Relevant bibliographies by topics / Self-assembly of Organic Nanostructures

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Self-assembly of Organic Nanostructures'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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Journal articles on the topic "Self-assembly of Organic Nanostructures"

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Maerz, Andrew K., Drew A. Fowler, Andrew V. Mossine, et al. "Solvent mediated self-assembly of organic nanostructures." New Journal of Chemistry 35, no. 4 (2011): 784. http://dx.doi.org/10.1039/c1nj00005e.

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Mandal, Dindyal, Amir Nasrolahi Shirazi, and Keykavous Parang. "Self-assembly of peptides to nanostructures." Org. Biomol. Chem. 12, no. 22 (2014): 3544–61. http://dx.doi.org/10.1039/c4ob00447g.

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The formation of well-ordered nanostructures through self-assembly of diverse organic and inorganic building blocks has drawn much attention owing to their potential applications in biology and chemistry.
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Mi, Yong Sheng, Zhou Yang, Dong Wang, Peng Xia Liang, and Zhao Kui Jin. "Self-Assembly Micro-Nanostructures of Discotic Organic Molecules." Applied Mechanics and Materials 331 (July 2013): 567–71. http://dx.doi.org/10.4028/www.scientific.net/amm.331.567.

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A series of discotic organic molecules with different substituents have been successfully synthesized. The structures of these compounds were fully characterized by 1H-NMR, FT-IR and MS. Their optical and electrical properties were investigated by means of Uv-vis absorption, fluorescence emission and cyclic voltammogram. By exploring the self-assembly behavior of different substituted discotic molecules through method of solvent exchange-evaporation, organic micro-nanostructures such as nanoparticles, nanotubes and nanorods were obtained through supramolecular self-assembly. In order to investigate the applications of these discotic organic molecules, the relationship of molecular design, structural design and material properties has been studied based on the experimental work.
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Nguyen, Thuc-Quyen, Richard Martel, Mark Bushey, et al. "Self-assembly of 1-D organic semiconductor nanostructures." Physical Chemistry Chemical Physics 9, no. 13 (2007): 1515. http://dx.doi.org/10.1039/b609956d.

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Lund, Kyle, Yan Liu, and Hao Yan. "Combinatorial self-assembly of DNA nanostructures." Organic & Biomolecular Chemistry 4, no. 18 (2006): 3402. http://dx.doi.org/10.1039/b605208h.

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Kumari, Rina, Shib Shankar Banerjee, Anil K. Bhowmick, and Prolay Das. "DNA–melamine hybrid molecules: from self-assembly to nanostructures." Beilstein Journal of Nanotechnology 6 (June 30, 2015): 1432–38. http://dx.doi.org/10.3762/bjnano.6.148.

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Single-stranded DNA–melamine hybrid molecular building blocks were synthesized using a phosphoramidation cross-coupling reaction with a zero linker approach. The self-assembly of the DNA–organic hybrid molecules was achieved by DNA hybridization. Following self-assembly, two distinct types of nanostructures in the form of linear chains and network arrays were observed. The morphology of the self-assembled nanostructures was found to depend on the number of DNA strands that were attached to a single melamine molecule.
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Aljabri, Mahmood D., Nilesh M. Gosavi, Lathe A. Jones, Pranay P. Morajkar, Duong D. La, and Sheshanath V. Bhosale. "Arginine-Induced Self-Assembly of Protoporphyrin to Obtain Effective Photocatalysts in Aqueous Media Under Visible Light." Molecules 24, no. 22 (2019): 4172. http://dx.doi.org/10.3390/molecules24224172.

