Bibliografías temáticas / Heteroatomic1

Literatura académica sobre el tema "Heteroatomic1"

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Publicado: 6 de septiembre de 2023

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Artículos de revistas sobre el tema "Heteroatomic1"

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Lin, Jin-Yi, Bin Liu, Meng-Na Yu, Chang-Jin Ou, Zhen-Feng Lei, Feng Liu, Xu-Hua Wang et al. "Understanding the molecular gelation processes of heteroatomic conjugated polymers for stable blue polymer light-emitting diodes". Journal of Materials Chemistry C 5, n.º 27 (2017): 6762–70. http://dx.doi.org/10.1039/c7tc01541k.

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Ovchinnikov, V. V., L. R. Khazieva, L. I. Lapteva y A. I. Konovalov. "Thermochemistry of heteroatomic compounds". Russian Chemical Bulletin 49, n.º 1 (enero de 1990): 33–38. http://dx.doi.org/10.1007/bf02499061.

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Ovchinnikov, V. V., T. B. Makeeva, L. I. Lapteva, V. A. Valiullina, L. M. Pilishkina y A. I. Konovalov. "Thermochemistry of heteroatomic compounds". Journal of Thermal Analysis 45, n.º 4 (octubre de 1995): 735–39. http://dx.doi.org/10.1007/bf02548889.

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Ovchinnikov, V. V., L. I. Lapteva, E. Yu Sitnikova y A. I. Konovalov. "Thermochemistry of heteroatomic compounds". Russian Chemical Bulletin 49, n.º 9 (septiembre de 2000): 1522–25. http://dx.doi.org/10.1007/bf02495153.

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Ovchinnikov, V. V., L. I. Lapteva y M. G. Kireev. "Thermochemistry of heteroatomic compounds". Russian Chemical Bulletin 53, n.º 8 (agosto de 2004): 1761–62. http://dx.doi.org/10.1007/s11172-005-0031-z.

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Zhang, Kai, Benjamin B. Noble, Adam C. Mater, Michael J. Monteiro, Michelle L. Coote y Zhongfan Jia. "Effect of heteroatom and functionality substitution on the oxidation potential of cyclic nitroxide radicals: role of electrostatics in electrochemistry". Physical Chemistry Chemical Physics 20, n.º 4 (2018): 2606–14. http://dx.doi.org/10.1039/c7cp07444a.

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Roy, Matthew M. D., Michael J. Ferguson, Robert McDonald, Yuqiao Zhou y Eric Rivard. "A vinyl silylsilylene and its activation of strong homo- and heteroatomic bonds". Chemical Science 10, n.º 26 (2019): 6476–81. http://dx.doi.org/10.1039/c9sc01192g.

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Lv, Jing-Hui, Xian-Yong Wei, Ying-Hua Wang, Tie-Min Wang, Jing Liu, Dong-Dong Zhang y Zhi-Min Zong. "Characterization of condensed aromatics and heteroatomic species in Yanshan petroleum coke through ruthenium ion-catalyzed oxidation using three mass spectrometers". RSC Advances 6, n.º 66 (2016): 61758–70. http://dx.doi.org/10.1039/c6ra09194f.

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Chen, Jiazhi, Fang Lu y Jie Xu. "Formation of uniform hollow nanocages with heteroatom-doped MCM-41 structures". RSC Advances 5, n.º 7 (2015): 5068–71. http://dx.doi.org/10.1039/c4ra13959c.

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Li, Caixia, Shihua Dong, Rui Tang, Xiaoli Ge, Zhiwei Zhang, Chengxiang Wang, Yupeng Lu y Longwei Yin. "Heteroatomic interface engineering in MOF-derived carbon heterostructures with built-in electric-field effects for high performance Al-ion batteries". Energy & Environmental Science 11, n.º 11 (2018): 3201–11. http://dx.doi.org/10.1039/c8ee01046c.

