Gotowa bibliografia na temat „Porphyrin”
Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych
Spis treści
Zobacz listy aktualnych artykułów, książek, rozpraw, streszczeń i innych źródeł naukowych na temat „Porphyrin”.
Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.
Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.
Artykuły w czasopismach na temat "Porphyrin"
Stölzel, Ulrich, Thomas Stauch i Ilja Kubisch. "Porphyrien". Der Internist 62, nr 9 (29.06.2021): 937–51. http://dx.doi.org/10.1007/s00108-021-01066-1.
Pełny tekst źródłaHindmarsh, J. Thomas, Linda Oliveras i Donald C. Greenway. "Plasma Porphyrins in the Porphyrias". Clinical Chemistry 45, nr 7 (1.07.1999): 1070–76. http://dx.doi.org/10.1093/clinchem/45.7.1070.
Pełny tekst źródłaWoolf, Jacqueline, Joanne T. Marsden, Timothy Degg, Sharon Whatley, Paul Reed, Nadia Brazil, M. Felicity Stewart i Michael Badminton. "Best practice guidelines on first-line laboratory testing for porphyria". Annals of Clinical Biochemistry: International Journal of Laboratory Medicine 54, nr 2 (19.01.2017): 188–98. http://dx.doi.org/10.1177/0004563216667965.
Pełny tekst źródłaPuzikova, А. I., Е. А. Litvin, D. А. Kildyushkin i А. Е. Druy. "Application of high-performance liquid chromatography in porphyrias diagnostics". Pediatric Hematology/Oncology and Immunopathology 20, nr 3 (8.10.2021): 140–44. http://dx.doi.org/10.24287/1726-1708-2021-20-3-140-144.
Pełny tekst źródłaKrivosheev, Alexander B., L. Ya Kupriyanova i M. A. Kondratova. "DOUBLE PORPHYRIA: LITERATURE REVIEW AND ANALYSIS OF CLINICAL OBSERVATION". Russian Journal of Skin and Venereal Diseases 21, nr 2 (15.04.2018): 120–24. http://dx.doi.org/10.18821/1560-9588-2018-21-2-120-124.
Pełny tekst źródłaCarson, R. W., E. J. Dunnigan, T. D. DuBose, D. E. Goeger i 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, nr 9 (marzec 1992): 1445–50. http://dx.doi.org/10.1681/asn.v291445.
Pełny tekst źródłaEgemen, Gamze, Mustafa Hayvalı, Zeynel Kılıç, A. Osman Solak i Zafer Üstündağ. "Phosphorus-nitrogen compounds Part 17: The synthesis, spectral and electrochemical investigations of porphyrino-phosphazenes". Journal of Porphyrins and Phthalocyanines 14, nr 03 (marzec 2010): 227–34. http://dx.doi.org/10.1142/s1088424610001945.
Pełny tekst źródłaHindmarsh, J. T. "The porphyrias: recent advances." Clinical Chemistry 32, nr 7 (1.07.1986): 1255–63. http://dx.doi.org/10.1093/clinchem/32.7.1255.
Pełny tekst źródłaLockwood, W. H., V. Poulos, E. Rossi i D. H. Curnow. "Rapid procedure for fecal porphyrin assay." Clinical Chemistry 31, nr 7 (1.07.1985): 1163–67. http://dx.doi.org/10.1093/clinchem/31.7.1163.
Pełny tekst źródłaPerkins, S. L., i 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, nr 7 (1.07.1989): 1508–12. http://dx.doi.org/10.1093/clinchem/35.7.1508.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaGuo, Rong. "Porphyrin metabolism in congenital erythropoietic porphyria". Thesis, Open University, 1992. http://oro.open.ac.uk/57392/.
Pełny tekst źródłaLefley, 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.
Pełny tekst źródłaWessendorf, Florian. "Supramolecular fullerene-porphyrin architectures = Supramolekulare Fulleren-Porphyrin-Architekturen". kostenfrei, 2010. http://d-nb.info/1000613593/34.
Pełny tekst źródłaBeavington, Richard. "Porphyrin arrays". Thesis, University of Oxford, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.388909.
Pełny tekst źródłaPromarak, Vinich. "Porphyrin arrays". Thesis, University of Oxford, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.249614.