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The fabrication of controlled supramolecular nanostructures via self-assembly of protoporphyrin IX (PPIX) was studied with enantiomerically pure l-arginine and d-arginine, and we have shown that stoichiometry controlled the morphology formed. The nanostructure morphology was mainly influenced by the delicate balance of π-π stacking interactions between PPIX cores, as well as H-bonding between the deprotonated acidic head group of PPIX with the guanidine head group of arginine. PPIX self-assembled with l-/d-arginine to create rose-like nanoflower structures for four equivalents of arginine that were 5–10 μm in length and 1–4 μm diameter. We employed UV-vis, fluorescence spectroscopy, scanning electron microscopy (SEM), X-ray diffraction (XRD), dynamic light scattering (DLS) and Fourier transform infrared spectroscopy (FT-IR) techniques to characterize the resulting self-assembled nanostructures. Furthermore, we investigated the catalytic activity of PPIX and arginine co-assembled materials. The fabricated PPIX–arginine nanostructure showed high enhancement of photocatalytic activity through degradation of rhodamine B (RhB) with a decrease in dye concentration of around 78–80% under simulated visible radiation.
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Gholami, Ahmad, Seyyed Alireza Hashemi, Khadije Yousefi, et al. "3D Nanostructures for Tissue Engineering, Cancer Therapy, and Gene Delivery." Journal of Nanomaterials 2020 (November 30, 2020): 1–24. http://dx.doi.org/10.1155/2020/1852946.

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The self-assembling is a spontaneous progression through which objects of nanophase/molecules materialize into prepared collections. Several biomolecules can interact and assemble into highly structured supramolecular structures, for instance, proteins and peptides, with fibrous scaffolds, helical ribbons, and many other functionalities. Various self-assembly systems have been established, from copolymers in blocks to three-dimensional (3D) cell culture scaffolds. Another advantage of self-assembly is its ability to manage a large variety of materials, including metals, oxides, inorganic salts, polymers, semiconductors, and various organic semiconductors. The most basic self-assembly of 3D nanomaterials is three primary forms of nanostructured carbon-based materials that perform a critical role in the progress of modern nanotechnologies, such as carbon nanotubes (CNTs), graphene, and fullerene. This review summarized important information on the 3D self-assembly nanostructure, such as peptide hydrogel, graphene, carbon nanotubes (CNTs), and fullerene for application in gene delivery, cancer therapy, and tissue engineering.
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SONG, XIN, HUIHUI KONG, LACHENG LIU, XIAOQING LIU, MINGDONG DONG, and LI WANG. "TERRACE INDUCED HOMOCHIRAL SELF-ASSEMBLY OF ZINC PHTHALOCYANINEON COPPER (111) SURFACE." Surface Review and Letters 23, no. 06 (2016): 1650047. http://dx.doi.org/10.1142/s0218625x16500475.

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It is still a challenge to find a suitable method to fabricate a well-defined homochiral surface from achiral molecules, and one of the possible methods is to modify surfaces with organic molecular assemblies. Large-area chiral self-assembly nanostructures have been observed at room temperature by depositing ZnPc molecules on a Cu(111) surface. The growth process has been investigated. ZnPc molecules get adsorbed first at the terrace steps, and then extend over the lower terrace until the whole terrace is covered with ZnPc molecules; such growth process would be stopped when the self-assembly nanostructure run into a decorated upper terrace step edge. We found that the terrace steps with specific directions with respect to the close-packed directions of the substrate can induce homochiral self-assembly on the lower terraces. So we can propose a possible way to fabricate a well-defined homochiral surface from achiral organic molecules.
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Li, Bing, Jiosep Puigmartí-Luis, Alain M. Jonas, David B. Amabilino, and Steven De Feyter. "Hierarchical growth of curved organic nanowires upon evaporation induced self-assembly." Chem. Commun. 50, no. 87 (2014): 13216–19. http://dx.doi.org/10.1039/c4cc03676j.

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Dissertations / Theses on the topic "Self-assembly of Organic Nanostructures"

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Chang, Ming-Hua. "Organic semiconductor nanostructures based on supramolecular self-assembly." Thesis, University of Oxford, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.489419.

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This thesis is concerned with two important photophysical questions in the area of organic semiconductors. One is the influence of intermolecular interactions on the excitation transfer and excitonic relaxation dynamics. The other is how dynamic changes of the excited-state excitonic wavefunction may be caused by intramolecular geometric relaxations.
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Sun, Yuan. "Self-assembly of Organic Nanostructures for Biomedical Applications." The Ohio State University, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=osu1480526082654358.

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Balakrishnan, Kaushik. "Self-assembly of organic semiconducting molecules into one-dimensional nanostructures /." Available to subscribers only, 2008. http://proquest.umi.com/pqdweb?did=1594481341&sid=10&Fmt=2&clientId=1509&RQT=309&VName=PQD.

