Artículos de revistas sobre el tema "Extended porphyrin"
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Yan, Jia Ying, Ya Qing Feng, Fang Qun Zhou, Yi Wen Chang y Bao Zhang. "Studies on Sonogashira Coupling Reaction of Dibenzoporphyrin". Advanced Materials Research 581-582 (octubre de 2012): 317–21. http://dx.doi.org/10.4028/www.scientific.net/amr.581-582.317.
Texto completoCheprakov, Andrei V. y Mikhail A. Filatov. "The dihydroisoindole approach to linearly annelated π-extended porphyrins". Journal of Porphyrins and Phthalocyanines 13, n.º 03 (marzo de 2009): 291–303. http://dx.doi.org/10.1142/s1088424609000383.
Texto completoBrewer, Ashley, Matthew Lacey, John R. Owen, Iris Nandhakumar y Eugen Stulz. "Supramolecular hetero-porphyrin SWNT complexes". Journal of Porphyrins and Phthalocyanines 15, n.º 04 (abril de 2011): 257–63. http://dx.doi.org/10.1142/s1088424611003227.
Texto completoWang, Hong, Yi Hu, Michael Thomas, Ajyal Alsaleh y Francis D'Souza. "(Invited) Pi-Extended Porphyrins: Synthesis, Functionalization and Applications in Dye-Sensitized Solar Cells". ECS Meeting Abstracts MA2022-01, n.º 13 (7 de julio de 2022): 903. http://dx.doi.org/10.1149/ma2022-0113903mtgabs.
Texto completode Torres, Miriam, Sergey Semin, Ilya Razdolski, Jialiang Xu, Johannes A. A. W. Elemans, Theo Rasing, Alan E. Rowan y Roeland J. M. Nolte. "Extended π-conjugated ruthenium zinc–porphyrin complexes with enhanced nonlinear-optical properties". Chemical Communications 51, n.º 14 (2015): 2855–58. http://dx.doi.org/10.1039/c4cc09592h.
Texto completoChevrier, Michèle, Sébastien Richeter, Olivier Coulembier, Mathieu Surin, Ahmad Mehdi, Roberto Lazzaroni, Rachel C. Evans, Philippe Dubois y Sébastien Clément. "Expanding the light absorption of poly(3-hexylthiophene) by end-functionalization with π-extended porphyrins". Chemical Communications 52, n.º 1 (2016): 171–74. http://dx.doi.org/10.1039/c5cc06290j.
Texto completoThomas, Michael B., R. G. Waruna Jindasa, Yi Hu, Benjamin Schmitz, Hong Wang y Francis D’Souza. "Investigation of the push–pull effects on β-functionalized zinc porphyrin coordinated to C60 donor–acceptor conjugates". Canadian Journal of Chemistry 96, n.º 9 (septiembre de 2018): 881–89. http://dx.doi.org/10.1139/cjc-2017-0416.
Texto completoWarrener, Ronald N., Hongsui Sun y Martin R. Johnston. "Position-Addressable Nano-Scaffolds. II. The Introduction of One, Two, or Three Addressable Succinimide Linkage Points onto the Under-Surface of ‘Southern’ Cavity Bis-Porphyrins". Australian Journal of Chemistry 56, n.º 4 (2003): 269. http://dx.doi.org/10.1071/ch02219.
Texto completoHamer, Mariana, Rolando M. Caraballo, Peter J. Eaton y Craig Medforth. "Nanoparticles as template for porphyrin nanostructure growth". Journal of Porphyrins and Phthalocyanines 23, n.º 04n05 (abril de 2019): 526–33. http://dx.doi.org/10.1142/s1088424619500469.
Texto completoVannelli, Tommaso A. y Timothy B. Karpishin. "Neocuproine-Extended Porphyrin Coordination Complexes". Inorganic Chemistry 38, n.º 10 (mayo de 1999): 2246–47. http://dx.doi.org/10.1021/ic9812914.
