Статті в журналах з теми "Tetra phenyl porphyrins"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Tetra phenyl porphyrins".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Ion, R. M., A. Planner, K. Wiktorowicz, and D. Frackowiak. "The incorporation of various porphyrins into blood cells measured via flow cytometry, absorption and emission spectroscopy." Acta Biochimica Polonica 45, no. 3 (September 30, 1998): 833–45. http://dx.doi.org/10.18388/abp.1998_4279.
Повний текст джерелаScheldt, W. Robert, Beisong Cheng, Allen G. Oliver, and John A. Goodwin. "Solid-state porphyrin interactions with oppositely charged peripheral groups." Journal of Porphyrins and Phthalocyanines 19, no. 12 (December 2015): 1256–61. http://dx.doi.org/10.1142/s1088424615501084.
Повний текст джерелаION, Chim Rodica-Mariana, and Cristina MANDRAVEL. "THE PHOTODEGRADATION REACTION OF SOME PORPHYRINS." SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY 5, no. 5 (December 20, 1997): 111–29. http://dx.doi.org/10.48141/sbjchem.v5.n5.1997.109_1997.pdf.
Повний текст джерелаGeorge, Reama Chinedu, Nkem Torimiro, Oluwafemi Bamidele Daramola, and 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, no. 2 (June 1, 2022): 187–207. http://dx.doi.org/10.4314/ejst.v15i2.6.
Повний текст джерелаLi, Yang, Hannah M. Rhoda, Anthony M. Wertish, and Victor N. Nemykin. "Organometallic pyrene-containing porphyrins: Synthesis, characterization, and non-covalent interactions with C60 fullerenes." Journal of Porphyrins and Phthalocyanines 20, no. 08n11 (August 2016): 1098–113. http://dx.doi.org/10.1142/s1088424616500735.
Повний текст джерелаAlemohammad, Tahereh, Nasser Safari, and Samira Osati. "Effect of hydrogen bonding on catalytic activity of some manganese porphyrins in epoxidation reactions." Journal of Porphyrins and Phthalocyanines 15, no. 03 (March 2011): 181–87. http://dx.doi.org/10.1142/s1088424611003094.
Повний текст джерелаHALVORSEN, INGAR, ERIK STEENE та ABHIK GHOSH. "Resonance Raman marker bands of β-octahalogeno-meso-tetraarylmetalloporphyrins". Journal of Porphyrins and Phthalocyanines 05, № 10 (жовтень 2001): 721–30. http://dx.doi.org/10.1002/jpp.378.
Повний текст джерелаShen, Liang, Xiaomei Wang, Bo Li, Wanli Jiang, Ping Yang, Shixiong Qian, Xutang Tao, and Minhua Jiang. "Two-photon absorption properties of substituted porphyrins." Journal of Porphyrins and Phthalocyanines 10, no. 03 (March 2006): 160–66. http://dx.doi.org/10.1142/s1088424606000193.
Повний текст джерелаSu, Qiwen, and Tamara D. Hamilton. "Extending mechanochemical porphyrin synthesis to bulkier aromatics: tetramesitylporphyrin." Beilstein Journal of Organic Chemistry 15 (May 22, 2019): 1149–53. http://dx.doi.org/10.3762/bjoc.15.111.
Повний текст джерелаNasrollahi, Rahele, and 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, no. 3 (2018): 1806–15. http://dx.doi.org/10.1039/c7nj04233g.
Повний текст джерелаLopez, Marco A., and Martha A. De La Rosa. "Electronic effects on carbon monoxide dissociation from iron(II) tetraphenylporhyrins." Journal of Porphyrins and Phthalocyanines 09, no. 12 (December 2005): 821–29. http://dx.doi.org/10.1142/s1088424605000939.
Повний текст джерелаMakarska-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, no. 8 (August 1, 2013): 1360–67. http://dx.doi.org/10.2478/s11532-013-0267-7.
Повний текст джерелаOu, Zhongping, Xueyan Chen, Lina Ye, Songlin Xue, Yuanyuan Fang, Xiaoqin Jiang, and 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, no. 01-03 (January 2015): 251–60. http://dx.doi.org/10.1142/s1088424614501132.