Pełny tekst źródłaZhang, Wei. "Porphyrin arrays". Thesis, University of Oxford, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.494395.
Pełny tekst źródłaTannert, 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.
Pełny tekst źródłaThis 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.
Pełny tekst źródłaIakushev, 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.
Pełny tekst źródłaPolymacrocyclic 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
Książki na temat "Porphyrin"
R, Moore Michael, i Wintrobe Maxwell Myer 1901-, red. Disorders of porphyrin metabolism. New York: Plenum Medical Book Co., 1987.
Znajdź pełny tekst źródłaDobhal, M. P. Porphyrins - Spectral Data of Porphyrin Isomers and Expanded Porphyrins. Redaktorzy V. Gupta, M. D. Lechner i R. Gupta. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-47224-8.
Pełny tekst źródłaA, Sheldon Roger, red. Metalloporphyrins in catalytic oxidations. New York: M. Dekker, 1994.
Znajdź pełny tekst źródłaA, Sheldon Roger, red. Metalloporphyrins in catalyticoxidations. New York: M. Dekker, 1994.
Znajdź pełny tekst źródła1945-, Kadish Karl M., Smith Kevin M i Guilard Roger, red. The porphyrin handbook. San Diego, Calif: Academic Press, 2003.
Znajdź pełny tekst źródła1945-, Kadish Karl M., Smith Kevin M i Guilard Roger, red. The porphyrin handbook. San Diego: Academic Press, 2000.
Znajdź pełny tekst źródłaMa, Shengqian, i Gaurav Verma, red. Porphyrin-based Supramolecular Architectures. Cambridge: Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781839164934.
Pełny tekst źródłaKessel, David, red. Methods in Porphyrin Photosensitization. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2165-1.
Pełny tekst źródłaMoore, Michael R., Kenneth E. L. McColl, Claude Rimington i Abraham Goldberg. Disorders of Porphyrin Metabolism. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-1277-2.
Pełny tekst źródłaDavid, Kessel, red. Methods in porphyrin photosensitization. New York: Plenum Press, 1985.
Znajdź pełny tekst źródłaCzęści książek na temat "Porphyrin"
Cleaves, Henderson James. "Porphyrin". W Encyclopedia of Astrobiology, 1326. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_1258.
Pełny tekst źródłaCleaves, Henderson James. "Porphyrin". W Encyclopedia of Astrobiology, 2000. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_1258.
Pełny tekst źródłaCleaves, Henderson James. "Porphyrin". W Encyclopedia of Astrobiology, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-642-27833-4_1258-4.
Pełny tekst źródłaCleaves, Henderson James. "Porphyrin". W Encyclopedia of Astrobiology, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27833-4_1258-3.
Pełny tekst źródłaCleaves, Henderson James. "Porphyrin". W Encyclopedia of Astrobiology, 2445–46. Berlin, Heidelberg: Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65093-6_1258.
Pełny tekst źródłaDobhal, M. P. "Spectral data of porphyrin derivative C48H33N3S2". W 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.
Pełny tekst źródłaDobhal, M. P. "Spectral data of porphyrin derivative C50H38N4O2". W 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.
Pełny tekst źródłaDobhal, M. P. "Spectral data of porphyrin derivative C50H38N4O4". W 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.
Pełny tekst źródłaDobhal, M. P. "Spectral data of porphyrin derivative C50H38N4O6". W 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.
Pełny tekst źródłaDobhal, M. P. "Spectral data of porphyrin derivative C50H38N4O6". W 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.
Pełny tekst źródłaStreszczenia konferencji na temat "Porphyrin"
Ahmed, Md Soif, Chinmoy Biswas, Dipanjan Banerjee, Botta Bhavani, S. Prasanthkumar, Lingamallu Giribabu, Venugopal Rao Soma i Sai Santosh Kumar Raavi. "Ultrafast Photoexcited Molecular Dynamics of Metalated Porphyrin – Napthalimide Based Donor-Acceptor Systems". W CLEO: Applications and Technology. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/cleo_at.2022.jw3b.4.
Pełny tekst źródłaNeumann, Laurie. "Synthesis of 5,15-A2BC-Type Porphyrins to Modify a Field-Effect Transistor for Detection of Gram-Negative Bacteria". W 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.
