Готові списки джерел за темами / Photophysical Chemistry

Добірка наукової літератури з теми "Photophysical Chemistry"

Автор: Grafiati
Опубліковано: 10 грудня 2022
Оновлено: 29 січня 2023

Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями

Оберіть тип джерела:

Зміст

Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Photophysical Chemistry".

Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.

Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.

Статті в журналах з теми "Photophysical Chemistry"

1

Arad, Ofir, Noemí Rubio, David Sánchez-García, José I. Borrell, and Santi Nonell. "Asymmetric porphycenes: synthesis and photophysical properties of 9-substituted 2,7,12,17-tetraphenylporphycenes." Journal of Porphyrins and Phthalocyanines 13, no. 03 (March 2009): 376–81. http://dx.doi.org/10.1142/s1088424609000462.

Повний текст джерела
Анотація:
The effects of 9-substitution on the photophysical properties of tetraphenylporphycenes (TPPo) have been examined using an electron acceptor, an electron donor, and an electroneutral substituent as model compounds. Introduction of the acetoxy group enhances the fluorescence ability of the compound, with only a small reduction in the singlet oxygen quantum yield. The optical and photophysical properties of a nitro-porphycene are reported for the first time. The compound is emerald green, contrasting with the typical blue color of porphycenes. While this compound is much less fluorescent than unsubstituted TPPo, its singlet oxygen quantum yield is only slightly lower, almost identical to that of the 9-acetoxy compound (9-AcOTPPo). Finally, the electron-donor amino group is found to induce the greatest changes in the porphycene photophysics, decreasing strongly its fluorescence and singlet oxygen quantum yields. With the exception of such electron donors, introduction of substituents at the 9 (meso) position of tetraphenylporphycenes is not detrimental to their photophysics and photosensitizing ability and thus can be exploited for targeted photodynamic therapy purposes.
Стилі APA, Harvard, Vancouver, ISO та ін.
2

Luh, Tien-Yau. "Alternating dialkylsilylene-divinylarene copolymers." Pure and Applied Chemistry 82, no. 3 (February 24, 2010): 613–24. http://dx.doi.org/10.1351/pac-con-09-08-07.

Повний текст джерела
Анотація:
A summary of recent advances in the chemistry and photophysics of alternating dialkylsilylene-divinylarene copolymers is presented. The silicon moieties are considered to be insulating tetrahedral spacers in these copolymers. The substituents on silicon can readily be tuned, and the steric environment of these substituents around the silicon may dictate the conformation (or helicity) of the copolymers (the Thorpe–Ingold effect) and hence their photophysical properties. Because different chromophores can be regioregularly introduced into the polymeric chain, these copolymers have been used as models to study energy transfer and photoinduced electron transfer (PET), as well as chiroptical transfer.
Стилі APA, Harvard, Vancouver, ISO та ін.
3

Ge, Yuan, and Donal F. O'Shea. "Azadipyrromethenes: from traditional dye chemistry to leading edge applications." Chemical Society Reviews 45, no. 14 (2016): 3846–64. http://dx.doi.org/10.1039/c6cs00200e.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
4

Auwalu, Muhammad Aminu, and Shanshan Cheng. "Diketopyrrolopyrrole Fluorescent Probes, Photophysical and Biological Applications." Chemosensors 9, no. 3 (February 26, 2021): 44. http://dx.doi.org/10.3390/chemosensors9030044.

Повний текст джерела
Анотація:
Biological applications of fluorescent probes are rapidly increasing in the supramolecular chemistry research field. Several organic dyes are being utilized currently in developing and advancing this attractive research area, of which diketopyrrolopyrrole (DPP) organic dyes show an exceptional photophysical features (high-fluorescence quantum yield (FQY), good photochemical and thermal stability) that are essential properties for biological applications. Great efforts have been made in recent years towards developing novel fluorescent DPPs by different chemists for such applications, and some positive results have been reported. As a result, this review article gives an account of the progress that has so far been made very recently, mainly within the last decade, in that we selectively focus on and discuss more from 2015 to present on some recent scholarly achievements of fluorescent DPPs: quantum yield, aggregation-induced emission (AIE), solid-state emission, bio-imaging, cancer/tumor therapy, mitochondria staining and some polymeric fluorescent DPPs. Finally, this review article highlights researchers working on luminescent DPPs and the future prospects in some key areas towards designing DPP-based fluorescent probes in order to boost their photophysical and biological applications more effectively.
Стилі APA, Harvard, Vancouver, ISO та ін.
5

Anandkumar, Devaraj, Shanmugam Ganesan, Perumal Rajakumar, and Pichai Maruthamuthu. "Synthesis, photophysical and electrochemical properties and DSSC applications of triphenylamine chalcone dendrimers via click chemistry." New Journal of Chemistry 41, no. 19 (2017): 11238–49. http://dx.doi.org/10.1039/c7nj01059a.

