Готові списки джерел за темами / Macromolecular and materials chemistry

Добірка наукової літератури з теми "Macromolecular and materials chemistry"

Автор: Grafiati
Опубліковано: 10 грудня 2022
Оновлено: 28 січня 2023

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Статті в журналах з теми "Macromolecular and materials chemistry"

1

Lutz, Jean-François, and Hans G. Börner. "Precision Macromolecular Chemistry." Macromolecular Rapid Communications 32, no. 2 (December 14, 2010): 113–14. http://dx.doi.org/10.1002/marc.201000728.

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2

Suter, Ulrich W. "Materials science — a challenge to macromolecular chemistry." Macromolecular Chemistry and Physics 195, no. 1 (January 1994): 29–34. http://dx.doi.org/10.1002/macp.1994.021950104.

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3

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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4

Balsam, Martin, Peter Barghoorn, and Uwe Stebani. "Trends in applied macromolecular chemistry." Die Angewandte Makromolekulare Chemie 267, no. 1 (June 1, 1999): 1–9. http://dx.doi.org/10.1002/(sici)1522-9505(19990601)267:1<1::aid-apmc1>3.0.co;2-1.

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5

Hata, Yuuki, Toshiki Sawada, and Takeshi Serizawa. "Macromolecular crowding for materials-directed controlled self-assembly." Journal of Materials Chemistry B 6, no. 40 (2018): 6344–59. http://dx.doi.org/10.1039/c8tb02201a.

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6

Heeger, Alan J. "Semiconducting and Metallic Polymers: The Fourth Generation of Polymeric Materials." MRS Bulletin 26, no. 11 (November 2001): 900–904. http://dx.doi.org/10.1557/mrs2001.232.

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Анотація:
Prior to receiving the Nobel Prize in chemistry in 2000 for my work in polymers, polymer science had been recognized three times. The first Nobel Prize in chemistry for polymer science was awarded in 1953 to Hermann Staudinger, for his pioneering work in the 1920s. At that time, the concept of macromolecules was new, and his ideas were controversial. However, the data prevailed, and he was awarded the Prize “for his discoveries in the field of macromolecular chemistry.” The next major event in polymer science was the discovery and invention of nylon by Wallace Carothers at the Dupont Company in 1935. Although Carothers died as a young man, his discoveries created an industry. I have little doubt that his work was deserving of a Nobel Prize and probably would have been awarded. The next related Prize went to Karl Ziegler and Giulio Natta in 1963 for their work on polymer synthesis in the 1950s. The Ziegler–Natta catalysts made possible the large-scale production of polymers such as polypropylene. They were awarded the Nobel Prize in chemistry “for their discoveries in the field of chemistry and technology of high polymers.” In 1974, the Prize for chemistry went to Paul J. Flory, who was a giant in this field. He was awarded the Nobel “for his fundamental achievements, both theoretical and experimental, in the physical chemistry of macromolecules.”
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Zaikov, G. E. "Colloquium on Macromolecular Chemistry: Report." Polymer-Plastics Technology and Engineering 31, no. 3-4 (March 1992): 359–61. http://dx.doi.org/10.1080/03602559208017752.

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8

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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9

Gandini, Alessandro, Armando J. D. Silvestre, and Dora Coelho. "Reversible click chemistry at the service of macromolecular materials." Polymer Chemistry 2, no. 8 (2011): 1713. http://dx.doi.org/10.1039/c1py00125f.

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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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Дисертації з теми "Macromolecular and materials chemistry"

1

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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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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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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5

Van, Schalkwyk Welmarie. "Self-assembly of amphiphilic discotic materials." Thesis, Stellenbosch : Stellenbosch University, 2013. http://hdl.handle.net/10019.1/79799.

