Literatura académica sobre el tema "Porphyrin"
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Artículos de revistas sobre el tema "Porphyrin"
Stölzel, Ulrich, Thomas Stauch y Ilja Kubisch. "Porphyrien". Der Internist 62, n.º 9 (29 de junio de 2021): 937–51. http://dx.doi.org/10.1007/s00108-021-01066-1.
Texto completoHindmarsh, J. Thomas, Linda Oliveras y Donald C. Greenway. "Plasma Porphyrins in the Porphyrias". Clinical Chemistry 45, n.º 7 (1 de julio de 1999): 1070–76. http://dx.doi.org/10.1093/clinchem/45.7.1070.
Texto completoWoolf, Jacqueline, Joanne T. Marsden, Timothy Degg, Sharon Whatley, Paul Reed, Nadia Brazil, M. Felicity Stewart y Michael Badminton. "Best practice guidelines on first-line laboratory testing for porphyria". Annals of Clinical Biochemistry: International Journal of Laboratory Medicine 54, n.º 2 (19 de enero de 2017): 188–98. http://dx.doi.org/10.1177/0004563216667965.
Texto completoPuzikova, А. I., Е. А. Litvin, D. А. Kildyushkin y А. Е. Druy. "Application of high-performance liquid chromatography in porphyrias diagnostics". Pediatric Hematology/Oncology and Immunopathology 20, n.º 3 (8 de octubre de 2021): 140–44. http://dx.doi.org/10.24287/1726-1708-2021-20-3-140-144.
Texto completoKrivosheev, Alexander B., L. Ya Kupriyanova y M. A. Kondratova. "DOUBLE PORPHYRIA: LITERATURE REVIEW AND ANALYSIS OF CLINICAL OBSERVATION". Russian Journal of Skin and Venereal Diseases 21, n.º 2 (15 de abril de 2018): 120–24. http://dx.doi.org/10.18821/1560-9588-2018-21-2-120-124.
Texto completoCarson, R. W., E. J. Dunnigan, T. D. DuBose, D. E. Goeger y K. E. Anderson. "Removal of plasma porphyrins with high-flux hemodialysis in porphyria cutanea tarda associated with end-stage renal disease." Journal of the American Society of Nephrology 2, n.º 9 (marzo de 1992): 1445–50. http://dx.doi.org/10.1681/asn.v291445.
Texto completoEgemen, Gamze, Mustafa Hayvalı, Zeynel Kılıç, A. Osman Solak y Zafer Üstündağ. "Phosphorus-nitrogen compounds Part 17: The synthesis, spectral and electrochemical investigations of porphyrino-phosphazenes". Journal of Porphyrins and Phthalocyanines 14, n.º 03 (marzo de 2010): 227–34. http://dx.doi.org/10.1142/s1088424610001945.
Texto completoHindmarsh, J. T. "The porphyrias: recent advances." Clinical Chemistry 32, n.º 7 (1 de julio de 1986): 1255–63. http://dx.doi.org/10.1093/clinchem/32.7.1255.
Texto completoLockwood, W. H., V. Poulos, E. Rossi y D. H. Curnow. "Rapid procedure for fecal porphyrin assay." Clinical Chemistry 31, n.º 7 (1 de julio de 1985): 1163–67. http://dx.doi.org/10.1093/clinchem/31.7.1163.
Texto completoPerkins, S. L. y P. M. Johnson. "Loss of porphyrins from solution during analysis: effect of sample pH and matrix on porphyrin quantification in urine by "high-performance" liquid chromatography." Clinical Chemistry 35, n.º 7 (1 de julio de 1989): 1508–12. http://dx.doi.org/10.1093/clinchem/35.7.1508.
Texto completoTesis sobre el tema "Porphyrin"
Luo, Jin-Li. "Porphyrin metabolism in porphyria cutanea tarda". Thesis, Open University, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315308.
Texto completoGuo, Rong. "Porphyrin metabolism in congenital erythropoietic porphyria". Thesis, Open University, 1992. http://oro.open.ac.uk/57392/.
Texto completoLefley, Colin Richard. "Raman spectroscopic studies of porphyrins and porphyrin-protein complexes". Thesis, University of York, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.239782.
Texto completoWessendorf, Florian. "Supramolecular fullerene-porphyrin architectures = Supramolekulare Fulleren-Porphyrin-Architekturen". kostenfrei, 2010. http://d-nb.info/1000613593/34.
Texto completoBeavington, Richard. "Porphyrin arrays". Thesis, University of Oxford, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.388909.
Texto completoPromarak, Vinich. "Porphyrin arrays". Thesis, University of Oxford, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.249614.
