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Relevant bibliographies by topics / Macromolecular materials

Academic literature on the topic 'Macromolecular materials'

Author: Grafiati

Published: 10 December 2022

Last updated: 28 January 2023

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Journal articles on the topic "Macromolecular materials"

1

Webber, Matthew J., Neha P. Kamat, Phillip B. Messersmith, and Sébastien Lecommandoux. "Bioinspired Macromolecular Materials." Biomacromolecules 22, no. 1 (January 11, 2021): 1–3. http://dx.doi.org/10.1021/acs.biomac.0c01614.

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Bazunova, Marina, Valentina Chernova, Roman Lazdin, Angela Shurshina, Anna Bazunova, Mariya Elinson, and Elena Kulish. "Cosolvents Impact on some Properties of the Solutions and the Films of Succinamide Chitosan." Chemistry & Chemical Technology 14, no. 4 (December 15, 2020): 481–86. http://dx.doi.org/10.23939/chcht14.04.481.

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The article deals with the method of the medical purpose materials creation with the controlled physico-chemical and mechanical deformation properties on the basis of water-soluble derivative of amino polysaccharide chitosan – succinamide chitosan. The essence of the method is the macromolecules aggregation processes regulation in the initial solutions by the injection of organic cosolvents – acetone and ethanol. It has been stated that in a mixed solvent succinamide chitosan molecules are not in the form of the isolated macromolecular balls but as the macromolecules interacting (aggregated) systems. It has been proved that the presence of cosolvents decreases the polymer macromolecule links capability to interact with an enzyme and increases physico-mechanical characteristics of the film materials.

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Zimmermann, Markus, and Alan Wineman. "On the Elastic Behavior of Scission Materials." Mathematics and Mechanics of Solids 10, no. 1 (February 2005): 63–88. http://dx.doi.org/10.1177/1081286504033008.

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Constitutive equations have recently been developed which account for changes in the mechanical response of an elastomer due to changes in its macromolecular structure. The changes consist of scission of macromolecular network junctions, recoiling of macromolecules and their subsequent cross linking to form new networks with new stress-free reference configurations. This work discusses changes caused by large deformations. For each deformation history, there is a range of deformations in which the microstructure is fixed, with no further scission or cross linking. The elastomer has a modified elastic behavior and a new stress-free reference configuration. The constitutive equation for this post-scission elastic range is developed. Two subclasses of this constitutive equation are defined: Mooney-Rivlin based and neo-Hookean based scission materials. The strain energy density function for each subclass is derived. It is shown how the new material symmetry is determined from the preceding deformation history and the scission and cross linking processes. The effect of scission on the stability behavior of a neo-Hookean based scission material is discussed and a cube under triaxial load is considered.

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Kato, Takashi, Takeshi Sakamoto, and Tatsuya Nishimura. "Macromolecular Templating for the Formation of Inorganic-Organic Hybrid Structures." MRS Bulletin 35, no. 2 (February 2010): 127–32. http://dx.doi.org/10.1557/mrs2010.632.

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AbstractBiominerals such as the nacre of shells, spicules of sea urchins, teeth, and bones are inorganic-organic hybrids that have highly controlled hierarchical and complex structures. These structures are formed in mild conditions, and the processes are controlled by macromolecular templates of proteins, peptides, and polysaccharides. Materials scientists can obtain ideas from the structures, properties, and formation processes of biominerals for use in creating synthetic, biomimetic materials. This article highlights bioinspired synthetic approaches to the development of organic/CaCO3 hybrids using macromolecular templates. These hybrids have oriented, patterned, and 3D complex structures, as well as thin films with smooth surfaces. The structures are formed by templating synthetic and semisynthetic macromolecules. These materials have great potential for new functional materials.

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Chen, Biqiong, Suprakas Sinha Ray, and Mohan Edirisinghe. "Sustainable Macromolecular Materials and Engineering." Macromolecular Materials and Engineering 307, no. 6 (June 2022): 2200242. http://dx.doi.org/10.1002/mame.202200242.

