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Artykuły w czasopismach na temat "Extended porphyrin"
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 źródłaRozprawy doktorskie na temat "Extended porphyrin"
Mori, Hirotaka. "Studies on Novel π-Extended Porphyrins". 京都大学 (Kyoto University), 2016. http://hdl.handle.net/2433/215337.
Pełny tekst źródłaHu, Yi. "Synthesis and Characterization of β-Functionalized π-Extended Porphyrins". Thesis, University of North Texas, 2019. https://digital.library.unt.edu/ark:/67531/metadc1609167/.
Pełny tekst źródłaAltundas, 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.
Pełny tekst źródłaJiang, Lin. "Functionalized pi-Extended Porphyrins". Miami University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=miami1373974099.
Pełny tekst źródłaFukui, Norihito. "Development of Novel π-Extended Porphyrins". Kyoto University, 2018. http://hdl.handle.net/2433/232280.
Pełny tekst źródłaKumar, Siddhartha. "Synthesis and Characterization of π-Extended Benzoporphyrins". Thesis, University of North Texas, 2019. https://digital.library.unt.edu/ark:/67531/metadc1505216/.
Pełny tekst źródłaIordache, Adriana. "Activation par transfert d'électron : applications aux systèmes commutables et à l'ingénierie moléculaire". Phd thesis, Grenoble, 2010. http://www.theses.fr/2010GRENV056.
Pełny tekst źródłaOne of the most important key to the development of nanosciences lies in our ability to monitor, modify or control nanometric materials. The addition or removal of electrons to or from given molecular objects can find useful applications in numerous arena of nanosciences: as signal transcription of interactions processes, as impulse to trigger conformational, configurational or directional mechanical changes at the molecular level or even as a way to control and activate the reactivity of molecular building blocks in organic synthesis. This work deals with two complementary processes associated to electron transfer: molecular movements in switchable architectures and activation of molecular building blocks to form conjugated macrocyclic structures The first part of this research work is devoted to the synthesis of porphyrin-based molecular tweezers and of ferrocene-based molecular pivots. The dynamic properties of these switchable molecular objects; relying on reversible π-dimerization processes, have been investigated by spectroscopic, electrochemical and spectroelectrochemical methods. In the second part of this manuscript we show few examples of electrochemically driven synthetic procedures for preparation of expanded porphyrins. Unlike chemical oxidants, which must often be tested empirically for a given transformation, under electrochemical conditions, one has the opportunity to tune the reactivity of the pyrrole-based reagent via the choice of anodic voltage. We especially established that the use of bipyrrole allows for the clean and high-yield production of cyclo[8]pyrrole; the requisite electrochemically-induced cyclization of four bipyrrole building blocks likely involving an electrolyte-based templating effect. The success of this approach leads us to propose that analogous electrochemical oxidation processes could be used to generate a range of new expanded porphyrin products
Roznyatovskiy, Vladimir. "From old porphyrins to novel materials". Thesis, 2011. http://hdl.handle.net/2152/ETD-UT-2011-08-4050.
Pełny tekst źródłatext
Lin, Rong-Shin, i 林榮新. "The synthesis of the fully conjugated of extended bimetal-porphyrin and application". Thesis, 2007. http://ndltd.ncl.edu.tw/handle/57214063528479044596.
Pełny tekst źródła臺灣大學
化學研究所
95
To synthesize a conjugation system of porphyrins and to study their properties with metal ions are the major work of this thesis. With the assists of microwave technology, the target molecule was easily achieved. In the presence of the diketone porphyrin with 5,6-diamino-1,l0-phenanthroline in a co-solvent system (CH2Cl2:Et2O: MeOH:H2O) proceeded smoothly to yield the p-diketoone prophyrin (A9). Complexation of A9 with various metal ions were investigated. In a typical example, reaction of CoCl2 with A9 in the DMF, produced a metal-prophyrin species C1. This cobalt prophyrin complex can be used as a catalyst in oxidation olefin, benzaldehydes and sulfides under mild conditions.
Kung, Hsiang-Ho, i 孔祥禾. "Synthesis of Various π-Extended Push-Pull Porphyrin Dimers for Dye-Sensitized Solar Cells". Thesis, 2013. http://ndltd.ncl.edu.tw/handle/34772354196540897275.
Pełny tekst źródła國立中興大學
化學系所
101
Energy is the prime need of human being but their sources is limited in nature. So, the development of alternative clean and renewable energy sources is a priority in the research field to solve the problem of energy shortages and green house effect. Among numbers of alternative energy, infinite and inexhaustible solar energy is a good candidate to meet a rapidly increasing global demand for energy. Recently, the development of solar cells especially to the third generation solar cells is dye-sensitized solar cells (DSSC). DSCC are currently attracting considerable attention because of their high light-to-electricity conversion efficiencies, ease of fabrication, and low production costs. However, we focused on application of DSCC especially for dye design that is based on porphyrin structure. In addition of porphyrin monomers as dyes, we have synthesized a series of porphyrin dimers due to their wider Soret band and Q band caused by exciton coupling. Moreover, the increasing of extinction coefficient and bathochromic shift in absorption spectrum is also notable application for porphyrin dimers. We expect these advantages are useful in DSCC. Therefore, we designed and successfully synthesized various of π-extended push-pull porphyrin dimers by single bond or ethynyl group as linker to combine two porphyrin monomers. In addition, we are also committed to study device for dye-sensitized solar cells, hope that we can get achievements well in the future.