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Alam, Md Shah. "Development of Multicomponent Nanostructures by Self-assembly of Graphene Oxide and Organic Nanotubes." The Ohio State University, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu159500274123902.

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Nardi, Elena. "Growth of organic nanostructures through on-surface reactions : from phthalocyanines self-assembly to polymeric phthalocyanines." Thesis, Aix-Marseille, 2015. http://www.theses.fr/2015AIXM4351/document.

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Le couplage covalent de précurseurs moléculaires spécialement conçus, assisté par une surface métallique, a récemment émergé comme nouvelle voie pour la création de nouvelles architectures moléculaires prometteuses pour l’électronique moléculaire. Les phtalocyanines et leurs dérivés ont attiré beaucoup d’intérêt à cause de leurs propriétés chimiques et optoélectroniques. Dans cette thèse la synthèse de composés de phtalocyanine est présentée. Les composés sont obtenus par une réaction en surface entre précurseurs fonctionnalisés avec quatre groupements carbonitriles et des atomes métalliques. L’étude expérimentale est faite par microscopie à effet tunnel et spectroscopie de photoémission X. Les précurseurs moléculaires de TCN-DBTTF et de PPCN ont été étudiés. Les TCN-DBTTF ont été déposés avec les atomes de Mn, Fe ou Cu sur Ag(111) et Au(111). La réaction de cyclotetramerization a été activée par recuits. Dans le cas le plus favorable (TCN-DBTTF avec Fe sur Ag(111)), la réaction peut être activée à 200°C et permet la synthèse de phtalocyanines individuelles. Un recuit à plus haute température permet de continuer la réaction en 1D (250°C) et en 2D (275°C). Des résultats similaires ont été obtenus pour le dépôt de PPCN avec Mn ou Cu sur Au(111). L’évolution des spectres des niveaux de coeur permet d’obtenir une preuve de la réaction. Les différents facteurs qui influencent la cyclotetramerisation ont été étudiés.L'étude démontre la versatilité de la méthode: la synthèse en surface permet la création de polymères 2D originaux connectés par des macrocycles de phtalocyanine susceptibles d’être étendus à un grand nombre de précurseurs et d’atomes métalliques<br>Surface-assisted covalent coupling of suitably designed molecular precursors on metal surfaces has recently emerged as a new route towards the design of novel molecular architectures promising for future applications. Phthalocyanines and their derivatives have been widely studied for their chemical and optoelectronic properties. In this thesis the synthesis of phthalocyanine compounds is presented. The compounds are obtained through an on-surface reaction between tetracarbonitrile-functionalized precursors and metals. The experimental investigation is carried out by means of scanning tunnelling microscopy and X-Ray photoemission spectroscopy. Two molecular precursors, TCN-DBTTF and PPCN, are studied. TCN-DBTTF molecules are deposited with metal atoms (Mn, Fe, or Cu) on Ag(111) and Au(111). Annealing is used to activate the reaction of cyclotetramerization between precursors and metals. In the most favourable case (TCN-DBTTF with Fe on Ag(111)) the reaction can be activated at 200°C and leads to the synthesis of individual phthalocyanines. Increasing the temperature allows the synthesis of polymeric lines, at 250°C, and small 2D domains, at 275°C. Similar results are obtained for PPCN deposition with Mn or Cu on Au(111). In this latter case, the evolution of core level spectra allows a chemical proof of the on-surface reaction. The factors affecting on-surface cyclotetramerization have also been studied. This study demonstrates the versatility of the method: on-surface cyclotetramerization allows creating original 2D polymers connected by phthalocyanine macrocycles, and may work with a wide range of tetracarbonitrile-functionalized precursors and metallic atoms
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Kazantsev, Roman V. "Self-Assembled, Crystalline Organic Nanostructures for Photocatalysis." Thesis, Northwestern University, 2016. http://pqdtopen.proquest.com/#viewpdf?dispub=3741384.