Повний текст джерела
Анотація:
Fluorene-cored dendrimers containing a triphenylamine chalcone unit at the periphery have been synthesized by click chemistry approach, and their photophysical and electrochemical properties have been investigated.
Стилі APA, Harvard, Vancouver, ISO та ін.
6

Hoyle, Charles E., Isaac B. Rufus, and Himanshu Shah. "Solvent effect on the photophysics of bisphenol-A-based polycarbonate and diphenylcarbonate." Canadian Journal of Chemistry 73, no. 11 (November 1, 1995): 2062–68. http://dx.doi.org/10.1139/v95-254.

Повний текст джерела
Анотація:
Polycarbonate and diphenylcarbonate exhibit an anomalous fluorescence emission with peak maximum around 350 nm in polar solvents that may be attributed to the association of diarylcarbonate moieties in a polar solvent cage. The red-shifted emission is attributed to intermolecular interactions in polar solvents and intramolecular interactions in polycarbonate. The photophysical behavior of polycarbonate and diphenylcarbonate is different from that of 1,3-diphenylpropane where a red-shifted emission is due to excimers formed by phenyl groups separated by three carbon atoms and is independent of the polarity of the solvent. Keywords: diphenylcarbonate, polycarbonate, aggregates, photophysics.
Стилі APA, Harvard, Vancouver, ISO та ін.
7

Hou, X., S. R. Abrams, J. J. Balsevich, N. Irvine, T. Norstrom, M. Sikorski, H. K. Sinha, and R. P. Steer. "Synthesis and photophysical properties of fluorophore-labeled abscisic acid." Canadian Journal of Chemistry 78, no. 7 (July 1, 2000): 963–74. http://dx.doi.org/10.1139/v00-087.

Повний текст джерела
Анотація:
The 8'-benzophenone, 8'-dansylhydrazone, 3'-S-(2-ethyldansylamide), and 3'-S-acetamidofluorescein derivatives of the plant hormone abscisic acid (ABA) have been synthesized for use in photoaffinity labeling (the benzophenone derivative) or fluorescence probe experiments and have been spectroscopically characterized. One of the three fluorescent compounds, the 3'-tethered fluorescein derivative, exhibits spectroscopic and photophysical properties which indicate that it could be an excellent fluorescent probe of ABA interactions in vivo. The 3'-tethered fluorescein and ABA moieties do not interact strongly, so that the fluorescence properties of the fluorescein-labelled hormone are very similar to those of fluorescein itself. Measurements of the absorption, emission, and fluorescence excitation spectra, fluorescence quantum yields, and fluorescence decay parameters of this derivative as a function of pH indicate that the photophysics is dominated by ground and excited state prototropic equilibria involving only the fluorescein moiety. The fluorescein dianion is the only significant absorber and emitter at pH > 6.7, whereas only the cation absorbs and emits at pH < 0. In the intervening pH range, strong emission from the monoanion and weak emission from two neutral species, tentatively assigned to the zwitterion and the lactone of the fluorescein moiety, is observed.Key words: abscisic acid, fluorescein, synthesis, photophysics.
Стилі APA, Harvard, Vancouver, ISO та ін.
8

Moodelly, Davina, Patrycja Kowalik, Piotr Bujak, Adam Pron, and Peter Reiss. "Synthesis, photophysical properties and surface chemistry of chalcopyrite-type semiconductor nanocrystals." Journal of Materials Chemistry C 7, no. 38 (2019): 11665–709. http://dx.doi.org/10.1039/c9tc03875b.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
9

Li, Chengjie, and Bernhard Kräutler. "Transition metal complexes of phyllobilins – a new realm of bioinorganic chemistry." Dalton Transactions 44, no. 22 (2015): 10116–27. http://dx.doi.org/10.1039/c5dt00474h.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
10

Steinbrück, Dörte, Claudia Rasch, and Michael U. Kumke. "Photophysics of Ochratoxin A in Aqueous Solution." Zeitschrift für Naturforschung B 63, no. 11 (November 1, 2008): 1321–26. http://dx.doi.org/10.1515/znb-2008-1111.

