Relevant bibliographies by topics / Carbon chemistry

Contents

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

Academic literature on the topic 'Carbon chemistry'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Carbon chemistry"

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Li, Xiaoxian, Tongxing Liu, Beibei Zhang, et al. "Formation of Carbon-Carbon Bonds Mediated by Hypervalent Iodine Reagents Under Metal-free Conditions." Current Organic Chemistry 24, no. 1 (2020): 74–103. http://dx.doi.org/10.2174/1385272824666200211093103.

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During the past several decades, hypervalent iodine reagents have been widely used in various organic transformations. Specifically, these exclusive classes of reagents have been extensively used for the construction of carbon-carbon bonds. This review aims to cover all the reactions involving the construction of carbon-carbon bonds mediated by hypervalent iodine reagents, providing references and highlights for synthetic chemists who are interested in hypervalent iodine chemistry.
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Langer, W. D. "Carbon Isotopic Chemistry." Symposium - International Astronomical Union 150 (1992): 193–97. http://dx.doi.org/10.1017/s0074180900090008.

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Isotopic molecular abundances are used to interpret Galactic chemical evolution and the properties of interstellar clouds. The isotopic chemistry of carbon plays an important role in the interpretation of these measurements. This paper reviews the recent measurements of the carbon twelve to thirteen ratio across the Galaxy and the isotopic chemistry.
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Olchowski, Rafał, Emil Zięba, Dimitrios A. Giannakoudakis, Ioannis Anastopoulos, Ryszard Dobrowolski, and Mariusz Barczak. "Tailoring Surface Chemistry of Sugar-Derived Ordered Mesoporous Carbons towards Efficient Removal of Diclofenac from Aquatic Environments." Materials 13, no. 7 (2020): 1625. http://dx.doi.org/10.3390/ma13071625.

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Ordered mesoporous carbon (CMK-3), obtained from an abundant natural source, sugar, was thermochemically modified with dicyandiamide and thiourea as well as by classical oxidization with hydrogen peroxide to introduce specific surface groups. Thermochemical modifications resulted in carbon with almost unchanged porosity and altered surface chemistry while porosity of H2O2-treated carbon was seriously deteriorated. The obtained carbons were tested as sorbents of diclofenac, considered as one of the emerging water contaminants. Changes in porosity and surface chemistry of modified carbons result
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Chen, Xiang, Xiao-Ru Chen, Ting-Zheng Hou, et al. "Lithiophilicity chemistry of heteroatom-doped carbon to guide uniform lithium nucleation in lithium metal anodes." Science Advances 5, no. 2 (2019): eaau7728. http://dx.doi.org/10.1126/sciadv.aau7728.

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The uncontrollable growth of lithium (Li) dendrites seriously impedes practical applications of Li metal batteries. Various lithiophilic conductive frameworks, especially carbon hosts, are used to guide uniform Li nucleation and thus deliver a dendrite-free composite anode. However, the lithiophilic nature of these carbon hosts is poorly understood. Herein, the lithiophilicity chemistry of heteroatom-doped carbon is investigated through both first principles calculations and experimental verifications to guide uniform Li nucleation. The electronegativity, local dipole, and charge transfer are
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Lin, Tong, Vardhan Bajpai, Tao Ji, and Liming Dai. "Chemistry of Carbon Nanotubes." Australian Journal of Chemistry 56, no. 7 (2003): 635. http://dx.doi.org/10.1071/ch02254.

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Judicious application of site-selective reactions to non-aligned and aligned carbon nanotubes has opened a rich field of carbon nanotube chemistry. In order to meet specific requirements demanded by particular applications (e.g. biocompatibility for nanotube biosensors and interfacial strength for blending with polymers), chemical modification of carbon nanotubes is essential. The tips of carbon nanotubes are more reactive than their sidewalls, allowing a variety of chemical reagents to be attached at the nanotube tips. Recently, some interesting reactions have also been devised for chemical m
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Oliva-Enrich, Josep M., Ibon Alkorta, and José Elguero. "Hybrid Boron-Carbon Chemistry." Molecules 25, no. 21 (2020): 5026. http://dx.doi.org/10.3390/molecules25215026.

