Artículos de revistas sobre el tema "Tetra phenyl porphyrins"
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Ion, R. M., A. Planner, K. Wiktorowicz y D. Frackowiak. "The incorporation of various porphyrins into blood cells measured via flow cytometry, absorption and emission spectroscopy." Acta Biochimica Polonica 45, n.º 3 (30 de septiembre de 1998): 833–45. http://dx.doi.org/10.18388/abp.1998_4279.
Texto completoScheldt, W. Robert, Beisong Cheng, Allen G. Oliver y John A. Goodwin. "Solid-state porphyrin interactions with oppositely charged peripheral groups". Journal of Porphyrins and Phthalocyanines 19, n.º 12 (diciembre de 2015): 1256–61. http://dx.doi.org/10.1142/s1088424615501084.
Texto completoION, Chim Rodica-Mariana y Cristina MANDRAVEL. "THE PHOTODEGRADATION REACTION OF SOME PORPHYRINS". SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY 5, n.º 5 (20 de diciembre de 1997): 111–29. http://dx.doi.org/10.48141/sbjchem.v5.n5.1997.109_1997.pdf.
Texto completoGeorge, Reama Chinedu, Nkem Torimiro, Oluwafemi Bamidele Daramola y Afusat Ajoke Olajide. "Zinc, Tin and Silver Porphyrins (TPP, TCPP, TMPP, THPP, TPPS, TMPyP) as photosensitizers in antibacterial photodynamic therapy for chronic wounds: A screening study". Ethiopian Journal of Science and Technology 15, n.º 2 (1 de junio de 2022): 187–207. http://dx.doi.org/10.4314/ejst.v15i2.6.
Texto completoLi, Yang, Hannah M. Rhoda, Anthony M. Wertish y Victor N. Nemykin. "Organometallic pyrene-containing porphyrins: Synthesis, characterization, and non-covalent interactions with C60 fullerenes". Journal of Porphyrins and Phthalocyanines 20, n.º 08n11 (agosto de 2016): 1098–113. http://dx.doi.org/10.1142/s1088424616500735.
Texto completoAlemohammad, Tahereh, Nasser Safari y Samira Osati. "Effect of hydrogen bonding on catalytic activity of some manganese porphyrins in epoxidation reactions". Journal of Porphyrins and Phthalocyanines 15, n.º 03 (marzo de 2011): 181–87. http://dx.doi.org/10.1142/s1088424611003094.
Texto completoHALVORSEN, INGAR, ERIK STEENE y ABHIK GHOSH. "Resonance Raman marker bands of β-octahalogeno-meso-tetraarylmetalloporphyrins". Journal of Porphyrins and Phthalocyanines 05, n.º 10 (octubre de 2001): 721–30. http://dx.doi.org/10.1002/jpp.378.
Texto completoShen, Liang, Xiaomei Wang, Bo Li, Wanli Jiang, Ping Yang, Shixiong Qian, Xutang Tao y Minhua Jiang. "Two-photon absorption properties of substituted porphyrins". Journal of Porphyrins and Phthalocyanines 10, n.º 03 (marzo de 2006): 160–66. http://dx.doi.org/10.1142/s1088424606000193.
Texto completoSu, Qiwen y Tamara D. Hamilton. "Extending mechanochemical porphyrin synthesis to bulkier aromatics: tetramesitylporphyrin". Beilstein Journal of Organic Chemistry 15 (22 de mayo de 2019): 1149–53. http://dx.doi.org/10.3762/bjoc.15.111.
Texto completoNasrollahi, Rahele y Saeed Zakavi. "Kinetics and mechanistic studies on the formation and reactivity of high valent MnO porphyrin species: mono-ortho or para-substituted porphyrins versus a di-ortho-substituted one". New Journal of Chemistry 42, n.º 3 (2018): 1806–15. http://dx.doi.org/10.1039/c7nj04233g.
Texto completoLopez, Marco A. y Martha A. De La Rosa. "Electronic effects on carbon monoxide dissociation from iron(II) tetraphenylporhyrins". Journal of Porphyrins and Phthalocyanines 09, n.º 12 (diciembre de 2005): 821–29. http://dx.doi.org/10.1142/s1088424605000939.
