0000000001306971
AUTHOR
Kirill P. Birin
showing 14 related works from this author
On the synthesis of functionalized porphyrins and porphyrin conjugates via β-aminoporphyrins
2016
International audience; The synthesis of functionalized porphyrins and their conjugates from meso-tetraarylporphyrins through the acylation and the oxidation of beta-aminoporphyrins was investigated. 2,3-Dioxochlorins were prepared by the oxidation of a variety of beta-aminoporphyrins and subsequently used in a condensation reaction with functionalized aromatic aldehydes and ammonium acetate to form beta-functionalized porphyrins bearing a fused imidazole ring. Under optimized experimental conditions both reactions tolerate various functional groups and afford the products in an appropriate overall yield. The mildness and usefulness of this methodology are illustrated by several examples in…
Post-synthetic methods for functionalization of imidazole-fused porphyrins
2018
Several methods for the post-synthetic modification of imidazo[4,5-[Formula: see text]]porphyrins are reported. First, a synthetic approach to the isomeric difunctionalized porphyrins, containing two [Formula: see text]-fused 2-aryl-1[Formula: see text]-imidazole cycles at adjacent or opposite pyrrole rings of the macrocycle is developed. The core chemistry of this synthetic route is the transformation of 2-aryl-1[Formula: see text]-imidazo[4,5-[Formula: see text]]porphyrins into corresponding imidazodioxochlorins followed by Debus–Radziszewski condensation with aromatic aldehyde. Next, 2-(4-bromophenyl)-1[Formula: see text]-imidazo[4,5-[Formula: see text]]-5,10,15,20-tetramesitylporphyrin…
Imidazoporphyrins as supramolecular tectons: synthesis and self-assembly of zinc 2-(4-pyridyl)-1H-imidazo[4,5-b]porphyrinate
2019
International audience; 5,10,15,20-Tetramesityl-2-(4-pyridyl)-1H-imidazo[4,5-b]porphyrin (PyPor) bearing a pyridine donor site connected to the tetrapyrrolic macrocycle by a rigid imidazole linker was prepared in high yield by the condensation of the corresponding 2,3-dioxochlorin and 4-formylpyridine in the presence of ammonium acetate. After the insertion of a metal ion capable of metal–ligand axial coordination, namely Zn(II), this compound afforded self-complementary porphyrin PyPorZn which was suitable for self-assembly. In the crystals, this complex exists as a zigzag coordination polymer formed through the axial coordination of the pyridine nitrogen atom to the zinc ion of the neighb…
Coordination self-assembly through weak interactions in meso-dialkoxyphosphoryl-substituted zinc porphyrinates.
2019
International audience; The self-assembly of seven zinc 10-(dialkoxyphosphoryl)-5,15-diarylporphyrinates Zn5-Zn11 containing different substituents at the phosphonate and aryl groups was investigated. Single crystals of Zn5-Zn9 complexes were grown under the same conditions and analyzed by X-ray structural analysis. A supramolecular self-assembly is observed in all crystals through weak coordinative bonding of the phosphoryl group of one porphyrin molecule to the zinc(II) ion of a second porphyrin molecule. The geometry of the porphyrin macrocycle is similar in all of the studied crystals and the central zinc atom in each case adopts a distorted tetragonal pyramidal environment. However, th…
Heterocycle-appended porphyrins: synthesis and challenges
2020
Abstract Porphyrin and their versatile metal complexes represent a special class of coordination compounds possessing unique physical-chemical properties. The achievements in the development of the synthetic approaches for the modification of the porphyrin macrocycle allowed the preparation of a variety of functional derivatives for diverse applications. Among a broad diversity of synthetically available metalloporphyrins meso-substituted tetrapyrroles are comprehensively investigated. However, β-substituted porphyrins could be considered as the most suitable models for mimicking the key roles of naturally occurring dyes in vital processes. The introduction of various substituents to the β-…
Synthesis of porphyrin-bis(polyazamacrocycle) triads via Suzuki coupling reaction
2014
Suzuki–Miyaura cross-coupling reaction has been used for the synthesis of tricyclic architectures based on trans-A2B2-porphyrins and bisaminal-protected polyazamacrocycles which are linked directly or by a p-phenylene spacer. This modular approach allowed the synthesis of ligands with various substituted porphyrin macrocycles and bisaminal-protected tetraazamacrocycles possessing different cavity sizes. These molecules can be assembled into dimers using a DABCO linker. Deprotection of these compounds afforded porphyrin-bis(polyazamacrocycle) triads.