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The recently proved one-to-one structural equivalence between a conjugated hydrocarbon CnHm and the corresponding borane BnHm+n is applied here to hybrid systems, where each C=C double bond in the hydrocarbon is consecutively substituted by planar B(H2)B moieties from diborane(6). Quantum chemical computations with the B3LYP/cc-pVTZ method show that the structural equivalences are maintained along the substitutions, even for non-planar systems. We use as benchmark aromatic and antiaromatic (poly)cyclic conjugated hydrocarbons: cyclobutadiene, benzene, cyclooctatetraene, pentalene, benzocyclobu
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Tasis, Dimitrios, Nikos Tagmatarchis, Alberto Bianco, and Maurizio Prato. "Chemistry of Carbon Nanotubes." Chemical Reviews 106, no. 3 (2006): 1105–36. http://dx.doi.org/10.1021/cr050569o.

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Sakai, Nami, and Satoshi Yamamoto. "Warm Carbon-Chain Chemistry." Chemical Reviews 113, no. 12 (2013): 8981–9015. http://dx.doi.org/10.1021/cr4001308.

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Alcarazo, Manuel, Christian W. Lehmann, Anakuthil Anoop, Walter Thiel, and Alois Fürstner. "Coordination chemistry at carbon." Nature Chemistry 1, no. 4 (2009): 295–301. http://dx.doi.org/10.1038/nchem.248.

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Uppenbrink, J. "CHEMISTRY: Carbon Chain Gangs." Science 287, no. 5457 (2000): 1365c—1365. http://dx.doi.org/10.1126/science.287.5457.1365c.

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Dissertations / Theses on the topic "Carbon chemistry"

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Sirokman, Gergely. "(N-heterocyclic-carbene)Copper(I)-catalyzed carbon-carbon bond formation using carbon dioxide." Thesis, Massachusetts Institute of Technology, 2007. http://hdl.handle.net/1721.1/39584.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2007.<br>Vita.<br>Includes bibliographical references.<br>This thesis presents work towards the development of a new catalytic C-C bond forming reaction. Alkynes and olefins insert into [(IPr)CuH]2 (IPr = N,N-bis-(2,6-diisopropylphenyl)-1,3-imidazol-2-ylidene) to give copper vinyl and copper alkyl complexes. These copper complexes insert CO2 into the Cu-C bond to form copper acrylate and copper carboxylate complexes. Acrylic and carboxylic acids can be isolated by hydrolysis. A catalytic cycle based on (IPr)copper(I) w
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Abbott, Jennifer Ileana. "Carbon chemistry of giant impacts." Thesis, Open University, 2000. http://oro.open.ac.uk/19046/.

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Impact diamonds were found in several impactites from the Ries crater, Germany including fallout and fallback (crater fill) suevites. a glass bomb, impact melt rock and shocked gneiss. These diamonds formed two distinct grain size populations: 50-300?m apographitic. platy aggregates with surface ornamentation and etching that were observed using optical and scanning electron microscopy and 5-20?m diamonds which displayed two different morphologies identified using transmission electron microscopy and selected area electron diffraction. These 5-20?m grains comprised apographitic. platy grains w
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Abbott, Jennifer Ileana. "Carbon chemistry of giant impacts." n.p, 1999. http://library7.open.ac.uk/abstracts/page.php?thesisid=31.

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Sau, Roca Míriam. "From Click Chemistry to catalytic cleavage of unstrained C-C bonds." Doctoral thesis, Universitat Rovira i Virgili, 2016. http://hdl.handle.net/10803/396080.