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<p> The goal of this thesis was to integrate light-absorbing supramolecular materials into a photocatalytic system for solar-to-fuel conversion. Toward this end, a series of perylene-based chromophore amphiphiles was synthesized and their self-assembly properties explored. Characterization of these materials by electron microscopy and x-ray scattering techniques revealed molecular assembly into 1D ribbon nanostructures. Surprisingly, these ribbons were observed to spontaneously crystallize in solution, as observed by wide-angle and grazing incidence X-ray scattering. These crystalline nanostructures could be gelled with oppositely charged electrolytes, forming a 3D light-absorbing scaffold. By designing and synthesizing oppositely charged proton reduction catalysts to electrostatically bind to the light-absorbing scaffold, hydrogen gas was detected by gas chromatography after white light illumination of the scaffold / catalyst system. As a direct result of their crystalline nature, the exciton properties of these materials and the photocatalytic properties of the system could be tuned by slight modification in their molecular packing arrangement. These changes were achieved by creating a library of chromophores with small functional groups directly attached to the PMI core. Some amphiphiles in this library were observed to undergo a crystalline phase transition between two unique packing arrangements as evidenced by variable temperature absorbance and x-ray scattering experiments. This transition involved a substantial change in the exciton properties of the material. Surprisingly, some crystalline phases carried the distinct spectral signature of charge-transfer (CT) excitons, an excitation that is shared among multiple chromophores. Characterization of this CT state was accomplished by ground state and transient absorption spectroscopy, transient electron paramagnetic resonance spectroscopy, and second-order harmonic generation microscopy. The crystalline nanostructures of the library that yielded evidence for CT-excitons were the most photocatalytically active. This observation is consistent with established theories developed elsewhere that connect CT-exciton formation with an enhancement in exciton mobility.</p>
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Jha, Kshitij Chandra. "Polarization and Self-Assembly at Metal-Organic Interfaces: Models and Molecular-Level Processes." University of Akron / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=akron1333644685.

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Zhang, Hongyang. "Synthesis, characterization and properties of self-assembled metal complex nanosheets heterostructured organic microrods." HKBU Institutional Repository, 2019. https://repository.hkbu.edu.hk/etd_oa/607.

