Relevant bibliographies by topics / Fundamental chemistry

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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 'Fundamental chemistry'

Author: Grafiati
Published: 4 June 2021
Last updated: 18 February 2022

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Journal articles on the topic "Fundamental chemistry"

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KATO, Masayoshi. "Fundamental chemistry of etching." Journal of the Metal Finishing Society of Japan 38, no. 5 (1987): 172–79. http://dx.doi.org/10.4139/sfj1950.38.172.

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MATSUMOTO, Osamu. "Fundamental aspects of plasma chemistry." Jitsumu Hyomen Gijutsu 34, no. 10 (1987): 379–90. http://dx.doi.org/10.4139/sfj1970.34.379.

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LÜ, Ping, and Yanguang WANG. "Stereoelectronic Effects in Fundamental Organic Chemistry." University Chemistry 33, no. 12 (2018): 113–20. http://dx.doi.org/10.3866/pku.dxhx201811001.

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ISHIKAWA, Masamichi. "Fundamental Physics and Chemistry under Microgravity." Journal of the Society of Mechanical Engineers 107, no. 1025 (2004): 258–60. http://dx.doi.org/10.1299/jsmemag.107.1025_258.

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Canac, Yves. "Carbon Ligands: From Fundamental Aspects to Applications." Molecules 26, no. 8 (April 8, 2021): 2132. http://dx.doi.org/10.3390/molecules26082132.

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Chaloner, Penny A. "Organotransition metal chemistry; fundamental concepts and applications." Journal of Organometallic Chemistry 317, no. 1 (December 1986): C17—C18. http://dx.doi.org/10.1016/s0022-328x(00)99355-0.

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ROSS, LINDA. "UNDERGRADUATE CHEMISTRY NSF to promote fundamental changes." Chemical & Engineering News 71, no. 21 (May 24, 1993): 4–5. http://dx.doi.org/10.1021/cen-v071n021.p004.

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S, S. J. "Organotransition Metal Chemistry, Fundamental Concepts and Applications." Journal of Molecular Structure 172 (February 1988): 437. http://dx.doi.org/10.1016/0022-2860(88)87036-4.

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Skull, Alan. "Eurozone crisis, green chemistry, and fundamental research." Focus on Surfactants 2012, no. 9 (September 2012): 1. http://dx.doi.org/10.1016/s1351-4210(12)70237-8.

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Krebs, Bernt, and Jan Reedijk. "Bioinorganic Chemistry - From Fundamental Research to Applications." Zeitschrift für anorganische und allgemeine Chemie 639, no. 8-9 (July 2013): 1295–96. http://dx.doi.org/10.1002/zaac.201310001.

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Dissertations / Theses on the topic "Fundamental chemistry"

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Tun, Zin-Min. "Fundamental Chlorophosphazene Chemistry." University of Akron / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=akron1321278169.

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Wheatley, James Ernest. "Fundamental chemistry of carbon dioxide capture." Thesis, University of Leeds, 2017. http://etheses.whiterose.ac.uk/18363/.

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Carbon dioxide capture is an urgently needed pathway to mitigation of climate change, yet the amine-based solvents currently considered the leading industrial technologies suffer from many shortcomings; namely their high operating cost, poor stability and potentially damaging environmental impact from emission of degradation products. This work is a study of possible routes to improved CO2 capture technologies from a fundamental chemistry perspective. Initial work focused on the development of a straightforward and adaptable protocol for studying the species formed by CO2 capture into amine solvents, using 1H NMR spectroscopy for its combination of speed and accuracy. The applicability of this approach to diverse blended-amine solvents was demonstrated. This method was then applied to the study of phenoxide as a novel possible capture agent in conjunction with amines. Blends of potassium phenoxide with monoethanolamine were found to have an excellent capture capacity and favourable speciation that suggests a low energy consumption in practical use. This demonstrates the feasibility of blended solvents with a reduced amine component. Finally, a possible amine-free route to CO2 capture, exploiting the high susceptibility of carboxylate acidity to solvation, was explored. The first systematic study of the pKa of CO2 in mixtures of organic solvent and water was carried out, finding that this value is relatively insensitive to the makeup of the solvent and therefore in organic-rich solutions, carboxylate salts can be used as a CO2-absorbing base. CO2 capture using a system developed along these principles was demonstrated, and the possible basis for the observed insensitivity was discussed with particular emphasis given to the thermodynamics of the process.
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Stiel, Jason A. "Fundamental Chemistry of Chlorophosphazenes and Polysilanes." University of Akron / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=akron1467990664.