Texto completoMakarska-Bialokoz, Magdalena. "Spectroscopic study of associated systems formed between water-soluble cationic porphyrins or their copper (II) complexes and nucleic building blocks". Open Chemistry 11, n.º 8 (1 de agosto de 2013): 1360–67. http://dx.doi.org/10.2478/s11532-013-0267-7.
Texto completoOu, Zhongping, Xueyan Chen, Lina Ye, Songlin Xue, Yuanyuan Fang, Xiaoqin Jiang y Karl M. Kadish. "N-confusedmeso-tetraaryl-substituted free-base porphyrins: determination of protonation and deprotonation constants in nonaqueous media". Journal of Porphyrins and Phthalocyanines 19, n.º 01-03 (enero de 2015): 251–60. http://dx.doi.org/10.1142/s1088424614501132.
Texto completoChen, Jian, Ji-Ming Hu, Zhi-San Xu y Rong-Sheng Sheng. "Surface-Enhanced Resonance Raman Spectra Study of α,β,γ,δ-Tetra-(4-Trimethyl Ammonium Phenyl) Porphyrin". Applied Spectroscopy 47, n.º 3 (marzo de 1993): 292–95. http://dx.doi.org/10.1366/0003702934066659.
Texto completoMojarrad, Aida G. y Saeed Zakavi. "Simple low cost porphyrinic photosensitizers for large scale chemoselective oxidation of sulfides to sulfoxides under green conditions: targeted protonation of porphyrins". Catalysis Science & Technology 8, n.º 3 (2018): 768–81. http://dx.doi.org/10.1039/c7cy02308a.
Texto completoPavanelli, André L. S., Leandro N. C. Máximo, Roberto S. da Silva y Iouri E. Borissevitch. "Effect of Serum Albumin on Porphyrin-Quantum Dot Complex Formation, Characteristics and Spectroscopic Analysis". Nanomaterials 11, n.º 7 (25 de junio de 2021): 1674. http://dx.doi.org/10.3390/nano11071674.
Texto completoSălăgeanu, Luminița, Delia Muntean, Horhat Florin George, Anca Lascu, Diana Anghel, Iulia Cristina Bagiu y Eugenia Fagadar-Cosma. "Antimicrobial activity of different substituted meso-porphyrin derivatives". Revista Romana de Medicina de Laborator 28, n.º 2 (1 de abril de 2020): 205–16. http://dx.doi.org/10.2478/rrlm-2020-0014.
Texto completoIon, Rodica-Mariana. "Synthesis, photophysical properties and photocatalytic activity of tungsten porphyrin (TPPWCl4)". Journal of Porphyrins and Phthalocyanines 17, n.º 06n07 (junio de 2013): 460–72. http://dx.doi.org/10.1142/s108842461350034x.
Texto completoAl-Shewiki, Rasha K., Carola Mende, Roy Buschbeck, Pablo F. Siles, Oliver G. Schmidt, Tobias Rüffer y Heinrich Lang. "Synthesis, spectroscopic characterization and thermogravimetric analysis of two series of substituted (metallo)tetraphenylporphyrins". Beilstein Journal of Nanotechnology 8 (2 de junio de 2017): 1191–204. http://dx.doi.org/10.3762/bjnano.8.121.
Texto completoWang, Bei-Bei, Huiping Zuo, John Mack, Poulomi Majumdar, Tebello Nyokong, Kin Shing Chan y Zhen Shen. "Optical properties and electronic structures of axially-ligated group 9 porphyrins". Journal of Porphyrins and Phthalocyanines 19, n.º 08 (agosto de 2015): 973–82. http://dx.doi.org/10.1142/s108842461550073x.
Texto completoGuergueb, Mouhieddinne, Soumaya Nasri, Jihed Brahmi, Frédérique Loiseau, Florian Molton, Thierry Roisnel, Vincent Guerineau, Ilona Turowska-Tyrk, Kaïss Aouadi y Habib Nasri. "Effect of the coordination of π-acceptor 4-cyanopyridine ligand on the structural and electronic properties of meso-tetra(para-methoxy) and meso-tetra(para-chlorophenyl) porphyrin cobalt(ii) coordination compounds. Application in the catalytic degradation of methylene blue dye". RSC Advances 10, n.º 12 (2020): 6900–6918. http://dx.doi.org/10.1039/c9ra08504a.