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Molecular self-assembly or ligand-metal assembly is a process in which several individual molecules and metal ions organize themselves into an ordered arrangement without external stimuli, the defined structures can lead to distinctive electronic and photonic performances. In the meantime, as the scale of materials decreases, various unique properties arise from their minute scaled dimensions, such as surface effect, volume effect, quantum effect and dielectric confinement effect, etc. Therefore, the design and fabrication of the micro- and nanomaterial via the technique of molecular self-assembly or ligand-metal assembly is becoming an emerging research field, for the purpose of meeting the increased demands of multi-functional materials. Chapter 1 gives an overview of the advanced materials prepared by either molecular self-assembly or ligand-metal assembly. We described the interaction nature in detail, and enumerated the applications as well as developments of this scientific field. Furthermore, the detailed classifications as well as previous work of these advanced materials we researched on, such as two dimensional nanosheets, hetero-structured materials and cyclometalated iridium(Ⅲ) complexes were also amply summarized. Two-dimensional nanosheets have always been a research hotspot since graphene was discovered and isolated. In contrast, molecule-based organometallic nanosheets through bottom-up method exhibit more inner structures. In Chapter 2, we constructed two classes of organometallic nanosheets with different intermolecular forces, one is metal-ligand coordination, while the other one is the aromatic (π-π) interaction. Two-dimensional nanosheets with Hg-acetylide linkages, bis(dipyrrinato)metal linkages as well as bis(terpyridine)metal linkages were synthesized and characterized by UV-Vis absorption spectroscopy, FT-IR spectroscopy, optical and electron microscopy, photoluminescence spectroscopy, thermal gravimetric analysis, X-ray photoelectron spectroscopy and so on. In addition, the potential applications were explored as well, including the tests of charge mobility and current capacitance. Meanwhile we also investigated the two-dimensional nanosheets self-assembled by aromatic (π-π) interaction. The morphology characterizations, crystal form measurements, besides elemental analyses were conducted. By means of surface control, the hybrid nanosheets could achieve many superior performances, like super hydrophobicity, high conductivity and soft magnetism. In Chapter 3, we firstly mentioned that organic hetero-structured micro- or nanomaterials are widely attractive on account of its extensive applications in lasers, bipolar transistors, field effect transistors and solar cells. In our work, we focus on the diverse microrods assembled from π-conjugated small molecules, especially in the construction of heterogeneous organic heterojunction materials with specific components distribution. Two novel kinds of heterostructure, multilayer core-shell structured heterojunction and heterogeneous rod-tail helix were fabricated and developed both via a stepwise seeded-growth route, in which the different constituents possess different colors of luminescence. Through the media of fluorescence microscopy and confocal microscopy, the core-shell hetero- structures can be observed, testified and recorded quite distinctly. Furthermore, the prepared method by employing seeded-precursor could give us a revelation about constructing more sophisticated and functional organic luminescent heterogeneous materials. Chapter 4 focuses on the syntheses and characterization of eight cyclometalated iridium(Ⅲ) complexes, Ir(TPY)2(Dipyrrinato), Ir(PIQ)2(Dipyrrinato), Ir(Ligand 1)2(Dipyrrinato), Ir(Ligand 2)2(Dipyrrinato), Ir(Ligand 3)2(Dipyrrinato), Ir(PPY)2 (Dipyrrinato), Ir(m-PPY)2(Dipyrrinato) and Ir(PPY-m)2(Dipyrrinato). As is known, iridium(Ⅲ) complexes can exploit the energy of both 25% singlet and 75% triplet excited states. Due to their highly efficient applications in phosphorescent OLEDs, these materials are considered as one of the potential candidates for flexible display screen as well as clearing luminary. Among those full-color light-emitting iridium(Ⅲ) phosphors, near-infrared (NIR) phosphors are broadly utilized in phototherapy as well as biosensors. Herein, our eight synthetic cyclometalated iridium(Ⅲ) complexes all gave photoluminescence at 680 - 700 nm in solution, which could be attributed to the NIR region. We continuously tune the extensive conjugation on the C^N ligands in order to make longer wavelength emitting phosphors. The HOMO and LUMO of eight synthetic iridium(Ⅲ) phosphors were also calculated according to their cyclic voltamograms (CV). The design and preparation strategy in this thesis can inspire us to develop near-infrared as well as higher-performance organometallic phosphors.
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Masuda, Koji. "Design and Fabrication of Nanostructures by Layer-by-Layer Assembly for Organic Photovoltaic Devices." 京都大学 (Kyoto University), 2010. http://hdl.handle.net/2433/123342.

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Peyrot, David. "Engineering 2D organic nanoarchitectures on Au(111) by self-assembly and on-surface reactions." Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLX007/document.

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Ces dernières années ont été marquées par de grandes évolutions technologiques à travers notamment une course à la miniaturisation. De gros efforts de recherche se concentrent en particulier sur le domaine de l’électronique organique mais aussi sur de nouveaux matériaux bidimensionnels comme le graphène. Ces matériaux 2D présentent des propriétés physiques exceptionnelles et sont des candidats prometteurs pour le développement de futurs dispositifs électroniques. Au cours de cette thèse, l’approche ascendante, qui consiste à assembler ensemble des petites briques élémentaires, a été utilisée pour élaborer des nanostructures bidimensionnelles originales sur des surfaces. Des états électroniques localisés dus à un couplage électronique latéral particulier entre les molécules ont été observés. Quatre nanoarchitectures hybrides ioniques-organiques différentes ont été réalisées en faisant varier la température de la surface. Des nanostructures organiques covalentes ont aussi été élaborées par une réaction de couplage d’Ullmann sur la surface. Deux précurseurs différents en forme d’étoile avec des substituants iodés et bromés respectivement, ont été étudiés. De grandes nanostructures carbonées hexagonales poreuses ont notamment été synthétisées en faisant varier la température du substrat. Ces travaux ouvrent de nouvelles perspectives pour la réalisation de matériaux organiques bidimensionnels aux propriétés contrôlées<br>Over the last few years, important technological developments were made following a trend towards miniaturization. In particular, lots of research efforts are put into the research on organic electronics and on 2D materials like graphene. Such 2D materials show great physical properties and are promising candidates for the development of future electronic devices.In this project, bottom-up approach consisting in assembling elementary building blocks together, was used to engineer novel twodimensional nanostructures on metal surfaces. The properties of these two-dimensional nanostructures were investigated using Scanning Tunneling Microscopy (STM) and X-ray Photoemission Spectroscopy (XPS). Two-dimensional nanostructures based on the self-assembly of organic building blocks stabilized by intermolecular interactions were engineered. In particular, nanostructures stabilized by hydrogen bonds, halogen bonds and ionic-organic interactions were investigated. Localized electronic states due to specific molecular lateral electronic coupling were observed. Four different ionic-organic nanoarchitectures were engineered varying the substrate temperature. Covalent organic nanostructures were also engineered by onsurface Ullmann coupling reaction. Two different star-shaped precursors with iodine and bromine substituents respectively, were investigated. Large periodic porous 2D covalent hexagonal carbon nanostructures weresuccessfully engineered by temperature driven hierarchal Ullmann coupling. These results open new perspectives for the development of 2D organic materials with controlled structures and properties
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Books on the topic "Self-assembly of Organic Nanostructures"

