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Relevant bibliographies by topics / Tetraphenylporphyrin synthesis

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Academic literature on the topic 'Tetraphenylporphyrin synthesis'

Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

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Journal articles on the topic "Tetraphenylporphyrin synthesis"

1

Önal, Emel, Ismail Fidan, Dominique Luneau, and Catherine Hirel. "Through the challenging synthesis of tetraphenylporphyrin derivatives bearing nitroxide moieties." Journal of Porphyrins and Phthalocyanines 23, no. 04n05 (2019): 584–88. http://dx.doi.org/10.1142/s1088424619500500.

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Tetraphenylporphyrin derivatives a synthetic heterocycles with convenient preparation and a richness of properties which make them attractive in broad fields such as energy, life and materials sciences. Thus, in the quest for new radical architectures, tetraphenylporphyrins are prime candidates. To this end, we designed free-base tetraphenylporphyrins bearing nitronyl and imino nitroxide moieties covalently bonded to the para-position of the meso-phenyl substituent. Their detailed synthesis and characterization are reported here.

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Peters, Morten K., Christian Näther та Rainer Herges. "Crystal structure of a polymorph of μ-oxido-bis[(5,10,15,20-tetraphenylporphyrinato)iron(III)]". Acta Crystallographica Section E Crystallographic Communications 75, № 6 (2019): 930–33. http://dx.doi.org/10.1107/s2056989019007576.

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The title compound, [Fe2(C44H28N4O)2O], was obtained as a by-product during the synthesis of FeIII tetraphenylporphyrin perchlorate. It crystallizes as a new polymorphic modification in addition to the orthorhombic form previously reported [Hoffman et al. (1972). J. Am. Chem. Soc. 94, 3620–3626; Swepston & Ibers (1985) Acta Cryst. C41, 671–673; Kooijmann et al. (2007). Private Communication (refcode 667666). CCDC, Cambridge, England]. In its crystal structure, the two crystallographically independent FeIII cations are coordinated in a square-planar environment by the four N atoms of a tetr

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3

GOH, GERARD KIAN-MENG, and LESZEK CZUCHAJOWSKI. "The Synthesis of Isomeric Dithymidyl-phosphorus(V)-meso-tetraphenylporphyrins." Journal of Porphyrins and Phthalocyanines 01, no. 03 (1997): 281–85. http://dx.doi.org/10.1002/(sici)1099-1409(199707)1:3<281::aid-jpp32>3.0.co;2-l.

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The synthesis of three novel axial dinucleosides was successfully accomplished. The compounds are 5″- O , 5″- O -dithymidylphosphorus(V)-meso-tetraphenylporphyrin, 5″- O , 3″- O -dithymi-dylphosphorus(V)-meso-tetraphenylporphyrin, and 3″- O , 3″- O -dithymidylphosphorus(V)tetraphenylporo-phyrin. These compounds could provide a lead toward the synthesis of an oligo-porphyrinyl DNA analogue that represents a system containing phosphorus(V)porphine units axially connected through the 5″- O -thymidine-3″- O bridges.

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4

Morales, Paula, Laura Moreno, Javier Fernández-Ruiz, and Nadine Jagerovic. "Synthesis of a novel CB2 cannabinoid-porphyrin conjugate based on an antitumor chromenopyrazoledione." Journal of Porphyrins and Phthalocyanines 21, no. 01 (2017): 67–76. http://dx.doi.org/10.1142/s1088424617500092.

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With the objective of developing an antitumor agent, the synthesis of a chromenopyrazoledione conjugated to a tetraphenylporphyrin is described. A complete conformational analysis of the novel porphyrin conjugate was performed using ab initio Hartree–Fock calculations at the 6-31G* level. The novel conjugate (14) shows stronger absorption intensity for both Soret and Q-bands than the free meso-tetraphenylporphyrin. It binds weakly but selectively to the cannabinoid receptor type-2. During the synthetic approach, a new tetraphenylporphyrin, 5-[4-(3,5-dioxomorpholino)phenyl]-10,15,20-triphenylpo

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5

Fedulova, Irina N., Natalya A. Bragina, Nikita V. Novikov, et al. "Synthesis and mesomorphism of tetraphenylporphyrin derivatives." Mendeleev Communications 18, no. 6 (2008): 324–26. http://dx.doi.org/10.1016/j.mencom.2008.11.013.

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6

İşci, Ümit, Sevinc Zehra Topal, Emel Önal, et al. "Synthesis and characterization of a new meso-tetra-dihydro benzocyclobutacenaphthylene free-base porphyrin." Journal of Porphyrins and Phthalocyanines 22, no. 01n03 (2018): 173–80. http://dx.doi.org/10.1142/s1088424618500062.

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A meso-tetra-6b,10b-dihydrobenzo[j]cyclobut[a]acenaphthylene free-base porphyrin was synthesised and its photophysical, photochemical and electrochemical properties were compared with those of free-base meso-tetraphenylporphyrin. The frontier orbitals and the HOMO–LUMO energy gaps of both compounds were also determined. It was demonstrated that the meso6b,10b-Dihydrobenzo[j]cyclobut[a]acenaphthylene porphyrin retained the same properties as the tetraphenylporphyrin.

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7

Stopka, Pavel, and Dana M. Wagnerová. "Photochemical generation of porphyrin. ESR and absorption spectroscopic studies." Collection of Czechoslovak Chemical Communications 54, no. 6 (1989): 1630–39. http://dx.doi.org/10.1135/cccc19891630.

