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1047684-56-9

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1047684-56-9 Usage

Description

4,4'-Bis(5-hexylthiophen-2-yl)-2,2'-bipyridine is an organic compound that features a bipyridine core with two 5-hexylthiophen-2-yl groups attached to the 4,4' positions. This molecule is known for its electronic properties and is commonly utilized in the development of materials for electronic devices.

Uses

Used in Photovoltaic Industry:
4,4'-Bis(5-hexylthiophen-2-yl)-2,2'-bipyridine is used as a reactant for the synthesis of ruthenium(II) ligand complexes, which serve as sensitizers in dye-sensitized solar cells. These complexes play a crucial role in enhancing the light-harvesting capabilities and overall efficiency of the solar cells by facilitating the transfer of electrons from the excited dye molecules to the semiconductor surface.

Check Digit Verification of cas no

The CAS Registry Mumber 1047684-56-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,7,6,8 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1047684-56:
(9*1)+(8*0)+(7*4)+(6*7)+(5*6)+(4*8)+(3*4)+(2*5)+(1*6)=169
169 % 10 = 9
So 1047684-56-9 is a valid CAS Registry Number.

1047684-56-9 Well-known Company Product Price

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  • TCI America

  • (B4420)  4,4'-Bis(5-hexyl-2-thienyl)-2,2'-bipyridyl  >98.0%(HPLC)(N)

  • 1047684-56-9

  • 200mg

  • 1,490.00CNY

  • Detail

1047684-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(5-hexylthiophen-2-yl)-2-[4-(5-hexylthiophen-2-yl)pyridin-2-yl]pyridine

1.2 Other means of identification

Product number -
Other names 4,4'-dihexylthiophene-2,2'-bipyridine

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:1047684-56-9 SDS

1047684-56-9Downstream Products

1047684-56-9Relevant articles and documents

Enhance the optical absorptivity of nanocrystalline TiO2 film with high molar extinction coefficient ruthenium sensitizers for high performance dye-sensitized solar cells

Gao, Feifei,Wang, Yuan,Shi, Dong,Zhang, Jing,Wang, Mingkui,Jing, Xiaoyan,Humphry-Baker, Robin,Wang, Peng,Zakeeruddin, Shaik M.,Graetzel, Michael

, p. 10720 - 10728 (2008)

We report two new heteroleptic polypyridyl ruthenium complexes, coded C101 and C102, with high molar extinction coefficients by extending the π-conjugation of spectator ligands, with a motivation to enhance the optical absorptivity of mesoporous titania film and charge collection yield in a dye-sensitized solar cell. On the basis of this C101 sensitizer, several DSC benchmarks measured under the air mass 1.5 global sunlight have been reached. Along with an acetonitrile-based electrolyte, the C101 sensitizer has already achieved a strikingly high efficiency of 11.0-11.3%, even under a preliminary testing. More importantly, based on a low volatility 3-methoxypropionitrile electrolyte and a solvent-free ionic liquid electrolyte, cells have corresponding >9.0% and ~7.4% efficiencies retained over 95% of their initial performances after 1000 h full sunlight soaking at 60°C. With the aid of electrical impedance measurements, we further disclose that, compared to the cell with an acetonitrile-based electrolyte, a dye-sensitized solar cell with an ionic liquid electrolyte shows a feature of much shorter effective electron diffusion lengths due to the lower electron diffusion coefficients and shorter electron lifetimes in the mesoporous titania film, explaining the photocurrent difference between these two type devices. This highlights the next necessary efforts to further improve the efficiency of cells with ionic liquid electrolytes, facilitating the large-scale production and application of flexible thin film mesoscopic solar cells.

4,4′-Unsymmetrically substituted-2,2′-bipyridines: Novel bidentate ligands on ruthenium(II) [3 + 2 + 1] mixed ligand complexes for efficient sensitization of nanocrystalline TiO2 in dye solar cells

Chandrasekharam,Kumar, Ch. Pavan,Singh, Surya Prakash,Anusha,Bhanuprakash,Islam,Han

, p. 26035 - 26046 (2013)

A series of five new ruthenium [3 + 2 + 1] complexes coded as MC107-MC111, with novel unsymmetrical bipyridines as ancillary ligands and terpyridine tricarboxylic acid as an anchoring ligand have been successfully synthesized and characterized by 1H NMR, 13C NMR and UV-Visible spectrometry. Improvement in the molar extinction coefficient of all these sensitizers was observed compared with reference standard N749 dye under comparable conditions. Among all the new sensitizers MC108 exhibited a maximum solar to electrical conversion efficiency of 5.573% (Jsc = 16.81 mA cm-2, Voc = 0.50 V. FF = 0.65) under standard global AM 1.5 G solar condition, when compared to the N749 dye with an efficiency of 6.29% (Jsc = 13.74 mA cm-2, Voc = 0.67 V. FF = 0.68) under similar fabrication and evaluation conditions. Density functional theory (DFT) and time-dependent DFT calculations are carried out for MC107-MC111 to understand their structural, electronic and photophysical properties.

A process for preparing 2,2 the 4-dipyridyl- [...], the 4 [...] -(5-hexyl-2-thiophene) method

-

Paragraph 0025-0027, (2017/03/08)

The invention discloses a method for preparing 2,2'-bipyridyl-4,4-(5-hexyl-2-thiophene), and belongs to the field of organic synthesis. The method comprises the following steps: 1, reacting zinc chloride, tetrahydrofuran and a grignard reagent to prepare a zinc reagent for later use; 2, reacting 4,4-dibromo-2,2-bipyridyl with the zinc reagent under a catalytic system comprising 1,2-bis(diphenylphosphino)ethane nickel chloride, triphenylphosphine and dimethyl formamide in a nitrogen protective environment, and performing cooling, filtering, washing, recrystallizing and the like to refine an obtained product to obtain a 2,2'-bipyridyl-4,4-(5-hexyl-2-thiophene) product. According to the method, the raw materials are low in cost, a generated intermediate is nontoxic, the reaction process is easy to control, the environment pollution is less, and the method has high industrial value.

CYCLOMETALATED TRANSITION METAL DYES

-

, (2012/12/13)

The present invention provides substituted cyclometalated dyes with wider absorbance bands in the visible spectrum. The compounds have hexacoordinate structures as shown in formula (I) where the central transition metal (M) is bonded to two substituted bi

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