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Статті в журналах з теми "Conjugated and cumulated molecules"
Sarbadhikary, Prodipta, Suranjan Shil та Anirban Misra. "Magnetic and transport properties of conjugated and cumulated molecules: the π-system enlightens part of the story". Physical Chemistry Chemical Physics 20, № 14 (2018): 9364–75. http://dx.doi.org/10.1039/c7cp06113g.
Повний текст джерелаHorká, Petra, Vladimír Vrkoslav, Jiří Kindl, Karolina Schwarzová-Pecková, and Josef Cvačka. "Structural Characterization of Unusual Fatty Acid Methyl Esters with Double and Triple Bonds Using HPLC/APCI-MS2 with Acetonitrile In-Source Derivatization." Molecules 26, no. 21 (October 26, 2021): 6468. http://dx.doi.org/10.3390/molecules26216468.
Повний текст джерелаRenard, Emma, Olivier Raguin, Victor Goncalves, Celine Mothes, Mathieu Moreau, Claire Bernhard, Peggy Provent, et al. "Abstract 1401: Lead optimization of radiopharmaceuticals for molecular radiotherapy and preclinical evaluation." Cancer Research 82, no. 12_Supplement (June 15, 2022): 1401. http://dx.doi.org/10.1158/1538-7445.am2022-1401.
Повний текст джерелаvan Dongen, J. P. C. M., A. J. de Jong, H. A. Selling, P. P. Montijn, J. H. van Boom, and L. Brandsma. "Isomerization of conjugated and cumulated systems." Recueil des Travaux Chimiques des Pays-Bas 86, no. 10 (September 2, 2010): 1077–81. http://dx.doi.org/10.1002/recl.19670861008.
Повний текст джерелаSchonk, Ruud M., Bert H. Bakker, and Hans Cerfontain. "Reactions of cumulated and conjugated dienes with sulfur trioxide." Recueil des Travaux Chimiques des Pays-Bas 112, no. 3 (September 2, 2010): 201–9. http://dx.doi.org/10.1002/recl.19931120301.
Повний текст джерелаZhu, Xiao-Qing, Hao Liang, Yan Zhu, and Jin-Pei Cheng. "Hydride Affinities of Cumulated, Isolated, and Conjugated Dienes in Acetonitrile." Journal of Organic Chemistry 73, no. 21 (November 7, 2008): 8403–10. http://dx.doi.org/10.1021/jo801536m.
Повний текст джерелаH. Muhammad, G. Tastemirova, and K. Abdibekova. "STRUCTURES OF ALKANDIENES IN HYDROCARBONS." Bulletin of Toraighyrov University. Chemistry & Biology series, no. 4.2022 (December 28, 2022): 19–33. http://dx.doi.org/10.48081/rglj8585.
Повний текст джерелаNuckolls, Colin, Thomas J. Katz, and Louis Castellanos. "Aggregation of Conjugated Helical Molecules." Journal of the American Chemical Society 118, no. 15 (January 1996): 3767–68. http://dx.doi.org/10.1021/ja960145z.
Повний текст джерелаDias, Jerry Ray. "Almost-isospectral conjugated polyene molecules." Chemical Physics Letters 253, no. 3-4 (May 1996): 305–12. http://dx.doi.org/10.1016/0009-2614(96)00258-8.
Повний текст джерелаFox, J., Z. Dong, X. Liu, and G. Yap. "Parallel Alignment of Conjugated Rod Molecules." Synfacts 2007, no. 4 (April 2007): 0384. http://dx.doi.org/10.1055/s-2007-968319.
Повний текст джерелаДисертації з теми "Conjugated and cumulated molecules"
Sarbadhikary, Prodipta. "Magnetic and transport properties of spin polarized molecular systems: theoretical perspective." Thesis, University of North Bengal, 2021. http://ir.nbu.ac.in/handle/123456789/4668.
Повний текст джерелаO'Connor, M. P. "Electronic properties of conjugated molecules." Thesis, Lancaster University, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.379188.
Повний текст джерелаSamori, Paolo. "Self-assembly of conjugated (macro)molecules." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2000. http://dx.doi.org/10.18452/14604.