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Aquesta tesi doctoral es basa principalment amb la síntesis de molècules petites potencialment útils per investigacions avançades. S'han utilitzat diferents metodologies per obtenir-les: 1) Cicloaddicions intramoleculars entre un alkí i una azida lliures de coure per l'obtenció de derivats de benzodiazepines. Obtenint-se una gran varietat de triazols fusionats a heterocicles de set membres. Posteriorment, s'han dut a terme proves d'activitat biològica. 2) a) Trencament d'enllaços carboni-carboni no activats d'amino alcohols i utilització d'aquest com a nucleòfil juntament amb bromurs d'ari
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Ye, Yuxuan Ph D. Massachusetts Institute of Technology. "Development of new transition metal-catalyzed carbon-fluorine, carbon-nitrogen, and carbon-carbon bond forming processes." Thesis, Massachusetts Institute of Technology, 2018. http://hdl.handle.net/1721.1/118281.

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Thesis: Ph. D. in Organic Chemistry, Massachusetts Institute of Technology, Department of Chemistry, 2018.<br>Cataloged from PDF version of thesis.<br>Includes bibliographical references.<br>Chapter 1. Palladium-Catalyzed Fluorination of Cyclic Vinyl Triflates: Dramatic Effect of TESCF₃ as an Additive A method for the synthesis of cyclic vinyl fluorides with high levels of regiochemical fidelity has been achieved by Pd-catalysis employing a new biarylphosphine ligand and TESCF₃ as a crucial additive. Five, six, and seven-membered vinyl triflate substrates, as well as a few acyclic substrates u
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Koutsantonis, George Anthony. "Some organotransition metal chemistry of the carbon-carbon triple bond /." Title page, contents and summary only, 1989. http://web4.library.adelaide.edu.au/theses/09PH/09phk876.pdf.

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Raymer, Julia. "Carbon-Carbon Bond Formation Via o-Lithiointermediates." TopSCHOLAR®, 2004. http://digitalcommons.wku.edu/theses/512.

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The process of C-C bond formation via Directed ort/zo-Metalation (DoM) consists of two separate steps. Utilizing fractional equivalents of TMEDA in hydrocarbon solvents at 60°C, o-lithiation of anisole and dimethylaniline can be effected in >95% yields. The first step in the DoM process involves preparation of solid samples of these o-lithiointermediates. Completing the sequence, the second step concerns formation of a new arene-derivative bond at the reactive site. For this thesis the arene-derivative bond formed is to carbon. Various carbon electrophiles have been studied using different sol
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Billingsley, Kelvin L. "Recent advances in palladium-catalyzed carbon-carbon and carbon-boron bond forming processes." Thesis, Massachusetts Institute of Technology, 2008. http://hdl.handle.net/1721.1/43777.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2008.<br>Vita.<br>Includes bibliographical references.<br>Chapter 1. Highly active and efficient catalyst systems derived from palladium precatalysts and monophosphine ligands for the Suzuki-Miyaura cross-coupling reaction of heteroaryl boronic acids and esters has been developed. This method allows for the preparation of a wide variety of heterobiaryls in good to excellent yields and displays a high level of activity for the coupling of heteroaryl chlorides as well as hindered aryl and heteroaryl halides. Specific fac
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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 so
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Altman, Ryan A. (Ryan Alan). "Recent advances in copper- and palladium-catalyzed carbon-heteroatom and carbon-carbon bond-formation." Thesis, Massachusetts Institute of Technology, 2008. http://hdl.handle.net/1721.1/43779.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2008.<br>Vita.<br>Includes bibliographical references.<br>Metal-catalyzed nucleophilic substitution reactions of aryl halides have become one of the most valuable and useful classes of reactions developed in the last 30 years. Foremost among these processes are the classes of palladium- and copper-catalyzed reactions, which employ heteroatom-based nucleophiles. Herein, newly designed catalyst systems are presented for the palladium- and/or copper-catalyzed nucleophilic substitution reactions of aryl halides with a vari
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Books on the topic "Carbon chemistry"

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West, Krista. Carbon chemistry. Chelsea House, 2009.