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Irradiation by a high-pressure mercury arc of a mixture containing pyrrole, benzaldehyde, and Fe(III) in the medium of glacial acetic acid results in the formation of Fe(III)-meso-tetraphenylporphyrin and some amount of free meso-tetraphenylporphyrin. The products were identified by means of ESR and absorption spectra. When irradiated for long periods of time, the products undergo photochemical degradation. Since the photochemical incorporation of Fe(III) into the free meso-tetraphenylporphyrin ligand yields a complex with a structure different from that in the previous case, it may be conclud

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8

Silva, Eduarda M. P., Catarina I. V. Ramos, Patrícia M. R. Pereira та ін. "Cationic β-vinyl substitutedmeso-tetraphenylporphyrins: synthesis and non-covalent interactions with a short poly(dGdC) duplex". Journal of Porphyrins and Phthalocyanines 16, № 01 (2012): 101–13. http://dx.doi.org/10.1142/s1088424611004373.

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Several cationic beta-vinyl-pyridinium and beta-vinyl-quinolinium-meso-tetraphenylporphyrin derivatives were synthesized starting from 2-formyl-meso-tetraphenylporphyrin, and the corresponding Zn(II) complex, and different N-alkyl derivatives of 2- and 4-methylpyridine and 2- and 4-methylquinoline. The new compounds were obtained in a one-step process via base catalyzed aldol-type condensation reactions. Electrospray ionization mass spectrometry (ESI-MS) and ultraviolet-visible (UV-vis) spectroscopy were used to investigate the binding mode of the synthesized cationic beta-vinyl-pyridinium and

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9

Foley, Timothy J., Khalil A. Abboud, and James M. Boncella. "Synthesis of Ln(III) Chloride Tetraphenylporphyrin Complexes." Inorganic Chemistry 41, no. 7 (2002): 1704–6. http://dx.doi.org/10.1021/ic015612e.

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10

Kotsuba, Vasily E., Nadezhda M. Kolyadina, Anatoly T. Soldatenkov, and Victor N. Khrustalev. "Synthesis of a Novel Crown-Fused Tetraphenylporphyrin." Macroheterocycles 6, no. 1 (2013): 74–76. http://dx.doi.org/10.6060/mhc130223k.

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Dissertations / Theses on the topic "Tetraphenylporphyrin synthesis"

1

Ladd, Richard Maurice. "Synthesis of the zinc and cobalt derivatives of meso-(4-sulphonatophenyl)-porphyrin for use as diamagnetic shift reagents in nuclear magnetic resonance studies." Thesis, Manchester Metropolitan University, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.238379.

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Hatcher, Jancie Stinecipher. "Synthesis, characterization, and monolayer formation of sulfur-substituted tetraphenylporphyrins." Thesis, Georgia Institute of Technology, 1990. http://hdl.handle.net/1853/29977.

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3

Altundas, Abdullah Bilal. "Synthesis of XZH-5 Derivatives as Inhibitors of Signal Transducer and Activator of Transcription 3 (STAT3) and Synthesis of π-Extended Tetraphenylporphyrins". Miami University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=miami1473201129.

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楊富安. "Synthesis and spectroscopic studies on cadmium complexes of N-benzamidoporphyrin, thallium complexes of pentafluoropropionato-tetraphenylporphyrin and heptafluorobutyrato- tetraphenylporphyrin." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/18836860180365465826.

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Dahal, Sanjay. "Synthesis Structure And Photophysical Properties Of Beta-Pyrrole Substituted Tetraphenylporphyrins." Thesis, 1995. http://etd.iisc.ernet.in/handle/2005/1845.

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6

Maurer-Chronakis, Katja [Verfasser]. "Synthesis of cyanuric acid and Hamilton receptor functionalized tetraphenylporphyrins : investigation on the chiroptical and photophysical properties of their self-assembled superstructures with depsipeptide and fullerene dendrimers / vorgelegt von Katja Maurer-Chronakis." 2010. http://d-nb.info/1010576658/34.

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Book chapters on the topic "Tetraphenylporphyrin synthesis"

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Emmert, H., R. Sailer, W. S. L. Strauss, D. G. Kieback, and R. Steiner. "Synthese, Zytotoxizität und Intrazelluläre Akkumulation eines lipophilen Meso-Tetraphenylporphyrins." In Laser in der Medizin Laser in Medicine. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-60306-8_41.

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2

Önal, Emel, Ismail Fidan, Dominique Luneau, and Catherine Hirel. "Through the challenging synthesis of tetraphenylporphyrin derivatives bearing nitroxide moieties." In Porphyrin Science by Women. WORLD SCIENTIFIC, 2021. http://dx.doi.org/10.1142/9789811223556_0040.

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Conference papers on the topic "Tetraphenylporphyrin synthesis"

1

Richert, Clemens, and Kendra Dombi. "Relative Reactivities of Activated Carboxylic Acids in Amide-Forming Reactions Employed for the Synthesis of Tetraphenylporphyrin Libraries." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01909.

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2

Berezin, Dmitry B., Raymond Bonnett, Maria A. de Madariaga, et al. "Gd-meso-tetraphenylporphyrins: synthesis, encapsulation into liposomes, and characterization of the resulting preparations." In BiOS Europe '97, edited by Kristian Berg, Benjamin Ehrenberg, Zvi Malik, Johan Moan, and Abraham Katzir. SPIE, 1997. http://dx.doi.org/10.1117/12.297829.

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