Повний текст джерелаIn this thesis the self-assembly of pi-conjugated (macro)molecular architectures, either through chemisorption or via physisorption, into highly ordered supramolecular nanoscopic and microscopic structures has been studied. On solid substrates structure and dynamics has been investigated on the molecular scale making use primarily of Scanning Probe Microscopies, in particular Scanning Tunneling Microscopy and Scanning Force Microscopy. This allowed to characterize a variety of phenomena occurring both at the solid-liquid interface, such as the dynamics of the single molecular nanorods (known as Ostwald ripening), the fractionation of a solution of rigid-rod polymers upon physisorption on graphite; and in dry films, i.e. the self-assembly of rigid-rod polymers into nanoribbons with molecular cross sections which can be epitaxially oriented at surfaces and the formation ordered layered architectures of disc-like molecules. In addition the electronic properties of the investigated moieties have been studied by means of Photoelectron Spectroscopies. The nanostructures that have been developed are not only of interest for nanoconstructions on solid surfaces, but also exhibit properties that render them candidates for applications in the field of molecular electronics, in particular for building molecular nanowire devices.
Winfield, Jessica Mary. "Spectroscopy of conjugated polymers and small molecules." Thesis, University of Cambridge, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.611577.
Повний текст джерелаWildman, Jack. "Molecular dynamics simulations of conjugated semiconducting molecules." Thesis, Heriot-Watt University, 2017. http://hdl.handle.net/10399/3261.
Повний текст джерелаJäckel, Frank. "Self-Assembly and Electronic Properties of Conjugated Molecules." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2005. http://dx.doi.org/10.18452/15267.
Повний текст джерелаThe use of single molecules as active components in electronic devices is presently considered a potential alternative to semiconductor-based nano-scale electronics since it directly provides precisely-defined nano-scale components for electronic devices which eventually allows for simple processing and devicefabrication. In this thesis the self-assembly and electron transport properties of conjugated molecules are investigated by means of scanning tunneling microscopy (STM) and spectroscopy (STS) at solid-liquid interfaces and under ultrahigh vacuum conditions and low temperatures. The use of the molecules in hybrid-molecular electronic devices and potential approaches to a mono-molecular electronics are explored. In particular, electron-donor-acceptor-multiads are shown to exhibit a nano-phase-segregation at the solid-liquid interface which allows for the integration of different electronic functions at the nano-scale. Furthermore, the dependence of the electronic coupling of stacked disk-like molecules on the lateral off-set in the stack is demonstrated experimentally which offers new possibilities for the control of the electronic properties of these three-dimensional architectures. In addition the first STM/STS experiments on charge transfer in single organic donor-acceptor complexes are presented. Finally, charge transfer complexes are combined with the approach of nano-phase-segregation to realize the first single-molecule transistor with integrated nanometer-sized gates. In this prototypical device the current through a hybrid-molecular diode made from a hexa-peri-hexabenzocoronene (HBC) in the junction of the STM is modified by charge transfer complexes covalently attached to the HBC in the gap. Since the donor which complexes the covalently attached acceptor comes from the ambient fluid the set-up represents a single-molecule chemical field-effect transistor with nanometer-sized gates. This is considered a major step towards mono-molecular electronics.
Vogel, Jörn-Oliver. "Co-deposited films of rod-like conjugated molecules." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2009. http://dx.doi.org/10.18452/15978.
Повний текст джерелаThis thesis is centered on studies of phase separation and mixing in co-deposited thin films of rod-like conjugated molecules. The main focus is to determine which molecular properties lead to phase separation and/or mixing of two materials. To address this question I used five materials, of importance in the context of “organic electronics”: pentacene (PEN), quaterthiophene (4T), sexithiophene (6T), p-sexiphenylene (6P), alpha,omega-dihexylsexithiophene (DH6T). With these it was possible to form material pairs which differ in the parameters: energy levels, length of the conjugated core, and alkyl-end-chain-substitution. All films were deposited by organic molecular beam deposition onto the chemically inert substrates silicon oxide and Mylar, a polyethylene terephthalate (PET) foil. The material pairs were deposited simultaneously from two thermal sublima-tion sources. The mixing ratio was controlled by the individual deposition rates, which were measured online by a microbalance. The total deposition rate was 0.5 nm/min, and the film thicknesses ranged from 4 nm to 40 nm. Phase separation is observed for material pairs with dissimilar conjugated core sizes, i.e. [4T/6T]. Noteworthy, the co-deposition of material pairs with similarly sized conju-gated cores [4T/PEN] and [6T/6P] lead to well ordered layered structures. The mole-cules show mixing within layers on a molecular scale and the long molecular axis is ori-ented almost perpendicular to the substrate surface. Material pairs with similarly sized conjugated core and alkyl-end-chain-substitution [6T/DH6T] and [6P/DH6T] show also growth in mixed layered structures. An especially appealing fact is that the interlayer distance increases proportional to the DH6T content in the film. This can be explained with a phase separation into an aromatic and an alkyl domain vertically to the substrate surface. A decrease of the DH6T content in the film leads to a less dense packing in the alkyl domain. This leads, due to the flexibility of the alkyl chains, to a decrease of the overall interlayer distance. The low surface corrugation and the interconnected islands render the material pair [6T/DH6T] well suitable for the use as active layer in organic field effect transistors. It is shown that it is possible to tune the charge carrier density in the channel by changing the ratio between 6T and DH6T. This effect enables switching the transistor from en-hancement to depletion mode, while maintaining a high charge carrier mobility. This is comparable to p-type doping of inorganic semiconductors.