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West, Krista. Carbon chemistry. Chelsea House, 2009.

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West, Krista. Carbon chemistry. Chelsea House, 2009.

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Muellen, Klaus, and Xinliang Feng, eds. Chemistry of Carbon Nanostructures. De Gruyter, 2017. http://dx.doi.org/10.1515/9783110284645.

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Basiuk, Vladimir A., and Elena V. Basiuk. Chemistry of carbon nanotubes. American Scientific Publishers, 2008.

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Giese, Bernd. Radicals in organic synthesis: Formation of carbon-carbon bonds. Pergamon, 1986.

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Giese, Bernd. Radicals in organic synthesis: Formation of carbon-carbon bonds. Franklin, 1995.

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Giese, Bernd. Radicals in organic synthesis: Formation of carbon-carbon bonds. Franklin, 1996.

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Urry, Grant. Elementary equilibrium chemistry of carbon. Wiley, 1989.

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The chemistry of carbon compounds. Open University, 1988.

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Book chapters on the topic "Carbon chemistry"

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Roussak, O. V., and H. D. Gesser. "Carbon-Based Polymers, Activated Carbons." In Applied Chemistry. Springer US, 2012. http://dx.doi.org/10.1007/978-1-4614-4262-2_16.

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O’Neill, Peter. "Carbon." In Environmental Chemistry. Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-010-9318-7_4.

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Shia, George A., and Ganpat Mani. "Fluorinated Carbon." In Organofluorine Chemistry. Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-1202-2_24.

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Ehrenfreund, P., and M. Spaans. "Cosmic Carbon Chemistry." In ACS Symposium Series. American Chemical Society, 2008. http://dx.doi.org/10.1021/bk-2008-0981.ch012.

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Langer, W. D. "Carbon Isotopic Chemistry." In Astrochemistry of Cosmic Phenomena. Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2761-5_45.

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Barker, Alan, and Kathryn Knapp. "Carbon." In Work Out Chemistry GCSE. Macmillan Education UK, 1990. http://dx.doi.org/10.1007/978-1-349-11950-9_13.

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Turova, Nataliya. "Carbon." In Inorganic Chemistry in Tables. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-20487-6_18.

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Tobe, Yoshito, and Tomonari Wakabayashi. "Carbon-Rich Compounds: Acetylene-Based Carbon Allotropes." In Acetylene Chemistry. Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527605487.ch9.

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Jutand, Anny, and Guillaume Lefèvre. "Transition Metal-Catalyzed Carbon-Carbon Cross-Coupling." In Arene Chemistry. John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118754887.ch19.

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Montchamp, Jean-Luc. "Carbon–Hydrogen to Carbon–Phosphorus Transformations." In Phosphorus Chemistry II. Springer International Publishing, 2014. http://dx.doi.org/10.1007/128_2014_558.

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Conference papers on the topic "Carbon chemistry"

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Anikeeva, I. V., A. B. Arbuzov, M. V. Trenikhin, and Yu G. Kryazhev. "Formation of carbon-carbon composite materials with nanoglobular carbon particles embedded in amorphous carbon matrix." In 21ST CENTURY: CHEMISTRY TO LIFE. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5122941.

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Lodders, Katharina, and Bruce Fegley. "Condensation chemistry of carbon stars." In ASTROPHYSICAL IMPLICATIONS OF THE LABORATORY STUDY OF PRESOLAR MATERIALS. ASCE, 1997. http://dx.doi.org/10.1063/1.53317.

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Callista, Xena, Imam Prasetyo, and Teguh Ariyanto. "Adsorption of carbon dioxide in porous carbon containing monoethanolamine (MEA): The effect of carbon surface pre-treatment." In 4TH INTERNATIONAL SEMINAR ON CHEMISTRY. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0052535.