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Han, Bo. Interfacial electrochemistry and in situ SEIRAS investigations of self assembled organic monolayers on Au-electrolyte interfaces. Forschungszentrum, Zentralbibliothek, 2006.

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Bellucci, Stefano, ed. Self-Assembly of Nanostructures. Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-0742-3.

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Guldin, Stefan. Inorganic Nanoarchitectures by Organic Self-Assembly. Springer International Publishing, 2013.

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Guldin, Stefan. Inorganic Nanoarchitectures by Organic Self-Assembly. Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-00312-2.

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Fuiita, Makoto, ed. Molecular Self-Assembly Organic Versus Inorganic Approaches. Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/3-540-46591-x.

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Lee, Yoon S. Self-assembly and nanotechnology systems: Design, characterization, and applications. Wiley, 2012.

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Mura, Manuela. Self-Assembly of Flat Organic Molecules on Metal Surfaces. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-30325-8.

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Complex macromolecular architectures: Synthesis, characterization, and self-assembly. Wiley, 2011.

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Russo, Nino. SelfOrganization of Molecular Systems: From Molecules and Clusters to Nanotubes and Proteins. Springer Netherlands, 2009.

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An introduction to ultrathin organic films: From Langmuir-Blodgett to self-assembly. Academic Press, 1991.

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Book chapters on the topic "Self-assembly of Organic Nanostructures"

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Qin, Long, Kai Lv, Zhaocun Shen, and Minghua Liu. "Self-Assembly of Organic Molecules into Nanostructures." In Soft Matter Nanotechnology. Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527682157.ch02.

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Kowerko, Danny. "Interrelation of Assembly Formation and Ligand Depletion in Colloidal Quantum Dots." In Self-Assembled Organic-Inorganic Nanostructures. CRC Press, 2016. http://dx.doi.org/10.1201/9781315364544-3.

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Zhang, Shaoyi, Yang Yang, and Zhihong Nie. "Controllable Self-Assembly of One-Dimensional Nanocrystals." In Functional Organic and Hybrid Nanostructured Materials. Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527807369.ch1.

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Fahmi, Amir. "Frontiers in Nanofabrication via Self-Assembly of Hybrid Materials into Low Dimensional Nanostructures." In Organic-Inorganic Hybrid Nanomaterials. Springer International Publishing, 2014. http://dx.doi.org/10.1007/12_2014_291.

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Zenkevich, Eduard, and Christian von. "Structural and Energetic Dynamics in Quantum Dot–Dye Nanoassemblies." In Self-Assembled Organic-Inorganic Nanostructures. CRC Press, 2016. http://dx.doi.org/10.1201/9781315364544-2.

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Blaudeck, Thomas. "Fluorescence Quenching of Semiconductor Quantum Dots by Multiple Dye Molecules." In Self-Assembled Organic-Inorganic Nanostructures. CRC Press, 2016. http://dx.doi.org/10.1201/9781315364544-4.

