Добірка наукової літератури з теми "Au-catalyzed"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Au-catalyzed".
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 "Au-catalyzed"
Pung, Swee Yong, Chee Chee Tee, Kwang Leong Choy, and Xiang Hui Hou. "Growth Mechanism of Au-Catalyzed Zno Nanowires: VLS or VS-VLS?" Advanced Materials Research 364 (October 2011): 333–37. http://dx.doi.org/10.4028/www.scientific.net/amr.364.333.
Повний текст джерелаRodriguez, Jessica, Nicolas Adet, Nathalie Saffon-Merceron, and Didier Bourissou. "Au(i)/Au(iii)-Catalyzed C–N coupling." Chemical Communications 56, no. 1 (2020): 94–97. http://dx.doi.org/10.1039/c9cc07666b.
Повний текст джерелаReeves, Ryan D., Caitlin N. Kinkema, Eleanor M. Landwehr, Logan E. Vine, and Jennifer M. Schomaker. "Stereodivergent Metal-Catalyzed Allene Cycloisomerizations." Synlett 31, no. 06 (February 4, 2020): 627–31. http://dx.doi.org/10.1055/s-0037-1610746.
Повний текст джерелаShi, Min, and Qiang Wang. "Synthesis of Cyclic and Heterocyclic Compounds via Gold-Catalyzed Reactions." Synlett 28, no. 17 (July 27, 2017): 2230–40. http://dx.doi.org/10.1055/s-0036-1590827.
Повний текст джерелаЛещенко, Е. Д., та В. Г. Дубровский. "Моделирование профиля состава осевой гетероструктуры InSb/GaInSb/InSb в нитевидных нанокристаллах". Письма в журнал технической физики 48, № 19 (2022): 20. http://dx.doi.org/10.21883/pjtf.2022.19.53590.19339.
Повний текст джерелаLeshchenko E. D. and Dubrovskii V. G. "Modeling the compositional profiles across axial InSb/GaInSb/InSb nanowire heterostructures." Technical Physics Letters 48, no. 10 (2022): 17. http://dx.doi.org/10.21883/tpl.2022.10.54790.19339.
Повний текст джерелаBhunia, Sabyasachi, and Rai-Shung Liu. "Access to molecular complexity via gold- and platinum-catalyzed cascade reactions." Pure and Applied Chemistry 84, no. 8 (March 31, 2012): 1749–57. http://dx.doi.org/10.1351/pac-con-11-09-13.
Повний текст джерелаDubrovskii, V. G., N. V. Sibirev, Y. Berdnikov, U. P. Gomes, D. Ercolani, V. Zannier, and L. Sorba. "Length distributions of Au-catalyzed and In-catalyzed InAs nanowires." Nanotechnology 27, no. 37 (August 8, 2016): 375602. http://dx.doi.org/10.1088/0957-4484/27/37/375602.
Повний текст джерелаXu, Shao Hong. "Au-Catalyzed Homocoupling of Terminal Alkynes." Applied Mechanics and Materials 184-185 (June 2012): 900–903. http://dx.doi.org/10.4028/www.scientific.net/amm.184-185.900.
Повний текст джерелаAponick, Aaron, Chuan-Ying Li, and Berenger Biannic. "Au-Catalyzed Cyclization of Monoallylic Diols." Organic Letters 10, no. 4 (February 2008): 669–71. http://dx.doi.org/10.1021/ol703002p.
Повний текст джерелаДисертації з теми "Au-catalyzed"
Ma, Ruoyu. "Chiral NHC-Au(I) Catalyzed Enantioselective Reactions." Miami University / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=miami1585432603722902.
Повний текст джерелаYaguchi, Momo. "The Effect of Lattice Strain in Electrochemical Oxidations Catalyzed by Au-PdPt Core-shell Octahedral Nanoparticles." Thesis, Boston College, 2012. http://hdl.handle.net/2345/2928.
