally, 3,8-Di(thien-2-yl)-1,10-phenanthroline has been the subject of research for its potential use in molecular electronics and as a building block for organic semiconductor materials.
Check Digit Verification of cas no
The CAS Registry Mumber 753491-32-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,3,4,9 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 753491-32:
(8*7)+(7*5)+(6*3)+(5*4)+(4*9)+(3*1)+(2*3)+(1*2)=176
176 % 10 = 6
So 753491-32-6 is a valid CAS Registry Number.
753491-32-6Relevant articles and documents
Bridging nanogap electrodes by in situ electropolymerization of a bis(terthiophenylphenanthroline)ruthenium complex
Araki, Koiti,Endo, Hiroaki,Masuda, Gou,Ogawa, Takaji
, p. 3331 - 3340 (2004)
A novel complex containing a 3,8-bis[terthiophenyl-(1,10-phenanthroline)] ligand coordinated to [Ru(bpy)2] was synthesized and characterized by electrochemical and spectroscopic techniques. The complex was shown to be a suitable starting material for the electrode position of functionalized molecular wires between nanogap electrodes to generate stable molecular nanodevices. Temperature-dependent nonlinear I-V curves were obtained at 80-300 K. The material can also be deposited on indium tin oxide (ITO) to form compact electrochromic films at surface concentrations lower than ≈ 1 × 10 -8 mol cm2; however, a more loosely bond fibrous form is preferentially deposited at higher surface concentrations.
