Artykuły w czasopismach na temat „Extended porphyrin”
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Yan, Jia Ying, Ya Qing Feng, Fang Qun Zhou, Yi Wen Chang i Bao Zhang. "Studies on Sonogashira Coupling Reaction of Dibenzoporphyrin". Advanced Materials Research 581-582 (październik 2012): 317–21. http://dx.doi.org/10.4028/www.scientific.net/amr.581-582.317.
Pełny tekst źródłaCheprakov, Andrei V., i Mikhail A. Filatov. "The dihydroisoindole approach to linearly annelated π-extended porphyrins". Journal of Porphyrins and Phthalocyanines 13, nr 03 (marzec 2009): 291–303. http://dx.doi.org/10.1142/s1088424609000383.
Pełny tekst źródłaBrewer, Ashley, Matthew Lacey, John R. Owen, Iris Nandhakumar i Eugen Stulz. "Supramolecular hetero-porphyrin SWNT complexes". Journal of Porphyrins and Phthalocyanines 15, nr 04 (kwiecień 2011): 257–63. http://dx.doi.org/10.1142/s1088424611003227.
Pełny tekst źródłaWang, Hong, Yi Hu, Michael Thomas, Ajyal Alsaleh i Francis D'Souza. "(Invited) Pi-Extended Porphyrins: Synthesis, Functionalization and Applications in Dye-Sensitized Solar Cells". ECS Meeting Abstracts MA2022-01, nr 13 (7.07.2022): 903. http://dx.doi.org/10.1149/ma2022-0113903mtgabs.
Pełny tekst źródłade Torres, Miriam, Sergey Semin, Ilya Razdolski, Jialiang Xu, Johannes A. A. W. Elemans, Theo Rasing, Alan E. Rowan i Roeland J. M. Nolte. "Extended π-conjugated ruthenium zinc–porphyrin complexes with enhanced nonlinear-optical properties". Chemical Communications 51, nr 14 (2015): 2855–58. http://dx.doi.org/10.1039/c4cc09592h.
Pełny tekst źródłaChevrier, Michèle, Sébastien Richeter, Olivier Coulembier, Mathieu Surin, Ahmad Mehdi, Roberto Lazzaroni, Rachel C. Evans, Philippe Dubois i Sébastien Clément. "Expanding the light absorption of poly(3-hexylthiophene) by end-functionalization with π-extended porphyrins". Chemical Communications 52, nr 1 (2016): 171–74. http://dx.doi.org/10.1039/c5cc06290j.
Pełny tekst źródłaThomas, Michael B., R. G. Waruna Jindasa, Yi Hu, Benjamin Schmitz, Hong Wang i 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, nr 9 (wrzesień 2018): 881–89. http://dx.doi.org/10.1139/cjc-2017-0416.
Pełny tekst źródłaWarrener, Ronald N., Hongsui Sun i 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, nr 4 (2003): 269. http://dx.doi.org/10.1071/ch02219.
Pełny tekst źródłaHamer, Mariana, Rolando M. Caraballo, Peter J. Eaton i Craig Medforth. "Nanoparticles as template for porphyrin nanostructure growth". Journal of Porphyrins and Phthalocyanines 23, nr 04n05 (kwiecień 2019): 526–33. http://dx.doi.org/10.1142/s1088424619500469.
Pełny tekst źródłaVannelli, Tommaso A., i Timothy B. Karpishin. "Neocuproine-Extended Porphyrin Coordination Complexes". Inorganic Chemistry 38, nr 10 (maj 1999): 2246–47. http://dx.doi.org/10.1021/ic9812914.
Pełny tekst źródłaOu, Zhongping, Wenbo E, Jianguo Shao, Paul L. Burn, Craig S. Sheehan, Robin Walton, Karl M. Kadish i 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, nr 02 (luty 2005): 142–51. http://dx.doi.org/10.1142/s1088424605000216.
Pełny tekst źródłaPoddutoori, Premaladha, Prashanth Kumar Poddutoori i 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, nr 01 (styczeń 2006): 1–12. http://dx.doi.org/10.1142/s1088424606000028.
Pełny tekst źródłaChae, Seung Hyun, Kicheon Yoo, Yo Sub Lee, Min Ju Cho, Jong Hak Kim, Min Jae Ko, Suk Joong Lee i Dong Hoon Choi. "Novel π-extended porphyrin derivatives for use in dye-sensitized solar cells". Journal of Porphyrins and Phthalocyanines 18, nr 07 (lipiec 2014): 569–78. http://dx.doi.org/10.1142/s1088424614500308.