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Reneker, D. H., W. L. Mattice, R. P. Quirk, and S. J. Kim. "Macromolecular smart materials and structures." Smart Materials and Structures 1, no. 1 (March 1, 1992): 84–90. http://dx.doi.org/10.1088/0964-1726/1/1/013.

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Binder, K. "Computer simulation of macromolecular materials." Colloid & Polymer Science 266, no. 10 (October 1988): 871–85. http://dx.doi.org/10.1007/bf01410842.

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Spiegel, Stefan. "Recent Developments in Macromolecular Materials." Macromolecular Materials and Engineering 296, no. 1 (December 27, 2010): 6–7. http://dx.doi.org/10.1002/mame.201000439.

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Narupai, Benjaporn, and Alshakim Nelson. "100th Anniversary of Macromolecular Science Viewpoint: Macromolecular Materials for Additive Manufacturing." ACS Macro Letters 9, no. 5 (April 15, 2020): 627–38. http://dx.doi.org/10.1021/acsmacrolett.0c00200.

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Grube, Mandy, Gizem Cinar, Ulrich S. Schubert, and Ivo Nischang. "Incentives of Using the Hydrodynamic Invariant and Sedimentation Parameter for the Study of Naturally- and Synthetically-Based Macromolecules in Solution." Polymers 12, no. 2 (January 31, 2020): 277. http://dx.doi.org/10.3390/polym12020277.

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The interrelation of experimental rotational and translational hydrodynamic friction data as a basis for the study of macromolecules in solution represents a useful attempt for the verification of hydrodynamic information. Such interrelation originates from the basic development of colloid and macromolecular science and has proven to be a powerful tool for the study of naturally- and synthetically-based, i.e., artificial, macromolecules. In this tutorial review, we introduce this very basic concept with a brief historical background, the governing physical principles, and guidelines for anyone making use of it. This is because very often data to determine such an interrelation are available and it only takes a set of simple equations for it to be established. We exemplify this with data collected over recent years, focused primarily on water-based macromolecular systems and with relevance for pharmaceutical applications. We conclude with future incentives and opportunities for verifying an advanced design and tailored properties of natural/synthetic macromolecular materials in a dispersed or dissolved manner, i.e., in solution. Particular importance for the here outlined concept emanates from the situation that the classical scaling relationships of Kuhn–Mark–Houwink–Sakurada, most frequently applied in macromolecular science, are fulfilled, once the hydrodynamic invariant and/or sedimentation parameter are established. However, the hydrodynamic invariant and sedimentation parameter concept do not require a series of molar masses for their establishment and can help in the verification of a sound estimation of molar mass values of macromolecules.

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Dissertations / Theses on the topic "Macromolecular materials"

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Zhang, Borui. "Novel Dynamic Materials Tailored by Macromolecular Engineering." Miami University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=miami1564157701522666.

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Reinsel, Anna Michele. "Spectroscopic Characterization of Organic and Inorganic Macromolecular Materials." University of Akron / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=akron1312823530.

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Eden, E. G. "Analysis of solution-phase macromolecular materials by diffusion NMR." Thesis, University of Liverpool, 2017. http://livrepository.liverpool.ac.uk/3006567/.

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Molecules such as covalent cages can adopt several shapes, in which the ratio of starting materials is the same, but the number of starting materials, and the shape of the resulting molecule is different. However, determining this in the absence of a crystal structure can be challenging. Pulsed field gradient (PFG) NMR has been used for two decades to characterise large macromolecules in solution, but it is still difficult to determine precise structural information, because of the rotational-averaging experienced in experimental measurements. Here, we develop experimental techniques for collecting PFG-NMR data that break this barrier, and allow characterisation of several useful molecular descriptors. By measuring the diffusion coefficients of molecules in a range of solvents, incurvate surfaces are probed to map the outer surface of nanometre-sized molecular species. This technique allows details about the geometrical shape of covalent cages to be determined without the need for isolation. Furthermore, we compare experimental PFG-NMR data to structures produced by computational modelling and produce a new molecular descriptor, ρr, which describes the isotropy of covalent cages. This descriptor is used to determine the quality of agreement between proposed structures and experimental PFG-NMR data. In analysing polymers, we develop a new mathematical model for determining the molar-mass dispersity (ÐM) by PFG-NMR. We find a single parameter is sufficient to determine the dispersity of a system, which eliminates the need for data modelling and enhances the reliability of analysis. We hope this will make the technique more accessible to polymer scientists, and will help test the validity of molar-mass dispersity measurements made by other means. Finally, we synthesise five novel dodecaamide cages, which contain functional groups that offer the opportunity to extend functionality beyond the cage via further reaction. We take significant steps towards producing singly functionalised species, which could be incorporated into polymeric materials for the development of robust membranes and coatings.