Texto completoZhang, Wei. "Porphyrin arrays". Thesis, University of Oxford, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.494395.
Texto completoTannert, Sebastian. "Energy and electron transfer in porphyrin-phthalocyanin-porphyrin heterotrimers". Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2013. http://dx.doi.org/10.18452/16850.
Texto completoThis thesis contributes to the comprehension of energy and electron transfer within novel supra-molecular structures, denominated triads, consisting of a central phthalocyanine axially-coupled to two porphyrins. In the course of this thesis, two of the trimers, were quantitatively characterized regarding their intramolecular transfer processes. Both feature a dative bond between the porphyrins and the phthalocyanine via the central silicium atom of the latter. These investigations aimed at answering whether this class of compounds allows the desired combination of light harvesting and charge separation. The rate constants of both investigated trimers in two solvents with different polarity were determined by the combination of data from a variety of measurement methods. An efficient charge transfer from the porphyrins to the phthalocyanine and a hole transfer from the phthalocyanine to one of the porphyrins occurs in all investigated cases. This result confirms the prospect that light harvesting and charge separation can occur combined in one molecule. Depending on solvent polarity and the structure of the porphyrines, electron transfer parallel to the energy transfer and a charge back transfer takes place in addition to both above-mentioned processes. However, the charge-separated state of the investigated substances decays to fast, still preventing a practical utilization of these compounds in solar cells and necessitating further developments.
Sek, Sau Yin. "The synthesis of haematoporphyrin derivative III and other novel porphyrins /". Title page, table of contents and abstract only, 1990. http://web4.library.adelaide.edu.au/theses/09PH/09phs4622.pdf.
Texto completoIakushev, Aleksei A. "Amination catalysée par des sels de palladium ou de cuivre pour la synthèse de polymacrocycliques contenant des fragments aza éthers-couronnes, porphyrines et calix[4]arènes". Thesis, Montpellier, 2016. http://www.theses.fr/2016MONTT221/document.
Texto completoPolymacrocyclic compounds are of great interest due to their unique coordination properties. The first convenient synthetic approach to various polycyclic compounds containing several azacrown-ether moieties, to cryptands and supercryptands, based on azacrown-ethers, has been developed by Krakowiak and coworkers in the beginning of 1990s using simple nucleophilic substitution reactions. At present time heteropolytopic polymacrocyclic compounds, capable of forming polynuclear complexes with various metals, attract the utmost interest. In the majority of publications dealing with the synthesis of polymacrocyclic compounds non-catalytic approaches were applied, except for several porphyrin dyads and triads, which were obtained using Suzuki, Sonogashira and Heck reactions. The laboratory of organoelement compounds of Chemistry Department of Lomonosov Moscow State University has a great experience of the application of Pd-catalyzed amination reactions for the synthesis of polymacrocyclic compounds, nowadays Cu-catalyzed arylation of di- and polyamines is under investigation. Bearing it in mind we have found the research for Cu-catalyzed amination to be important in synthesis of polymacrocyclic compounds containing di- and polyamine linkers; as well as the synthesis of new types of polytopic polymacrocyclic conjugates, bearing azacrown-ether, porphyrin and calixarene moieties, by means of Pd- and Cu-catalyzed reactions; and studying their properties as metal cations detectors.The aim of the research is to develop catalytic synthetic approaches to polymacrocyclic conjugates, bearing azacrown-ether, porphyrin and calix[4]arene moieties, and to study their abilities as detectors for metal cations. For this purpose it is necessary to carry out the following investigations: 1) to study the regularities of Cu(I)-catalyzed amination of halogen derivatives of azacrown-ethers and porphyrins and to synthesize corresponding amino derivatives; 2) to develop the methods for the catalytic macrocyclization aimed at the synthesis of macrobicyclic and macrotricyclic compounds, containing diazacrown-ether, cyclen, cyclam and calix[4]arene moieties; 3) to introduce fluorophoric fragments (including porphyrins) into macrocyclic and macrobicyclic compounds; 4) to investigate metal cations binding by thus synthesized polymacrocycles using UV and fluorescent spectroscopy, and to find possible fluorescent and colorimetric detectors among them
Libros sobre el tema "Porphyrin"
R, Moore Michael y Wintrobe Maxwell Myer 1901-, eds. Disorders of porphyrin metabolism. New York: Plenum Medical Book Co., 1987.
Buscar texto completoDobhal, M. P. Porphyrins - Spectral Data of Porphyrin Isomers and Expanded Porphyrins. Editado por V. Gupta, M. D. Lechner y R. Gupta. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-47224-8.