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Thesis (MSc)--Stellenbosch University, 2013.
ENGLISH ABSTRACT: The creation of nanometer-scale (nanoscale) materials has fascinated and inspired the scientific community for more than a quarter of a century because of the wide range of applications of these materials, e.g. applications in drug delivery, medicine, tissue engineering, memory storage, display and audio devices, semiconductors, etc. π-Conjugated dendrimers have a proposed flat packing arrangement. An alternating phenyl isoxazole dendrimer system was developed to investigate this phenomenon. The synthesis of this dendritic system was attempted by divergent and convergent approaches. Preparation of the second generation failed because some functional groups inhibited the monomers to react to the first generation. Other examples of nano materials that have attracted a vast amount of interest are the so-called discotic amphiphiles. Discotic amphiphilic molecules have the potential to self-assemble into helical architectures. Discotic systems bearing chiral polar side chains (one and three respectively) were developed. Their self-assembly was investigated in variable concentration and variable solvent composition experiments. These systems did show signs of aggregation in UV-vis and CD spectroscopy experiments. Thread-like helical structures were observed with transmission electron microscopy.
AFRIKAANSE OPSOMMING: Nanometer-skaal materiale inspireer en fassineer wetenskaplikes al vir meer as 25 jaar as gevolg van hulle wye verskeidenheid toepassings bv.: die vervoer van geneesmiddels, weefsel ontwerp, geheue stoorspasie, digitale skerms, klank toerusting, geleiers, ens. π-Gekonjugeerde dendrimere het 'n plat drie dimmensionele rangskikking. 'n Afwisselende feniel isoxazole dendrimer stelsel was ontwikkel om hierdie verskynsel te ondersoek. Die sintese van hierdie dendritiese stelsel is aangepak deur divergerende en konvergerende benaderings. Sintese van die tweede generasie het misluk omdat sommige funksionele groepe die monomere geïnhibeer het om te reageer met die eerste generasie. Ander interessante voorbeelde van nano materiale, is die sogenaamde skyfvormige amphiphiles. Skyfvormige amphiphiles het die potensiaal om spontaan te versamel in heliese strukture. Skyfvormige molekules met chirale polêre sykettings (een en drie onderskeidelik) is ontwikkel. Hulle potensiaal om spontaan te versamel is ondersoek met wisselende konsentrasie en wisselende oplosmiddel samestelling eksperimente. Hierdie stelsels het tekens van versameling gewys in UV-vis en CD-spektroskopiese eksperimente. Staaf-vormige heliese strukture is waargeneem met transmissie-elektronmikroskopie.
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6

Lenart, William R. "EXPANDING EXPERIMENTAL AND ANALYTICAL TECHNIQUES FOR THE CHARACTERIZATION OF MACROMOLECULAR STRUCTURES." Case Western Reserve University School of Graduate Studies / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1584358701735061.

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7

Wu, Haiyan. "Design and Development of New Chemistry for Biosensing." University of Akron / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=akron1502459975409826.

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Ehrlich, Deborah J. C. "Synthetic strategies for control of structure from individual macromolecules to nanoscale materials to networks." Thesis, Massachusetts Institute of Technology, 2019. https://hdl.handle.net/1721.1/122451.