Повний текст джерелаChen, Jian, Ji-Ming Hu, Zhi-San Xu та Rong-Sheng Sheng. "Surface-Enhanced Resonance Raman Spectra Study of α,β,γ,δ-Tetra-(4-Trimethyl Ammonium Phenyl) Porphyrin". Applied Spectroscopy 47, № 3 (березень 1993): 292–95. http://dx.doi.org/10.1366/0003702934066659.
Повний текст джерелаMojarrad, Aida G., and 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, no. 3 (2018): 768–81. http://dx.doi.org/10.1039/c7cy02308a.
Повний текст джерелаPavanelli, André L. S., Leandro N. C. Máximo, Roberto S. da Silva, and Iouri E. Borissevitch. "Effect of Serum Albumin on Porphyrin-Quantum Dot Complex Formation, Characteristics and Spectroscopic Analysis." Nanomaterials 11, no. 7 (June 25, 2021): 1674. http://dx.doi.org/10.3390/nano11071674.
Повний текст джерелаSălăgeanu, Luminița, Delia Muntean, Horhat Florin George, Anca Lascu, Diana Anghel, Iulia Cristina Bagiu, and Eugenia Fagadar-Cosma. "Antimicrobial activity of different substituted meso-porphyrin derivatives." Revista Romana de Medicina de Laborator 28, no. 2 (April 1, 2020): 205–16. http://dx.doi.org/10.2478/rrlm-2020-0014.
Повний текст джерелаIon, Rodica-Mariana. "Synthesis, photophysical properties and photocatalytic activity of tungsten porphyrin (TPPWCl4)." Journal of Porphyrins and Phthalocyanines 17, no. 06n07 (June 2013): 460–72. http://dx.doi.org/10.1142/s108842461350034x.
Повний текст джерелаAl-Shewiki, Rasha K., Carola Mende, Roy Buschbeck, Pablo F. Siles, Oliver G. Schmidt, Tobias Rüffer, and Heinrich Lang. "Synthesis, spectroscopic characterization and thermogravimetric analysis of two series of substituted (metallo)tetraphenylporphyrins." Beilstein Journal of Nanotechnology 8 (June 2, 2017): 1191–204. http://dx.doi.org/10.3762/bjnano.8.121.
Повний текст джерелаWang, Bei-Bei, Huiping Zuo, John Mack, Poulomi Majumdar, Tebello Nyokong, Kin Shing Chan, and Zhen Shen. "Optical properties and electronic structures of axially-ligated group 9 porphyrins." Journal of Porphyrins and Phthalocyanines 19, no. 08 (August 2015): 973–82. http://dx.doi.org/10.1142/s108842461550073x.
Повний текст джерелаGuergueb, Mouhieddinne, Soumaya Nasri, Jihed Brahmi, Frédérique Loiseau, Florian Molton, Thierry Roisnel, Vincent Guerineau, Ilona Turowska-Tyrk, Kaïss Aouadi та 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, № 12 (2020): 6900–6918. http://dx.doi.org/10.1039/c9ra08504a.
Повний текст джерелаAlbani, Guglielmo, Alberto Calloni, Madan S. Jagadeesh, Alberto Brambilla, Andrea Picone, Alessandro Lodesani, Lamberto Duò, Franco Ciccacci, Marco Finazzi, and Gianlorenzo Bussetti. "Ordered Porphyrin Arrays on Fe(001): An Enabling Technology for Future Spintronics." Proceedings 56, no. 1 (December 19, 2020): 25. http://dx.doi.org/10.3390/proceedings2020056025.
Повний текст джерелаVicente, M. Graça H., Benjamin F. Edwards, Shankar J. Shetty, Yongjin Hou, and James E. Boggan. "Syntheses and preliminary biological studies of four meso-Tetra[(nido-carboranylmethyl)phenyl]porphyrins." Bioorganic & Medicinal Chemistry 10, no. 3 (March 2002): 481–92. http://dx.doi.org/10.1016/s0968-0896(01)00300-5.
Повний текст джерелаSrinivasan, Alagar, Bashyam Sridevi, Mereddy Venkat Ram Reddy, Seenichamy Jeyaprakash Narayanan, and Tavarekere K. Chandrashekar. "Improved synthesis of meso substituted 21-Oxa and 21-Thia tetra phenyl porphyrins." Tetrahedron Letters 38, no. 23 (June 1997): 4149–52. http://dx.doi.org/10.1016/s0040-4039(97)00807-1.