Części książek na temat "Extended porphyrin"
Vinogradov, Sergei A., i David F. Wilson. "Extended Porphyrins". W Advances in Experimental Medicine and Biology, 597–603. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-5865-1_74.
Pełny tekst źródłaCrow, John P. "Administration of Mn Porphyrin and Mn Texaphyrin at Symptom Onset Extends Survival of ALS Mice". W ACS Symposium Series, 295–318. Washington, DC: American Chemical Society, 2005. http://dx.doi.org/10.1021/bk-2005-0903.ch017.
Pełny tekst źródłaCheprakov, Andrei V. "58 The Synthesis of π-Extended Porphyrins". W Handbook of Porphyrin Science, 1–149. World Scientific Publishing Company, 2011. http://dx.doi.org/10.1142/9789814322386_0010.
Pełny tekst źródła"Metal Complexes Containing Redox-active Ligands". W Inorganic Electrochemistry Theory, Practice and Application, 335–401. Wyd. 2. The Royal Society of Chemistry, 2011. http://dx.doi.org/10.1039/bk9781849730716-00335.
Pełny tekst źródłaTaber, Douglass. "Construction of Alkenes, Alkynes and Allenes". W Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0020.
Pełny tekst źródłaLeys, Clyde, Adam Schwarz, Mark Cloos, Sugeng Widodo, J. Richard Kyle i Julius Sirait. "Chapter 29: Grasberg Copper-Gold-(Molybdenum) Deposit: Product of Two Overlapping Porphyry Systems". W Geology of the World’s Major Gold Deposits and Provinces, 599–620. Society of Economic Geologists, 2020. http://dx.doi.org/10.5382/sp.23.29.
Pełny tekst źródłaLaZella, Andrew. "The Real Concept of Being". W The Singular Voice of Being, 41–60. Fordham University Press, 2019. http://dx.doi.org/10.5422/fordham/9780823284573.003.0003.
Pełny tekst źródłaTurner, Stephen J., Graeme Reynolds i Steffen G. Hagemann. "Chapter 13: Boddington: An Enigmatic Giant Archean Gold-Copper (Molybdenum-Silver) Deposit in the Southwest Yilgarn Craton, Western Australia". W Geology of the World’s Major Gold Deposits and Provinces, 275–88. Society of Economic Geologists, 2020. http://dx.doi.org/10.5382/sp.23.13.
Pełny tekst źródłaDromundo, Omar, Sigfrido Robles, Thomas Bissig, Claudio Flores, Maria del Carmen Alfaro i Lorenzo Cardona. "Chapter 19: The Peñasquito Gold-(Silver-Lead-Zinc) Deposit, Zacatecas, Mexico". W Geology of the World’s Major Gold Deposits and Provinces, 399–414. Society of Economic Geologists, 2020. http://dx.doi.org/10.5382/sp.23.19.
Pełny tekst źródłaHayes, Timothy S., James G. Brown, Stephen J. Sutley i Joseph F. Whelan. "Geology and Rock-Water Geochemistry of Exotic Copper Deposits, Ferricretes, and Manganocretes Associated with Porphyry Copper Deposits in Arizona, New Mexico, and Sonora (Extended Abstract)". W Supergene Environments, Processes, and Products. Society of Economic Geologists, 2009. http://dx.doi.org/10.5382/sp.14.13.
Pełny tekst źródłaStreszczenia konferencji na temat "Extended porphyrin"
Avramenko, Aleksandr G., i Aaron S. Rury. "Dynamics of Cavity Multipolaritons formed from Quasi-degenerate Porphyrin Excitons". W Laser Science. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/ls.2022.lw6f.3.
Pełny tekst źródłaDrobizhev, M., A. Karotki, H. L. Anderson i A. Rebane. "Very efficient multi-photon absorption in porphyrins with extended /spl pi/-conjugation". W Quantum Electronics and Laser Science (QELS). Postconference Digest. IEEE, 2003. http://dx.doi.org/10.1109/qels.2003.237846.
Pełny tekst źródłaAlfano, Robert F., G. C. Tang, Asima Pradhan, D. J. Choy i E. Opher. "Fluorescence spectra from cancerous and normal human breast and lung tissues". W OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1987. http://dx.doi.org/10.1364/oam.1987.thq3.
Pełny tekst źródłaRaporty organizacyjne na temat "Extended porphyrin"
Wang, Hong, i Lei Kerr. Pi-Extended Porphyrins: Functionalization and applications in DSSC. SC0010800-Final. Office of Scientific and Technical Information (OSTI), sierpień 2018. http://dx.doi.org/10.2172/1417036.
Pełny tekst źródłaIsrael, Alvaro, i John Merrill. Production of Seed Stocks for Sustainable Tank Cultivation of the Red Edible Seaweed Porphyra. United States Department of Agriculture, 2006. http://dx.doi.org/10.32747/2006.7696527.bard.
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