Insights into the Synthesis and the Solution Behavior ofmeso-Aryloxy- and Alkoxy-Substituted Porphyrins
2015
meso-RO-appended (R = alkyl, aryl) porphyrins bearing one or two OR substituents at the tetrapyrrolic macrocycle were synthesized in good yields from 5,15-dibromo-10,20-diphenylporphyrins 2H(Br2DPP), Ni(Br2DPP) and Zn(Br2DPP) using an SNAr reaction. By varying the solvent, the base, the temperature, and the time of the reaction, the optimum conditions were established, and the selective introduction of one or two meso-RO substituents at the periphery of the macrocycle was achieved. Moreover, monofunctionalization of Ni(Br2DPP) according to an SNAr reaction was used as a key step for the synthesis of rarely explored unsymmetrical porphyrinyl alkyl ethers. 1H NMR studies of these ethers in CD…
Synthesis and Self-Organization of Zinc β-(Dialkoxyphosphoryl)porphyrins in the Solid State and in Solution
2012
The first synthesis and self-organization of zinc β-phosphorylporphyrins in the solid state and in solution are reported. β-Dialkoxyphosphoryl-5,10,15,20-tetraphenylporphyrins and their Zn(II) complexes have been synthesized in good yields by using Pd- and Cu-mediated carbon-phosphorous bond-forming reactions. The Cu-mediated reaction allowed to prepare the mono-β-(dialkoxyphosphoryl)porphyrins 1 Zn-3 Zn starting from the β-bromo-substituted zinc porphyrinate ZnTPPBr (TPP = tetraphenylporphyrin) and dialkyl phosphites HP(O)(OR)(2) (R = Et, iPr, nBu). The derivatives 1 Zn-3 Zn were obtained in good yields by using one to three equivalents of CuI. When the reaction was carried out in the pres…
CCDC 1871295: Experimental Crystal Structure Determination
2019
Related Article: Inna A. Abdulaeva, Kirill P. Birin, Anna A. Sinelshchikova, Mikhail S. Grigoriev, Konstantin A. Lyssenko, Yulia G. Gorbunova, Aslan Yu. Tsivadze, Alla Bessmertnykh-Lemeune|2019|CrystEngComm|21|1488|doi:10.1039/C8CE01992D
CCDC 1844989: Experimental Crystal Structure Determination
2019
Related Article: Sergey E. Nefedov, Kirill P. Birin, Alla Bessmertnykh-Lemeune, Yulia Y. Enakieva, Anna A. Sinelshchikova, Yulia G. Gorbunova, Aslan Y. Tsivadze, Christine Stern, Yuanyuan Fang, Karl M. Kadish|2019|Dalton Trans.|48|5372|doi:10.1039/C9DT00706G
CCDC 1844993: Experimental Crystal Structure Determination
2019
Related Article: Sergey E. Nefedov, Kirill P. Birin, Alla Bessmertnykh-Lemeune, Yulia Y. Enakieva, Anna A. Sinelshchikova, Yulia G. Gorbunova, Aslan Y. Tsivadze, Christine Stern, Yuanyuan Fang, Karl M. Kadish|2019|Dalton Trans.|48|5372|doi:10.1039/C9DT00706G
CCDC 1844991: Experimental Crystal Structure Determination
2019
Related Article: Sergey E. Nefedov, Kirill P. Birin, Alla Bessmertnykh-Lemeune, Yulia Y. Enakieva, Anna A. Sinelshchikova, Yulia G. Gorbunova, Aslan Y. Tsivadze, Christine Stern, Yuanyuan Fang, Karl M. Kadish|2019|Dalton Trans.|48|5372|doi:10.1039/C9DT00706G
CCDC 1844992: Experimental Crystal Structure Determination
2019
Related Article: Sergey E. Nefedov, Kirill P. Birin, Alla Bessmertnykh-Lemeune, Yulia Y. Enakieva, Anna A. Sinelshchikova, Yulia G. Gorbunova, Aslan Y. Tsivadze, Christine Stern, Yuanyuan Fang, Karl M. Kadish|2019|Dalton Trans.|48|5372|doi:10.1039/C9DT00706G
CCDC 1844990: Experimental Crystal Structure Determination
2019
Related Article: Sergey E. Nefedov, Kirill P. Birin, Alla Bessmertnykh-Lemeune, Yulia Y. Enakieva, Anna A. Sinelshchikova, Yulia G. Gorbunova, Aslan Y. Tsivadze, Christine Stern, Yuanyuan Fang, Karl M. Kadish|2019|Dalton Trans.|48|5372|doi:10.1039/C9DT00706G