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Tesis sobre el tema "Heteroatomic1"

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Hilmey, David George. "Synthesis and study of heteroatomic spirocyclic scaffolds". Columbus, Ohio : Ohio State University, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1141334542.

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Shen, Chengshuo. "Heteroatomic and organometallic helicenes : synthesis and chiroptical properties". Thesis, Rennes 1, 2015. http://www.theses.fr/2015REN1S159.

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Mes travaux de thèse se sont portés sur la synthèse d'hélicènes organométalliques et hétéroatomiques, et se divisent suivant trois axes majeurs. Le premier sujet est l'étude des hélicènes avec un centre métallique redox. Nous avons introduit un motif chimique contenant un atome de fer sur l'hélicène connecté par une liaison C≡C. Dans ce sujet, nous avons étudié les propriétés chiroptiques avec le changement d'état redox du centre métallique. Pour cela, nous avons utilisé des techniques spectroscopiques chiroptiques comme le dichroïsme circulaire vibrationnel, le spectre d'activité optique Raman qui opèrent dans la région infrarouge. Le deuxième sujet est l'étude d'hélicènes avec un centre rédox et un centre photochrome. Nous avons introduit l'hélicène sur un bloc chimique contenant du ruthénium connecté par liaison une C≡C, puis introduit le motif photochrome DTE (dithiényléthène) sur le ruthénium. La molécule contient donc trois parties : un centre chiral, un centre rédox et un centre photochrome. Dans ce sujet, nous avons étudié l'activité d'interrupteur chiroptique provoquée par un stimulus redox et/ou par la lumière. Le troisième sujet est l'étude de platinahélicènes et de borahélicènes qui sont issus de l'incorporation d'un ou deux platinacycles ou cycles azaboroles dans le squelette de l'hélicène. Dans ce sujet, nous avons examiné les propriétés optiques et chiroptiques, et étudié l'influence du nombre de cycles et du nombre d'hétérocycles. Ces produits ont également révélé des propriétés d'émission et de la luminescence polarisée circulairement
My PhD work has focused on the synthesis of organometallic and heteroatomic helicenes and is separated into three subjects. The first subject is the study of helicene with one redox metal center. We have introduced a building block containing an iron atom on the helicene connected by a C≡C bond. In this subject, we have studied the chiroptical properties with the change of the redox state of the metal center. Besides, we have used the techniques of chiroptical spectroscopies such as the vibrational circular dichroism, the Raman optical activity which occur in the infrared region. The second subject is the study of helicenes with one redox center and one photochromic center. We have introduced the helicene on the ruthenium building block, and then introduced a photochromic unit DTE (dithienylethene) on the ruthenium through C≡C bonds. This molecule contains three parts: one chiral center, one redox center and one photochromic center. In this subject, we have studied the redox- and/or light-triggered chiroptical switching activity. The third subject is the study on the platinahelicenes and borahelicenes which show one or two platinacycles or azaborole cycles incorporated in the helicene skeleton. In this subject, we have studied the optical and chiroptical properties, and also studied the influence of the number of cycles and number of the heterocycles. These compounds are also studied in the emission properties and circularly polarized luminescence
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Ratcliffe, Giles Stuart. "NMR of heteroatomic structures of coal and coal products". Thesis, University of Warwick, 1988. http://wrap.warwick.ac.uk/107456/.