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Lamm, Ashley, and Ashley Lamm. "Fundamental Chemistry of 1,2-Dihydro-1,2-Azaborines." Thesis, University of Oregon, 2012. http://hdl.handle.net/1794/12514.

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Benzene and its derivatives are ubiquitous in chemical research, with applications ranging from material science to biomedical research. 1,2-Dihydro-1,2-azaborine is a benzene mimic which replaces a CC bond with a BN bond. The basic science and applications of 1,2-azaborines is relatively underdeveloped. This thesis expands the fundamental understanding of 1,2-azaborines. Chapter I describes the air and moisture stability of 1,2-azaborines. Chapter II introduces nucleophilic aromatic substitution reactions that the parent 1,2-dihydro-1,2-azaborine will undergo. Chapter III discusses a trimerization reaction that 1,2-dihydro-1,2-azaborine can perform, which is unique from benzene. Chapter IV examines a novel protection free synthesis of 1,2-azaborines, which provides a more direct route to functionalized 1,2-azaborines. Chapter V discusses the novel deprotection of the N-silicon using an amide, giving one of the first 1,2-azaborine pharmaceutical mimics. Finally, chapter VI summarized miscellaneous contributions I have made to the basic science of 1,2-azaborines. This dissertation includes previously published and unpublished co-authored material.
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Saleh, Nidal. "Chiral complexes : from fundamental chirality to helicene chemistry." Thesis, Rennes 1, 2013. http://www.theses.fr/2013REN1S112/document.

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Au cours de ce travail de doctorat, nous avons d'abord étudié un aspect fondamental de la chiralité au niveau moléculaire visant à observer des différences d'énergie entre deux énantiomères provenant d'effets de violation de la parité (PV). Nous avons en particulier examiné les complexes oxorhénium chiraux dont les deux énantiomères présentent théoriquement des énergies d'absorption infrarouge différentes. Leur propriétés chiroptiques, en particulier leur dichroïsme circulaire vibrationnel (VCD), ont été examinées. D'autres complexes métalliques chiraux comme des complexes de platine portant un carbone asymétrique fluoré ont été préparés. Par ailleurs, nous avons étudié la chiralité hélicoïdale provenant de la fusion en ortho de plusieurs cycles aromatiques. Ainsi, des hélicènes portant des fonctionnalités bi-pyridines ont été synthétisés et ont montré des propriétés photophysiques et chiroptiques intéressantes. La présence d'unité chélatantes de type N^N’ ou N-C nous a permis d'étudier l'influence de la coordination de divers métaux de transition (Re(I) et Pt(II)) sur les propriétés et de concevoir de nouveaux commutateurs chiroptiques acido-basiques
In this PhD work, we first investigated a fundamental aspect of chirality at the molecular level aiming to determine the parity violation (PV) energy difference between two enantiomers. We focused on chiral oxorhenium complexes for which the two corresponding enantiomers show theoretically different infrared absorption energies. Their chiroptical properties and especially their vibrational circular dichroism (VCD) were examined. Other chiral metal complexes such as platinum complexes bearing an asymmetric fluorinated carbon have also been prepared. Furthermore, we have investigated the helical chirality derived from the skew shape of ortho-fused aromatic ring. Indeed, helicenes bearing 2,2’-bipyridine functionalities were synthesized and they showed interesting photophysical and chiroptical properties. The presence of N^N’ or N-C chelating moieties enabled us to study the coordination effect of different transition metals (Re(I) and Pt(II)) on their properties and to conceive new acid-base triggered chiroptical switches
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McKay, Hayley. "Fundamental studies of surface reaction mechanisms." Thesis, University of Cambridge, 2010. https://www.repository.cam.ac.uk/handle/1810/252213.