Повний текст джерелаPt-based alloy and core-shell nanoparticles have been intensively studied to regulate its size and shape. It has known that these nanoparticles show enhanced catalytic activity in various important fields such as heterogeneous catalysis, and electrochemical energy storage including fuel cells and metal-air batteries. Here, we report a facile hydrothermal synthesis of sub-10 nm PdPt alloy and sub-20 nm Au@PdPt core-shell structures. By using a mild reducing agent in aqueous solution, metal precursors are co-reduced. Specific gases are introduced during the synthesis to optimize the reaction conditions. The PdPt alloy and Au@PdPt core-shell nanostructures were characterized and confirmed by TEM, HRTEM, EDS, ICP-OES and XRD. The resulting PdPt and Au@PdPt particles are monodispersed single crystalline and octahedral shape enclosed by (111) facets. The electrocatalytic activity for the oxidation of formic acid was tested. It was found that the catalytic activity toward the formic acid oxidation of Au@PdPt core-shell particles were much higher than those of PdPt alloy particles. In addition, Pt-rich compositions were the most active in both PdPt alloy and Au@PdPt core-shell nanoparticles. Further studies on thinner alloy-shell core-shell nanoparticles reveal that there is a volcano-curve relationship between the lattice strain strength related to alloy-shell thickness and the catalytic performance. It is proposed that there are three key parameters that can determine the catalytic activity: the alloy composition, the presence of the gold core, and the thickness of alloy-shell
Thesis (MS) — Boston College, 2012
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Cera, Gianpiero <1985>. "Au(I) Catalyzed Manipulation of Propargylic Alcohols: A New Route Towards the Synthesis of Indole Alkaloids." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2014. http://amsdottorato.unibo.it/6417/1/Cera_Gianpiero_Tesi-1.pdf.
Повний текст джерелаIn questo lavoro di tesi abbiamo presentato diversi aspetti riguardanti la possibilità di utilizzare alcoli propargilici come precursori aciclici nello sviluppo di nuove reazioni a cascata stereoselettive [Au(I)] catalizzate per la sintesi di architetture indoliche altamente funzionalizzate. Alcoli propargilici su base indolica di tipo 1, sono stati utilizzati per sviluppare un processo a cascata per la sintesi di una nuova classe di indoline tetra cicliche, diidropiranilindoline A e furoindoline B. Un protocollo enantioselettivo è stato successivamente studiato per la sintesi di tali strutture con buone rese ed elevati eccessi enantiomerici. Diversi alcoli propargilici sono stati studiati nello sviluppare reazioni a cascata [Au(I)] catalizzate per la sintesi e funzionalizzazione di anelli indolici. Precursori su base anilinica di tipo 2, si sono rivelati essere precursori di eccellenza per la sintesi di [1,2-a]-azepino-indoli di tipo C. Nel descrivere quest’ultima reattività abbiamo riportato evidenze sperimentali di una nuova specie [Au(I)]-carbenica in grado di dirigere la chiusura dell’anello a sette termini in maniera altamente chemoselettiva. La flessibilità chimica degli alcoli propargilici è stata infine studiata cambiata la natura dell’intorno chimico con differenti gruppi N-alchilati in precursori di tipo 3. Utilizzando come catena un alcol primario, la selettività della reazione si è dimostrata completamente rivolta verso la sintesi della classe dei [4,3-a]-ossazino-indoli D, mentre utilizzando alcoli allilici abbiamo riportato il primo esempio di sintesi e funzionalizzazione enantioselettiva [Au(I)]catalizzata, di questa classe di molecole (D*). Concludendo, in questo lavoro abbiamo stabilito gli alcoli propargilici, essere precursori d’eccezione in reazioni a cascata Au(I) catalizzate riportando nuovi strumenti sintetici per la sintesi stereo selettiva di architetture indoliche ed indoliniche estremamente complesse.
Cera, Gianpiero <1985>. "Au(I) Catalyzed Manipulation of Propargylic Alcohols: A New Route Towards the Synthesis of Indole Alkaloids." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2014. http://amsdottorato.unibo.it/6417/.