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This thesis describes various applications of high field n.m.r. for the elucidation of coal structure, and concentrates on discovering the chemical environments of the heteroatoms in coal i.e. those elements other than carbon and hydrogen. Chapter 2 describes how hydroxyl groups may be converted to trimethyl siloxyl groups, observation of which by 29si n.m.r. allows one to determine the types of hydroxyl functionalities present in the original material. Such derivatization methods are well known. However trimethyl siloxyl groups give 29si resonances that have predictable chemical shifts and so the derivative spectra of complex coal tars and extracts are easy to interpret. Using this technique we have investigated the nature of hydroxyl groups in a rank series of coal tars. This has given us some insight into the way the hydroxyls are affected by coalification. Chapter 3 is a demonstration of the use of n.m.r. as a detector for H.P.L.C. This has two principle novelties over previous work. Firstly it does not involve building a special probe and secondly, the data is presented as a contour plot of intensity vs. retention time and chemical shift. This method has been used to investigate the nature of several tar fractions and complements the derivatization technique of chapter 2. The final chapter shows how the nature of sodium in coal was determined by 23Na MAS-NMR. By using the information contained in the chemical shift and linewidths of raw and dried coal it was concluded that sodium exists bound to the surface of coal pores by oxygen functions such as carboxylates and phenoxides. It does not exist as sodium chloride microcrystals as once thought.
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Aoki, Dan. "Functional Developments of Cellulose Derivatives by Heteroatomic Modification and Multicomposition". Kyoto University, 2011. http://hdl.handle.net/2433/152019.

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Kyoto University (京都大学)
0048
新制・課程博士
博士(農学)
甲第16412号
農博第1897号
新制||農||994(附属図書館)
学位論文||H23||N4637(農学部図書室)
29043
京都大学大学院農学研究科森林科学専攻
(主査)教授 西尾 嘉之, 教授 木村 恒久, 教授 髙野 俊幸
学位規則第４条第１項該当
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Mulhall, Steven Eric. "I. Rearrangements of beta-heteroatomic carbenes ; II. Chemistry of 2-tert-butyl-4-diazobenzopyran /". The Ohio State University, 1989. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487675687173776.

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Reuter, Kirsten [Verfasser] y Carsten von [Akademischer Betreuer] Hänisch. "Synthesis of Disila-Crown Ether Complexes and Heteroatomic Bridged Paracyclophanes / Kirsten Reuter ; Betreuer: Carsten von Hänisch". Marburg : Philipps-Universität Marburg, 2017. http://d-nb.info/1131253302/34.

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Fix, Aaron. "Synthesis and Properties of Indenofluorene and Diindenothiophene Derivatives for Use as Semiconducting Materials in Organic Electronic Devices". Thesis, University of Oregon, 2013. http://hdl.handle.net/1794/13444.

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Organic electronic devices are becoming commonplace in many academic and industrial materials laboratories, and commercial application of these technologies is underway. To maximize our fundamental understanding of organic electronics, a wide array of molecular frameworks is necessary, as it allows for a variety of optical and electronic properties to be systematically investigated. With the ability to further tune each individual scaffold via derivatization, access to a broad spectrum of interesting materials is possible. Of particular interest in the search for organic semiconducting materials are the cyclopenta-fused polyaromatic hydrocarbons, including those based on the fully conjugated indenofluorene (IF) system, which is comprised of five structural isomers. This dissertation represents my recent contributions to this area of research. Chapter I serves as a historical perspective on early indenofluorene research and a review of more current research on their synthesis and applications in organic electronic devices. Chapters II and III cover our early work developing the synthesis of the fully-reduced indeno[1,2-b]fluorene scaffold, with the latter of these chapters showing the first example of its application in an organic electronic device, a field effect transistor. Chapter IV demonstrates the first syntheses of fully-reduced indeno[2,1-c]fluorene derivatives. Chapter V expands our research to encompass isoelectronic heteroatomic derivatives of that same scaffold, introducing the fully-reduced diindeno[2,1-b:1',2'-d]thiophene scaffold and showing that our synthetic methodology also can be used to produce a quinoidal thiophene core. Chapter VI concludes with a review of the similarities between the indeno[2,1-c]fluorene and diindeno[2,1-b:1',2'-d]thiophene molecular architectures and introduces benzo[a]indeno[2,1-b]fluorene derivatives, demonstrating the first example of a fully-reduced indenofluorene that possesses a non-quinoidal core, illustrating that the quinoidal core is not a prerequisite for the strong electron affinities seen across the families of fully-reduced indenofluorenes. This dissertation encompasses previously published and unpublished co-authored material.
2015-10-10
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Waibel, Markus [Verfasser], Thomas F. [Akademischer Betreuer] Fässler, Kai-Olaf [Akademischer Betreuer] Hinrichsen y Klaus [Akademischer Betreuer] Köhler. "Investigations on the Reactivity of Homo- and Heteroatomic Group 14 Zintl Ions / Markus Waibel. Gutachter: Thomas F. Fässler ; Kai-Olaf Hinrichsen ; Klaus Köhler. Betreuer: Thomas F. Fässler". München : Universitätsbibliothek der TU München, 2012. http://d-nb.info/105843456X/34.