Повний текст джерелаŞen, 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, no. 8 (August 23, 2010): 4446–75. http://dx.doi.org/10.3390/ma3084446.
Повний текст джерелаAng-Yang Yu. "Density Functional Theory Study of Meso-Tetra-Substituted Porphyrins: 3-Pyridyl Substitution for Phenyl." Russian Journal of Physical Chemistry A 94, no. 3 (March 2020): 604–7. http://dx.doi.org/10.1134/s0036024420030036.
Повний текст джерелаDahal, Sanjay, and 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, no. 7 (2000): 382–87. http://dx.doi.org/10.1002/1099-1395(200007)13:7<382::aid-poc266>3.0.co;2-5.
Повний текст джерелаAlbani, Guglielmo, Alberto Calloni, Andrea Picone, Alberto Brambilla, Michele Capra, Alessandro Lodesani, Lamberto Duò, Marco Finazzi, Franco Ciccacci, and 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, no. 2 (February 13, 2021): 191. http://dx.doi.org/10.3390/mi12020191.
Повний текст джерелаGarcía-Pérez, César A., Carmina Menchaca-Campos, Miguel A. García-Sánchez, and 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, no. 2 (March 30, 2022): 81–86. http://dx.doi.org/10.24018/ejeng.2022.7.2.2775.
Повний текст джерелаAghabali, Amineh, and Nasser Safari. "Effects of methoxy-substituted metalloporphyrins in catalytic alkene epoxidation by n-Bu4NHSO5." Journal of Porphyrins and Phthalocyanines 14, no. 04 (April 2010): 335–42. http://dx.doi.org/10.1142/s1088424610002136.
Повний текст джерелаLi, Jianzhong, Tao Tang, Fan Li, and Min Li. "The synthesis and characterization of novel liquid crystalline, meso-tetra[4-(3,4,5-trialkoxybenzoate)phenyl]porphyrins." Dyes and Pigments 77, no. 2 (January 2008): 395–401. http://dx.doi.org/10.1016/j.dyepig.2007.07.008.
Повний текст джерелаPeng, Su-Hong, Li-Li Wang, Sha-Sha Cai, Hui-Qing Xiao, Xin-Tong Zhao, Hui Wang, and Hai-Yang Liu. "UV, FL and IR spectroscopic analysis of N-confused meso-tetra(methoxyphenyl)porphyrins." Journal of Porphyrins and Phthalocyanines 26, no. 03 (December 22, 2021): 195–202. http://dx.doi.org/10.1142/s1088424622500031.
Повний текст джерелаZolghadri, Samaneh, Hassan Yousefnia, Amir Reza Jalilian, and 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, no. 2 (June 2015): 339–48. http://dx.doi.org/10.1590/s1984-82502015000200011.
Повний текст джерелаYun, Lin, Ling Zhen, Zikuan Wang, and Xuefeng Fu. "Aerobic oxidative N-dealkylation of secondary amines in aqueous solution catalyzed by rhodium porphyrins." Journal of Porphyrins and Phthalocyanines 18, no. 10n11 (October 2014): 937–43. http://dx.doi.org/10.1142/s108842461450076x.
Повний текст джерелаYu, Miao, Yu J. Zhang, Jian H. Shi, Guo F. Liu, and 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, no. 6 (July 13, 2010): 404–9. http://dx.doi.org/10.1080/15533174.2010.492552.
Повний текст джерелаWu, Ya-hong, Lin Chen, Jian Yu, Shan-ling Tong, and Yan Yan. "Synthesis and spectroscopic characterization of meso-tetra (Schiff-base substituted phenyl) porphyrins and their zinc complexes." Dyes and Pigments 97, no. 3 (June 2013): 423–28. http://dx.doi.org/10.1016/j.dyepig.2012.12.032.
Повний текст джерелаKurochkin, Ivan Yu, Valentina A. Olshevskaya, Andrei V. Zaitsev, Nina I. Girichevac, and 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, no. 4 (2021): 334–41. http://dx.doi.org/10.6060/mhc224109g.
Повний текст джерелаZheng, Wen Q., Wen Y. Liu, and 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, no. 2 (December 28, 2012): 175–77. http://dx.doi.org/10.1080/15533174.2012.684254.