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Kuttner, Christian [Verfasser]. "Macromolecular Interphases and Interfaces in Composite Materials / Christian Kuttner." München : Verlag Dr. Hut, 2014. http://d-nb.info/1063222036/34.

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Price, Erik Joshua. "EXTREME-ENVIRONMENT PROTECTION USING MACROMOLECULAR COMPOSITE TECHNOLOGY." Case Western Reserve University School of Graduate Studies / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=case1617027732923331.

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Mohin, Jacob W. "Nanostructured π-Electron Materials for Energy Applications Derived from Macromolecular Self-Assembly." Research Showcase @ CMU, 2015. http://repository.cmu.edu/dissertations/1045.

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Globalization and climate change have driven the need to develop new technologies which can provide clean, plentiful energy from renewable sources. This work was focused on the application of nanostructured π-electron materials derived from carbon-based macromolecules towards capturing, converting, and storing energy. Nanostructures are beneficial in this role as they provide high interfacial area and unique electronic properties which can be harnessed to perform chemistry relevant to energy conversion and storage. This work was focused on the characterization, materials development, and device application of two nanostructured systems: (i) poly(3-hexyl)thiophene (P3HT) blended with phenyl(C-61)butyric acid methyl ester (PCBM), and (ii) copolymer-templated nitrogen-doped nanoporous carbons (CTNCs). In both systems, nanomorphology has pronounced impact on the performance of devices made from such materials. P3HT/PCBM blends find application as a photovoltaic material, where the phase-separated morphology is crucial for efficient photogenerated charge collection. Despite widespread recognition of the importance of morphology in P3HT/PCBM photovoltaics, a robust understanding of the unique packing motif of P3HT on the morphology of blended structures has yet to emerge. This thesis addresses this deficiency by developing methods which connects real-space atomic force microscopy images with inverse space x-ray scattering patterns to analyze poorly ordered two-phase systems. The application of this method allowed for quantitative measurement of the phase ratios of P3HT/PCBM nanostructured blends, utilizing the Porod length of inhomogeneity and the Bragg length associated with pseudo-fibrillar P3HT morphologies. The results showed that P3HT possesses void space originating from molecular weight dispersity inherent to polymerization, which accounts for solid-phase solubility of PCBM in P3HT. X-ray scattering and atomic force microscopy were also used in part to characterize CTNCs. Past success using CTNCs as electrocatalysts and supercapacitors motivated research towards increasing their surface area by utilizing a lower molecular weight precursor polymer. Atom-transfer radical polymerization was utilized to synthesize block copolymers consisting of polystyrene and polyacrylonitrile, but it was found their surface areas were lower than those achieved in previous work. Careful structural analysis by variable temperature x-ray scattering showed that crystallization of polyacrylonitrile drives morphological changes on heating, increasing domain spacing. Further thermal analysis showed that polystyrene interferes with the crosslinking of polyacrylonitrile, which may cause morphological collapse leading to low surface area. A feature of CTNCs noted in past and present studies is their sizeable surface area consisting of pores <1 nanometer (micropores). Differential scanning calorimetry showed that reactive chain ends left behind by polymerization might play a role in disrupting the crosslinking process, resulting in a material with sizeable microporosity, which could be used to engineer dual pore-size materials. Finally, CTNCs were utilized for heterogeneous catalytic production of hydrogen from water, with electrons provided by both light and external circuitry. Their performance was correlated with nitrogen heteroatom content, conductivity, and nanomorphology, and shown to match that of noble metals. The lessons learned about nanomorphology in P3HT/PCBM and CTNCs highlight the importance of nanomorphology in energy devices and will serve as insight for materials design in future studies.