Texto completoAlbani, Guglielmo, Alberto Calloni, Madan S. Jagadeesh, Alberto Brambilla, Andrea Picone, Alessandro Lodesani, Lamberto Duò, Franco Ciccacci, Marco Finazzi y Gianlorenzo Bussetti. "Ordered Porphyrin Arrays on Fe(001): An Enabling Technology for Future Spintronics". Proceedings 56, n.º 1 (19 de diciembre de 2020): 25. http://dx.doi.org/10.3390/proceedings2020056025.
Texto completoVicente, M. Graça H., Benjamin F. Edwards, Shankar J. Shetty, Yongjin Hou y James E. Boggan. "Syntheses and preliminary biological studies of four meso-Tetra[(nido-carboranylmethyl)phenyl]porphyrins". Bioorganic & Medicinal Chemistry 10, n.º 3 (marzo de 2002): 481–92. http://dx.doi.org/10.1016/s0968-0896(01)00300-5.
Texto completoSrinivasan, Alagar, Bashyam Sridevi, Mereddy Venkat Ram Reddy, Seenichamy Jeyaprakash Narayanan y Tavarekere K. Chandrashekar. "Improved synthesis of meso substituted 21-Oxa and 21-Thia tetra phenyl porphyrins". Tetrahedron Letters 38, n.º 23 (junio de 1997): 4149–52. http://dx.doi.org/10.1016/s0040-4039(97)00807-1.
Texto completoŞen, Pınar, Catherine Hirel, Chantal Andraud, Christophe Aronica, Yann Bretonnière, Abdelsalam Mohammed, Hans Ågren et al. "Fluorescence and FTIR Spectra Analysis of Trans-A2B2-Substituted Di- and Tetra-Phenyl Porphyrins". Materials 3, n.º 8 (23 de agosto de 2010): 4446–75. http://dx.doi.org/10.3390/ma3084446.
Texto completoAng-Yang Yu. "Density Functional Theory Study of Meso-Tetra-Substituted Porphyrins: 3-Pyridyl Substitution for Phenyl". Russian Journal of Physical Chemistry A 94, n.º 3 (marzo de 2020): 604–7. http://dx.doi.org/10.1134/s0036024420030036.
Texto completoDahal, Sanjay y Israel Goldberg. "Solid-state supramolecular chemistry of porphyrins. Hydrogen-bonded networks and porous crystals ofmeso-tetra[4-(3,5-diaminotriazino)phenyl]porphyrin". Journal of Physical Organic Chemistry 13, n.º 7 (2000): 382–87. http://dx.doi.org/10.1002/1099-1395(200007)13:7<382::aid-poc266>3.0.co;2-5.
Texto completoAlbani, Guglielmo, Alberto Calloni, Andrea Picone, Alberto Brambilla, Michele Capra, Alessandro Lodesani, Lamberto Duò, Marco Finazzi, Franco Ciccacci y Gianlorenzo Bussetti. "An In-Depth Assessment of the Electronic and Magnetic Properties of a Highly Ordered Hybrid Interface: The Case of Nickel Tetra-Phenyl-Porphyrins on Fe(001)–p(1 × 1)O". Micromachines 12, n.º 2 (13 de febrero de 2021): 191. http://dx.doi.org/10.3390/mi12020191.
Texto completoGarcía-Pérez, César A., Carmina Menchaca-Campos, Miguel A. García-Sánchez y Jorge Uruchurtu. "Electrochemical Capacitive Properties of Ny/PP/GO Electro-spun Composite Coating on Stainless Steel in Acid Media". European Journal of Engineering and Technology Research 7, n.º 2 (30 de marzo de 2022): 81–86. http://dx.doi.org/10.24018/ejeng.2022.7.2.2775.
Texto completoAghabali, Amineh y Nasser Safari. "Effects of methoxy-substituted metalloporphyrins in catalytic alkene epoxidation by n-Bu4NHSO5". Journal of Porphyrins and Phthalocyanines 14, n.º 04 (abril de 2010): 335–42. http://dx.doi.org/10.1142/s1088424610002136.
Texto completoLi, Jianzhong, Tao Tang, Fan Li y Min Li. "The synthesis and characterization of novel liquid crystalline, meso-tetra[4-(3,4,5-trialkoxybenzoate)phenyl]porphyrins". Dyes and Pigments 77, n.º 2 (enero de 2008): 395–401. http://dx.doi.org/10.1016/j.dyepig.2007.07.008.