Повний текст джерела
Анотація:
Abstract The photophysics of Ochratoxin A (OTA) in aqueous solution strongly depends on the pH. Due to its molecular structure OTA is prone to an excited state proton transfer reaction, which rules the photophysical properties. Based on results of absorption and fluorescence measurements the rate constants of the proton transfer reactions (forward and back reaction) were determined and subsequently, the pK*a value was calculated. Based on the results, optimized experimental conditions for the analysis can be determined e. solvent conditions (HPLC chromatography) or excitation and emission wavelength (fluorescence spectroscopy).
Стилі APA, Harvard, Vancouver, ISO та ін.
Більше джерел

Дисертації з теми "Photophysical Chemistry"

1

Conn, Pauline Frances. "Photophysical chemistry of carotenoids." Thesis, Keele University, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315187.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
2

Dosche, Carsten, Hans-Gerd Löhmannsröben, A. Bieser, P. I. Dosa, S. Han, M. Iwamoto, A. Schleifenbaum, and K. Peter C. Vollhardt. "Photophysical properties of [N]phenylenes." Universität Potsdam, 2002. http://opus.kobv.de/ubp/volltexte/2007/1193/.

Повний текст джерела
Анотація:
In the present study, photophysical properties of [N]phenylenes were studied by means of stationary and time-resolved absorption and fluorescence spectroscopy (in THF at room temperature). For biphenylene (1) and linear [3]phenylene (2a), internal conversion (IC) with quantum yields ΦIC > 0.99 is by far the dominant mechanism of S1 state deactivation. Angular [3]phenylene (3a), the zig-zag [4]- and [5]phenylenes (3b), (3c), and the triangular [4]phenylene (4) show fluorescence emission with fluorescence quantum yieds and lifetimes between ΦF = 0.07 for (3a) and 0.21 for (3c) and τF = 20 ns for (3a) and 81 ns for (4). Also, compounds (3) and (4) exhibit triplet formation upon photoexcitation with quantum yields as high as ΦISC = 0.45 for (3c). The strong differences in the fluorescence properties and in the triplet fromation efficiencies between (1) and (2a) on one hand and (3) and (4) on the other are related to the remarkable variation of the internal conversion (IC) rate constants kIC. A tentative classification of (1) and (2a) as “fast IC compounds”, with kIC > 109 s-1, and of (3) and (4) as “slow IC compounds”, with kIC ≈ 107 s-1, is suggested. This classification cannot simply be related to Hückel’s rule-type concepts of aromaticity, because the group of “fast IC compounds” consists of “antiaromatic” (1) and “aromatic” (2a), and the group of “slow IC compounds” consists of “antiaromatic” (3b), (4) and “aromatic” (3a), (3c). The IC in the [N]phenylenes is discussed within the framework of the so-called energy gap law established for non-radiative processes in benzenoid hydrocarbons.
Стилі APA, Harvard, Vancouver, ISO та ін.
3

Lin, Liangbih. "Photophysical studies of ring containing conjugated polymers." The Ohio State University, 1995. http://rave.ohiolink.edu/etdc/view?acc_num=osu1343061430.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
4

Mickenberg, Seth F. (Seth Fox). "Tuning the photophysical properties of amidophosphine complexes of copper." Thesis, Massachusetts Institute of Technology, 2009. http://hdl.handle.net/1721.1/49753.

Повний текст джерела
Анотація:
Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2009.
Vita.
Includes bibliographical references (leaves 23-24).
A series of monomeric copper complexes that allow for the tuning of the emission properties is reported. Luminescence lifetimes up to 150 [mu]s are observed in benzene solution at ambient temperature, which are comparable to the lifetimes of the longest-lived previously reported copper luminophores. These complexes also exhibit quantum yields up to 0 = 0.70 at 298 K. The results of time-dependent density functional theory (TDDFT) calculations indicate emission from a triplet state in all cases. The calculations also successfully correlate the energy of the transition from this triplet state to the energy of the observed emission. Such luminescence from a first-row metal is highly unusual, especially when considering the phosphine-based ligand framework used.
by Seth F. Mickenberg.
S.M.
Стилі APA, Harvard, Vancouver, ISO та ін.
5

