159726-85-9 Usage
Description
1,10-Phenanthroline, 2,2'-(1,3-phenylene)bis[9-(4-methoxyphenyl)is a chemical compound derived from 1,10-phenanthroline, featuring a 1,3-phenylene linker and two 9-(4-methoxyphenyl) substituents. 1,10-Phenanthroline, 2,2'-(1,3-phenylene)bis[9-(4-methoxyphenyl)is known for its ability to chelate with various metal ions, making it a valuable asset in coordination chemistry and metal complexation. Its unique structure and metal-binding properties contribute to its versatility and potential for a broad spectrum of applications in research and industry.
Uses
Used in Coordination Chemistry:
1,10-Phenanthroline, 2,2'-(1,3-phenylene)bis[9-(4-methoxyphenyl)is used as a chelating ligand for forming stable complexes with a variety of metal ions. Its application in this field is due to its ability to selectively bind to certain metal ions, which is crucial for the study and manipulation of metal complexes.
Used in Analytical Chemistry:
In analytical chemistry, 1,10-Phenanthroline, 2,2'-(1,3-phenylene)bis[9-(4-methoxyphenyl)is utilized for its selective metal ion binding capabilities. This property is essential for the detection, identification, and quantification of specific metal ions in various samples, contributing to the accuracy and reliability of analytical results.
Used in Biochemistry:
1,10-Phenanthroline, 2,2'-(1,3-phenylene)bis[9-(4-methoxyphenyl)is also employed in biochemistry, where its metal-binding properties can be harnessed for studying the role of metal ions in biological systems. This application is valuable for understanding metal ion interactions with biomolecules and their implications in biological processes.
Used in Research and Development:
1,10-Phenanthroline, 2,2'-(1,3-phenylene)bis[9-(4-methoxyphenyl)-'s versatility and potential applications make it a valuable tool in research and development across various industries. Its ability to form stable complexes with metal ions can lead to the discovery of new materials, catalysts, and other advancements in chemical and materials science.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, the compound's metal-binding properties could potentially be applied in the pharmaceutical industry for the development of drugs that target metal ion-dependent biological processes or for the creation of metal-based therapeutics.
Check Digit Verification of cas no
The CAS Registry Mumber 159726-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,7,2 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 159726-85:
(8*1)+(7*5)+(6*9)+(5*7)+(4*2)+(3*6)+(2*8)+(1*5)=179
179 % 10 = 9
So 159726-85-9 is a valid CAS Registry Number.
159726-85-9Relevant articles and documents
A dicopper(I) trefoil knot with m-phenylene bridges between the ligand subunits: Synthesis, resolution, and absolute configuration
Dietrich-Buchecker, Christiane,Rapenne, Gwenael,Sauvage, Jean-Pierre,De Cian, Andre,Fischer, Jean
, p. 1432 - 1439 (1999)
A molecular trefoil knot, constructed around two copper(I) centres used as a template, has been synthesized in 29% yield (cyclization step) by the use of 1,3-phenylene spacers between the 1,10-phenanthroline subunits; the double stranded helical precursor
Molecular composite knots
Carina, Riccardo F.,Dietrich-Buchecker, Christiane,Sauvage, Jean-Pierre
, p. 9110 - 9116 (2007/10/03)
Molecular composite knots have been prepared from transition metal-assembled precursors via a Glaser acetylenic coupling reaction. The templating metal is copper(I), and the coordinating fragments incorporated into the final structure are 1,10-phenanthroline-type chelates. The compounds are composite knots as opposed to prime knots such as the classical trefoil knot. By combining two tied open-chain fragments in a cyclodimerization reaction, the simplest composite knots are obtained as a mixture of two topological diastereomers. The minimum number of crossing points used to represent the molecules in a plane is six. Due to the complexity of the entangled precursors and to the several cyclization possibilities, the formation yield of composite knots is only modest (~3%). On the other hand, the compound has been fully characterized by ES-MS (molecular weight, 4037.8) and by 1H NMR spectroscopy, including 2D NMR (NOESY).