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Trenkmann, Ines, Thomas Blaudeck, and Christian von. "Static and Dynamic Quenching of Quantum Dot Photoluminescence by Organic Semiconductors and Dye Molecules." In Self-Assembled Organic-Inorganic Nanostructures. CRC Press, 2016. http://dx.doi.org/10.1201/9781315364544-5.

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Zenkevich, Eduard, and Christian von. "Selected Applications of QDs and QD-Based Nanoassemblies." In Self-Assembled Organic-Inorganic Nanostructures. CRC Press, 2016. http://dx.doi.org/10.1201/9781315364544-6.

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Graaf, Harald, and Thomas Baumgärtel. "Nanolithography and Decoration of Generated Nanostructures by Dye Molecules." In Self-Assembled Organic-Inorganic Nanostructures. CRC Press, 2016. http://dx.doi.org/10.1201/9781315364544-7.

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Täuber, Daniela, and Christian von. "Identification of Heterogeneous Surface Properties via Fluorescent Probes." In Self-Assembled Organic-Inorganic Nanostructures. CRC Press, 2016. http://dx.doi.org/10.1201/9781315364544-8.

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Conference papers on the topic "Self-assembly of Organic Nanostructures"

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Lu, Wei. "Self-Assembled Nanostructures." In 2008 Second International Conference on Integration and Commercialization of Micro and Nanosystems. ASMEDC, 2008. http://dx.doi.org/10.1115/micronano2008-70067.

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A binary monolayer on an elastic substrate may self-organize into ordered nanoscale phase patterns. Here we report a work of using a substrate strain field to guide the self-assembly process. The study shows that straining a substrate uniformly does not influence the pattern. However, a non-uniform strain field significantly influences the size, shape and distribution of self-assembled features. The study suggests a method of strain field design to make various monolayer patterns.
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Adams, Sarah M., and Regina Ragan. "Gold Nanoparticle Self Assembly on Diblock Copolymers for Application as Biomolecular Sensors." In ASME 2010 First Global Congress on NanoEngineering for Medicine and Biology. ASMEDC, 2010. http://dx.doi.org/10.1115/nemb2010-13126.

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Current efforts in medical diagnostic technology focus toward developing biological sensors with the capacity for detecting trace quantities of specified organic molecules. In this study, metallic nanoparticles were investigated for the development of field-enhanced chemical and biological detection devices with the capacity to achieve single-molecule level detection resulting from surface enhanced Raman scattering (SERS) associated with closely spaced noble metal nanostructures.[1, 2] Localized surface plasmon resonance (LSPR) sensors likewise benefit from the incorporation of ordered metal nanoparticles on surfaces, providing increased shift in minimum of reflectivity with biological binding event (figure 1).[3]
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FUCHS, H. "ADVANCED SCANNING PROBES AS APPLIED TO SELF ORGANIZED ORGANIC SYSTEMS." In Physics, Chemistry and Application of Nanostructures - Reviews and Short Notes to Nanomeeting 2003. WORLD SCIENTIFIC, 2003. http://dx.doi.org/10.1142/9789812796738_0106.

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Cui, Tianhong, Yuri Lvov, Feng Hua, and Jingshi Shi. "Novel Lithography-Based Approaches to Pattern Layer-by-Layer Self-Assembled Thin Films." In ASME 2002 International Mechanical Engineering Congress and Exposition. ASMEDC, 2002. http://dx.doi.org/10.1115/imece2002-32731.

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Layer-by-layer self-assembly is a key enabling technique in nanotechnology. It is very crucial to pattern the self-assembled thin films for the realization of nano/microelectronics devices or NEMS (Nano Electro Mechanical Systems). Two approaches to generate spatially separated patterns comprised of organic or inorganic nanoparticles are demonstrated. The processes are based on the lithographic patterning of the nanoparticle-based thin films which are layer-by-layer assembled. This opens to industrial applications of popular layer-by-layer method to produce multilayers for polymers, nanoparticles and protein organized in nanometer scale. These two methods are referred to by us as “lift-off” and “metal mask”, respectively. Sharp and clear patterns are created with both methods and images are recorded by scanning electron microscope. Their advantages and disadvantages are discussed and potential usage in 3-D nanostructure fabrication is investigated. In addition, temperature-dependent experiment has first been carried out to make this techniques more practical for micro/naoelectronics or NEMS devices.
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Rebane, Aleksander, and Alexander Mikhaylov. "Femtosecond light-induced macromolecular self-assembly." 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/10.1117/12.2237867.