Texto completoOu, Zhongping, Wenbo E, Jianguo Shao, Paul L. Burn, Craig S. Sheehan, Robin Walton, Karl M. Kadish y Maxwell J. Crossley. "Electrochemical and spectroelectrochemical properties of building blocks for molecular arrays: reactions of quinoxalino[2,3-b]porphyrins containing metal(II) ions". Journal of Porphyrins and Phthalocyanines 09, n.º 02 (febrero de 2005): 142–51. http://dx.doi.org/10.1142/s1088424605000216.
Texto completoPoddutoori, Premaladha, Prashanth Kumar Poddutoori y Bhaskar G. Maiya. "Nucleobase (A, T, G and C) appended tri-cationic water-soluble porphyrins: synthesis, characterization, binding and photocleavage studies with DNA". Journal of Porphyrins and Phthalocyanines 10, n.º 01 (enero de 2006): 1–12. http://dx.doi.org/10.1142/s1088424606000028.
Texto completoChae, Seung Hyun, Kicheon Yoo, Yo Sub Lee, Min Ju Cho, Jong Hak Kim, Min Jae Ko, Suk Joong Lee y Dong Hoon Choi. "Novel π-extended porphyrin derivatives for use in dye-sensitized solar cells". Journal of Porphyrins and Phthalocyanines 18, n.º 07 (julio de 2014): 569–78. http://dx.doi.org/10.1142/s1088424614500308.
Texto completoThomas, Michael B., Siddhartha Kumar, Timothy Esquivel, Hong Wang y Francis D’Souza. "Excited state electron transfer in A2 and A2B2 functionalized zinc porphyrins carrying rigid and flexible β-pyrrole π-extended substituents". Journal of Porphyrins and Phthalocyanines 24, n.º 05n07 (mayo de 2020): 904–19. http://dx.doi.org/10.1142/s1088424620500017.
Texto completoYaseen, Muhammad, Muhammad A. Rashid, Muhammad A. Iqbal, Zahid Farooq, Muhammad Idrees, Muhammad A. Qayyum, Azeem Intisar, Mian HR Mahmood, Ibrahim Khan y Muhammad Latif. "Synthesis, photoinduced amination and topological indices of novel porphyrin dyads". Journal of Porphyrins and Phthalocyanines 24, n.º 08 (agosto de 2020): 1054–65. http://dx.doi.org/10.1142/s1088424620500200.
Texto completoBaytaeva, D. A. y S. S. Bessmeltsev. "The metabolitic role of the iron porphyrin complex in the development of anemic syndrome in patients with minor form of β-thalassemia". Kazan medical journal 93, n.º 1 (15 de febrero de 2012): 7–11. http://dx.doi.org/10.17816/kmj2135.
Texto completoBarbe, Jean-Michel, Fabien Burdet, Enrique Espinosa, Claude P. Gros y Roger Guilard. "New insights into the synthesis of porphyrin-corrole and biscorrole systems". Journal of Porphyrins and Phthalocyanines 07, n.º 05 (mayo de 2003): 365–74. http://dx.doi.org/10.1142/s1088424603000471.
Texto completoOtieno, Sebastian, Anabel E. Lanterna, John Mack, Solomon Derese, Edith K. Amuhaya, Tebello Nyokong y Juan C. Scaiano. "Solar Driven Photocatalytic Activity of Porphyrin Sensitized TiO2: Experimental and Computational Studies". Molecules 26, n.º 11 (24 de mayo de 2021): 3131. http://dx.doi.org/10.3390/molecules26113131.
Texto completoElliott, Rory, Aoife A. Ryan, Aviral Aggarwal, Nianyong Zhu, Friedrich W. Steuber, Mathias O. Senge y Wolfgang Schmitt. "2D Porphyrinic Metal-Organic Frameworks Featuring Rod-Shaped Secondary Building Units". Molecules 26, n.º 10 (16 de mayo de 2021): 2955. http://dx.doi.org/10.3390/molecules26102955.
Texto completoMongwaketsi, Nametso, Noluthando Mayedwa, Nolubabalo Matinise, Kasinathan Kaviyarasu, Raymond Sparrow y Malik Maaza. "Polymer matrices for porphyrin nanorods incorporation. Artificial light harvesting applications". Journal of Porphyrins and Phthalocyanines 22, n.º 04 (abril de 2018): 303–17. http://dx.doi.org/10.1142/s1088424618500268.