Повний текст джерелаIn questo lavoro di tesi abbiamo presentato diversi aspetti riguardanti la possibilità di utilizzare alcoli propargilici come precursori aciclici nello sviluppo di nuove reazioni a cascata stereoselettive [Au(I)] catalizzate per la sintesi di architetture indoliche altamente funzionalizzate. Alcoli propargilici su base indolica di tipo 1, sono stati utilizzati per sviluppare un processo a cascata per la sintesi di una nuova classe di indoline tetra cicliche, diidropiranilindoline A e furoindoline B. Un protocollo enantioselettivo è stato successivamente studiato per la sintesi di tali strutture con buone rese ed elevati eccessi enantiomerici. Diversi alcoli propargilici sono stati studiati nello sviluppare reazioni a cascata [Au(I)] catalizzate per la sintesi e funzionalizzazione di anelli indolici. Precursori su base anilinica di tipo 2, si sono rivelati essere precursori di eccellenza per la sintesi di [1,2-a]-azepino-indoli di tipo C. Nel descrivere quest’ultima reattività abbiamo riportato evidenze sperimentali di una nuova specie [Au(I)]-carbenica in grado di dirigere la chiusura dell’anello a sette termini in maniera altamente chemoselettiva. La flessibilità chimica degli alcoli propargilici è stata infine studiata cambiata la natura dell’intorno chimico con differenti gruppi N-alchilati in precursori di tipo 3. Utilizzando come catena un alcol primario, la selettività della reazione si è dimostrata completamente rivolta verso la sintesi della classe dei [4,3-a]-ossazino-indoli D, mentre utilizzando alcoli allilici abbiamo riportato il primo esempio di sintesi e funzionalizzazione enantioselettiva [Au(I)]catalizzata, di questa classe di molecole (D*). Concludendo, in questo lavoro abbiamo stabilito gli alcoli propargilici, essere precursori d’eccezione in reazioni a cascata Au(I) catalizzate riportando nuovi strumenti sintetici per la sintesi stereo selettiva di architetture indoliche ed indoliniche estremamente complesse.
Charpenay, Mélanie. "Fenestradiènes et cyclooctatriènes : synthèse directe par réaction en cascade palladocatalysée." Phd thesis, Université de Strasbourg, 2012. http://tel.archives-ouvertes.fr/tel-00836869.
Повний текст джерелаZhang, Man. "Design, synthesis, and evaluation of bioactive molecules; Chiral polyvinylpyrrolidones supported Cu/Au nanoclusters catalyzed cyclization of 5-substituted nona-1,8-dien-5-ols." Diss., Kansas State University, 2017. http://hdl.handle.net/2097/35470.
Повний текст джерелаDepartment of Chemistry
Duy H. Hua
Small molecules are of great importance in drug discovery currently. The first three chapters discussed the design, synthesis and bio-evaluation of three different classes of small molecules and exploration of their biological targets. Triacsin C analogs were designed as long chain fatty acyl-CoA synthetase (ACSL) inhibitors for attenuating ischemia and reperfusion (I/R) injury. Oxadiazole derivatives were designed as T-type calcium channel inhibitors, which have potential application in the treatment of seizure and epilepsy. Tricyclic pyrone derivatives were reported as anti-Alzheimer lead compounds in previous research done by the Hua group. TP70 and CP2 were synthesized to explore their pharmacokinetics properties. Chapter 4 described chiral-substituted poly-N-vinylpyrrolidones (CSPVP) supported Cu/Au nanoclusters mediation of cyclization reaction of 5-substituted nona-1,8-dien-5-ols. A five-member cyclized lactone possessing a stereogenic tetrasubstituted carbon center was formed in a one-step Cu/Au nanoclusters-hydrogen peroxide oxidation reaction. This developed a novel and simple method to synthesize tetrasubstituted carbon stereogenic center. Drawbacks of the method in my initial study were low reaction yield and moderate enantioselectivity. The chemical yield and enantioselectivity have been significantly improved by introducing bulkier substitution in C3 and C4 positions of CSPVP according to the updates of ongoing research.
Li, Jihui. "Copper-Catalyzed Domino C-N Bond Formation for Synthesis of N-Containing Compounds (Benzimidazoles, Imidazoles, and Guanidines) - Approach toward Total Synthesis of Natural Product Raputindoles." Thesis, Paris 11, 2013. http://www.theses.fr/2013PA112130.
