1542234-40-1 Usage
Description
2,6-Di(2H-1,2,3-triazol-4-yl)pyridine, also known as DTP, is a chemical compound characterized by its molecular formula C11H7N9. It is a pyridine derivative featuring two triazolyl groups attached at the 2 and 6 positions of the pyridine ring. DTP is recognized for its role in coordination chemistry, where it is utilized for the synthesis of metal-organic frameworks and coordination polymers due to its capacity to form stable complexes with metal ions. Its versatility and significance in the field of coordination chemistry extend to potential applications in catalysis, luminescent materials, and molecular recognition, making it an important chemical for various industrial and research purposes.
Uses
Used in Coordination Chemistry:
2,6-Di(2H-1,2,3-triazol-4-yl)pyridine is used as a ligand in coordination chemistry for the synthesis of metal-organic frameworks and coordination polymers. Its ability to form stable complexes with metal ions makes it a valuable component in creating structures with specific properties and applications.
Used in Catalyst Development:
In the field of catalysis, 2,6-Di(2H-1,2,3-triazol-4-yl)pyridine is being researched for its potential as a catalyst or a component in catalytic systems. Its unique structure and coordination capabilities can contribute to the development of new catalysts that enhance reaction efficiency and selectivity.
Used in Luminescent Materials:
2,6-Di(2H-1,2,3-triazol-4-yl)pyridine is utilized in the development of luminescent materials. Its chemical properties can be harnessed to create materials that exhibit light emission, which can be applied in various technologies such as sensors, displays, and lighting.
Used in Molecular Recognition:
In molecular recognition, 2,6-Di(2H-1,2,3-triazol-4-yl)pyridine is employed for its potential to interact with specific molecules, which can be useful in the design of molecular sensors, drug delivery systems, and other applications that rely on the selective binding of molecules.
Used in Research Applications:
2,6-Di(2H-1,2,3-triazol-4-yl)pyridine is used as a research chemical to explore its properties and potential uses in various scientific fields. Its unique structure and reactivity make it a subject of interest for studies aimed at understanding and exploiting its capabilities in different chemical and material systems.
Check Digit Verification of cas no
The CAS Registry Mumber 1542234-40-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,4,2,2,3 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1542234-40:
(9*1)+(8*5)+(7*4)+(6*2)+(5*2)+(4*3)+(3*4)+(2*4)+(1*0)=131
131 % 10 = 1
So 1542234-40-1 is a valid CAS Registry Number.
1542234-40-1Relevant articles and documents
A heteroleptic bis(tridentate) ruthenium(II) platform featuring an anionic 1,2,3-triazolate-based ligand for application in the dye-sensitized solar cell
Sinn, Stephan,Schulze, Benjamin,Friebe, Christian,Brown, Douglas G.,Jaeger, Michael,Kuebel, Joachim,Dietzek, Benjamin,Berlinguette, Curtis P.,Schubert, Ulrich S.
, p. 1637 - 1645 (2014)
A series of bis(tridentate) ruthenium(II) complexes featuring new anionic 1,2,3-triazolate-based tridentate ligands and 2,2′:6′, 2′′-terpyridine is presented. For a complex equipped with carboxy anchoring groups, the performance in a dye-sensitized solar cell is evaluated. The title complexes are readily synthesized and can be decorated with alkyl chains utilizing azide-alkyne cycloaddition methods, in order to improve the device stability and allow the use of alternative electrolytes. On account of the strong electron donation from the 1,2,3-triazolates, the complexes exhibit a broad metal-to-ligand charge-transfer absorption (up to 700 nm), leading to an electron transfer toward the anchoring ligand. The lifetimes of the charge-separated excited states are in the range of 50 to 80 ns. In addition, the ground- and excited-state redox potentials are appropriate for the application in dye-sensitized solar cells, as demonstrated by power conversion efficiencies of up to 4.9% (vs 6.1% for N749).