Pełny tekst źródłaThomas, Michael B., Siddhartha Kumar, Timothy Esquivel, Hong Wang i 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, nr 05n07 (maj 2020): 904–19. http://dx.doi.org/10.1142/s1088424620500017.
Pełny tekst źródłaYaseen, Muhammad, Muhammad A. Rashid, Muhammad A. Iqbal, Zahid Farooq, Muhammad Idrees, Muhammad A. Qayyum, Azeem Intisar, Mian HR Mahmood, Ibrahim Khan i Muhammad Latif. "Synthesis, photoinduced amination and topological indices of novel porphyrin dyads". Journal of Porphyrins and Phthalocyanines 24, nr 08 (sierpień 2020): 1054–65. http://dx.doi.org/10.1142/s1088424620500200.
Pełny tekst źródłaBaytaeva, D. A., i 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, nr 1 (15.02.2012): 7–11. http://dx.doi.org/10.17816/kmj2135.
Pełny tekst źródłaBarbe, Jean-Michel, Fabien Burdet, Enrique Espinosa, Claude P. Gros i Roger Guilard. "New insights into the synthesis of porphyrin-corrole and biscorrole systems". Journal of Porphyrins and Phthalocyanines 07, nr 05 (maj 2003): 365–74. http://dx.doi.org/10.1142/s1088424603000471.
Pełny tekst źródłaOtieno, Sebastian, Anabel E. Lanterna, John Mack, Solomon Derese, Edith K. Amuhaya, Tebello Nyokong i Juan C. Scaiano. "Solar Driven Photocatalytic Activity of Porphyrin Sensitized TiO2: Experimental and Computational Studies". Molecules 26, nr 11 (24.05.2021): 3131. http://dx.doi.org/10.3390/molecules26113131.
Pełny tekst źródłaElliott, Rory, Aoife A. Ryan, Aviral Aggarwal, Nianyong Zhu, Friedrich W. Steuber, Mathias O. Senge i Wolfgang Schmitt. "2D Porphyrinic Metal-Organic Frameworks Featuring Rod-Shaped Secondary Building Units". Molecules 26, nr 10 (16.05.2021): 2955. http://dx.doi.org/10.3390/molecules26102955.
Pełny tekst źródłaMongwaketsi, Nametso, Noluthando Mayedwa, Nolubabalo Matinise, Kasinathan Kaviyarasu, Raymond Sparrow i Malik Maaza. "Polymer matrices for porphyrin nanorods incorporation. Artificial light harvesting applications". Journal of Porphyrins and Phthalocyanines 22, nr 04 (kwiecień 2018): 303–17. http://dx.doi.org/10.1142/s1088424618500268.
Pełny tekst źródłaCrossley, Maxwell J., Craig S. Sheehan, Tony Khoury, Jeffery R. Reimers i 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, nr 2 (2008): 340–52. http://dx.doi.org/10.1039/b712643c.
Pełny tekst źródłaMatlachowski, Corinna, i Matthias Schwalbe. "Photochemical CO2-reduction catalyzed by mono- and dinuclear phenanthroline-extended tetramesityl porphyrin complexes". Dalton Transactions 44, nr 14 (2015): 6480–89. http://dx.doi.org/10.1039/c4dt03846k.
Pełny tekst źródłaShiu, Jia-Wei, Yen-Cheng Chang, Chien-Yi Chan, Hui-Ping Wu, Hung-Yu Hsu, Chin-Li Wang, Ching-Yao Lin i 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, nr 4 (2015): 1417–20. http://dx.doi.org/10.1039/c4ta06589a.
Pełny tekst źródłaNalaoh, Phattananawee, Sareeya Bureekaew, Vinich Promarak i 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, nr 7 (5.06.2020): 647–54. http://dx.doi.org/10.1107/s2053229620007172.
Pełny tekst źródłaSatake, Akiharu, Toshimasa Sugimura i Yoshiaki Kobuke. "Coordination-induced sliding motion of a complementary porphyrin-phthalocyanine dimer: fluorescence-based molecular switch". Journal of Porphyrins and Phthalocyanines 13, nr 03 (marzec 2009): 326–35. http://dx.doi.org/10.1142/s1088424609000450.
Pełny tekst źródłaHooper, Riley W., Angel Zhang, Dominik Koszelewski, Jan P. Lewtak, Beata Koszarna, Christopher J. Levy, Daniel T. Gryko i 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, nr 12 (grudzień 2018): 1111–28. http://dx.doi.org/10.1142/s1088424618501110.