Повний текст джерелаThis thesis consists in three parts: bibliographic background, copper-catalyzed reactions for synthesis of N-containing compounds, approach to the synthesis of raputindoles.The first part introduces the domino reactions and their applications, then, copper-mediated reactions for construction of C-N bond formation are reviewed including Ullmann, Goldberg and Chan-Lam coupling, oxidative C-H activation/C-N formation, insertion of nitrenes and carbenoids, and hydroamination of multi-C-C bonds. This can be used as guides to design domino reaction. Following these copper-mediated single C-N bond formation reactions, recent developments of copper-catalyzed domino reactions for synthesis of heterocycles are described.The second part can be divided into three sections: 1) synthesis of benzimidazoles, 2) synthesis of imidazoles and 3) synthesis of guanidines. Each section summarizes the existing methods used for their synthesis. Following it, our synthetic work involving copper-catalyzed C-N bond formation domino reactions is discussed in detail. Our objectives include the synthesis of benzimidazoles through copper-catalyzed sequential reaction of benzamidines and boronic acids, synthesis of imidazoles via copper-catalyzed domino reaction of benzamidines and acetylenes, and synthesis of guanidines and 2-aminobenzimidazoles by Cu-catalyzed three-component reaction of cyanamides, boronic acids and amines. These copper-catalyzed domino reactions show high efficiencies from readily available and simple starting materials.The last part is about the total synthesis of raputindoles. The structure and bioactivities of raputindoles and key reactions for the total synthesis of raputindoles are introduced first, the synthetic strategies are then proposed on basis of relative synthetic methods. The key reactions we use for the synthesis of raputindoles are iridium catalyzed [3+2] annulation of o-formylarylboronic acids and 1,3-dienes, Leimgruber-Batcho indole synthesis, transition-metal catalyzed SN2 substitution and alkylborylation-protondeborylation. According to the three strategies we proposed, lots of relative reactions were investigated. The results show that it is possible to synthesize the raputindole molecules based on the iridium catalyzed [3+2] annulation of 2-formylarylboronic acids and 1,3-dienes
Gomes, Umesh Prasad. "Catalyst-assisted and catalyst-free growth of III-V semiconductor nanowires." Doctoral thesis, Scuola Normale Superiore, 2017. http://hdl.handle.net/11384/85884.
Повний текст джерелаZhou, Edouard. "Nouveaux systèmes catalytiques appliqués aux formations de liaisons C—C par couplage croisé catalysé par des sels de fer : applications, mécanismes." Thesis, Paris Sciences et Lettres (ComUE), 2018. http://www.theses.fr/2018PSLEC008.
Повний текст джерелаJabeen, Fauzia. "III-V semiconducting nanowires by molecular beam epitaxy." Doctoral thesis, Università degli studi di Trieste, 2009. http://hdl.handle.net/10077/3097.
Повний текст джерелаThis thesis is devoted to the study of the growth of III-V nanowires (NWs) by catalyst assisted and catalyst free molecular beam epitaxy (MBE). The nanostructures have been routinely characterized by scanning electron microscopy (SEM) and, to a minor extent by transmission electron microscopy (TEM). X-ray photoemission spectroscopy (XPS), scanning photoemission microscopy (SPEM), extended X-ray absrorption fi ne structure analysis (EXAFS), photoluminescence (PL) and trans- port measurements have given an important contribution on specifi c topics. The first section of this thesis reports on GaAs, InAs, and InGaAs NWs growth by Au assisted MBE. A substrate treatment is proposed that improves uniformity in the NWS morphology. Thanks to a careful statistical analysis of the NWs shape and dimensions as a function of growth temperature and duration, evidence is found of radial growth of the NWs taking place together with the axial growth at the tip. This eff ect is interpreted in term of temperature dependent diff usion length of the cations on the NWs lateral surface. The control of the NWs radial growth allowed to grow core shell InGaAs/GaAs NWs, displaying superior optical quality. A new procedure is proposed to protect NWs surface from air exposure. This procedure allowed to perform ex-situ SPEM studies of electronic properties of the NWs. The second part of this thesis is devoted to Au-free NWs growth. GaAs and InAs NWs were successfully grown for the first time using Mn as catalyst. Incorporation of Mn in the NW is studied using EXAFS technique. It is shown that Mn atoms are incorporated in the body of GaAs NWs. Use of low growth temperature is suggested in order to improve the Mn incorporation inside GaAs NWs and obtain NWs with magnetic properties. Finally, growth of GaAs and InAs NWs on cleaved Si subtrate is demonstrated without the use of any outside metal catalyst. Two kinds of nanowires have been obtained. The experimental findings suggest that the two types of nanowires grow after di fferent growth processes.
