57412-08-5Relevant articles and documents
Poly(arylene ether ketone)s with pendant porphyrins: Synthesis and investigation on optical limiting properties
Du, Yinlong,Zhu, Kai,Fang, Yu,Zhang, Shuling,Zhang, Xingrui,Lu, Yaning,Yang, Yanchao,Song, Yinglin,Wang, Guibin
, p. 48311 - 48322 (2015)
This paper describes the synthesis and characterization of a novel series of poly(arylene ether ketone)s bearing porphyrin pendants, along with the demonstration of their nonlinear optical and optical limiting properties at 532 nm in both THF and films. T
One-Photon Excitation Followed by a Three-Step Sequential Energy–Energy–Electron Transfer Leading to a Charge-Separated State in a Supramolecular Tetrad Featuring Benzothiazole–Boron-Dipyrromethene–Zinc Porphyrin–C60
Badgurjar, Deepak,Seetharaman, Sairaman,D'Souza, Francis,Chitta, Raghu
supporting information, p. 2184 - 2195 (2020/12/25)
A panchromatic triad, consisting of benzothiazole (BTZ) and BF2-chelated boron-dipyrromethene (BODIPY) moieties covalently linked to a zinc porphyrin (ZnP) core, has been synthesized and systematically characterized by using 1H NMR s
Self‐assembled nanomaterials based on complementary sn(Iv) and zn(ii)‐porphyrins, and their photocatalytic degradation for rhodamine b dye
Kim, Hee-Joon,Shee, Nirmal K.
, (2021/06/26)
A series of porphyrin triads (1–6), based on the reaction of trans‐dihydroxo‐[5,15‐bis(3‐ pyridyl)‐10,20‐bis(phenyl)porphyrinato]tin(IV) (SnP) with six different phenoxy Zn(II)‐porphyrins (ZnLn), was synthesized. The cooperative metal–ligand co
Synthesis and cancer cell cytotoxicity of gold(III) tetraarylporphyrins with a C5-carboxylate substituent
Liu, Jinliang,Chen, Huasheng,Li, Yan,Chen, Ying,Mao, Leilei,Xu, Aihua,Wang, Cunde
experimental part, p. 698 - 702 (2012/03/12)
Gold(III) tetraarylporphyrins with a C5-carboxylate substituent have been synthesised and their in vitro cytotoxic activity against SGC-7901 human gastric cancer cell line panel evaluated. The compound 5-[4-(4-ethoxycarbonylbut oxy)phenyl]-10,15,20-tri(4-
Synthesis and photophysical properties of a conformationally flexible mixed porphyrin star-pentamer
Bell, Toby D. M.,Bhosale, Sheshanath V.,Ghiggino, Kenneth P.,Langford, Steven J.,Woodward, Clint P.
experimental part, p. 692 - 699 (2010/02/28)
The synthesis of a porphyrin star-pentamer bearing a free-base porphyrin core and four zinc(ii) metalloporphyrins, which are tethered by a conformationally flexible linker about the central porphyrin's antipody, is described. The synthetic strategy is hig
Surface-functionalised nano-beads as novel supports for organic synthesis
Cammidge, Andrew N.,Downing, Stuart,Ngaini, Zainab
, p. 6633 - 6634 (2007/10/03)
A novel polymer support has been prepared in which functional link points are located on the surface of polymer nano-beads; the use of the support has been demonstrated in the syntheses of unsymmetrical porphyrins.
Synthesis of Porphyrinyl-Nucleosides
Czuchajowski, Leszek,Habdas, Jan,Niedbala, Halina,Wandrekar, Vinay
, p. 479 - 486 (2007/10/02)
Several porphyrinyl-nucleosides were prepared in the reaction of the OH group of one, two or four meso-p-hydroxyphenyl substituents of porphyrin with 5'-O-tosylates of 2',3'-O-isopropylidene-adenosine or -uridine, or 5'-O-tosylthymidine; the remaining porphyrin meso-substituents were p-tolyl, p-hydroxyphenyl or 4-pyridyl.The following porphyrinyl-nucleosides were obtained with 8-17percent yield: meso-di(p-tolyl)di(p-phenylene-5'-O-2',3'-O-isopropylidene-adenosine) (or -uridine)porphyrins 1,2, the respective meso-tetranucleosideporphyrins 3,4-meso-mono(p-phenylene-5'-O-thymidine)porphyrins 5-7, meso-di(p-tolyl)di(p-phenylene-5'-O-thymidine)porphyrins 8,9 and the meso-di(p-hydroxyphenyl)di(p-phenylene-5'-O-thymidine)porphyrins 10.Other compounds prepared belonged to the series: meso(4-pyridyl)4-n(p-phenylene-5'-O-2',3'-O-isopropylideneuridine)nporphyrin, n = 1,2 or 4, 11-13.N-Methylation gave the water soluble iodide salts: (N-methyl-4-pyridinium)4-n(p-phenylene-5'-O-2',3'-isopropylideneuridine)nporphyrins, n = 1,2 or 4, 14-16.The ms fab showed in most cases stepwise detachment of the CH2(5')-nucleoside fragments.The porphyrins meso disubstituted by thymidine represent a convenient substrate for the build-up of both nucleoside units into the oligo/polynucleotide chains.
Light-Induced Electron Transfer of Porphyrin Triad for Photoelectric Conversion
Wang, Xiang Dong,Zhang, Bao Wen,Bai, Jian Wei,Cao, Yi,Xiao, Xu Rui,Xu, Jing Mei
, p. 2886 - 2891 (2007/10/02)
Two new triad model compounds of porphyrin-viologen-carbazole (1a and 1b) with different chain length were synthesized to mimic photosynthesis.The absorption and fluorescence spectra in solution, in micelle solution as well as in binary solvent, were inve
SYNTHESIS OF HYBRID "METALLOPORPHYRIN-ELLIPTICINE" MOLECULES
Etemad-Moghadam, Guita,Ding, Li,Tadj, Fatemeh,Meunier, Bernard
, p. 2641 - 2648 (2007/10/02)
The synthesis of hybrid "metalloporphyrin-ellipticine" molecules is reported.These molecules are based on 9-methoxyellipticine and porphyrin linked by a ten-bond chain, -(CH2)4-CO-NH-(CH2)3-, between the hydroxy