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Pambudi, Agung Bagus, Riskaviana Kurniawati, Ani Iryani, and Djoko Hartanto. "Effect of calcination temperature in the synthesis of carbon doped TiO2 without external carbon source." In THE 3RD INTERNATIONAL SEMINAR ON CHEMISTRY: Green Chemistry and its Role for Sustainability. Author(s), 2018. http://dx.doi.org/10.1063/1.5082479.

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Baklanova, O. N., O. A. Knyazheva, A. V. Vasilevich, and A. V. Lavrenov. "From mesopores to micropores: A new way to control the porous structure of carbon-carbon composites." In 21ST CENTURY: CHEMISTRY TO LIFE. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5122903.

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Widyanto, Alvin R., Irmariza S. Caralin, Nurul Widiastuti, et al. "Improvement N2/SF6 separation performance on P84 derived carbon membrane by incorporating of zeolite-carbon composite." In 4TH INTERNATIONAL SEMINAR ON CHEMISTRY. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0052171.

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Alexey, Sukhorukov, Pavel Ushakov, Yana Naumovich, and Sema Ioffea. "NEW METHODS FOR THE CONSTRUCTION OF CARBON-CARBON AND CARBON-HETEROATOM BONDS UTILIZING NITRO-DERIVATIVES." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m721.aks-2019/53-55.

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Voropay, A. N., Yu V. Surovikin, and I. V. Rezanov. "Electrochemical studies of modified carbon black in supercapacitors." In 21ST CENTURY: CHEMISTRY TO LIFE. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5122947.

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Haddon, Robert. "Chemistry and Applications of Single-Walled Carbon Nanotubes." In 2006 International Conference on Nanoscience and Nanotechnology. IEEE, 2006. http://dx.doi.org/10.1109/iconn.2006.340556.

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Makino, H., and N. Noda. "Reduction technology of carbon dioxide emission from a coal utilized power generation system." In SUSTAINABLE CHEMISTRY 2011. WIT Press, 2011. http://dx.doi.org/10.2495/chem110091.

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Reports on the topic "Carbon chemistry"

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Menawat, A. S. Carbon dioxide, climate and the deep ocean circulation: Carbon chemistry model. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/6994048.

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Menawat, A. S. Carbon dioxide, climate and the deep ocean circulation: Carbon chemistry model. Final report. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/10105035.

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DesMarteau, Darryl D. Novel Developments in Organonitrogen Fluorine Chemistry from Carbon- Nitrogen. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada244426.

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Reynolds, J. G. Nitrogen and carbon oxides chemistry in the HRS retorting process. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10189713.

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Barry, Brian M., Richard Alan Kemp, Constantine A. Stewart, and Diane A. Dickie. Main group adducts of carbon dioxide and related chemistry (LDRD 149938). Office of Scientific and Technical Information (OSTI), 2010. http://dx.doi.org/10.2172/1005035.

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DePuy, C. H., and V. M. Bierbaum. Gas Phase Ion-Molecule Chemistry of Carbon, Nitrogen and Oxygen Compounds. Defense Technical Information Center, 1985. http://dx.doi.org/10.21236/ada152876.

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Brewer, P. G., T. Takahashi, and R. T. Williams. Transient Tracers in the Oceans (TTO) - hydrographic data and carbon dioxide systems with revised carbon chemistry data. Office of Scientific and Technical Information (OSTI), 1986. http://dx.doi.org/10.2172/538035.

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Dignon, J., H. E. Eddleman, and J. E. Penner. A black carbon emission data base for atmospheric chemistry and climate studies. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/28275.

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Gibson, D. H. Organometallic Chemistry of Carbon Dioxide. Final Report for June 1, 1986 - March 31, 2002. Office of Scientific and Technical Information (OSTI), 2002. http://dx.doi.org/10.2172/825899.

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Podzorov, Vitaly. Basic surface chemistry and physics of carbon-based electronic materials modified by silane molecular layers. Office of Scientific and Technical Information (OSTI), 2012. http://dx.doi.org/10.2172/1162113.

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