Questa tesi e' dedicata allo studio della crescita di nanofili di semiconduttori III- V tramite epitassia da fasci molecolari (MBE) assistita da catalizzatore e senza l'uso di catalizzatori. Le nanostrutture sono state caratterizzate sistematicamente tramite microscopia elettronica a scansione (SEM), e in maniera minore microscopia elettronica in trasmissione (TEM). Altre tecniche come la spettroscopia di fotoemissione da raggi x (XPS), la microscopia da fotoemissione in scansione (SPEM), la spettroscopia di assorbimento x (in particolare la extended X-ray absorpition fine structure analysis (EXAFS)) la fotoluminescenza (PL), e il trasporto elettrico hanno dato importanti contributi su problematiche specifiche. La prima parte di questa tesi riguarda la crescita di nanofili di GaAs, InAs e InGaAs tramite MBE assistita da oro. Viene proposto un trattamento del substrato che migliora nettamente l'omogeneita' morfologica dei nanofili. Grazie ad un'attenta analisi statistica della forma e delle dimensioni dei nanofili in funzione della temperatura e del tempo di crescita e' stata dimostrata la crescita radiale dei nanofili, che avviene insieme alla crescita assiale che ha luogo alla punta del nanofilo. Le osservazioni sperimentali sono state interpretate in termini di dipendenza dalla temperatura della lunghezza di diffusione dei cationi sulle super ci laterali dei nanofili. Il controllo della crescita radiale ha permesso di crescere nanofili di InGaAs/GaAs core shell, costituiti cioe' da una anima centrale di InGaAs (core) e uno strato esterno di GaAs (shell) , che hanno dimostrato eccellente qualita' ottica. Viene quindi proposta una nuova procedura per proteggere la super ficie dei nanofili durante l'esposizione all'aria. Grazie a questa e' stato possibile realizzare ex-situ uno studio SPEM delle proprieta' elettroniche dei nanofili. La seconda parte della tesi riguarda la crescita di nanofili senza l'uso di oro. Viene per la prima volta dimostrata la possibilita' di crescere nanofili di GaAs e InAs usando il manganese come catalizzatore. L'incorporazione del Mn come impurezza nei nanofili e' stata studiata tramite EXAFS. Le misure hanno dimostrato che atomi di Mn sono effettivamente incorporate nel corpo dei nano fili. La crescita delle nanostrutture a temperatura piu' bassa potrebbe migliorare qualitativamente l'incorporazione del Mn e permettere la crescita di nanofili con proprieta' magnetiche. Viene in fine dimostrata la crescita di nanofili di GaAs e di InAs senza l'utilizzo di materiali diversi da quelli costituenti il semiconduttore. Tale risultato e' ottenuto su superfici sfaldate di silicio. Sono state osservate nanostrutture di due tipi, che sulla base dei dati sperimentali sembrano essere dovuti a due diversi meccanismi di crescita.
XXI Ciclo
1977
Книги з теми "Au-catalyzed"
Bandini, Marco, ed. Au-Catalyzed Synthesis and Functionalization of Heterocycles. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-35144-5.
Повний текст джерелаSoriano, Elena, and José Marco-Contelles, eds. Computational Mechanisms of Au and Pt Catalyzed Reactions. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-21083-9.
Повний текст джерелаElena, Soriano, José Marco-Contelles, and B. Alcaide. Computational mechanisms of Au and Pt catalyzed reactions. Heidelberg: Springer, 2011.
Знайти повний текст джерелаBandini, Marco. Au-Catalyzed Synthesis and Functionalization of Heterocycles. Springer London, Limited, 2016.
Знайти повний текст джерелаBandini, Marco. Au-Catalyzed Synthesis and Functionalization of Heterocycles. Springer International Publishing AG, 2016.
Знайти повний текст джерелаBandini, Marco. Au-Catalyzed Synthesis and Functionalization of Heterocycles. Springer, 2018.
Знайти повний текст джерелаSoriano, Elena, and José Marco-Contelles. Computational Mechanisms of Au and Pt Catalyzed Reactions. Springer, 2013.
Знайти повний текст джерелаSoriano, Elena, and José Marco-Contelles. Computational Mechanisms of Au and Pt Catalyzed Reactions. Springer, 2011.
Знайти повний текст джерелаЧастини книг з теми "Au-catalyzed"
Xiao, Yuanjing, and Junliang Zhang. "Au- and Pt-Catalyzed CH Activation/Functionalizations for the Synthesis of Heterocycles." In Transition Metal-Catalyzed Heterocycle Synthesis via CH Activation, 359–402. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527691920.ch12.
Повний текст джерелаLiu, Zhiming, and Wenjian Wu. "COMPLEX OXIDATION OF TMB CATALYZED WITH PEROXIDASE-LIKE AU NANOPARTICLES." In Nanociências e Nanotecnologia: Pesquisa e Aplicações, 87–97. Editora Artemis, 2022. http://dx.doi.org/10.37572/edart_2908226686.