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Анотація:
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemistry, 2019
Cataloged from PDF version of thesis.
Includes bibliographical references.
Chapter 1. Aqueous self-assembly of prodrug macromonomers. A series of highly tunable micelles for drug delivery were made from norbornene based poly(ethylene glycol) macromonomers with covalently linked drugs. A total of five macromonomers were made using three different drugs (telmisartan, paclitaxel, and SN-38) and three different drug loadings. Combinations of these macromonomers were then allowed to self assemble into micellar aggregates. The size, stability, and shape of these micellar aggregates were controlled with the highly versatile structure. Chapter 2. Post micellization modification of norbornene-containing prodrug macromonomers. Highly tunable micelles for drug delivery were functionalized after their selfassembly. Post-micellization inverse electron demand Diels-Alder reactions of norbornenes and tetrazines were used to signal changes in micelle size and stability through the addition of either hydrophilic or hydrophobic tetrazines.
Thiol-ene additions reactions were used to increase micelle size and form chemically crosslinked nanoparticles. These modifications of norbornene-containing prodrug macromonomer assemblies illustrate their versatility. Chapter 3. Synthesis of polymers by iterative exponential growth. A scalable synthetic route that enables absolute control over polymer sequence and structure has remained a key challenge in polymer chemistry. Here, we report an iterative exponential growth plus side-chain functionalization (IEG+) strategy for the production of macromolecules with defined sequence, length, and stereoconfiguration. Each IEG+ cycle begins with the azide opening of an enantiopure epoxide, followed by side chain functionalization, alkyne deprotection, and copper-catalyzed azide-alkyne cycloaddition (CuAAC). These cycles have been conducted to form unimolecular macromolecules with molar masses of over 6,000 g/mol.
Subsequent modifications to IEG+ allow for the functionalization of monomers prior to the IEG+ cycle, expanding the library of compatible side chain chemistries. Chapter 4. Introduction to elastomer toughening strategies. Silicone elastomers are ubiquitous. Here, silicone elastomers are discussed in terms of network structure, the impact of network structure upon physical properties, and modifications of network structure in order to achieve desired physical properties. Fillers, the standard toughening strategy, are discussed in conjunction with entanglement density. Focus is placed on the impact of entanglement density on material properties. Topological networks are discussed and noted for their stress dissipative properties. Chapter 5. Topology modification of polydimethylsiloxane elastomers through loop formation. Topological networks are well known for their stress dissipation through the pulley effect leading to soft, extensible materials.
Combining these properties with a traditionally crosslinked network to produce a hybrid material allows for enhanced extensibility without a loss in modulus. Here, such hybrid networks were made with poly(dimethyl siloxane) polymers of a range of molecular weights. Side-loop polymer brushes were synthesized and then crosslinked to create hybrid networks with the statistical formation of topological bonds. These materials were characterized through tensile testing. Elastomers formed with the same molecular weight polymer in both side-loops and network formation did not show mechanical properties that depended upon the fraction of networks used for brush formation. Elastomers made with long polymers in brush formation and shorter polymers for network formation resulted in highly extensible systems without significant loss in modulus.
by Deborah J.C. Ehrlich.
Ph. D.
Ph.D. Massachusetts Institute of Technology, Department of Chemistry
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9

Etok, S. E. "Structural characterisation and in vitro behaviour of apatite coatings and powders." Thesis, Faculty of Medicine and Biosciences, 2009. http://hdl.handle.net/1826/3973.

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Hydroxyapatite (HAP) coatings are used in orthopaedic surgery for bone regeneration. Current methods of phase quantification of HAP coatings suffer from drawbacks. A novel methodology of quantitative phase analysis of HAP coatings has been devised and validated. This method, based on whole pattern fitting with a fundamental parameters approach, incorporates amorphous calcium phosphate (ACP) and apatite phases into structural refinements. A comparison of the structural and chemical properties of plasma sprayed (PS) and novel electrodeposited (ED) HAP coatings has been conducted. ED coatings contained less ACP and more preferred orientation than the PS coatings, although the stoichiometry was similar. In vitro investigations of PS and ED coatings in simulated body fluid and foetal calf serum revealed that both are bioactive. A carbonated apatite layer produced on the ED coatings was -0.7μm thick with a stoichiometry and chemical constituents similar to that of natural bone apatite. PS coatings produced a nanocrystalline carbonated apatite layer (-4μm). For the first time it has been possible to model crystalline HAP and nanocrystalline apatite as independent phases and obtain accurate lattice parameters for each. A positive linear correlation has been made between microstrain and the solubility of HAP and carbonated apatites. Dissolution studies have shown that the behaviour of HAP and carbonated apatite is dominated by crystallite size at low undersaturation and by crystallite size and microstrain at high undersaturation for crystallites between -30OA- 1000A. Metastable equilibrium occurred for crystallites <_400A at low undersaturation. Carbonate content did not affect the solubility or dissolution behaviour. A novel technology for coating polymeric tape with HAP for potential use in anterior cruciate ligament reconstruction has been devised. Mechanical tests have demonstrated that no adverse properties are induced by the coating technology. Cell culture studies have shown that the HAP layer is capable of enhanced attachment, proliferation and differentiation of osteoblast cells compared to uncoated tape.
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10

Etok, Susan Essien. "Structural characterisation and in vitro behaviour of apatite coatings and powders." Thesis, Cranfield University, 2005. http://dspace.lib.cranfield.ac.uk/handle/1826/3973.