Samorí, Paolo. "Self-assembly of conjugated (macro)molecules nanostructures for molecular electronics /." [S.l. : s.n.], 2000. http://deposit.ddb.de/cgi-bin/dokserv?idn=962281530.
Повний текст джерелаWright, Helen. "Fused ring conjugated polymers and small molecules for organic-semiconductors." Thesis, University of Manchester, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542784.
Повний текст джерелаWiebeler, Christian [Verfasser]. "Photophysics and photochemistry of conjugated systems and photochromic molecules / Christian Wiebeler." Paderborn : Universitätsbibliothek, 2015. http://d-nb.info/1073201570/34.
Повний текст джерелаКниги з теми "Conjugated and cumulated molecules"
Pietila, Lars-Olof. Molecular mechanics and force field studies of weakly coupled conjugated molecules and molecular crystals. Helsinki: Societas Scientiarum Fennica, 1988.
Знайти повний текст джерелаEland, John H. D., and Raimund Feifel. Conjugated and aromatic molecules. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198788980.003.0006.
Повний текст джерелаDaudel, Raymond. Electronic Structure of Molecules: Diatomic Molecules, Small Molecules, Saturated Hydrocarbons, Conjugated Molecules, Molecules of Biochemical Interest. Elsevier Science & Technology Books, 2017.
Знайти повний текст джерелаChen, Pengle, та Bin Wu, ред. Functional Supramolecular Nanoassemblies of Π-Conjugated Molecules. Frontiers Media SA, 2020. http://dx.doi.org/10.3389/978-2-88963-360-9.
Повний текст джерелаGraovac, A., I. Gotman, and N. Trinajstic. Topological Approach to the Chemistry of Conjugated Molecules. Springer, 2012.
Знайти повний текст джерелаЧастини книг з теми "Conjugated and cumulated molecules"
Gutman, Ivan, and Oskar E. Polansky. "Thermodynamic Stability of Conjugated Molecules." In Mathematical Concepts in Organic Chemistry, 135–54. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-70982-1_13.
Повний текст джерелаDelysse, S., J. M. Nunzi, P. Raimond, and F. Kajzar. "Nonlinear Spectroscopy in Conjugated Molecules." In Electrical and Related Properties of Organic Solids, 339–58. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5790-2_20.
Повний текст джерелаYergey, Alfred L., Charles G. Edmonds, Ivor A. S. Lewis, and Marvin L. Vestal. "LC/MS of Conjugated Molecules." In Liquid Chromatography/Mass Spectrometry, 127–35. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3605-9_7.
Повний текст джерелаAkaike, Kouki, and Kaname Kanai. "Solar Cell Applications of π-Conjugated Molecules." In Physics and Chemistry of Carbon-Based Materials, 293–332. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-3417-7_10.
Повний текст джерелаSixl, H. "Electronic Structures of Conjugated Polydiacetylene Oligomer Molecules." In Springer Series in Solid-State Sciences, 240–45. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-82569-9_43.
Повний текст джерелаLesk, Arthur M. "Molecular Orbital Theory of Planar Conjugated Molecules." In Introduction to Symmetry and Group Theory for Chemists, 103–17. Dordrecht: Springer Netherlands, 2004. http://dx.doi.org/10.1007/1-4020-2151-8_11.
Повний текст джерелаHannah, Robert W., and Foil A. Miller. "Characteristic Frequencies of Molecules with Triple Bonds and Cumulated Double Bonds." In Course Notes on the Interpretation of Infrared and Raman Spectra, 85–99. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2004. http://dx.doi.org/10.1002/0471690082.ch4.
Повний текст джерелаMorley, J. O. "Design of Novel Conjugated Molecules with Large Hyperpolarizabilities." In Springer Proceedings in Physics, 86–97. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-93426-1_13.
Повний текст джерелаZhang, Fuji, and Huaien Li. "On maximal energy ordering of acyclic conjugated molecules." In Discrete Mathematical Chemistry, 385–92. Providence, Rhode Island: American Mathematical Society, 2000. http://dx.doi.org/10.1090/dimacs/051/29.