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Wood, David John. "Fundamental studies on ionomer glasses." Thesis, University of Greenwich, 1993. http://gala.gre.ac.uk/6347/.

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Composition-structure-property relationships were studied in glasses of the type used to produce glass lonomer dental cements. These materials are currently being developed as a bone cement in joint replacement surgery. Initially, a simple quaternary (25i02-Al203-CaO-CaF2) glass was produced and was found to undergo minimal fluorine loss. This results in a glass whose composition is reproducible between batches. This composition, however, was too reactive to form a glass ionomer cement. A glass-ceramic approach was pursued to deactivate the glass and following heat treatments, cements were produced whose properties varied depending upon the precise heat treatment used. The heat treatments above the glass transition temperature resulted in amorphous phase separation, probably by a spinodal decomposition mechanism, followed by a two stage crystallization of calcium fluoride (fluorite) and anorthite. The anorthite phase crystallized from fluorite nuclei and, in effect, crystallization occurred by a bulk nucleation mechanism. The glass will also undergo significant crystallization to fluorite below the glass transition temperature, with surface nucleation the dominant mechanism. This explains the deactivation of ionomer glasses used commercially to control the setting properties of dental glass ionomer cements. The structural role of fluorine in these glasses was also investigated. It seems that fluorine is present in the glass network, rather than existing as a discreet entity bonded to a modifying cation. There is evidence that the fluoride ions are bonded only to aluminium sites and act to disrupt network connectivity. A commercial glass was examined and was found to be clearly phase separated. This glass was found to crystallize to apatite and mullite. Apatite is the mineral phase of bone and enamel and this may explain the excellent biocornpatability of glass ionomer cements. Glasses containing sodium and phosphate ions have also been produced. The sodium containing glasses were all found to crystallize from the melt to calcium fluoride. The phosphate containing glasses formed cements without any subsequent modification, and following a simple heat treatment, all of the phosphate containing glasses were found again to crystallize initially to an apatite phase. Selected compositions additionally crystallized to mullite. These glass-ceramics were tougher than the base glasses and this is attributed to the presence of interlocking needles of the two phases. Some of the glasses were easily castable to produce optically clear glasses, and in addition the glasses underwent bulk nucleation via prior amorphous phase separation, to give needles of apatite and mullite. These glass-ceramics thus show tremendous potential for use as a bloactive bone substitute material or as a castable crown.
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Han, Qi. "Electrocatalysis at the Electrode-Adsorbate-Solution Interface: Fundamental Studies." Case Western Reserve University School of Graduate Studies / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1574855036013662.

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Pappas, Iraklis. "Fundamental investigations into dinitrogen fixation by group 4 metals." Thesis, Princeton University, 2016. http://pqdtopen.proquest.com/#viewpdf?dispub=10120357.

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Addition of terminal or internal alkynes to a base free titanocene oxide results in synthesis of the corresponding oxometallocyclobutene. With appropriate cyclopentadienyl substitution, these compounds undergo reversible C-C reductive elimination offering a unique approach to cyclopentadienyl modification. Subsequent reactivity demonstrates the complete scission of the Ti=O multiple bond.

Cycloaddition of monosubstituted allenes with a monomeric, base free titanocene oxide resulted in isolation and crystallographic characterization of the corresponding oxatitanacyclobutanes. In solution these compounds are a mixture of (E) and (Z) isomers and interconvert by mechanisms that are dependent on the specific substitution of the allene. Facile carbonylation of the oxatitanacyclobutanes was also observed to yield rare examples of structurally characterized oxatitanacyclopentanones. These studies highlight the new chemistry available from synthesis of base free titanocene oxide compounds enabled by appropriate cyclopentadienyl substitution.