Bradley, Patricia Marie. "Photochemistry and photophysical properties of metal-metal dimer complexes /." The Ohio State University, 2002. http://rave.ohiolink.edu/etdc/view?acc_num=osu1486461246814571.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
6

Liska, Tadeas. "Bis(imidazolyl)carbazolide Platinum(II) Alkynyls: Synthesis, Characterization, and Photophysical Properties." Case Western Reserve University School of Graduate Studies / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=case1626960987919156.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
7

Rogge, Carsten. "Photophysical studies of organic dyes in polymer matrices." Thesis, Cranfield University, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266485.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
8

Kelly, Graeme P. "Photochemical and photophysical properties of various triaryl-2-pyrazolines." Thesis, Loughborough University, 1987. https://dspace.lboro.ac.uk/2134/28194.

Повний текст джерела
Анотація:
The main aim of the research was to obtain a detailed insight into the photochemical and photophysical properties of various triaryl-2- pyrazolines, with a view to understanding better their role in photoconductive materials. The technique of laser flash photolysis, in both transmission and diffuse reflectance mode, was employed to study the compounds as microcrystalline powders, within polymer films, on fabrics and in solution. In those media where the triplet state was not directly observed it was sensitized with a suitable triplet energy donor such as benzophenone.
Стилі APA, Harvard, Vancouver, ISO та ін.
9

Wallace, Sheena J. L. "Photophysical studies of hydrophobically-modified poly(N,N-dimethylacrylamide)." Thesis, Lancaster University, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.242818.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
10

Chretien, Michelle N. "Photochemical, photophysical, and photobiological studies of zeolite guest-host complexes." Thesis, University of Ottawa (Canada), 2005. http://hdl.handle.net/10393/29205.

Повний текст джерела
Анотація:
This thesis focuses on the photochemistry and photophysics of a variety of zeolite complexes, from catalysts to sunscreens. The first chapter describes the preparation and photophysical and photochemical characterization of two new photocatalytic materials. The catalysts are based on a multi-component zeolite, host-guest complex and the interaction between components was probed using time-resolved spectroscopic techniques. The catalytic efficiency, in terms of the ability to photodegrade biological contaminants, was also investigated. These studies were performed with the aim of developing efficient catalysts for wastewater remediation which can be used with solar (visible) radiation. In subsequent chapters, zeolite materials have been used as matrices for the stabilization of various transient or reactive species. In the case of ZSM-5-type zeolite, the dibenzotropylium cation was rendered indefinitely persistent allowing the examination of its excited-state behaviour. The geometric restriction within the cavities also permits the observation of electron transfer chemistry in the absence of a nucleophilic addition reaction with the electron donor. In a second example, ketoprofen (a non-steroidal anti-inflammatory drug) was found to undergo intrazeolite photodecarboxylation to generate a benzylic carbanion. The lifetime of the zeolite-encapsulated carbanion was found to be fifty times longer than in solution. The enhanced lifetime allows intermolecular nucleophilic addition chemistry to compete with protonation, effectively, a photo-initiated Grignard-type reaction is observed. In Chapter 6, fluorescence is used as tool to probe both intra- and interzeolite interactions. In the first part, a zeolite-entrapped radical probe was prepared by ship-in-a-bottle synthesis for the investigation of radical percolation in the zeolite matrix. The probe is a molecular dyad containing a persistent free-radical and a quenched fluorophore. When the probe radical couples with a carbon-centered radical, the probe fluorescence is restored and in this way free-radical species in heterogeneous systems can be conveniently examined. In the second section, zeolite particles were irreversibly labeled with a biologically-compatible fluorophore (also by ship-in-a-bottle synthesis). The last part of this thesis deals with a project relating to supramolecular sunscreens. (Abstract shortened by UMI.)
Стилі APA, Harvard, Vancouver, ISO та ін.
Більше джерел

Книги з теми "Photophysical Chemistry"

1

Wielopolski, Mateusz. Testing Molecular Wires: A Photophysical and Quantum Chemical Assay. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2010.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
2

Hänninen, Pekka. Lanthanide Luminescence: Photophysical, Analytical and Biological Aspects. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2011.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
3

Photophysics of organometallics. Heidelberg ; New York: Springer-Verlag, 2010.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
4

P, Lever A. B., American Chemical Society. Division of Inorganic Chemistry., Chemical Institute of Canada. Inorganic Chemistry Division., and Inorganic Chemical Symposium (1985 : Toronto, Ont.), eds. Excited states and reactive intermediates: Photochemistry, photophysics, and electrochemistry. Washington, DC: American Chemical Society, 1986.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
5