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Анотація:
Hydroxyapatite (HAP) coatings are used in orthopaedic surgery for bone regeneration. Current methods of phase quantification of HAP coatings suffer from drawbacks. A novel methodology of quantitative phase analysis of HAP coatings has been devised and validated. This method, based on whole pattern fitting with a fundamental parameters approach, incorporates amorphous calcium phosphate (ACP) and apatite phases into structural refinements. A comparison of the structural and chemical properties of plasma sprayed (PS) and novel electrodeposited (ED) HAP coatings has been conducted. ED coatings contained less ACP and more preferred orientation than the PS coatings, although the stoichiometry was similar. In vitro investigations of PS and ED coatings in simulated body fluid and foetal calf serum revealed that both are bioactive. A carbonated apatite layer produced on the ED coatings was -0.7μm thick with a stoichiometry and chemical constituents similar to that of natural bone apatite. PS coatings produced a nanocrystalline carbonated apatite layer (-4μm). For the first time it has been possible to model crystalline HAP and nanocrystalline apatite as independent phases and obtain accurate lattice parameters for each. A positive linear correlation has been made between microstrain and the solubility of HAP and carbonated apatites. Dissolution studies have shown that the behaviour of HAP and carbonated apatite is dominated by crystallite size at low undersaturation and by crystallite size and microstrain at high undersaturation for crystallites between -30OA- 1000A. Metastable equilibrium occurred for crystallites <_400A at low undersaturation. Carbonate content did not affect the solubility or dissolution behaviour. A novel technology for coating polymeric tape with HAP for potential use in anterior cruciate ligament reconstruction has been devised. Mechanical tests have demonstrated that no adverse properties are induced by the coating technology. Cell culture studies have shown that the HAP layer is capable of enhanced attachment, proliferation and differentiation of osteoblast cells compared to uncoated tape.
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Книги з теми "Macromolecular and materials chemistry"

1

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

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2

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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4

Howell, Bob A., ed. Introduction of Macromolecular Science/Polymeric Materials into the Foundational Course in Organic Chemistry. Washington, DC: American Chemical Society, 2013. http://dx.doi.org/10.1021/bk-2013-1151.

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5

N, Reinhoudt D., ed. Supramolecular materials and technologies. Chichester: Wiley, 1999.

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6

1945-, Mendenhall G. David, Greenberg Arthur, and Liebman Joel F, eds. Mesomolecules: From molecules to materials. New York, N.Y: Chapman & Hall, 1995.

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7

Click chemistry for biotechnology and materials science. Chichester, West Sussex: Wiley, 2009.

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8

OUMS '98 (3rd 1998 Osaka, Japan). Molecular interactions and time-space organization in macromolecular systems: Proceedings of the OUMS'98, Osaka, Japan, 3-6 June, 1998. Berlin: Springer-Verlag, 1999.

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9

H, Lima Arturo, ed. Biomimetic and supramolecular systems research. New York: Nova Science Publishers, 2008.

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10

Ekkehardt, Hahn, and SpringerLink (Online service), eds. Chemistry of Nanocontainers. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012.

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Частини книг з теми "Macromolecular and materials chemistry"

1

Hanabusa, Kenji. "Development of Organogelators Based on Supramolecular Chemistry." In Macromolecular Nanostructured Materials, 118–37. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-08439-7_7.

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2

Gronwald, Oliver, and Seiji Shinkai. "“Inorganic” Combinatorial Chemistry Utilizing Sol-Gel Transcription of Gelatinous Organic Superstructures." In Macromolecular Nanostructured Materials, 101–17. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-08439-7_6.