The hydrogenolysis of titanium nitrogen bonds in a family of bis(cyclopentadienyl) titanium amides, hydrazides, and imides via proton coupled electron transfer (PCET) is demonstrated. (η5-C5Me5)(py-Ph)Rh-H (py-Ph = 2-pyridylphenyl, [Rh]-H) and (η5- C5R5)(CO)3CrH ([Cr]R-H, R= H, Me) were used as catalysts for homolytic H2 activation followed by PCET to the nitrogen-containing fragment. Detailed mechanistic studies and an analysis of the underlying thermochemistry are employed to explain the decreased catalytic efficiency of [Cr]R-H compared to [Rh]-H. The N-H bond dissociation free energies (BDFEs) in 12 structurally similar compounds were determined through a combination of experimental and computational methods, providing a foundation for the use of N-H BDFEs as a metric to enable NH3 synthesis from H 2 and N2 at a well-defined metal center.

Combination of the readily available a-diimine ligand, ((ArN=C(Me)) 2 Ar = 2,6-iPr2-C6H3), (iPrDI) with air-stable nickel(II) bis(carboxylates) generated a highly active catalyst exhibiting anti-Markovnikov selectivity for the hydrosilylation of alkenes with (EtO)3SiH. The exclusive selectivity for formation of terminal alkyl silanes was also observed with internal alkenes via a tandem isomerization-hydrosilylation pathway. The hydrosilylation of 1-octene with triethoxysilane, a reaction performed commercially in the silicones industry on a scale of > 12,000,000 lbs/year, was performed on a 10 g scale with 96 % yield and >98 % selectivity for the desired product.

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Pastor, Michael B. "Bimetallic Complexes| The Fundamental Aspects of Metalmetal Interactions, Ligand Sterics and Application." Thesis, University of the Pacific, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=10932512.

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Metal containing complexes have been used to catalyze various organic transformations for the past few decades. The success of several mononuclear catalysts led to transition metal catalysts used in pharmaceuticals, environmental, and industrial processes. While mononuclear complexes have been used extensively, bimetallic systems have received far less attention. Bimetallic or polynuclear sites are commonly found in metalloenzymes that perform elegant transformation in biological systems, underlying their significance. Inorganic chemists take inspiration from nature and design model bimetallic complexes to further study this cooperativity effect. A bimetallic platform offers many structural and functional differences such as the identity of the metal atoms and the bonding interactions between metals, which have been reflected in their unique catalytic ability and reactivity.

This dissertation encompasses work related to the computational study of metal-metal interactions of bimetallic systems, the 1H NMR study of stereochemical and conformational changes in solution of N,N'-diarylformamidines, the synthesis of dizinc formamidinate complexes, and the synthesis and catalytic ability of dicopper formamidinate complexes.

In the first part, DFT calculations are used to study factors that influence metal-metal bond lengths in various complexes. Several experimentally obtained X-ray crystal structures were used as the basis for the study. Differences in metal-metal separations were investigated through various functionals, indicating the importance of charge, orbital interactions, and formal bond order. BH&HLYP SDD/aug-CC-PVDZ geometry optimizations of octahalodimetalate anions Tc2X8n- (X = Cl, Br; n=2, 3), Re2X82- (X = Cl, Br), and Mo2Cl 84- reproduced M-M bond distance trends observed experimentally. The study demonstrated that the increase in σ and π bond strength resulted in the shortening in Tc-Tc bond distance from Tc2X 82- to Tc2X83-, which was further supported by the short Mo-Mo bond in the Mo2Cl 84- ion. This study was expanded further through the inclusion of [M2Cl4(PMe3)4] n+ (M = Tc, Re, n = 0-2) and [Mo2E4] n- (E = HPO4 or SO4, n = 2-4), allowing a systematic study on the role of charge on the metal atoms. PBEO SDD/aug-CC-PVDZ calculations revealed that both formal bond order and formal charge on the metal atoms dictate the trends in M-M bond strength.

