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3,8-Di(thien-2-yl)-1,10-phenanthroline is a chemical compound characterized by the presence of two thien-2-yl groups and a phenanthroline moiety. It is known for its unique electronic and photophysical properties, making it a versatile ligand in coordination chemistry and a promising candidate for various applications in material science and optoelectronics.

753491-32-6

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753491-32-6 Usage

Uses

Used in Coordination Chemistry:
3,8-Di(thien-2-yl)-1,10-phenanthroline is used as a ligand for the formation of metal complexes in coordination chemistry. Its ability to chelate metal ions allows for the development of metal-organic frameworks with potential applications in catalysis, gas storage, and separation processes.
Used in Chemical Sensing:
3,8-Di(thien-2-yl)-1,10-phenanthroline is used as a fluorophore in chemical sensing applications. Its photophysical properties enable the detection and quantification of specific analytes, making it a valuable tool in analytical chemistry and environmental monitoring.
Used in Optoelectronic Devices:
3,8-Di(thien-2-yl)-1,10-phenanthroline is used in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices. Its electronic properties contribute to the efficient charge transport and light emission in these devices, enhancing their performance and potential for various display and lighting applications.
Used in Molecular Electronics:
3,8-Di(thien-2-yl)-1,10-phenanthroline is studied for its potential use in molecular electronics. Its electronic properties and ability to form stable complexes with metal ions make it a candidate for the development of molecular wires and other electronic components at the molecular level.
Used in Organic Semiconductor Materials:
3,8-Di(thien-2-yl)-1,10-phenanthroline is used as a building block for the synthesis of organic semiconductor materials. Its incorporation into the molecular structure of these materials can improve their electronic properties, such as charge mobility and stability, making them suitable for applications in organic field-effect transistors and solar cells.

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.

753491-32-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,8-dithiophen-2-yl-1,10-phenanthroline

1.2 Other means of identification

Product number -
Other names 3,8-di(thien-2-yl)-1,10-phenanthroline

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:753491-32-6 SDS

753491-32-6Downstream Products

753491-32-6Relevant academic research and scientific papers

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.

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