Texto completoA, Sheldon Roger, ed. Metalloporphyrins in catalytic oxidations. New York: M. Dekker, 1994.
Buscar texto completoA, Sheldon Roger, ed. Metalloporphyrins in catalyticoxidations. New York: M. Dekker, 1994.
Buscar texto completo1945-, Kadish Karl M., Smith Kevin M y Guilard Roger, eds. The porphyrin handbook. San Diego, Calif: Academic Press, 2003.
Buscar texto completo1945-, Kadish Karl M., Smith Kevin M y Guilard Roger, eds. The porphyrin handbook. San Diego: Academic Press, 2000.
Buscar texto completoMa, Shengqian y Gaurav Verma, eds. Porphyrin-based Supramolecular Architectures. Cambridge: Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781839164934.
Texto completoKessel, David, ed. Methods in Porphyrin Photosensitization. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2165-1.
Texto completoMoore, Michael R., Kenneth E. L. McColl, Claude Rimington y Abraham Goldberg. Disorders of Porphyrin Metabolism. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-1277-2.
Texto completoDavid, Kessel, ed. Methods in porphyrin photosensitization. New York: Plenum Press, 1985.
Buscar texto completoCapítulos de libros sobre el tema "Porphyrin"
Cleaves, Henderson James. "Porphyrin". En Encyclopedia of Astrobiology, 1326. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_1258.
Texto completoCleaves, Henderson James. "Porphyrin". En Encyclopedia of Astrobiology, 2000. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_1258.
Texto completoCleaves, Henderson James. "Porphyrin". En Encyclopedia of Astrobiology, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-642-27833-4_1258-4.
Texto completoCleaves, Henderson James. "Porphyrin". En Encyclopedia of Astrobiology, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27833-4_1258-3.
Texto completoCleaves, Henderson James. "Porphyrin". En Encyclopedia of Astrobiology, 2445–46. Berlin, Heidelberg: Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65093-6_1258.
Texto completoDobhal, M. P. "Spectral data of porphyrin derivative C48H33N3S2". En Porphyrins - Spectral Data of Porphyrin Isomers and Expanded Porphyrins, 21–22. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-47224-8_10.
Texto completoDobhal, M. P. "Spectral data of porphyrin derivative C50H38N4O2". En Porphyrins - Spectral Data of Porphyrin Isomers and Expanded Porphyrins, 189–90. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-47224-8_100.
Texto completoDobhal, M. P. "Spectral data of porphyrin derivative C50H38N4O4". En Porphyrins - Spectral Data of Porphyrin Isomers and Expanded Porphyrins, 191–92. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-47224-8_101.
Texto completoDobhal, M. P. "Spectral data of porphyrin derivative C50H38N4O6". En Porphyrins - Spectral Data of Porphyrin Isomers and Expanded Porphyrins, 193–94. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-47224-8_102.
Texto completoDobhal, M. P. "Spectral data of porphyrin derivative C50H38N4O6". En Porphyrins - Spectral Data of Porphyrin Isomers and Expanded Porphyrins, 195–96. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-47224-8_103.
Texto completoActas de conferencias sobre el tema "Porphyrin"
Ahmed, Md Soif, Chinmoy Biswas, Dipanjan Banerjee, Botta Bhavani, S. Prasanthkumar, Lingamallu Giribabu, Venugopal Rao Soma y Sai Santosh Kumar Raavi. "Ultrafast Photoexcited Molecular Dynamics of Metalated Porphyrin – Napthalimide Based Donor-Acceptor Systems". En CLEO: Applications and Technology. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/cleo_at.2022.jw3b.4.
Texto completoNeumann, Laurie. "Synthesis of 5,15-A2BC-Type Porphyrins to Modify a Field-Effect Transistor for Detection of Gram-Negative Bacteria". En SurfCoat Korea and Graphene Korea 2021 International Joint Virtual Conferences. Setcor Conferences and Events, 2021. http://dx.doi.org/10.26799/cp-surfcoat-graphene-korea-2021/2.
Texto completoKamitani, K., M. Uo, H. Inoue, A. Makishima, T. Suzuki y K. Horie. "Synthesis and Spectroscopy of TPP Derivative-Doped Silica Gels by Sol-Gel Process". En Spectral Hole-Burning and Related Spectroscopies: Science and Applications. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/shbs.1994.wd56.
Texto completoMorrow, D. I. J. y R. F. Donnelly. "Novel drug delivery strategies for porphyrins and porphyrin precursors". En 12th World Congress of the International Photodynamic Association, editado por David H. Kessel. SPIE, 2009. http://dx.doi.org/10.1117/12.822673.