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Gurkin, Joshua Taylor. "Synthesis and characterization of ruthenium(II) and platinum(IV) complexes with anionic heteroatomic ligands". 2009. http://www.lib.ncsu.edu/theses/available/etd-08102009-205055/unrestricted/etd.pdf.

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Feng, Yuee. "Synthesis and reactivity of ruthenium and platinum complexes with non-dative heteroatomic ligands studies of carbon-hydrogen bond activation /". 2007. http://www.lib.ncsu.edu/theses/available/etd-12132007-121728/unrestricted/etd.pdf.

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Libros sobre el tema "Heteroatomic1"

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Reineccius, Gary A. y Terry A. Reineccius, eds. Heteroatomic Aroma Compounds. Washington, DC: American Chemical Society, 2002. http://dx.doi.org/10.1021/bk-2002-0826.

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Gary, Reineccius, Reineccius Terry A. 1961-, American Chemical Society. Division of Agricultural and Food Chemistry y American Chemical Society Meeting, eds. Heteroatomic aroma compounds. Washington, D.C: American Chemical Society, 2002.

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Ligand coupling reactions with heteroatomic compounds. New York: Pergamon, 1998.

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Ratcliffe, Giles Stuart. NMR of heteroatomic structures of coal and coal products. [s.l.]: typescript, 1988.

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Block, Eric. Heteroatomic Chemistry. Wiley-VCH, 1990.

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Ligand Coupling Reactions with Heteroatomic Compounds. Elsevier, 1998. http://dx.doi.org/10.1016/s1460-1567(98)x8001-3.

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(Editor), Gary A. Reineccius y Terry A. Reineccius (Editor), eds. Heteroatomic Aroma Compounds (Acs Symposium Series). An American Chemical Society Publication, 2002.

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Finet. Ligand Coupling Reactions with Heteroatomic Compounds. Elsevier Science & Technology Books, 1998.

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Finet. Ligand Coupling Reactions with Heteroatomic Compounds. Elsevier Science & Technology Books, 1998.

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Chandrasekhar, Sosale. Rearrangements with Migration to Electrophilic Heteroatomic Centers: Timeless Classics in Organic Synthesis. Elsevier, 2022.

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Capítulos de libros sobre el tema "Heteroatomic1"

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Mustafa, Ahmed. "Photochemical Reactions of Sulfur and Nitrogen Heteroatomic Organic Compounds". En Advances in Photochemistry, 63–136. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470133323.ch3.

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Kharlamova, Ganna, Oleksii Kharlamov, Marina Bondarenko, Nadezhda Gubareni y Veneamin Fomenko. "Hetero-Carbon: Heteroatomic Molecules and Nano-structures of Carbon". En NATO Science for Peace and Security Series B: Physics and Biophysics, 339–57. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-7003-4_31.

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Buettner, A., A. Beer, C. Hannig, M. Settles y P. Schieberle. "Quantitation of the In-Mouth Release of Heteroatomic Odorants". En ACS Symposium Series, 296–311. Washington, DC: American Chemical Society, 2002. http://dx.doi.org/10.1021/bk-2002-0826.ch019.