Pełny tekst źródłaKamitani, K., M. Uo, H. Inoue, A. Makishima, T. Suzuki i K. Horie. "Synthesis and Spectroscopy of TPP Derivative-Doped Silica Gels by Sol-Gel Process". W 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.
Pełny tekst źródłaMorrow, D. I. J., i R. F. Donnelly. "Novel drug delivery strategies for porphyrins and porphyrin precursors". W 12th World Congress of the International Photodynamic Association, redaktor David H. Kessel. SPIE, 2009. http://dx.doi.org/10.1117/12.822673.
Pełny tekst źródłaEom, Hyo Soon, Cheon Min Kim, Sae Chae Jeoung i Dongho Kim. "Ultrafast Vibrational Relaxation and Ligand Photodissociation/Photoassociation Processes of Nickel(II) Porphyrins". W International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/up.1996.fe.54.
Pełny tekst źródłaПомыткина, Татьяна Евгеньевна, Виталия Андреевна Скрипко i Дарья Евгеньевна Фирстова. "CLINICAL CASE OF A PATIENT WITH VARIEGATED PORPHYRIA". W 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.
Pełny tekst źródłaZheng, Gang. "Porphyrin Nanophotonics". W Optical Molecular Probes, Imaging and Drug Delivery. Washington, D.C.: OSA, 2013. http://dx.doi.org/10.1364/omp.2013.mw1c.1.
Pełny tekst źródłaHarrison, R. J., G. S. Beddard, J. A. Cowan i J. K. M. Sanders. "Detection of the inverted region in photo-induced intramolecular electron transfer". W International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1986. http://dx.doi.org/10.1364/up.1986.mc8.
Pełny tekst źródłaSakoda, Kazuaki, i Masayuki Maeda. "Photochemical Hole Burning and Debye-Waller Factor in Polyvinylalcohol doped with Ionic Porphyrins". W 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.
Pełny tekst źródłaHuenerbein, M., Hanns-joerg Sinn, Hans-Hermann Schrenk, W. Maier-Borst i E. A. Friedrich. "Enhancement of porphyrin tumor accumulation by inhibition of porphyrin liver pathway". W International Conference on Photodynamic Therapy and Laser Medicine, redaktor Junheng Li. SPIE, 1993. http://dx.doi.org/10.1117/12.136985.
Pełny tekst źródłaRaporty organizacyjne na temat "Porphyrin"
Michl, J. Pyridinium-Coupled Porphyrin-Based Molecular Grid Membrane. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2001. http://dx.doi.org/10.21236/ada395522.
Pełny tekst źródłaBraden, Dale. Synthesis and Characterization of a Porphyrin Dyad. Portland State University Library, styczeń 2000. http://dx.doi.org/10.15760/etd.6852.
Pełny tekst źródłaKlunder, G., i 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), grudzień 1994. http://dx.doi.org/10.2172/86912.
Pełny tekst źródłaRebane, Aleksander. Two-Photon Porphyrin Core Dendrimers for Optical Power Limiting. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 2006. http://dx.doi.org/10.21236/ada495180.
Pełny tekst źródłaHays, James Allen. The coordination and atom transfer chemistry of titanium porphyrin complexes. Office of Scientific and Technical Information (OSTI), listopad 1993. http://dx.doi.org/10.2172/10194736.
Pełny tekst źródłaHoefler, Christoph. Preparation of electron donor and acceptor molecules for porphyrin derivatization. Portland State University Library, styczeń 2000. http://dx.doi.org/10.15760/etd.6201.
Pełny tekst źródłaKanan, Matthew W. Local Electric Field Effects on Rhodium-Porphyrin and NHC-Gold Catalysts. Fort Belvoir, VA: Defense Technical Information Center, styczeń 2015. http://dx.doi.org/10.21236/ad1013216.
Pełny tekst źródłaKlobukowski, 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), styczeń 2011. http://dx.doi.org/10.2172/1048517.
Pełny tekst źródłaEarnshaw, H. C., i 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.
Pełny tekst źródłaBeckett-Brown, C. E., A. M. McDonald i 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.
Pełny tekst źródła