Pełny tekst źródłaGonzalez, Monica C., i Alan C. Weedon. "Preparation and properties of a linked porphyrin–cyclodextrin". Canadian Journal of Chemistry 63, nr 3 (1.03.1985): 602–8. http://dx.doi.org/10.1139/v85-099.
Pełny tekst źródłaPijeat, Joffrey, Milos Baljozovic, Raphael Lamare, Karl-Heinz Ernst i Stephane Campidelli. "On-Surface Synthesis of Fused Anthracenyl Porphyrin Derivatives". ECS Meeting Abstracts MA2022-01, nr 14 (7.07.2022): 968. http://dx.doi.org/10.1149/ma2022-0114968mtgabs.
Pełny tekst źródłaChumakov, Denis, Anna Moiseeva, Alexander Anisimov, Boris Uzhinov i Andrey Khoroshutin. "Regioselective bromination of palladium tetraphenyltetrabenzoporphyrin to benzo-rings: Synthesis of mono- and octabromotetrabenzoporphyrins and their properties". Journal of Porphyrins and Phthalocyanines 14, nr 09 (wrzesień 2010): 815–24. http://dx.doi.org/10.1142/s1088424610002653.
Pełny tekst źródłaThomas, James O., Jakub K. Sowa, Bart Limburg, Xinya Bian, Charalambos Evangeli, Jacob L. Swett, Sumit Tewari i in. "Charge transport through extended molecular wires with strongly correlated electrons". Chemical Science 12, nr 33 (2021): 11121–29. http://dx.doi.org/10.1039/d1sc03050g.
Pełny tekst źródłaTakagi, Shigeru, Yoshio Kato, Hiroyuki Furuta, Satoru Onaka i T. Ken Miyamoto. "Metal-metal bonds extended over a porphyrin ring". Journal of Organometallic Chemistry 429, nr 3 (maj 1992): 287–99. http://dx.doi.org/10.1016/0022-328x(92)83180-p.
Pełny tekst źródłaRubio-Magnieto, Jenifer, Florent Di Meo, Mamadou Lo, Cécile Delcourt, Sébastien Clément, Patrick Norman, Sébastien Richeter, Mathieu Linares i Mathieu Surin. "Binding modes of a core-extended metalloporphyrin to human telomeric DNA G-quadruplexes". Organic & Biomolecular Chemistry 13, nr 8 (2015): 2453–63. http://dx.doi.org/10.1039/c4ob02097a.
Pełny tekst źródłaEpuran, Camelia, Ion Fratilescu, Ana-Maria Macsim, Anca Lascu, Catalin Ianasi, Mihaela Birdeanu i 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, nr 4 (1.04.2022): 133. http://dx.doi.org/10.3390/chemosensors10040133.
Pełny tekst źródłaFilatov, Mikhail A., Ernesta Heinrich, Katharina Landfester i Stanislav Baluschev. "meso-Tetraphenylporphyrin with a pi-system extended by fusion with anthraquinone". Organic & Biomolecular Chemistry 13, nr 25 (2015): 6977–83. http://dx.doi.org/10.1039/c5ob00884k.
Pełny tekst źródłaZurita, Adrián, Anna Duran, Josep M. Ribó, Zoubir El-Hachemi i Joaquim Crusats. "Hyperporphyrin effects extended into a J-aggregate supramolecular structure in water". RSC Advances 7, nr 6 (2017): 3353–57. http://dx.doi.org/10.1039/c6ra27441b.
Pełny tekst źródłaSatrialdi, Reina Munechika, Vasudevanpillai Biju, Yuta Takano, Hideyoshi Harashima i 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, nr 7 (2020): 1145–48. http://dx.doi.org/10.1039/c9cc08563g.
Pełny tekst źródłaLee, Chang Yeon, Chunxing She, Nak Cheon Jeong i Joseph T. Hupp. "Porphyrin sensitized solar cells: TiO2 sensitization with a π-extended porphyrin possessing two anchoring groups". Chemical Communications 46, nr 33 (2010): 6090. http://dx.doi.org/10.1039/c0cc00257g.
Pełny tekst źródłaSarabando, Sofia N., Cristina J. Dias, Cátia Vieira, Maria Bartolomeu, Maria G. P. M. S. Neves, Adelaide Almeida, Carlos J. P. Monteiro i Maria Amparo F. Faustino. "Sulfonamide Porphyrins as Potent Photosensitizers against Multidrug-Resistant Staphylococcus aureus (MRSA): The Role of Co-Adjuvants". Molecules 28, nr 5 (22.02.2023): 2067. http://dx.doi.org/10.3390/molecules28052067.