Texto completoEom, Hyo Soon, Cheon Min Kim, Sae Chae Jeoung y Dongho Kim. "Ultrafast Vibrational Relaxation and Ligand Photodissociation/Photoassociation Processes of Nickel(II) Porphyrins". En International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/up.1996.fe.54.
Texto completoПомыткина, Татьяна Евгеньевна, Виталия Андреевна Скрипко y Дарья Евгеньевна Фирстова. "CLINICAL CASE OF A PATIENT WITH VARIEGATED PORPHYRIA". En Science. Research. Practice (Наука. Исследования. Практика): сборник статей LXXIV International scientific conference (Санкт-Петербург, Февраль 2024). Crossref, 2024. http://dx.doi.org/10.37539/240216.2024.75.29.002.
Texto completoZheng, Gang. "Porphyrin Nanophotonics". En Optical Molecular Probes, Imaging and Drug Delivery. Washington, D.C.: OSA, 2013. http://dx.doi.org/10.1364/omp.2013.mw1c.1.
Texto completoHarrison, R. J., G. S. Beddard, J. A. Cowan y J. K. M. Sanders. "Detection of the inverted region in photo-induced intramolecular electron transfer". En International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1986. http://dx.doi.org/10.1364/up.1986.mc8.
Texto completoSakoda, Kazuaki y Masayuki Maeda. "Photochemical Hole Burning and Debye-Waller Factor in Polyvinylalcohol doped with Ionic Porphyrins". En Spectral Hole-Burning and Related Spectroscopies: Science and Applications. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/shbs.1994.wd38.
Texto completoHuenerbein, M., Hanns-joerg Sinn, Hans-Hermann Schrenk, W. Maier-Borst y E. A. Friedrich. "Enhancement of porphyrin tumor accumulation by inhibition of porphyrin liver pathway". En International Conference on Photodynamic Therapy and Laser Medicine, editado por Junheng Li. SPIE, 1993. http://dx.doi.org/10.1117/12.136985.
Texto completoInformes sobre el tema "Porphyrin"
Michl, J. Pyridinium-Coupled Porphyrin-Based Molecular Grid Membrane. Fort Belvoir, VA: Defense Technical Information Center, julio de 2001. http://dx.doi.org/10.21236/ada395522.
Texto completoBraden, Dale. Synthesis and Characterization of a Porphyrin Dyad. Portland State University Library, enero de 2000. http://dx.doi.org/10.15760/etd.6852.
Texto completoKlunder, G. y R. Silva. An expanded porphyrin approach toward transactinium chelation and the development of porphyrin-coated optical fibers as potential actinide sensors. Office of Scientific and Technical Information (OSTI), diciembre de 1994. http://dx.doi.org/10.2172/86912.
Texto completoRebane, Aleksander. Two-Photon Porphyrin Core Dendrimers for Optical Power Limiting. Fort Belvoir, VA: Defense Technical Information Center, septiembre de 2006. http://dx.doi.org/10.21236/ada495180.
Texto completoHays, James Allen. The coordination and atom transfer chemistry of titanium porphyrin complexes. Office of Scientific and Technical Information (OSTI), noviembre de 1993. http://dx.doi.org/10.2172/10194736.
Texto completoHoefler, Christoph. Preparation of electron donor and acceptor molecules for porphyrin derivatization. Portland State University Library, enero de 2000. http://dx.doi.org/10.15760/etd.6201.
Texto completoKanan, Matthew W. Local Electric Field Effects on Rhodium-Porphyrin and NHC-Gold Catalysts. Fort Belvoir, VA: Defense Technical Information Center, enero de 2015. http://dx.doi.org/10.21236/ad1013216.
Texto completoKlobukowski, Erik. Bulk gold catalyzed oxidation reactions of amines and isocyanides and iron porphyrin catalyzed N-H and O-H bond insertion/cyclization reactions of diamines and aminoalcohols. Office of Scientific and Technical Information (OSTI), enero de 2011. http://dx.doi.org/10.2172/1048517.
Texto completoEarnshaw, H. C. y B. D. Grant. The Porphyrin maturity parameter as an indicator of oil maturity and the onset of oil generation in the Cretaceous Slater River Formation, Fort Norman area, Northwest Territories. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1992. http://dx.doi.org/10.4095/133460.
Texto completoBeckett-Brown, C. E., A. M. McDonald y M. B. McClenaghan. Discovering a porphyry deposit using tourmaline: a case study from Yukon. Natural Resources Canada/CMSS/Information Management, 2023. http://dx.doi.org/10.4095/331349.
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