1931-, McGlynn S. P., Findley G. L. 1952-, Huebner R. H. 1931-, and North Atlantic Treaty Organization. Scientific Affairs Division., eds. Photophysics and photochemistry in the vacuum ultraviolet. Dordrecht, Holland: D. Reidel, 1985.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
6

Photophysics and photochemistry of metal-containing polymers. Hoboken, N.J: Wiley-Blackwell, 2010.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
7

Françoise, Lahmani, and Castex M. C, eds. Photophysics and photochemistry above 6eV: Proceedings of the 38th International Meeting of the Société de chimie physique, Bombannes, 17-21 September 1984. Amsterdam: Elsevier, 1985.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
8

Françoise, Lahmani, ed. Photophysics and photochemistry above 6 eV: Proceedings of the 38th International Meeting of the Société de chimie physique, Bombannes, 17-21 September 1984. Amsterdam: Elsevier, 1985.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
9

El-Zeiny M. Ebeid (Professor of Physical Chemistry, Tanta University). Photophysical and Laser Based Techniques in Chemistry, Biology, and Medicine. BookSurge Publishing, 2006.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
10

Hänninen, Pekka, and Harri Härmä. Lanthanide Luminescence: Photophysical, Analytical and Biological Aspects. Springer, 2013.

Знайти повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
Більше джерел

Частини книг з теми "Photophysical Chemistry"

1

Bäuerle, Dieter. "Thermal, Photophysical, and Photochemical Processes." In Laser Processing and Chemistry, 13–38. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-17613-5_2.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
2

Bäuerle, Dieter. "Thermal, Photophysical, and Photochemical Processes." In Laser Processing and Chemistry, 13–38. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-662-03253-4_2.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
3

Lehn, Jean-Marie. "Photophysical and Photochemical Aspects of Supramolecular Chemistry." In Supramolecular Photochemistry, 29–43. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3979-0_2.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
4

Leblanc, R. M. "Photophysical Properties of Supramolecular Assemblies in Organized Films." In Physical Supramolecular Chemistry, 199–212. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0317-3_13.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
5

Maity, Ramananda, and Biprajit Sarkar. "Redox and photochemical/photophysical properties of compounds containing mesoionic carbene ligands." In Organometallic Chemistry, 1–22. Cambridge: Royal Society of Chemistry, 2022. http://dx.doi.org/10.1039/9781839167713-00001.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
6

Kelly, J. M., E. M. Tuite, W. J. M. Putten, G. S. Beddard, and G. D. Reid. "Photophysical Properties of Thionine and Methylene Blue When Bound to Dna, Polynucleotides or Nucleotides." In Supramolecular Chemistry, 375–81. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2492-8_24.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
7

Scordino, Agata, Rosaria Grasso, Marisa Gulino, Luca Lanzano', Francesco Musumeci, Giuseppe Privitera, Maurizio Tedesco, Antonio Triglia, and Larissa Brizhik. "Hydration Effects on Photophysical Properties of Collagen." In NATO Science for Peace and Security Series A: Chemistry and Biology, 359–83. Dordrecht: Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-2590-6_17.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
8

Foote, Christopher S. "Photophysical, Photochemical, and Chemical Reactions of Fullerenes and Dihydrofullerene Derivatives." In Physics and Chemistry of the Fullerenes, 79–96. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0984-0_6.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
9

Leitl, Markus J., Daniel M. Zink, Alexander Schinabeck, Thomas Baumann, Daniel Volz, and Hartmut Yersin. "Copper(I) Complexes for Thermally Activated Delayed Fluorescence: From Photophysical to Device Properties." In Topics in Current Chemistry Collections, 141–74. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-59304-3_5.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
10

Arias-Rotondo, Daniela M., and James K. McCusker. "An Overview of the Physical and Photophysical Properties of [Ru(bpy)3 ]2+." In Visible Light Photocatalysis in Organic Chemistry, 1–24. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527674145.ch1.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.