Повний текст джерелаCollard, David M. "π-Stacked Oligomers as Models for Semiconducting Conjugated Organic Materials". У π-Stacked Polymers and Molecules, 185–243. Tokyo: Springer Japan, 2013. http://dx.doi.org/10.1007/978-4-431-54129-5_4.
Повний текст джерелаТези доповідей конференцій з теми "Conjugated and cumulated molecules"
LERICHE, P., A. LELIÈGE, E. RIPAUD, V. JEUX, D. DEMETER, P. BLANCHARD, and J. RONCALI. "PHOTOVOLTAICS BASED ON SMALL CONJUGATED MOLECULES." In Proceedings of International Conference Nanomeeting – 2013. WORLD SCIENTIFIC, 2013. http://dx.doi.org/10.1142/9789814460187_0115.
Повний текст джерелаKotkov, Sergei Y., Victor N. Zadkov, Boris A. Grishanin, Valentin D. Vachev, and John H. Frederick. "Ultrafast dynamics of surface-adsorbed conjugated molecules." In SPIE's 1995 International Symposium on Optical Science, Engineering, and Instrumentation, edited by Janice M. Hicks, Wilson Ho, and Hai-Lung Dai. SPIE, 1995. http://dx.doi.org/10.1117/12.221484.
Повний текст джерелаKubo, Takashi, Mitsuya Aoba, Akihiro Shimizu, Yasukazu Hirao, Kozo Matsumoto, Hiroyuki Kurata, and Masayoshi Nakano. "Singlet open-shell character of conjugated Kekulé molecules." In INTERNATIONAL CONFERENCE OF COMPUTATIONAL METHODS IN SCIENCES AND ENGINEERING 2009: (ICCMSE 2009). AIP, 2012. http://dx.doi.org/10.1063/1.4771836.
Повний текст джерелаVleugels, Rick, Ward Brullot, and Thierry Verbiest. "Giant faraday rotation in conjugated, rod-like molecules." In SPIE Organic Photonics + Electronics, edited by Joy E. Haley, Jon A. Schuller, Manfred Eich, and Jean-Michel Nunzi. SPIE, 2016. http://dx.doi.org/10.1117/12.2235685.
Повний текст джерелаSPANO, F. C., та S. SIDDIQUI. "EXCITONS IN PINWHEEL AGGREGATES OF π-CONJUGATED MOLECULES". У Proceedings of the 10th Annual Symposium of the NSF Center. WORLD SCIENTIFIC, 2000. http://dx.doi.org/10.1142/9789812793294_0006.
Повний текст джерелаAktas, Bengu, Lokman Uzun, Deniz Hur, and Bora Garipcan. "Amino acid conjugated self assembly molecules modified Si wafers." In 2014 18th National Biomedical Engineering Meeting (BIYOMUT). IEEE, 2014. http://dx.doi.org/10.1109/biyomut.2014.7026352.
Повний текст джерелаWang, Hong X., Akira Takahashi, M. Hartmann, and Shaul Mukamel. "Quantum confinement and nonlinear optical response of conjugated molecules." In OE/LASE'93: Optics, Electro-Optics, & Laser Applications in Science& Engineering, edited by Shahab Etemad. SPIE, 1993. http://dx.doi.org/10.1117/12.148452.
Повний текст джерелаFrederick, John H., Valentin D. Vachev, and J. E. Hadder. "Simple models for excited-state dynamics of conjugated molecules." In Laser Applications in Life Sciences: 5th International Conference, edited by Pavel A. Apanasevich, Nikolai I. Koroteev, Sergei G. Kruglik, and Victor N. Zadkov. SPIE, 1995. http://dx.doi.org/10.1117/12.197471.
Повний текст джерелаVivas, M. G., L. De Boni та C. R. Mendonca. "Polarization-dependent two-photon absorption of π-conjugated molecules". У Frontiers in Optics. Washington, D.C.: OSA, 2010. http://dx.doi.org/10.1364/fio.2010.jwa10.
Повний текст джерелаBronstein, Hugo. "Open-shell conjugated small molecules and polymers for optoelectronics." In MATSUS Fall 2023 Conference. València: FUNDACIO DE LA COMUNITAT VALENCIANA SCITO, 2023. http://dx.doi.org/10.29363/nanoge.matsus.2023.321.
Повний текст джерелаЗвіти організацій з теми "Conjugated and cumulated molecules"
Spiegel, Yitzhak, Michael McClure, Itzhak Kahane, and B. M. Zuckerman. Characterization of the Phytophagous Nematode Surface Coat to Provide New Strategies for Biocontrol. United States Department of Agriculture, November 1995. http://dx.doi.org/10.32747/1995.7613015.bard.
Повний текст джерела