The second half of this dissertation focuses on the synthesis and characterization of bimetallic Zn- and Cu-formamidinate complexes. The stereochemical exchange of substituted N,N'-diarylformamidines were studied through 1H NMR in various solvents. Alkyl substituents placed on the ortho positions were found to shift the isomeric equilibrium in solution through destabilization of the hydrogen-bond dimer evident in X-ray crystal structures. The Z-isomer of substituted N,N'-diarylformamidines is observed in CDCl3, C6D6, and DMSO-d6 when the ligands feature significant steric hinderance. Similar ortho substituted N,N'-diarylformamidines were also used to enforce steric interactions to limit the nuclearity of Zn-formamidinate complexes. Various dizinc formamidinate complexes were synthesized through direct and transmetalation routes. NMR and mass spectrometry were used alongside X-ray crystal structures to fully characterize the dizinc complexes. Dicopper formamidinates formed through a transmetallation route were synthesized and feature distinct short Cu …Cu separations thought to be brought about by metalophillic interactions. Preliminary results suggest catalytic ability of dicopper formamidinates in cyclopropanation and aziridination of styrene with various diazo compounds. The catalytic activity suggests the formation of dicopper carbene and nitrene intermediates, of which only few published experimentally observed examples exist in the literature.

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Books on the topic "Fundamental chemistry"

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Lukehart, Charles M. Fundamental transition metalorganometallic chemistry. Monterey, CA: Brooks/Cole, 1985.

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Brändas, Erkki J., and Eugene S. Kryachko, eds. Fundamental World of Quantum Chemistry. Dordrecht: Springer Netherlands, 2004. http://dx.doi.org/10.1007/978-94-017-0448-9.

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Brändas, Erkki J., and Eugene S. Kryachko, eds. Fundamental World of Quantum Chemistry. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-010-0113-7.

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Calbreath, Donald F. Clinical chemistry: A fundamental textbook. Philadelphia: Saunders, 1992.

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Fundamental transition metal organometallic chemistry. Monterey, Calif: Brooks/Cole, 1985.

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Physical organic chemistry: The fundamental concepts. 2nd ed. New York: M. Dekker, 1990.

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Organotransition metal chemistry: Fundamental concepts and applications. New York: Wiley, 1986.

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Lahaye, Jacques. Fundamental Issues in Control of Carbon Gasification Reactivity. Dordrecht: Springer Netherlands, 1991.

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Calbreath, Donald F. Instructor's manual to Clinical chemistry: A fundamental textbook. Philadelphia: W.B. Saunders, 1992.

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Brongersma, H. H. Fundamental Aspects of Heterogeneous Catalysis Studied by Particle Beams. Boston, MA: Springer US, 1991.

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Book chapters on the topic "Fundamental chemistry"

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Sartor, Klaus. "Fundamental Physics and Chemistry." In MR Imaging of the Skull and Brain, 1–32. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-75525-5_1.

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Iwasaki, Masayuki, and Yasushi Nishihara. "Mechanisms and Fundamental Reactions." In Lecture Notes in Chemistry, 17–39. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-32368-3_2.

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Fan, L. T., D. Neogi, and M. Yashima. "Fundamental Concepts and Definitions." In Lecture Notes in Chemistry, 3–15. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-45690-9_2.

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Hoffman, Donald B., Beth E. Zedeck, and Morris S. Zedeck. "Fundamental Issues of Postmortem Toxicology." In Forensic Chemistry Handbook, 457–81. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118062241.ch13.

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Tsuneda, Takao. "Appendix: Fundamental Conditions." In Density Functional Theory in Quantum Chemistry, 189–96. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54825-6_8.

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Kemp, William. "The Fundamental Basis of Magnetic Resonance." In NMR in Chemistry, 14–28. London: Macmillan Education UK, 1986. http://dx.doi.org/10.1007/978-1-349-18348-7_2.

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Fujita, Shinsaku. "Silver Halide Crystals. Fundamental Properties." In Organic Chemistry of Photography, 59–74. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-09130-2_3.

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Trubert, D., and C. Le Naour. "Fundamental Aspects of Single Atom Chemistry." In The Chemistry of Superheavy Elements, 95–116. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/0-306-48415-3_3.

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Joost, Maximilian. "Fundamental Elementary Steps in Gold Chemistry." In Synthesis and Original Reactivity of Copper and Gold Complexes, 31–81. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-18690-0_3.