Texto completoPeng, Su-Hong, Li-Li Wang, Sha-Sha Cai, Hui-Qing Xiao, Xin-Tong Zhao, Hui Wang y Hai-Yang Liu. "UV, FL and IR spectroscopic analysis of N-confused meso-tetra(methoxyphenyl)porphyrins". Journal of Porphyrins and Phthalocyanines 26, n.º 03 (22 de diciembre de 2021): 195–202. http://dx.doi.org/10.1142/s1088424622500031.
Texto completoZolghadri, Samaneh, Hassan Yousefnia, Amir Reza Jalilian y Yousef Fazaeli. "Production, quality control, biodistribution assessment and preliminary dose evaluation of [177Lu]-tetra phenyl porphyrin complex as a possible therapeutic agent". Brazilian Journal of Pharmaceutical Sciences 51, n.º 2 (junio de 2015): 339–48. http://dx.doi.org/10.1590/s1984-82502015000200011.
Texto completoYun, Lin, Ling Zhen, Zikuan Wang y Xuefeng Fu. "Aerobic oxidative N-dealkylation of secondary amines in aqueous solution catalyzed by rhodium porphyrins". Journal of Porphyrins and Phthalocyanines 18, n.º 10n11 (octubre de 2014): 937–43. http://dx.doi.org/10.1142/s108842461450076x.
Texto completoYu, Miao, Yu J. Zhang, Jian H. Shi, Guo F. Liu y Hong J. Zhang. "Meso-tetra[(p-alkoxyl-m-ethyloxy)phenyl]porphyrins and their Transition Metal Complexes: Synthesis and Characterization". Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 40, n.º 6 (13 de julio de 2010): 404–9. http://dx.doi.org/10.1080/15533174.2010.492552.
Texto completoWu, Ya-hong, Lin Chen, Jian Yu, Shan-ling Tong y Yan Yan. "Synthesis and spectroscopic characterization of meso-tetra (Schiff-base substituted phenyl) porphyrins and their zinc complexes". Dyes and Pigments 97, n.º 3 (junio de 2013): 423–28. http://dx.doi.org/10.1016/j.dyepig.2012.12.032.
Texto completoKurochkin, Ivan Yu, Valentina A. Olshevskaya, Andrei V. Zaitsev, Nina I. Girichevac y Georgy V. Girichev. "Vibrational Spectra of 5,10,15,20-Tetraphenylporphyrin (H2TPP) and Platinum(II) 5,10,15,20-Tetra(phenyl/pentafluorophenyl)porphyrins (PtTPP and PtTF5PP)". Macroheterocycles 14, n.º 4 (2021): 334–41. http://dx.doi.org/10.6060/mhc224109g.
Texto completoZheng, Wen Q., Wen Y. Liu y Miao Yu. "Liquid-Crystalline Properties of Meso-tetra [(p-alkoxyl-m-ethyloxy)phenyl]Porphyrins and Their Transition Metal Complexes". Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 43, n.º 2 (28 de diciembre de 2012): 175–77. http://dx.doi.org/10.1080/15533174.2012.684254.
Texto completoCrusats, Joaquim, Josep Claret, Ismael Díez-Pérez, Zoubir El-Hachemi, Héctor García-Ortega, Raimon Rubires, Francesc Sagués y Josep M. Ribó. "Chiral shape and enantioselective growth of colloidal particles of self-assembled meso-tetra(phenyl and 4-sulfonatophenyl)porphyrins". Chem. Commun., n.º 13 (2003): 1588–89. http://dx.doi.org/10.1039/b303273f.
Texto completoSHE, Yuanbin, Lianshun FENG, Aixin WANG y Xiuyan LI. "Synthesis of Substituted μ-Oxo-bis[tetra-phenyl porphyrinatoiron] Compounds from Free Base Porphyrins by a One-pot Method". Chinese Journal of Chemical Engineering 16, n.º 3 (junio de 2008): 369–72. http://dx.doi.org/10.1016/s1004-9541(08)60090-7.
Texto completoWang, Duo Yuan, Min Xue Hu, Ling Zhi Hu, Li Zheng Zhao, Zhen Zhong Lu, Yu Xin Nie, Kazuyuki Horie y Shinjiro Machida. "Photophysical Properties of MESO-Phenyl-Tetra-Benzo-Porphyrins and Photon-Gated Spectral Hole Burning in Mixed Donor-Acceptor Systems at Low Temperature". Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 291, n.º 1 (diciembre de 1996): 223–33. http://dx.doi.org/10.1080/10587259608042751.