Texto completoCrossley, Maxwell J., Craig S. Sheehan, Tony Khoury, Jeffery R. Reimers y Paul J. Sintic. "Construction of building blocks for extended porphyrin arrays by nitration of porphyrin-2,3-diones and quinoxalino[2,3-b]porphyrins". New J. Chem. 32, n.º 2 (2008): 340–52. http://dx.doi.org/10.1039/b712643c.
Texto completoMatlachowski, Corinna y Matthias Schwalbe. "Photochemical CO2-reduction catalyzed by mono- and dinuclear phenanthroline-extended tetramesityl porphyrin complexes". Dalton Transactions 44, n.º 14 (2015): 6480–89. http://dx.doi.org/10.1039/c4dt03846k.
Texto completoShiu, Jia-Wei, Yen-Cheng Chang, Chien-Yi Chan, Hui-Ping Wu, Hung-Yu Hsu, Chin-Li Wang, Ching-Yao Lin y Eric Wei-Guang Diau. "Panchromatic co-sensitization of porphyrin-sensitized solar cells to harvest near-infrared light beyond 900 nm". Journal of Materials Chemistry A 3, n.º 4 (2015): 1417–20. http://dx.doi.org/10.1039/c4ta06589a.
Texto completoNalaoh, Phattananawee, Sareeya Bureekaew, Vinich Promarak y Jonathan S. Lindsey. "Fourfold alkyl wrapping of a copper(II) porphyrin thwarts macrocycle π–π stacking in a compact supramolecular package". Acta Crystallographica Section C Structural Chemistry 76, n.º 7 (5 de junio de 2020): 647–54. http://dx.doi.org/10.1107/s2053229620007172.
Texto completoSatake, Akiharu, Toshimasa Sugimura y Yoshiaki Kobuke. "Coordination-induced sliding motion of a complementary porphyrin-phthalocyanine dimer: fluorescence-based molecular switch". Journal of Porphyrins and Phthalocyanines 13, n.º 03 (marzo de 2009): 326–35. http://dx.doi.org/10.1142/s1088424609000450.
Texto completoHooper, Riley W., Angel Zhang, Dominik Koszelewski, Jan P. Lewtak, Beata Koszarna, Christopher J. Levy, Daniel T. Gryko y Martin J. Stillman. "Differential quenching of the angular momentum of the B and Q bands of a porphyrin as a result of extended ring π-conjugation". Journal of Porphyrins and Phthalocyanines 22, n.º 12 (diciembre de 2018): 1111–28. http://dx.doi.org/10.1142/s1088424618501110.
Texto completoGonzalez, Monica C. y Alan C. Weedon. "Preparation and properties of a linked porphyrin–cyclodextrin". Canadian Journal of Chemistry 63, n.º 3 (1 de marzo de 1985): 602–8. http://dx.doi.org/10.1139/v85-099.
Texto completoPijeat, Joffrey, Milos Baljozovic, Raphael Lamare, Karl-Heinz Ernst y Stephane Campidelli. "On-Surface Synthesis of Fused Anthracenyl Porphyrin Derivatives". ECS Meeting Abstracts MA2022-01, n.º 14 (7 de julio de 2022): 968. http://dx.doi.org/10.1149/ma2022-0114968mtgabs.
Texto completoChumakov, Denis, Anna Moiseeva, Alexander Anisimov, Boris Uzhinov y Andrey Khoroshutin. "Regioselective bromination of palladium tetraphenyltetrabenzoporphyrin to benzo-rings: Synthesis of mono- and octabromotetrabenzoporphyrins and their properties". Journal of Porphyrins and Phthalocyanines 14, n.º 09 (septiembre de 2010): 815–24. http://dx.doi.org/10.1142/s1088424610002653.
Texto completoThomas, James O., Jakub K. Sowa, Bart Limburg, Xinya Bian, Charalambos Evangeli, Jacob L. Swett, Sumit Tewari et al. "Charge transport through extended molecular wires with strongly correlated electrons". Chemical Science 12, n.º 33 (2021): 11121–29. http://dx.doi.org/10.1039/d1sc03050g.