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Stimson, Lorna M. "Phase behaviour of macromolecular liquid crystalline materials : computational studies at the molecular level." Thesis, Durham University, 2003. http://etheses.dur.ac.uk/3144/.

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Molecular simulations provide an increasingly useful insight into the static and dynamic characteristics of materials. In this thesis molecular simulations of macro-molecular liquid crystalline materials are reported. The first liquid crystalline material that has been investigated is a side chain liquid crystal polymer (SCLCP). In this study semi-atomistic molecular dynamics simulations have been conducted at a range of temperatures and an aligning potential has been applied to mimic the effect of a magnetic field. In cooling the SCLCP from an isotropic melt, microphase separation was observed yielding a domain structure. The application of a magnetic field to this structure aligns the domains producing a stable smectic mesophase. This is the first study in which mesophases have been observed using an off-lattice model of a SCLCP. The second material that has been investigated is a dendrimer with terminal mesogenic functionalization. Here, a multi-scale approach has been taken with Monte Carlo studies of a single dendrimer molecule in the gas phase at the atomistic level, semi-atomistic molecular dynamics of a single molecule in liquid crystalline solvents and a coarse-grained molecular dynamics study of the dendrimer in the bulk. The coarse-grained model has been developed and parameterized using the results of the atomistic and semi-atomistic work. The single molecule studies showed that the liquid crystalline dendrimer was able to change its structure by conformational changes in the flexible chains that link the mesogenic groups to the core. Structural change was seen under the application of a mean field ordering potential in the gas phase, and in the presence of liquid crystalline solvents. No liquid crystalline phases were observed for the bulk phase studies of the coarse-grained model. However, when the length of the mesogenic units was increased there was some evidence for microphase separation in these systems.

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De, Alwis Watuthanthrige Nethmi Thanurika. "Application of Photochemistry and Dynamic Chemistry in Designing Materials tuned through Macromolecular Architecture." Miami University / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=miami1626694956739651.

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Zang, Xu. "Encapsulation of Proteinaceous materials in Macromolecular Organic Matter as a mechanism for environmental preservation /." The Ohio State University, 2001. http://rave.ohiolink.edu/etdc/view?acc_num=osu1486400446370061.

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Stark, Andreas. "Advancement and optimization of an electrospray injection based in-vacuum patterning system for macromolecular materials." [Tampa, Fla] : University of South Florida, 2008. http://purl.fcla.edu/usf/dc/et/SFE0002534.

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Books on the topic "Macromolecular materials"

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Ueyama, Norikazu, and Akira Harada, eds. Macromolecular Nanostructured Materials. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-08439-7.

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1942-, Ueyama Norikazu, and Harada A, eds. Macromolecular nanostructured materials. Tokyo: Kodansha, 2004.

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1934-, Hatada Koichi, Kitayama Tatsuki 1952-, and Vogl Otto 1927-, eds. Macromolecular design of polymeric materials. New York: M. Dekker, 1997.

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Dzhardimalieva, G. I. (Gulʹzhian Iskakovna) and Kestelʹman, V. N. (Vladimir Nikolaevich), eds. Macromolecular metal carboxylates and their nanocomposites. Heidelberg: Springer, 2010.

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Geckeler, Kurt E. Advanced Macromolecular and Supramolecular Materials and Processes. Boston, MA: Springer US, 2003.

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Geckeler, Kurt E., ed. Advanced Macromolecular and Supramolecular Materials and Processes. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4419-8495-1.

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Müller, Axel H. E. Complex Macromolecular Systems I. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2010.

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Hans-Werner, Schmidt, and SpringerLink (Online service), eds. Complex Macromolecular Systems II. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2010.