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Talapatra, Sunil Kumar, and Bani Talapatra. "Fundamental Stereochemical Concepts and Nomenclatures." In Chemistry of Plant Natural Products, 23–201. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-45410-3_2.

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Conference papers on the topic "Fundamental chemistry"

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HYDUTSKY, D. P., D. E. BERGERON, T. E. DERMOTA, J. R. STAIRS, K. L. KNAPPENBERGER, K. M. DAVIS, C. E. JONES, et al. "FUNDAMENTAL CLUSTER STUDIES OF MATERIALS AND ATMOSPHERIC CHEMISTRY." In Clusters and Nano-Assemblies - Physical and Biological Systems. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812701879_0011.

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Cooper, Valentino R. "Extending first principles modeling with crystal chemistry: a bond-valence based classical potential." In Fundamental Physics of Ferroelectrics 2003. AIP, 2003. http://dx.doi.org/10.1063/1.1609957.

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Lumetta, Gregg J., Brian M. Rapko, and Herman M. Cho. "Studies of the Fundamental Chemistry of Hanford Tank Sludges." In ASME 2003 9th International Conference on Radioactive Waste Management and Environmental Remediation. ASMEDC, 2003. http://dx.doi.org/10.1115/icem2003-4633.

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The U.S. Department of Energy has embarked on an effort to retrieve, immobilize, and dispose of the 2.1 × 105 m3 of radioactive tank wastes that were generated during weapons production and other operations at the Hanford Site in Washington State. One of the major challenges associated with this effort is the processing of the 4.2 × 104 m3 of high-level waste sludges. These sludges consist of a complex mixture of amorphous and crystalline mineral phases. The current plan for processing the sludge solids consists of leaching with aqueous NaOH, washing out the NaOH and dissolved components, then vitrifying the solids in borosilicate glass. The purpose of the NaOH leaching step is to remove components such as Al, Cr, and P that can lead to the production of an unacceptable quantity of high-level waste glass. In this paper, we will discuss the chemistry underlying the leaching and washing processes, focusing on the specific mineral phases present in the sludge solids and how these phases respond to the leaching process. The chemical phases present in the Hanford tank sludge solids have been identified through microscopy coupled with electron diffraction and through powder X-ray diffraction. We have also recently been applying nuclear magnetic resonance spectroscopy to characterize chemical species in tank sludge solids. Numerous chemical species have been identified including the aluminum oxy/hydroxides gibbsite and boehmite, aluminosilicates, iron oxy/hydroxides, and mixed Cr/Fe oxyhydroxides. Identification of these phases has led to a more fundamental understanding of the behavior of the various sludge components during leaching; in turn, this understanding will allow for improved process flow sheets. For example, we have shown that certain tank sludges are high in boehmite, Υ-AIOOH. This mineral phase is much more refractory than other AI phases such as gibbsite. Thus, more severe leaching conditions (e.g., increased temperature, NaOH concentration, and leaching duration) are required to remove AI from wastes high in boehmite.
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Ishikawa, Masamichi. "Japanese Programs of Fundamental Physics and Chemistry under Microgravity." In 54th International Astronautical Congress of the International Astronautical Federation, the International Academy of Astronautics, and the International Institute of Space Law. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2003. http://dx.doi.org/10.2514/6.iac-03-j.1.02.

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Ventzek, P. L. G. "Fundamental Atomic Plasma Chemistry for Semiconductor Manufacturing Process Analysis." In ATOMIC PROCESSES AND PLASMAS: 13th APS Topical Conference on Atomic Processes in Plasmas. AIP, 2002. http://dx.doi.org/10.1063/1.1516290.

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Jiang, Boquan, Ting Liu, Min Xu, Xu Li, and Zhengping Chen. "Establishment of Comprehensive Evaluation System of Fundamental Chemistry Experiment Course." In 2014 International Conference on Education, Management and Computing Technology (ICEMCT-14). Paris, France: Atlantis Press, 2014. http://dx.doi.org/10.2991/icemct-14.2014.108.