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Arenal, Raul y Annick Loiseau. "Heteroatomic Single-Wall Nanotubes Made of Boron, Carbon, and Nitrogen". En B-C-N Nanotubes and Related Nanostructures, 45–81. New York, NY: Springer New York, 2009. http://dx.doi.org/10.1007/978-1-4419-0086-9_3.

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Nagy, Sandor M., Mark P. Mack y Gregory G. Hlatky. "Modeling and Catalytic Performance of Group 4 Metal Complexes with Anionic Heteroatomic Ligands". En ACS Symposium Series, 76–85. Washington, DC: American Chemical Society, 2003. http://dx.doi.org/10.1021/bk-2003-0857.ch006.

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Kharlamov, O., M. Bondarenko, G. Kharlamova, P. Silenko, O. Khyzhun y N. Gubareni. "Carbon Nitride Oxide (g-C3N4)O and Heteroatomic N-Graphene (Azagraphene) as Perspective New Materials in CBRN Defense". En NATO Science for Peace and Security Series A: Chemistry and Biology, 279–92. Dordrecht: Springer Netherlands, 2018. http://dx.doi.org/10.1007/978-94-024-1304-5_20.

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Longfils, G., F. Ooms, J. Wouters, A. Olivier, M. Sevrin, P. George y F. Durant. "A Comparison of AB Initio, Semi-Empirical, and Molecular Mechanics Approaches to Compute Molecular Geometries and Electrostatic Descriptors of Heteroatomic Ring Fragments Observed in Drugs Molecules". En Molecular Modeling and Prediction of Bioactivity, 482–83. Boston, MA: Springer US, 2000. http://dx.doi.org/10.1007/978-1-4615-4141-7_129.

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Merino, P. "With Heteroatomic Multiple Bonds". En Heteroatom Analogues of Aldehydes and Ketones, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-027-00468.

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Inokuma, T. y Y. Takemoto. "Addition of Heteroatomic Compounds". En Brønsted Base and Acid Catalysts, and Additional Topics, 1. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-205-00330.

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Liu, R. H., M. G. Legendre, J. W. Kuan, A. J. St. Angelo y J. R. Vercellotti. "HETEROATOMIC COMPOUNDS ASSOCIATED WITH BEEF FLAVOR". En Warmed-over Flavor of Meat, 193–236. Elsevier, 1987. http://dx.doi.org/10.1016/b978-0-12-661605-7.50011-7.

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Actas de conferencias sobre el tema "Heteroatomic1"

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Obukhov, Alexandr E. "Excited electronic states of complex heteroatomic molecules in series and in different aggregation states of matter". En Laser Applications in Life Sciences: 5th International Conference, editado por Pavel A. Apanasevich, Nikolai I. Koroteev, Sergei G. Kruglik y Victor N. Zadkov. SPIE, 1995. http://dx.doi.org/10.1117/12.197452.

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Potapenko, O. V., T. V. Bobkova, P. V. Lipin, E. O. Altinkovich, K. S. Plekhova, T. P. Sorokina y V. P. Doronin. "Intermolecular hydrogen transfer reactions during the hydrocarbons conversion in the presence of heteroatomic compounds on zeolite-containing catalysts". En 21ST CENTURY: CHEMISTRY TO LIFE. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5122907.

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Krasnoyarova, Natalya A., Olga V. Serebrennikova y Ekaterina V. Kul’chakovskaya. "Laws of distribution of hydrocarbon and heteroatomic compounds in the dispersed organic matter of rocks of north of Western Siberia". En PROCEEDINGS OF THE INTERNATIONAL CONFERENCE ON ADVANCED MATERIALS WITH HIERARCHICAL STRUCTURE FOR NEW TECHNOLOGIES AND RELIABLE STRUCTURES 2019. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5132048.

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Informes sobre el tema "Heteroatomic1"

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Yoshida, T., P. D. Chantal y H. Sawatzky. Characterization of heteroatomic compounds in various synthetic crude naphthas. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1987. http://dx.doi.org/10.4095/302691.

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