Повний текст джерелаTaber, Douglass F. "The Trost Synthesis of Bryostatin 16." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0099.
Повний текст джерелаTaber, Douglass F. "Organic Functional Group Protection and Deprotection." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0016.
Повний текст джерелаTaber, Douglass F. "Heteroaromatic Synthesis: The Tokuyama Synthesis of (−)-Rhazinilam." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0066.
Повний текст джерелаTaber, Douglass. "Preparation of Heteroaromatic Derivatives." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0067.
Повний текст джерелаKnochel, P. "Palladium-Catalyzed Acylation." In Compounds of Groups 12 and 11 (Zn, Cd, Hg, Cu, Ag, Au), 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-003-00088.
Повний текст джерелаKnochel, P. "Copper-Catalyzed Reactions." In Compounds of Groups 12 and 11 (Zn, Cd, Hg, Cu, Ag, Au), 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-003-00116.
Повний текст джерелаZhang, L. "Gold-Catalyzed Propargylic Rearrangements." In Compounds of Groups 12 and 11 (Zn, Cd, Hg, Cu, Ag, Au), 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-103-00017.
Повний текст джерелаZhang, L. "Gold-Catalyzed Oxidative Homocoupling." In Compounds of Groups 12 and 11 (Zn, Cd, Hg, Cu, Ag, Au), 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-103-00030.
Повний текст джерелаТези доповідей конференцій з теми "Au-catalyzed"
Pung Swee Yong, Choy Kwang Leong, and Hou Xianghui. "Growth of Au-catalyzed and self-catalyzed ZnO nanowires using chemical vapor deposition technique." In 2010 International Conference on Enabling Science and Nanotechnology (ESciNano). IEEE, 2010. http://dx.doi.org/10.1109/escinano.2010.5700937.
Повний текст джерелаBerdnikov, Yury, Nikolay Sibirev, Jan Schmidtbauer, Mattias Borg, Jonas Johansson, and Vladimir Dubrovskii. "Broadening of length distributions of Au-catalyzed InAs nanowires." In MEDICAL PHYSICS: Fourteenth Mexican Symposium on Medical Physics. Author(s), 2016. http://dx.doi.org/10.1063/1.4954353.
Повний текст джерелаZou, Yichao, Zhi-Gang Chen, Yang Huang, John Drennan, and Jin Zou. "Au-catalyzed and catalyst-free growth of one-dimensional Bi2Se3 nanostructures." In 2014 Conference on Optoelectronic and Microelectronic Materials & Devices (COMMAD). IEEE, 2014. http://dx.doi.org/10.1109/commad.2014.7038638.
Повний текст джерелаPaiman, S., Q. Gao, H. J. Joyce, H. H. Tan, C. Jagadish, Y. Kim, Y. Guo, and J. Zou. "Au-catalyzed InP nanowires: The influence of growth temperature and V/III ratio." In Devices (COMMAD). IEEE, 2010. http://dx.doi.org/10.1109/commad.2010.5699767.
Повний текст джерелаYao, Luchi, Xiaohao Zhou, and Xiaoshuang Chen. "Configurations of nuclei in Au-catalyzed Si nanowire growth: a first-principles study." In Eighth International Symposium on Advanced Optical Manufacturing and Testing Technology (AOMATT2016), edited by Xiangang Luo, Tianchun Ye, Tingwen Xin, Song Hu, Minghui Hong, and Min Gu. SPIE, 2016. http://dx.doi.org/10.1117/12.2242625.
Повний текст джерелаZhou Zhang, Lai Mun Wong, Shijie Wang, and Tom Wu. "Si substrate controlled in-plane synthesis of self-assembled nanostructures catalyzed by Au nanoparticles." In 2010 IEEE 3rd International Nanoelectronics Conference (INEC). IEEE, 2010. http://dx.doi.org/10.1109/inec.2010.5424568.
Повний текст джерелаSolorio Alvarado, Cesar, Dipak Patil, María del Gamez Montano, and Marco Ramirez Morales. "SYNTHESIS OF BENZO[<em>b</em>]CARBAZOLS BY TANDEM Au(I)-CATALYZED CYCLIZATION/MIGRATION/CYCLIZATION." In The 24th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08402.
Повний текст джерела