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3

Wang, Hui, Dan-Wei Zhang, and Zhan-Ting Li. "Hydrogen Bonding for Molecular, Macromolecular, and Supramolecular Materials." In Lecture Notes in Chemistry, 185–231. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45780-1_6.

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4

Decker, Christian. "Photostabilization of Macromolecular Materials by UV-Cured Protective Coatings." In Advances in Chemistry, 319–34. Washington, DC: American Chemical Society, 1996. http://dx.doi.org/10.1021/ba-1996-0249.ch021.

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5

Sugiyasu, Kazunori, and Seiji Shinkai. "Supra-Macromolecular Chemistry: Toward Design of New Organic Materials from Supramolecular Standpoints." In Supramolecular Polymer Chemistry, 51–70. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527639786.ch3.

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6

Fundueanu, Gheorghe, Sanda Bucatariu, and Marieta Constantin. "Smart Polymeric Materials for Drug Delivery." In New Trends in Macromolecular and Supramolecular Chemistry for Biological Applications, 275–94. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-57456-7_14.

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7

Gandini, Alessandro, and Mohamed Naceur Belgacem. "Furan Chemistry at the Service of Functional Macromolecular Materials: The Reversible Diels-Alder Reaction." In ACS Symposium Series, 280–95. Washington, DC: American Chemical Society, 2007. http://dx.doi.org/10.1021/bk-2007-0954.ch018.

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8

Khosravi, Ezat, Thomas C. Castle, Margaret Kujawa, Jan Leejarkpai, Lian R. Hutchings, and Peter J. Hine. "Romp: The Method of Choice for Precise Macromolecular Engineering and Synthesis of Smart Materials." In NATO Science for Peace and Security Series A: Chemistry and Biology, 223–36. Dordrecht: Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-3278-2_14.

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9

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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10

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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Тези доповідей конференцій з теми "Macromolecular and materials chemistry"

1

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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2

NOGALES, EVA. "CRYO-EM VISUALIZATION OF MACROMOLECULAR STRUCTURE AND DYNAMICS." In 25th Solvay Conference on Chemistry. WORLD SCIENTIFIC, 2021. http://dx.doi.org/10.1142/9789811228216_0037.

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3

Nunes da Silva, Raquel, Roberto Dias, Catarina Costa, Maria Santos, Ana Sousa, Mariana Alves, Susana Braga, et al. "Bio-macromolecular detection: new organic vital dyes." In 6th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07509.

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4

Torrens, Francisco, and Gloria Castellano. "A NEW TOOL FOR THE INTERROGATION OF MACROMOLECULAR STRUCTURE." In The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-e006.

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5

Torrens, Francisco, and Gloria Castellano. "A New Tool for the Interrogation of Macromolecular Structure in Chemical Education." In The 12th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01279.

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6

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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7

González-Díaz, Humberto, Alcides Pérez-Bello, Eugenio Uriarte, and Yenny González-Díaz. "QSAR Study for Macromolecular RNA Folded Secondary Structures of Mycobacterial Promoters with Low Sequence Homology." In The 9th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01654.

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8

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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9

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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Звіти організацій з теми "Macromolecular and materials chemistry"

1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

Davies, Peter K., Peter K. Davies, and Robert S. Roth. Chemistry of electronic ceramic materials. Gaithersburg, MD: National Institute of Standards and Technology, 1991. http://dx.doi.org/10.6028/nist.sp.804.

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9

Fox, G. A., T. F. Baumann, L. J. Hope-Weeks, and A. L. Vance. Chemistry and Processing of Nanostructured Materials. Office of Scientific and Technical Information (OSTI), January 2002. http://dx.doi.org/10.2172/15005302.

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10

Rhodie, K., C. Mailhiot, D. Eaglesham, C. Hartmann-Siantar, L. Turpin, and P. Allen. Chemistry and Materials Science Strategic Plan. Office of Scientific and Technical Information (OSTI), April 2004. http://dx.doi.org/10.2172/15009835.

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