Texto completoZuo, Guofang, Xiaoquan Lu, Zhonghua Xue, Baoqiang Lv, Yongsheng Wang y Jingwan Kang. "Synthesis and Characterization of a Series of Thiol‐Derivatized Porphyrins and Electrocatalytic Reduction of Dioxygen by Cobalt(II)‐tetra‐[p‐(mercaptoprophyloxy)‐phenyl] Porphyrin (CoTMPP) on a Gold Support, Self‐Assembled Monolayers (SAMs)". Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 36, n.º 8 (1 de septiembre de 2006): 589–94. http://dx.doi.org/10.1080/15533170600908946.
Texto completoDesroches, Marie-Catherine, Sandrine Layac, Patrice Prognon, Philippe Maillard, David S. Grierson, Emmanuel Curis, Ioannis Nicolis y Athena Kasselouri. "Speciation of New Tri- and Tetra-Glucoconjugated Tetrapyrrolic Macrocycles (Porphyrins and Chlorins): An Electronic Molecular Spectroscopy Study". Applied Spectroscopy 57, n.º 8 (agosto de 2003): 950–59. http://dx.doi.org/10.1366/000370203322258913.
Texto completoPlotnikova, Anna O., Yulia B. Ivanova y Nugzar Zh Mamardashvili. "INVESTIGATION OF COORDINATION PROPERTIES OF 5,10,15,20-TETRA(4-OH-PHENYL) PORPHYRIN IN ACETONITRILE AND DIMETHYLFORMAMIDE". IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 60, n.º 6 (19 de julio de 2017): 65. http://dx.doi.org/10.6060/tcct.2017606.5550.
Texto completoSakthinathan, Subramanian, Subbiramaniyan Kubendhiran, Shen-Ming Chen y P. Tamizhdurai. "Reduced graphene oxide/gold tetraphenyl porphyrin (RGO/Au–TPP) nanocomposite as an ultrasensitive amperometric sensor for environmentally toxic hydrazine". RSC Advances 6, n.º 61 (2016): 56375–83. http://dx.doi.org/10.1039/c6ra09129f.
Texto completoYu, Miao, Guo F. Liu y Xiao L. Cui. "Synthesis, spectroscopy, surface photovoltage, and electrochemical properties of porphyrin compound liquid crystals". Journal of Porphyrins and Phthalocyanines 09, n.º 04 (abril de 2005): 231–39. http://dx.doi.org/10.1142/s1088424605000290.
Texto completoCheccoli, P., G. Conte, S. Salvatori, R. Paolesse, A. Bolognesi, M. Berliocchi, F. Brunetti, A. D’Amico, A. Di Carlo y P. Lugli. "Tetra-phenyl porphyrin based thin film transistors". Synthetic Metals 138, n.º 1-2 (junio de 2003): 261–66. http://dx.doi.org/10.1016/s0379-6779(02)01308-5.
Texto completoReddy, D. Raghunath y Bhaskar G. Maiya. "Bis(aryloxo) derivatives of tin(IV) porphyrins: synthesis, spectroscopy and redox activity". Journal of Porphyrins and Phthalocyanines 06, n.º 01 (enero de 2002): 3–11. http://dx.doi.org/10.1142/s1088424602000026.
Texto completoZakavi, Saeed, Aida Ghanbelanie Mojarrad y Saeed Rayati. "Substituent effects on the catalytic activity of a series of manganese meso-tetra(aryl)porphyrins: (2-, 3-, 4)-Pyridyl, 4-sulfonatophenyl and 3-sulfonato-4-methoxyphenyl groups compared to phenyl and 4-methoxyphenyl ones". Journal of Molecular Catalysis A: Chemical 363-364 (noviembre de 2012): 153–58. http://dx.doi.org/10.1016/j.molcata.2012.06.003.
Texto completoCalcavento, C., G. Conte, S. Salvatori, R. Paolesse, M. Berliocchi, A. Di Carlo, P. Lugli y A. Sassella. "Charge injection and transport in tetra-phenyl-porphyrin". Synthetic Metals 138, n.º 1-2 (junio de 2003): 255–60. http://dx.doi.org/10.1016/s0379-6779(02)01307-3.
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