Texto completoTakagi, Shigeru, Yoshio Kato, Hiroyuki Furuta, Satoru Onaka y T. Ken Miyamoto. "Metal-metal bonds extended over a porphyrin ring". Journal of Organometallic Chemistry 429, n.º 3 (mayo de 1992): 287–99. http://dx.doi.org/10.1016/0022-328x(92)83180-p.
Texto completoRubio-Magnieto, Jenifer, Florent Di Meo, Mamadou Lo, Cécile Delcourt, Sébastien Clément, Patrick Norman, Sébastien Richeter, Mathieu Linares y Mathieu Surin. "Binding modes of a core-extended metalloporphyrin to human telomeric DNA G-quadruplexes". Organic & Biomolecular Chemistry 13, n.º 8 (2015): 2453–63. http://dx.doi.org/10.1039/c4ob02097a.
Texto completoEpuran, Camelia, Ion Fratilescu, Ana-Maria Macsim, Anca Lascu, Catalin Ianasi, Mihaela Birdeanu y Eugenia Fagadar-Cosma. "Excellent Cooperation between Carboxyl-Substituted Porphyrins, k-Carrageenan and AuNPs for Extended Application in CO2 Capture and Manganese Ion Detection". Chemosensors 10, n.º 4 (1 de abril de 2022): 133. http://dx.doi.org/10.3390/chemosensors10040133.
Texto completoFilatov, Mikhail A., Ernesta Heinrich, Katharina Landfester y Stanislav Baluschev. "meso-Tetraphenylporphyrin with a pi-system extended by fusion with anthraquinone". Organic & Biomolecular Chemistry 13, n.º 25 (2015): 6977–83. http://dx.doi.org/10.1039/c5ob00884k.
Texto completoZurita, Adrián, Anna Duran, Josep M. Ribó, Zoubir El-Hachemi y Joaquim Crusats. "Hyperporphyrin effects extended into a J-aggregate supramolecular structure in water". RSC Advances 7, n.º 6 (2017): 3353–57. http://dx.doi.org/10.1039/c6ra27441b.
Texto completoSatrialdi, Reina Munechika, Vasudevanpillai Biju, Yuta Takano, Hideyoshi Harashima y Yuma Yamada. "The optimization of cancer photodynamic therapy by utilization of a pi-extended porphyrin-type photosensitizer in combination with MITO-Porter". Chemical Communications 56, n.º 7 (2020): 1145–48. http://dx.doi.org/10.1039/c9cc08563g.
Texto completoLee, Chang Yeon, Chunxing She, Nak Cheon Jeong y Joseph T. Hupp. "Porphyrin sensitized solar cells: TiO2 sensitization with a π-extended porphyrin possessing two anchoring groups". Chemical Communications 46, n.º 33 (2010): 6090. http://dx.doi.org/10.1039/c0cc00257g.
Texto completoSarabando, Sofia N., Cristina J. Dias, Cátia Vieira, Maria Bartolomeu, Maria G. P. M. S. Neves, Adelaide Almeida, Carlos J. P. Monteiro y Maria Amparo F. Faustino. "Sulfonamide Porphyrins as Potent Photosensitizers against Multidrug-Resistant Staphylococcus aureus (MRSA): The Role of Co-Adjuvants". Molecules 28, n.º 5 (22 de febrero de 2023): 2067. http://dx.doi.org/10.3390/molecules28052067.
Texto completoVentura, Barbara, Fabien Durola, Julien Frey, Valérie Heitz, Jean-Pierre Sauvage y Lucia Flamigni. "Near-infrared dual luminescence from an extended zinc porphyrin". Chem. Commun. 48, n.º 7 (2012): 1021–23. http://dx.doi.org/10.1039/c1cc16739a.