Тези доповідей конференцій з теми "Photophysical Chemistry"

1

Kramer, Stephanie N., Anthony J. Varni, Kevin J. T. Noonan, Tomasz Kowalewski, and Linda A. Peteanu. "Photophysical properties of novel photostable helical polyfurans." In Physical Chemistry of Semiconductor Materials and Interfaces IX, edited by Daniel Congreve, Christian Nielsen, and Andrew J. Musser. SPIE, 2020. http://dx.doi.org/10.1117/12.2567292.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
2

Barzykin, A. V., and M. Tachiya. "Elementary photophysical processes in microdisperse systems." In The 54th international meeting of physical chemistry: Fast elementary processes in chemical and biological systems. AIP, 1996. http://dx.doi.org/10.1063/1.50168.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
3

G. Costa, Susana P., Rosa M. F. Batista, and M. Manuela M. Raposo. "Synthesis and photophysical characterization of novel tri-(hetero)arylimidazoles." In The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a042.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
4

Yuen-Zhou, Joel Y., Luis A. Martínez-Martínez, Juan B. Pérez-Sánchez, and Kai Schwennicke. "Polariton chemistry: controlling organic photophysical processes with strong light-matter coupling." In Physical Chemistry of Semiconductor Materials and Interfaces IX, edited by Daniel Congreve, Christian Nielsen, and Andrew J. Musser. SPIE, 2020. http://dx.doi.org/10.1117/12.2569171.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
5

Raposo, M. Manuela, and M. Cidália Castro. "Synthesis and Characterization of the Photophysical Properties of Novel Heterocyclic Imines." In The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a048.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
6

Dimitrov, Stoichko D. "Dynamics of charge separation in polymer:fullerene blends, correlating structural and photophysical length scales." In Physical Chemistry of Semiconductor Materials and Interfaces IX, edited by Daniel Congreve, Christian Nielsen, and Andrew J. Musser. SPIE, 2020. http://dx.doi.org/10.1117/12.2569321.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
7

Vasilenko, Dmitry, Kirill Sadovnikov, Arina Tukhbatullina та Elena Averina. "NOVEL REACTION OF HETEROCYCLIZATION OF β-ARYL SUBSTITUTED α,β-UNSATURATED KETONES. SYNTHESIS OF 4-NITROISOXAZOLES AND π-CONJUGATED ISOXAZOLE-BASED SYSTEMS WITH VALUABLE PHOTOPHYSICAL PROPARTIESE PHOTOPHYSICAL PROPARTIES". У Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m731.aks-2019/102-104.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
8

Suntsova, Polina O., Aleksey A. Gagarin, Vladislav V. Chernenok, Pavel A. Slepukhin, and Nataliya P. Belskaya. "Synthesis and photophysical properties of new derivatives 4-oxothiazolidin-5-ylidenes." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0068954.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
9

Gonçalves, M., Carla Alves, and Paulo Coutinho. "Synthesis and photophysical characterisation of long alkyl side-chain derivatives of benzo[a]phenoxazinium salts." In The 12th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01229.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
10

Gonçalves, M. Sameiro, B. Rama Raju, Diogo Sampaio, and Paulo Coutinho. "Ultrasonic Mediated Synthesis of New Benzo[a]phenoxazinium Chlorides and Their Photophysical Studies." In The 16th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01112.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.

Звіти організацій з теми "Photophysical Chemistry"

1

Hollingsworth, Jennifer. Advanced Quantum Emitters: Chemistry, Photophysics, Integration and Application. Office of Scientific and Technical Information (OSTI), May 2021. http://dx.doi.org/10.2172/1781363.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
2

Webber, S. E. Polymers at liquid-liquid interfaces: Photophysics and photoredox chemistry. Office of Scientific and Technical Information (OSTI), November 1990. http://dx.doi.org/10.2172/6313119.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
3

Webber, S. E. Polymers at liquid-liquid interfaces: Photophysics and photoredox chemistry. Office of Scientific and Technical Information (OSTI), December 1991. http://dx.doi.org/10.2172/5890123.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
4

Webber, S. E. Polymers at liquid-liquid interfaces: Photophysics and photoredox chemistry. Progress report, April 1, 1991--March 31, 1992. Office of Scientific and Technical Information (OSTI), December 1991. http://dx.doi.org/10.2172/10114481.

Повний текст джерела
Стилі APA, Harvard, Vancouver, ISO та ін.
Також вас можуть зацікавити розширені добірки на тему "Photophysical Chemistry" для конкретних типів джерел:
Статті в журналах Дисертації Книги
Ми пропонуємо знижки на всі преміум-плани для авторів, чиї праці увійшли до тематичних добірок літератури. Зв'яжіться з нами, щоб отримати унікальний промокод!

До бібліографії