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5,15-bis(4-dioxylborylphenyl)porphyrin is a complex organic compound that belongs to the class of porphyrins, which are macrocyclic molecules with a central metal ion and a large conjugated π-system. This specific porphyrin derivative features two boron-containing substituents attached to the phenyl rings at positions 5 and 15. The presence of dioxylboryl groups enhances the compound's solubility and stability, making it suitable for various applications in materials science, catalysis, and medicinal chemistry. The unique structure and properties of 5,15-bis(4-dioxylborylphenyl)porphyrin allow it to interact with a wide range of molecules, making it a promising candidate for further research and development in these fields.

290356-48-8

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290356-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 290356-48-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,0,3,5 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 290356-48:
(8*2)+(7*9)+(6*0)+(5*3)+(4*5)+(3*6)+(2*4)+(1*8)=148
148 % 10 = 8
So 290356-48-8 is a valid CAS Registry Number.

290356-48-8Downstream Products

290356-48-8Relevant academic research and scientific papers

Meso-meso-linked porphyrin dimer as a novel scaffold for the selective binding of oligosaccharides

Ikeda, Masato,Shinkai, Seiji,Osuka, Atsuhiro

, p. 1047 - 1048 (2000)

A meso-meso-linked porphyrin dimer 1 bearing four boronic acid groups shows high selectivity for maltotetraose (n = 4) among maltooligosaccharides (n = 1-7), indicating that this class of porphyrins acts as a novel scaffold to design oligosaccharide recep

Design and studies of novel polyoxysterol-based porphyrin conjugates

Zhylitskaya, Halina A.,Zhabinskii, Vladimir N.,Litvinovskaya, Raisa P.,Lettieri, Raffaella,Monti, Donato,Venanzi, Mariano,Khripach, Vladimir A.,Draar, Pavel

, p. 1169 - 1175 (2012)

New types of steroid-porphyrin conjugates derived from 20-hydroxyecdysone (20E) and 24-epibrassinolide (EBl) were synthesized. An exceptional regioselectivity in the reaction of both steroids with porphyrin boronic acids was found to give side-chain-conjugated boronic esters as sole products. UV-Vis-, fluorescence and NMR spectroscopy yielded similar data for all the studied compounds confirming the solvent driven supramolecular assembly with formation of J-aggregates. CD measurements of water diluted solutions showed a clear difference between 20E and EBl conjugates. The latter showed a strong supramolecular chirality, whereas 20E J-aggregates did not.

Extraction of photogenerated electrons and holes from a covalent organic framework integrated heterojunction

Calik, Mona,Auras, Florian,Salonen, Laura M.,Bader, Kathrin,Grill, Irene,Handloser, Matthias,Medina, Dana D.,Dogru, Mirjam,L?bermann, Florian,Trauner, Dirk,Hartschuh, Achim,Bein, Thomas

, p. 17802 - 17807 (2015/02/19)

Covalent organic frameworks (COFs) offer a strategy to position molecular semiconductors within a rigid network in a highly controlled and predictable manner. The π-stacked columns of layered two-dimensional COFs enable electronic interactions between the COF sheets, thereby providing a path for exciton and charge carrier migration. Frameworks comprising two electronically separated subunits can form highly defined interdigitated donor-acceptor heterojunctions, which can drive the photogeneration of free charge carriers. Here we report the first example of a photovoltaic device that utilizes exclusively a crystalline organic framework with an inherent type II heterojunction as the active layer. The newly developed triphenylene-porphyrin COF was grown as an oriented thin film with the donor and acceptor units forming one-dimensional stacks that extend along the substrate normal, thus providing an optimal geometry for charge carrier transport. As a result of the degree of morphological precision that can be achieved with COFs and the enormous diversity of functional molecular building blocks that can be used to construct the frameworks, these materials show great potential as model systems for organic heterojunctions and might ultimately provide an alternative to the current disordered bulk heterojunctions.

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