Pełny tekst źródłaVentura, Barbara, Fabien Durola, Julien Frey, Valérie Heitz, Jean-Pierre Sauvage i Lucia Flamigni. "Near-infrared dual luminescence from an extended zinc porphyrin". Chem. Commun. 48, nr 7 (2012): 1021–23. http://dx.doi.org/10.1039/c1cc16739a.
Pełny tekst źródłaFinikova, Olga S., Andrei V. Cheprakov, Patrick J. Carroll, Sergio Dalosto i Sergei A. Vinogradov. "Influence of Nonplanarity and Extended Conjugation on Porphyrin Basicity". Inorganic Chemistry 41, nr 26 (grudzień 2002): 6944–46. http://dx.doi.org/10.1021/ic0260522.
Pełny tekst źródłaPasternack, Robert F., Cavan Fleming, Stephanie Herring, Peter J. Collings, Julio dePaula, Gerard DeCastro i Esther J. Gibbs. "Aggregation Kinetics of Extended Porphyrin and Cyanine Dye Assemblies". Biophysical Journal 79, nr 1 (lipiec 2000): 550–60. http://dx.doi.org/10.1016/s0006-3495(00)76316-8.
Pełny tekst źródłaBossa, Mario, Elena Cervone, Carmine Garzillo i Giuseppe Del Re. "On the electronic states of the extended porphyrin family". Journal of Molecular Structure: THEOCHEM 342 (październik 1995): 73–86. http://dx.doi.org/10.1016/0166-1280(95)90087-x.
Pełny tekst źródłaFeixas, Ferran, Miquel Solà i Marcel Swart. "Chemical bonding and aromaticity in metalloporphyrins",. Canadian Journal of Chemistry 87, nr 7 (lipiec 2009): 1063–73. http://dx.doi.org/10.1139/v09-037.
Pełny tekst źródłaKrishna, Jonnadula Venkata Suman, Devulapally Koteshwar, Towhid H. Chowdhury, Surya Prakash Singh, Idriss Bedja, Ashraful Islam i Lingamallu Giribabu. "Efficient near IR porphyrins containing a triphenylamine-substituted anthryl donating group for dye sensitized solar cells". Journal of Materials Chemistry C 7, nr 43 (2019): 13594–605. http://dx.doi.org/10.1039/c9tc03943k.
Pełny tekst źródłaAlam, Md M., F. Bolze, C. Daniel, L. Flamigni, C. Gourlaouen, V. Heitz, S. Jenni, J. Schmitt, A. Sour i B. Ventura. "π-Extended diketopyrrolopyrrole–porphyrin arrays: one- and two-photon photophysical investigations and theoretical studies". Physical Chemistry Chemical Physics 18, nr 31 (2016): 21954–65. http://dx.doi.org/10.1039/c6cp01844k.
Pełny tekst źródłaTakano, Yuta, Kazuaki Miyake, Jeladhara Sobhanan, Vasudevanpillai Biju, Nikolai V. Tkachenko i Hiroshi Imahori. "Near-infrared light control of membrane potential by an electron donor–acceptor linked molecule". Chemical Communications 56, nr 83 (2020): 12562–65. http://dx.doi.org/10.1039/d0cc05326k.
Pełny tekst źródłaKoner, Rajesh, i 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, nr 3 (25.02.2009): m139—m142. http://dx.doi.org/10.1107/s0108270109005691.
Pełny tekst źródłaDiskin-Posner, Yael, i Israel Goldberg. "Porphyrin sieves. Designing open networks of tetra(carboxyphenyl)porphyrins by extended coordination through sodium ion auxiliaries". New Journal of Chemistry 25, nr 7 (2001): 899–904. http://dx.doi.org/10.1039/b100580b.
Pełny tekst źródłaBabu, Balaji, John Mack i Tebello Nyokong. "A heavy-atom-free π-extended N-confused porphyrin as a photosensitizer for photodynamic therapy". New Journal of Chemistry 45, nr 12 (2021): 5654–58. http://dx.doi.org/10.1039/d1nj00112d.
Pełny tekst źródłaCrossley, Maxwell J., Linda J. Govenlock i 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, nr 23 (1995): 2379. http://dx.doi.org/10.1039/c39950002379.
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