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Swiderek, Petra, Markus Rohdenburg, Neha Thakur, and Sonia Castellanos. "Electron-induced chemistry fundamental to state-of-the-art nanotechnology." In Advances in Patterning Materials and Processes XXXVIII, edited by Douglas Guerrero and Daniel P. Sanders. SPIE, 2021. http://dx.doi.org/10.1117/12.2584166.

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Jarrahian, Khosro, Kenneth Sorbie, Michael Singleton, Lorraine Boak, and Alexander Graham. "Building a Fundamental Understanding of Scale Inhibitor Retention in Carbonate Formations." In SPE International Conference on Oilfield Chemistry. Society of Petroleum Engineers, 2019. http://dx.doi.org/10.2118/193635-ms.

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SEEBERGER, PETER H. "AUTOMATED OLIGOSACCHARIDE SYNTHESIS: FROM INSIGHTS INTO FUNDAMENTAL GLYCOBIOLOGY TO VACCINES AND DIAGNOSTICS." In 23rd International Solvay Conference on Chemistry. WORLD SCIENTIFIC, 2014. http://dx.doi.org/10.1142/9789814603836_0020.

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Luk′yanov, Oleg, Nina Shlykova, Vladimir Parakhin, Galina Pokhvisneva, Tatyana Ternikova, Sergey Nikitin, and Gennady Smirnova. "HIGH-ENERGY POLYNITRO HEXAAZAISOWURTZITANES: SYNTHESIS AND FUNDAMENTAL PHISICOCHEMICAL PROPERTIES." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m728.aks-2019/93-96.

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Reports on the topic "Fundamental chemistry"

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Simonson, John M., James G. Blencoe, Sheng Dai, Ariel A. Chialvo, and Peter T. Cummings. Fundamental Chemistry and Thermodynamics of Hydrothermal Oxidation Processes. Office of Scientific and Technical Information (OSTI), June 1999. http://dx.doi.org/10.2172/828161.

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Simonson, J. M. Fundamental Chemistry And Thermodynamics Of Hydrothermal Oxidation Processes. Office of Scientific and Technical Information (OSTI), December 2001. http://dx.doi.org/10.2172/828164.

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Shuh, David K., and Ian l. Pegg. Research Program to Investigate the Fundamental Chemistry of Technetium. Office of Scientific and Technical Information (OSTI), September 2005. http://dx.doi.org/10.2172/893269.

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Pegg, Ian. Research Program to Investigate the Fundamental Chemistry of Technetium. Office of Scientific and Technical Information (OSTI), June 2005. http://dx.doi.org/10.2172/884865.

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Edelstein, Norman M., Carol J. Burns, David D. Shuh, and Wayne Lukens. Research Program to Investigate the Fundamental Chemistry of Technetium. Office of Scientific and Technical Information (OSTI), June 2000. http://dx.doi.org/10.2172/829921.

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Edelstein, Norman M., Carol J. Burns, David K. Shuh, and Wayne Lukens. Research Program to Investigate the Fundamental Chemistry of Technetium. Office of Scientific and Technical Information (OSTI), June 2000. http://dx.doi.org/10.2172/829922.

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Shuh, David K., Carol J. Burns, and Wayne W. Lukens, Jr. Research Program to Investigate the Fundamental Chemistry of Technetium. Office of Scientific and Technical Information (OSTI), June 2001. http://dx.doi.org/10.2172/834461.

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Shuh, David K., Carol J. Burns, and Wayne W. Lukens, Jr. Research Programs to Investigate the Fundamental Chemistry of Technetium. Office of Scientific and Technical Information (OSTI), July 2002. http://dx.doi.org/10.2172/834462.

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Shuh, David K. Research Program to Investigate the Fundamental Chemistry of Technetium. Office of Scientific and Technical Information (OSTI), August 2004. http://dx.doi.org/10.2172/839285.

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Shuh, David K., and Ian L. Pegg. Research Program to Investigate the Fundamental Chemistry of Technetium. Office of Scientific and Technical Information (OSTI), August 2004. http://dx.doi.org/10.2172/839331.

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