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Tanabe, Yoshikazu. Macromolecular Science and Engineering: New Aspects. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999.

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Khosravi, Ezat, Yusuf Yagci, and Yuri Savelyev, eds. New Smart Materials via Metal Mediated Macromolecular Engineering. Dordrecht: Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-3278-2.

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Book chapters on the topic "Macromolecular materials"

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Dubois, G., R. D. Miller, and James L. Hedrick. "Microelectronic Materials with Hierarchical Organization." In Macromolecular Engineering, 2331–67. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527631421.ch56.

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Farmer, Robin S., Manoj B. Charati, and Kristi L. Kiick. "Biosynthesis of Protein-Based Polymeric Materials." In Macromolecular Engineering, 479–517. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527631421.ch11.

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Hirao, Toshikazu. "Macromolecular Conjugated Complexes." In Macromolecular Nanostructured Materials, 168–81. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-08439-7_10.

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Tseng, Hsian-Rong, Paul C. Celestre, and J. Fraser Stoddart. "An Integrated Systems-oriented Approach to Molecular Electronics." In Macromolecular Nanostructured Materials, 2–25. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-08439-7_1.

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Toshima, Naoki. "Polymer-capped Bimetallic Nanoclusters as Active and Selective Catalysts." In Macromolecular Nanostructured Materials, 182–96. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-08439-7_11.

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Kim, Kyung-Min, and Yoshiki Chujo. "Organic-Inorganic Hybrid Materials Based on Silsesquioxanes." In Macromolecular Nanostructured Materials, 197–208. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-08439-7_12.

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Nishihara, Hiroshi, and Masaki Murata. "Protonation-induced Intramolecular Electron Transfer in the Ferrocene-Quinone Conjugated System." In Macromolecular Nanostructured Materials, 209–23. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-08439-7_13.

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Okamura, Taka-aki, and Norikazu Ueyama. "Oligomers of Non-natural Metal Complex Amino Acids." In Macromolecular Nanostructured Materials, 224–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-08439-7_14.

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Reedijk, Jan. "Macromolecular Metal Complexes in Biological Systems." In Macromolecular Nanostructured Materials, 244–57. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-08439-7_15.

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Yamaguchi, Hiroyasu, and Akira Harada. "Direct Observation of Supramolecular Structures of Biorelated Materials by Atomic Force Microscopy." In Macromolecular Nanostructured Materials, 258–72. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-08439-7_16.

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Conference papers on the topic "Macromolecular materials"

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Cooper, Kristi L., Richard O. Claus, Jeffrey B. Mecham, Keith Huie, and Rochael Swavey. "Self-organization of macromolecular materials by self-assembly." In Complex Adaptive Structures, edited by William B. Spillman, Jr. SPIE, 2001. http://dx.doi.org/10.1117/12.446781.

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Rebane, Aleksander K., and Alexander Mikhaylov. "Polarized light scattering by macromolecular self-assembly of J-aggregates." In Organic Photonic Materials and Devices XX, edited by Christopher E. Tabor, François Kajzar, Toshikuni Kaino, and Yasuhiro Koike. SPIE, 2018. http://dx.doi.org/10.1117/12.2287881.

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ROSS-MURPHY, SIMON B. "THE RHEOLOGY OF MACROMOLECULAR AND SUPRAMOLECULAR BIOMATERIALS." In Proceedings of the Fifth Royal Society–Unilever Indo-UK Forum in Materials Science and Engineering. A CO-PUBLICATION OF IMPERIAL COLLEGE PRESS AND THE ROYAL SOCIETY, 2000. http://dx.doi.org/10.1142/9781848160163_0015.

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Liu, Pu, Haitao Zheng, Pingping Nie, Yaotian Wei, Zhenchao Feng, and Tao Sun. "Bioelectrochemical activity of an electroactive macromolecular weight coenzyme derivative." In Second International Conference on Smart Materials and Nanotechnology in Engineering, edited by Jinsong Leng, Anand K. Asundi, and Wolfgang Ecke. SPIE, 2009. http://dx.doi.org/10.1117/12.838551.