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Anthony, John E. "Exploring self-assembly in functionalized acenes." In Organic and Hybrid Field-Effect Transistors XX, edited by Oana D. Jurchescu and Iain McCulloch. SPIE, 2021. http://dx.doi.org/10.1117/12.2593830.

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Zhang, Cheng, Thuong H. Nguyen, and Emily M. Heckman. "Bioinspired self-assembly for organic elctro-optics." In SPIE NanoScience + Engineering, edited by Norihisa Kobayashi, Fahima Ouchen, and Ileana Rau. SPIE, 2010. http://dx.doi.org/10.1117/12.862235.

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Nielsen, Peter E., Wolfgang Fritzsche, and Frank Bier. "PNA Directed Sequence Addressed Self-Assembly of DNA Nanostructures." In DNA-BASED NANODEVICES: International Symposium on DNA-Based Nanodevices. AIP, 2008. http://dx.doi.org/10.1063/1.3012295.

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López-López, M., E. Cruz-Hernández, I. Martínez-Velis, et al. "Self-Assembly of Nanostructures on (631)-Oriented GaAs Substrates." In Advanced Summer School in Physics 2007. AIP, 2007. http://dx.doi.org/10.1063/1.2825122.

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Heflin, J. R., P. J. Neyman, C. Brands, et al. "Hybrid Covalent/Ionic Self-Assembly of Organic Second Order Nonlinear Optical Films." In Organic Thin Films. OSA, 2002. http://dx.doi.org/10.1364/otf.2001.otub5.

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Reports on the topic "Self-assembly of Organic Nanostructures"

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George, Thomas F., Lahsen Assoufid, G. A. Mansoori, and Guoping Zhang. Diamond-Like and Self-Assembling Organic Nanostructures: Measurement and Simulation of Intermolecular Interactions and Structural Characteristics. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada498551.

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Alexander-Katz, Alfredo. Biomimetic Templated Self-Assembly of Light Harvesting Nanostructures. Final report. Office of Scientific and Technical Information (OSTI), 2018. http://dx.doi.org/10.2172/1557669.

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Franco, Elisa. Final technical report: Programmable Dynamic Self-Assembly of DNA Nanostructures. Office of Scientific and Technical Information (OSTI), 2020. http://dx.doi.org/10.2172/1617110.

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Nitschke, Jonathan R. New Metal-organic Polymers Through Subcomponent Self-Assembly. Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ada582657.

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Zhang, Honghu. Bioinspired synthesis and self-assembly of hybrid organic–inorganic nanomaterials. Office of Scientific and Technical Information (OSTI), 2016. http://dx.doi.org/10.2172/1409201.

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Tavor, John. Self-assembly of pi-conjugated peptides in aqueous environments leading to energy-transporting bioelectronic nanostructures. Office of Scientific and Technical Information (OSTI), 2016. http://dx.doi.org/10.2172/1334524.

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Coker, Eric Nicholas, Raid Edward Haddad, Hongyou Fan, et al. Confined cooperative self-assembly and synthesis of optically and electrically active nanostructures : final LDRD report. Office of Scientific and Technical Information (OSTI), 2011. http://dx.doi.org/10.2172/1029766.

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Lai, Peng. Mesoporous Silicia Nanowires by Space-Confined Organic-Inorganic Hybrid Self-Assembly. Office of Scientific and Technical Information (OSTI), 2007. http://dx.doi.org/10.2172/990221.

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Swartzentruber, Brian Shoemaker. "Bottom-up" meets "top-down" : self-assembly to direct manipulation of nanostructures on length scales from atoms to microns. Office of Scientific and Technical Information (OSTI), 2009. http://dx.doi.org/10.2172/984156.

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Jen, Alex K. Molecular Self-Assembly and Interfacial Engineering for Highly Efficient Organic Field Effect Transistors and Solar Cells. Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ada581366.

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