Texto completoFinikova, Olga S., Andrei V. Cheprakov, Patrick J. Carroll, Sergio Dalosto y Sergei A. Vinogradov. "Influence of Nonplanarity and Extended Conjugation on Porphyrin Basicity". Inorganic Chemistry 41, n.º 26 (diciembre de 2002): 6944–46. http://dx.doi.org/10.1021/ic0260522.
Texto completoPasternack, Robert F., Cavan Fleming, Stephanie Herring, Peter J. Collings, Julio dePaula, Gerard DeCastro y Esther J. Gibbs. "Aggregation Kinetics of Extended Porphyrin and Cyanine Dye Assemblies". Biophysical Journal 79, n.º 1 (julio de 2000): 550–60. http://dx.doi.org/10.1016/s0006-3495(00)76316-8.
Texto completoBossa, Mario, Elena Cervone, Carmine Garzillo y Giuseppe Del Re. "On the electronic states of the extended porphyrin family". Journal of Molecular Structure: THEOCHEM 342 (octubre de 1995): 73–86. http://dx.doi.org/10.1016/0166-1280(95)90087-x.
Texto completoFeixas, Ferran, Miquel Solà y Marcel Swart. "Chemical bonding and aromaticity in metalloporphyrins",. Canadian Journal of Chemistry 87, n.º 7 (julio de 2009): 1063–73. http://dx.doi.org/10.1139/v09-037.
Texto completoKrishna, Jonnadula Venkata Suman, Devulapally Koteshwar, Towhid H. Chowdhury, Surya Prakash Singh, Idriss Bedja, Ashraful Islam y Lingamallu Giribabu. "Efficient near IR porphyrins containing a triphenylamine-substituted anthryl donating group for dye sensitized solar cells". Journal of Materials Chemistry C 7, n.º 43 (2019): 13594–605. http://dx.doi.org/10.1039/c9tc03943k.
Texto completoAlam, Md M., F. Bolze, C. Daniel, L. Flamigni, C. Gourlaouen, V. Heitz, S. Jenni, J. Schmitt, A. Sour y B. Ventura. "π-Extended diketopyrrolopyrrole–porphyrin arrays: one- and two-photon photophysical investigations and theoretical studies". Physical Chemistry Chemical Physics 18, n.º 31 (2016): 21954–65. http://dx.doi.org/10.1039/c6cp01844k.
Texto completoTakano, Yuta, Kazuaki Miyake, Jeladhara Sobhanan, Vasudevanpillai Biju, Nikolai V. Tkachenko y Hiroshi Imahori. "Near-infrared light control of membrane potential by an electron donor–acceptor linked molecule". Chemical Communications 56, n.º 83 (2020): 12562–65. http://dx.doi.org/10.1039/d0cc05326k.
Texto completoKoner, Rajesh y Israel Goldberg. "Square-grid coordination networks of (5,10,15,20-tetra-4-pyridylporphyrinato)zinc(II) in its clathrate with two guest molecules of 1,2-dichlorobenzene: supramolecular isomerism of the porphyrin self-assembly". Acta Crystallographica Section C Crystal Structure Communications 65, n.º 3 (25 de febrero de 2009): m139—m142. http://dx.doi.org/10.1107/s0108270109005691.
Texto completoDiskin-Posner, Yael y Israel Goldberg. "Porphyrin sieves. Designing open networks of tetra(carboxyphenyl)porphyrins by extended coordination through sodium ion auxiliaries". New Journal of Chemistry 25, n.º 7 (2001): 899–904. http://dx.doi.org/10.1039/b100580b.
Texto completoBabu, Balaji, John Mack y Tebello Nyokong. "A heavy-atom-free π-extended N-confused porphyrin as a photosensitizer for photodynamic therapy". New Journal of Chemistry 45, n.º 12 (2021): 5654–58. http://dx.doi.org/10.1039/d1nj00112d.
Texto completoCrossley, Maxwell J., Linda J. Govenlock y Jognandan K. Prashar. "Synthesis of porphyrin-2,3,12,13- and -2,3,7,8-tetraones: building blocks for the synthesis of extended porphyrin arrays". Journal of the Chemical Society, Chemical Communications, n.º 23 (1995): 2379. http://dx.doi.org/10.1039/c39950002379.
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