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Lakatos, Istvan Janos, Julianna Lakatos-Szabo, Gabriella Szentes, and Marianna Vadaszi. "Mitigation of Formation Damage Caused by Macromolecular Materials Using Liquid Polymers." In SPE European Formation Damage Conference & Exhibition. Society of Petroleum Engineers, 2013. http://dx.doi.org/10.2118/165176-ms.

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De Rossi, Danilo. "Polymer electromechanics: mechanical sensing and actuation properties of organic macromolecular systems." In Smart Structures and Materials: Second European Conference, edited by Alaster McDonach, Peter T. Gardiner, Ron S. McEwen, and Brian Culshaw. SPIE, 1994. http://dx.doi.org/10.1117/12.184822.

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Mykhaylyk, V., R. Duman, and A. Wagner. "Challenges and advances of long-wavelength macromolecular crystallography at Diamond Light Source." In 2014 IEEE International Conference on Oxide Materials for Electronic Engineering (OMEE). IEEE, 2014. http://dx.doi.org/10.1109/omee.2014.6912319.

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"MODELING AND ANALYSIS OF GENERALIZED PHOTOTHERMAL PULSE RESPONSE FOR CHARACTERIZATION OF THE MACROMOLECULAR MATERIALS." In Perspektivnye materialy s ierarkhicheskoy strukturoy dlya novykh tekhnologiy i nadezhnykh konstruktsiy, Khimiya nefti i gaza. Tomsk State University, 2018. http://dx.doi.org/10.17223/9785946217408/370.

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Akimov, A. S., N. N. Sviridenko, M. A. Morozov, S. V. Panin, V. O. Aleksenko, V. A. Vlasov, and A. V. Vosmerikov. "Structural changes and chemistry of petroleum macromolecular components during thermocatalytic processing." In 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/10.1063/1.5131874.

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Poulain, Xavier, Ramesh Talreja, and Amine Benzerga. "Prediction of Impact-Induced Damage Accumulation in a Composite Using a Macromolecular Polymer Model." In 50th AIAA/ASME/ASCE/AHS/ASC Structures, Structural Dynamics, and Materials Conference. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2009. http://dx.doi.org/10.2514/6.2009-2621.

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Reports on the topic "Macromolecular materials"

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Forest, M. G. High-Performance Macromolecular Materials. Fort Belvoir, VA: Defense Technical Information Center, March 2006. http://dx.doi.org/10.21236/ada444313.

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Forest, M. G. High-Performance Macromolecular Materials. Fort Belvoir, VA: Defense Technical Information Center, February 2010. http://dx.doi.org/10.21236/ada518688.

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Karasz, Frank E. Ultrastructure Processing of Macromolecular Materials. Fort Belvoir, VA: Defense Technical Information Center, November 1990. http://dx.doi.org/10.21236/ada230175.

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Wang, Qi. Hydrodynamics of Macromolecular and Nano-Composite Materials. Fort Belvoir, VA: Defense Technical Information Center, August 2005. http://dx.doi.org/10.21236/ada437262.

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Pang, Yi. Novel Macromolecular Materials for Electronic and Optical Applications. Fort Belvoir, VA: Defense Technical Information Center, October 1997. http://dx.doi.org/10.21236/ada339081.

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Forest, M. G. A Control Strategy for High-Performance Macromolecular Materials. Fort Belvoir, VA: Defense Technical Information Center, January 2007. http://dx.doi.org/10.21236/ada464293.

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Mandal, Braja K., Jan-Chan Huang, Jayant Kumar, and Sukant Tripathy. A Strategy for the Development of Macromolecular Nonlinear Optical Materials. Fort Belvoir, VA: Defense Technical Information Center, January 1990. http://dx.doi.org/10.21236/ada226325.

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Guo, Ruilan. Design, Synthesis and Characterization of Triptycene-Containing Macromolecules with Hierarchically Controlled Architectures as Functional Membrane Materials for Energy Applications. Office of Scientific and Technical Information (OSTI), March 2019. http://dx.doi.org/10.2172/1499993.

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