Повний текст джерелаCrusats, Joaquim, Josep Claret, Ismael Díez-Pérez, Zoubir El-Hachemi, Héctor García-Ortega, Raimon Rubires, Francesc Sagués, and Josep M. Ribó. "Chiral shape and enantioselective growth of colloidal particles of self-assembled meso-tetra(phenyl and 4-sulfonatophenyl)porphyrins." Chem. Commun., no. 13 (2003): 1588–89. http://dx.doi.org/10.1039/b303273f.
Повний текст джерелаSHE, Yuanbin, Lianshun FENG, Aixin WANG та 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, № 3 (червень 2008): 369–72. http://dx.doi.org/10.1016/s1004-9541(08)60090-7.
Повний текст джерелаWang, Duo Yuan, Min Xue Hu, Ling Zhi Hu, Li Zheng Zhao, Zhen Zhong Lu, Yu Xin Nie, Kazuyuki Horie, and 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, no. 1 (December 1996): 223–33. http://dx.doi.org/10.1080/10587259608042751.
Повний текст джерелаZuo, Guofang, Xiaoquan Lu, Zhonghua Xue, Baoqiang Lv, Yongsheng Wang, and 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, no. 8 (September 1, 2006): 589–94. http://dx.doi.org/10.1080/15533170600908946.
Повний текст джерелаDesroches, Marie-Catherine, Sandrine Layac, Patrice Prognon, Philippe Maillard, David S. Grierson, Emmanuel Curis, Ioannis Nicolis, and Athena Kasselouri. "Speciation of New Tri- and Tetra-Glucoconjugated Tetrapyrrolic Macrocycles (Porphyrins and Chlorins): An Electronic Molecular Spectroscopy Study." Applied Spectroscopy 57, no. 8 (August 2003): 950–59. http://dx.doi.org/10.1366/000370203322258913.
Повний текст джерелаPlotnikova, Anna O., Yulia B. Ivanova, and 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, no. 6 (July 19, 2017): 65. http://dx.doi.org/10.6060/tcct.2017606.5550.
Повний текст джерелаSakthinathan, Subramanian, Subbiramaniyan Kubendhiran, Shen-Ming Chen, and P. Tamizhdurai. "Reduced graphene oxide/gold tetraphenyl porphyrin (RGO/Au–TPP) nanocomposite as an ultrasensitive amperometric sensor for environmentally toxic hydrazine." RSC Advances 6, no. 61 (2016): 56375–83. http://dx.doi.org/10.1039/c6ra09129f.
Повний текст джерелаYu, Miao, Guo F. Liu, and Xiao L. Cui. "Synthesis, spectroscopy, surface photovoltage, and electrochemical properties of porphyrin compound liquid crystals." Journal of Porphyrins and Phthalocyanines 09, no. 04 (April 2005): 231–39. http://dx.doi.org/10.1142/s1088424605000290.
Повний текст джерелаCheccoli, P., G. Conte, S. Salvatori, R. Paolesse, A. Bolognesi, M. Berliocchi, F. Brunetti, A. D’Amico, A. Di Carlo, and P. Lugli. "Tetra-phenyl porphyrin based thin film transistors." Synthetic Metals 138, no. 1-2 (June 2003): 261–66. http://dx.doi.org/10.1016/s0379-6779(02)01308-5.
Повний текст джерелаReddy, D. Raghunath, and Bhaskar G. Maiya. "Bis(aryloxo) derivatives of tin(IV) porphyrins: synthesis, spectroscopy and redox activity." Journal of Porphyrins and Phthalocyanines 06, no. 01 (January 2002): 3–11. http://dx.doi.org/10.1142/s1088424602000026.
Повний текст джерелаZakavi, Saeed, Aida Ghanbelanie Mojarrad, and 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 (November 2012): 153–58. http://dx.doi.org/10.1016/j.molcata.2012.06.003.
Повний текст джерелаCalcavento, C., G. Conte, S. Salvatori, R. Paolesse, M. Berliocchi, A. Di Carlo, P. Lugli, and A. Sassella. "Charge injection and transport in tetra-phenyl-porphyrin." Synthetic Metals 138, no. 1-2 (June 2003): 255–60. http://dx.doi.org/10.1016/s0379-6779(02)01307-3.
Повний текст джерела